Faculty Collaboration Database

Medical College of Wisconsin

CTSI Research Informatics REDCap

Michael W. Lawlor PhD, MD

Adjunct Professor

Institution: Medical College of Wisconsin
Department: Pathology and Laboratory Medicine

Member of the Cardiovascular Research Center
Member of the Neuroscience Research Center

Send Message

Request Meeting

View Curriculum Vitae

Publications (107)

INCEPTUS Natural History, Run-in Study for Gene Replacement Clinical Trial in X-Linked Myotubular Myopathy. (Dowling JJ, Müller-Felber W, Smith BK, Bönnemann CG, Kuntz NL, Muntoni F, Servais L, Alfano LN, Beggs AH, Bilder DA, Blaschek A, Duong T, Graham RJ, Jain M, Lawlor MW, Lee J, Coats J, Lilien C, Lowes LP, MacBean V, Neuhaus S, Noursalehi M, Pitts T, Finlay C, Christensen S, Rafferty G, Seferian AM, Tsuchiya E, James ES, Miller W, Sepulveda B, Vila MC, Prasad S, Rico S, Shieh PB, INCEPTUS investigators) J Neuromuscul Dis 2022;9(4):503-516 PMID: 35694931 PMCID: PMC9398079 SCOPUS ID: 2-s2.0-85133659377 06/14/2022 24 Citations

Adherence to and changes in mental and physiological health during an 8-week yoga intervention: A pilot study. (Forseth B, Polfuss M, Brondino M, Hunter SD, Lawlor MW, Beatka MJ, Prom MJ, Eells J, Lyons JA) J Bodyw Mov Ther 2022 Apr;30:203-209 PMID: 35500972 SCOPUS ID: 2-s2.0-85126290657 05/03/2022 8 Citations

Adherence to and changes in mental and physiological health during an 8-week yoga intervention: A pilot study (Forseth B, Polfuss M, Brondino M, Hunter SD, Lawlor MW, Beatka MJ, Prom MJ, Eells J, Lyons JA) Journal of Bodywork and Movement Therapies April 2022;30:203-209 SCOPUS ID: 2-s2.0-85126290657 04/01/2022 8 Citations

A Long-Term Study Evaluating the Effects of Nicorandil Treatment on Duchenne Muscular Dystrophy-Associated Cardiomyopathy in mdx Mice. (Gartz M, Haberman M, Prom MJ, Beatka MJ, Strande JL, Lawlor MW) J Cardiovasc Pharmacol Ther 2022;27:10742484221088655 PMID: 35353647 SCOPUS ID: 2-s2.0-85127284016 03/31/2022 1 Citation

Muscle-directed gene therapy corrects Pompe disease and uncovers species-specific GAA immunogenicity (Eggers M, Vannoy CH, Huang J, Purushothaman P, Brassard J, Fonck C, Meng H, Prom MJ, Lawlor MW, Cunningham J, Sadhu C, Mavilio F) EMBO Molecular Medicine 11 January 2022;14(1) SCOPUS ID: 2-s2.0-85120325821 01/11/2022 42 Citations

Muscle-directed gene therapy corrects Pompe disease and uncovers species-specific GAA immunogenicity. (Eggers M, Vannoy CH, Huang J, Purushothaman P, Brassard J, Fonck C, Meng H, Prom MJ, Lawlor MW, Cunningham J, Sadhu C, Mavilio F) EMBO Mol Med 2022 Jan 11;14(1):e13968 PMID: 34850579 PMCID: PMC8749482 SCOPUS ID: 2-s2.0-85120325821 12/02/2021 42 Citations

Cardioprotective effect of nicorandil on isoproterenol induced cardiomyopathy in the Mdx mouse model (Sullivan RT, Lam NT, Haberman M, Beatka MJ, Afzal MZ, Lawlor MW, Strande JL) BMC Cardiovascular Disorders December 2021;21(1) SCOPUS ID: 2-s2.0-85107953538 12/01/2021 8 Citations

Erratum: Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice. (Hamm SE, Fathalikhani DD, Bukovec KE, Addington AK, Zhang H, Perry JB, McMillan RP, Lawlor MW, Prom MJ, Vanden Avond MA, Kumar SN, Coleman KE, Dupont JB, Mack DL, Brown DA, Morris CA, Gonzalez JP, Grange RW) Mol Ther Methods Clin Dev 2021 Dec 10;23:460 PMID: 34820472 PMCID: PMC8585580 SCOPUS ID: 2-s2.0-85118555887 11/26/2021

X-linked myotubular myopathy. (Lawlor MW, Dowling JJ) Neuromuscul Disord 2021 Oct;31(10):1004-1012 PMID: 34736623 SCOPUS ID: 2-s2.0-85118478299 11/06/2021 57 Citations

The Effect of Immunomodulatory Treatments on Anti-Dystrophin Immune Response After AAV Gene Therapy in Dystrophin Deficient mdx Mice. (Li N, Parkes JE, Spathis R, Morales M, Mcdonald J, Kendra RM, Ott EM, Brown KJ, Lawlor MW, Nagaraju K) J Neuromuscul Dis 2021;8(s2):S325-S340 PMID: 34569971 SCOPUS ID: 2-s2.0-85120957320 09/28/2021 14 Citations

Intrahepatic Cholestasis Is a Clinically Significant Feature Associated with Natural History of X-Linked Myotubular Myopathy (XLMTM): A Case Series and Biopsy Report. (Molera C, Sarishvili T, Nascimento A, Rtskhiladze I, Muñoz Bartolo G, Fernández Cebrián S, Valverde Fernández J, Muñoz Cabello B, Graham RJ, Miller W, Sepulveda B, Kamath BM, Meng H, Lawlor MW) J Neuromuscul Dis 2022;9(1):73-82 PMID: 34366366 PMCID: PMC8842755 SCOPUS ID: 2-s2.0-85122787622 08/10/2021 27 Citations

Cardiomyocyte-produced miR-339-5p mediates pathology in Duchenne muscular dystrophy cardiomyopathy. (Gartz M, Beatka M, Prom MJ, Strande JL, Lawlor MW) Hum Mol Genet 2021 Nov 16;30(23):2347-2361 PMID: 34270708 PMCID: PMC8600005 SCOPUS ID: 2-s2.0-85121129104 07/17/2021 14 Citations

Cardioprotective effect of nicorandil on isoproterenol induced cardiomyopathy in the Mdx mouse model. (Sullivan RT, Lam NT, Haberman M, Beatka MJ, Afzal MZ, Lawlor MW, Strande JL) BMC Cardiovasc Disord 2021 Jun 15;21(1):302 PMID: 34130633 PMCID: PMC8207777 SCOPUS ID: 2-s2.0-85107953538 06/17/2021 8 Citations

Clonally Focused Public and Private T Cells in Resected Brain Tissue From Surgeries to Treat Children With Intractable Seizures. (Chang JW, Reyes SD, Faure-Kumar E, Lam SK, Lawlor MW, Leventer RJ, Lew SM, Lockhart PJ, Pope K, Weiner HL, Salamon N, Vinters HV, Mathern GW, Fallah A, Owens GC) Front Immunol 2021;12:664344 PMID: 33889159 PMCID: PMC8056262 SCOPUS ID: 2-s2.0-85104563537 04/24/2021 13 Citations

Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice. (Hamm SE, Fathalikhani DD, Bukovec KE, Addington AK, Zhang H, Perry JB, McMillan RP, Lawlor MW, Prom MJ, Vanden Avond MA, Kumar SN, Coleman KE, Dupont JB, Mack DL, Brown DA, Morris CA, Gonzalez JP, Grange RW) Mol Ther Methods Clin Dev 2021 Jun 11;21:144-160 PMID: 33850950 PMCID: PMC8020351 SCOPUS ID: 2-s2.0-85102827954 04/15/2021 16 Citations

Association between yoga, physiologic and psychologic health: A cross sectional study. (Forseth B, Polfuss M, Brondino M, Lawlor MW, Beatka MJ, Prom MJ, Eells J, Lyons JA) Complement Ther Clin Pract 2021 May;43:101350 PMID: 33770740 SCOPUS ID: 2-s2.0-85103315703 03/27/2021 8 Citations

A Cross-Sectional Study of Nemaline Myopathy. (Amburgey K, Acker M, Saeed S, Amin R, Beggs AH, Bönnemann CG, Brudno M, Constantinescu A, Dastgir J, Diallo M, Genetti CA, Glueck M, Hewson S, Hum C, Jain MS, Lawlor MW, Meyer OH, Nelson L, Sultanum N, Syed F, Tran T, Wang CH, Dowling JJ) Neurology 2021 Mar 09;96(10):e1425-e1436 PMID: 33397769 PMCID: PMC8055318 SCOPUS ID: 2-s2.0-85102721587 01/06/2021 39 Citations

The nucleotide prodrug CERC-913 improves mtDNA content in primary hepatocytes from DGUOK-deficient rats. (Vanden Avond MA, Meng H, Beatka MJ, Helbling DC, Prom MJ, Sutton JL, Slick RA, Dimmock DP, Pertusati F, Serpi M, Pileggi E, Crutcher P, Thomas S, Lawlor MW) J Inherit Metab Dis 2021 Mar;44(2):492-501 PMID: 33368311 SCOPUS ID: 2-s2.0-85099334921 12/29/2020 10 Citations

Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function (Hall A, Fontelonga T, Wright A, Bugda Gwilt K, Widrick J, Pasut A, Villa F, Miranti CK, Gibbs D, Jiang E, Meng H, Lawlor MW, Gussoni E) Skeletal Muscle December 2020;10(1) SCOPUS ID: 2-s2.0-85096675863 12/01/2020 14 Citations

Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function. (Hall A, Fontelonga T, Wright A, Bugda Gwilt K, Widrick J, Pasut A, Villa F, Miranti CK, Gibbs D, Jiang E, Meng H, Lawlor MW, Gussoni E) Skelet Muscle 2020 Nov 27;10(1):34 PMID: 33243288 PMCID: PMC7693590 SCOPUS ID: 2-s2.0-85096675863 11/28/2020 14 Citations

Duchenne muscular dystrophy (DMD) cardiomyocyte-secreted exosomes promote the pathogenesis of DMD-associated cardiomyopathy. (Gartz M, Lin CW, Sussman MA, Lawlor MW, Strande JL) Dis Model Mech 2020 Nov 13;13(11) PMID: 33188007 PMCID: PMC7673361 SCOPUS ID: 2-s2.0-85096154674 11/15/2020 26 Citations

rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy. (Ross JA, Tasfaout H, Levy Y, Morgan J, Cowling BS, Laporte J, Zanoteli E, Romero NB, Lowe DA, Jungbluth H, Lawlor MW, Mack DL, Ochala J) Acta Neuropathol Commun 2020 Oct 19;8(1):167 PMID: 33076971 PMCID: PMC7574461 SCOPUS ID: 2-s2.0-85092799337 10/21/2020 16 Citations

Regulatory T Cells Contribute to Resistance against Lyme Arthritis. (Siebers EM, Liedhegner ES, Lawlor MW, Schell RF, Nardelli DT) Infect Immun 2020 Oct 19;88(11) PMID: 32778610 PMCID: PMC7573436 SCOPUS ID: 2-s2.0-85093883170 08/12/2020 7 Citations

Drug-impregnated, pressurized gas expanded liquid-processed alginate hydrogel scaffolds for accelerated burn wound healing. (Johnson KA, Muzzin N, Toufanian S, Slick RA, Lawlor MW, Seifried B, Moquin P, Latulippe D, Hoare T) Acta Biomater 2020 Aug;112:101-111 PMID: 32522716 SCOPUS ID: 2-s2.0-85086394204 06/12/2020 76 Citations

Conference report on contractures in musculoskeletal and neurological conditions. (Nuckolls GH, Kinnett K, Dayanidhi S, Domenighetti AA, Duong T, Hathout Y, Lawlor MW, Lee SSM, Magnusson SP, McDonald CM, McNally EM, Miller NF, Olwin BB, Raghavan P, Roberts TJ, Rutkove SB, Sarwark JF, Senesac CR, Vogel LF, Walter GA, Willcocks RJ, Rymer WZ, Lieber RL) Muscle Nerve 2020 Jun;61(6):740-744 PMID: 32108365 PMCID: PMC7229996 SCOPUS ID: 2-s2.0-85081550208 02/29/2020 18 Citations

Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb. (Laitila JM, McNamara EL, Wingate CD, Goullee H, Ross JA, Taylor RL, van der Pijl R, Griffiths LM, Harries R, Ravenscroft G, Clayton JS, Sewry C, Lawlor MW, Ottenheijm CAC, Bakker AJ, Ochala J, Laing NG, Wallgren-Pettersson C, Pelin K, Nowak KJ) Acta Neuropathol Commun 2020 Feb 17;8(1):18 PMID: 32066503 PMCID: PMC7027239 SCOPUS ID: 2-s2.0-85079597530 02/19/2020 12 Citations

AAV-Mediated Gene Transfer Restores a Normal Muscle Transcriptome in a Canine Model of X-Linked Myotubular Myopathy. (Dupont JB, Guo J, Renaud-Gabardos E, Poulard K, Latournerie V, Lawlor MW, Grange RW, Gray JT, Buj-Bello A, Childers MK, Mack DL) Mol Ther 2020 Feb 05;28(2):382-393 PMID: 31784415 PMCID: PMC7000997 SCOPUS ID: 2-s2.0-85075895675 12/01/2019 21 Citations

Disease burden of Crigler-Najjar syndrome: Systematic review and future perspectives. (Dhawan A, Lawlor MW, Mazariegos GV, McKiernan P, Squires JE, Strauss KA, Gupta D, James E, Prasad S) J Gastroenterol Hepatol 2020 Apr;35(4):530-543 PMID: 31495946 SCOPUS ID: 2-s2.0-85074581875 09/10/2019 37 Citations

NOD-like receptor protein 3 inflammasome drives postoperative mechanical pain in a sex-dependent manner. (Cowie AM, Menzel AD, O'Hara C, Lawlor MW, Stucky CL) Pain 2019 Aug;160(8):1794-1816 PMID: 31335648 PMCID: PMC6662742 SCOPUS ID: 2-s2.0-85069147648 07/25/2019 44 Citations

Intracranial Extraskeletal Mesenchymal Chondrosarcoma: Case Report and Review of the Literature of Reported Cases in Adults and Children. (Shabani S, Kaushal M, Kaufman B, Knipstein J, Lawlor MW, Lew S, Foy A) World Neurosurg 2019 Sep;129:302-310 PMID: 31158544 SCOPUS ID: 2-s2.0-85068562842 06/04/2019 9 Citations

Tissue Response and Biodistribution of Injectable Cellulose Nanocrystal Composite Hydrogels (De France KJ, Badv M, Dorogin J, Siebers E, Panchal V, Babi M, Moran-Mirabal J, Lawlor M, Cranston ED, Hoare T) ACS Biomaterials Science and Engineering 13 May 2019;5(5):2235-2246 SCOPUS ID: 2-s2.0-85065644124 05/13/2019 51 Citations

NOD-like receptor protein 3 inflammasome drives postoperative mechanical pain in a sex-dependent manner. (Cowie AM, Menzel AD, O'Hara C, Lawlor MW, Stucky CL) Pain 2019 Mar 08 PMID: 30870320 SCOPUS ID: 2-s2.0-85069147648 03/15/2019 44 Citations

Maintaining extraembryonic expression allows generation of mice with severe tissue factor pathway inhibitor deficiency. (Castillo MM, Yang Q, Zhan M, Pan AY, Lawlor MW, Mast AE, Sood R) Blood Adv 2019 Feb 12;3(3):489-498 PMID: 30755437 PMCID: PMC6373739 SCOPUS ID: 2-s2.0-85061474836 02/14/2019 11 Citations

Severe Neonatal RYR1 Myopathy With Pathological Features of Congenital Muscular Dystrophy. (Helbling DC, Mendoza D, McCarrier J, Vanden Avond MA, Harmelink MM, Barkhaus PE, Basel D, Lawlor MW) J Neuropathol Exp Neurol 2019 Mar 01;78(3):283-287 PMID: 30715496 PMCID: PMC6380315 SCOPUS ID: 2-s2.0-85063882669 02/05/2019 4 Citations

Ganglioglioma in a Survivor of Infantile Glioblastoma. (Scheuermann A, Belongia M, Lawlor MW, Suchi M, Kaufman B, Vasudevaraja V, Serrano J, Snuderl M, Knipstein J) J Pediatr Hematol Oncol 2020 Jan;42(1):e56-e60 PMID: 30676438 SCOPUS ID: 2-s2.0-85060368706 01/25/2019 2 Citations

Myostatin Inhibition Using ActRIIB-mFc Does Not Produce Weight Gain or Strength in the Nebulin Conditional KO Mouse. (Tinklenberg JA, Siebers EM, Beatka MJ, Fickau BA, Ayres S, Meng H, Yang L, Simpson P, Granzier HL, Lawlor MW) J Neuropathol Exp Neurol 2019 Feb 01;78(2):130-139 PMID: 30597051 PMCID: PMC6804412 SCOPUS ID: 2-s2.0-85060009246 01/01/2019 10 Citations

Injectable and Degradable Poly(Oligoethylene glycol methacrylate) Hydrogels with Tunable Charge Densities as Adhesive Peptide-Free Cell Scaffolds (Bakaic E, Smeets NMB, Badv M, Dodd M, Barrigar O, Siebers E, Lawlor M, Sheardown H, Hoare T) ACS Biomaterials Science and Engineering 12 November 2018;4(11):3713-3725 SCOPUS ID: 2-s2.0-85056870867 11/12/2018 26 Citations

Pathological Issues in Dystrophinopathy in the Age of Genetic Therapies. (Shahnoor N, Siebers EM, Brown KJ, Lawlor MW) Annu Rev Pathol 2019 Jan 24;14:105-126 PMID: 30148687 SCOPUS ID: 2-s2.0-85060528542 08/28/2018 8 Citations

Use Of Ankle Immobilization In Evaluating Treatments To Promote Longitudinal Muscle Growth In Mice. (Tinklenberg J, Beatka M, Bain JLW, Siebers EM, Meng H, Pearsall RS, Lawlor MW, Riley DA) Muscle Nerve 2018 Nov;58(5):718-725 PMID: 29981243 PMCID: PMC6246800 SCOPUS ID: 2-s2.0-85054337476 07/08/2018 6 Citations

TNNT1 nemaline myopathy: natural history and therapeutic frontier. (Fox MD, Carson VJ, Feng HZ, Lawlor MW, Gray JT, Brigatti KW, Jin JP, Strauss KA) Hum Mol Genet 2018 Sep 15;27(18):3272-3282 PMID: 29931346 PMCID: PMC6121192 SCOPUS ID: 2-s2.0-85055339707 06/23/2018 35 Citations

Sdha+/- Rats Display Minimal Muscle Pathology Without Significant Behavioral or Biochemical Abnormalities. (Siebers EM, Choi MJ, Tinklenberg JA, Beatka MJ, Ayres S, Meng H, Helbling DC, Takizawa A, Bennett B, Garces AM, Dias Duarte Machado LG, Dimmock D, Dwinell MR, Geurts AM, Lawlor MW) J Neuropathol Exp Neurol 2018 Aug 01;77(8):665-672 PMID: 29850869 PMCID: PMC6044411 SCOPUS ID: 2-s2.0-85054028838 06/01/2018 9 Citations

NINDS Common Data Elements for Congenital Muscular Dystrophy Clinical Research: A National Institute for Neurological Disorders and Stroke Project. (Lawlor MW, Iannaccone ST, Mathews K, Muntoni F, Alai-Hansen S, Odenkirchen JC, S Feldman R, CMD Working Group) J Neuromuscul Dis 2018;5(1):75-84 PMID: 29480213 SCOPUS ID: 2-s2.0-85043695419 02/27/2018 2 Citations

Intravenous Administration of a MTMR2-Encoding AAV Vector Ameliorates the Phenotype of Myotubular Myopathy in Mice. (Danièle N, Moal C, Julien L, Marinello M, Jamet T, Martin S, Vignaud A, Lawlor MW, Buj-Bello A) J Neuropathol Exp Neurol 2018 Apr 01;77(4):282-295 PMID: 29408998 PMCID: PMC5939852 SCOPUS ID: 2-s2.0-85045070041 02/07/2018 18 Citations

Myostatin inhibition using mRK35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice. (Tinklenberg JA, Siebers EM, Beatka MJ, Meng H, Yang L, Zhang Z, Ross JA, Ochala J, Morris C, Owens JM, Laing NG, Nowak KJ, Lawlor MW) Hum Mol Genet 2018 Feb 15;27(4):638-648 PMID: 29293963 PMCID: PMC5886278 SCOPUS ID: 2-s2.0-85041501214 01/03/2018 30 Citations

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy. (Konersman CG, Freyermuth F, Winder TL, Lawlor MW, Lagier-Tourenne C, Patel SB) Mol Genet Genomic Med 2017 Nov;5(6):678-691 PMID: 29178646 PMCID: PMC5702563 SCOPUS ID: 2-s2.0-85040707754 11/28/2017 28 Citations

Diaphragm Atrophy and Weakness in the Absence of Mitochondrial Dysfunction in the Critically Ill. (van den Berg M, Hooijman PE, Beishuizen A, de Waard MC, Paul MA, Hartemink KJ, van Hees HWH, Lawlor MW, Brocca L, Bottinelli R, Pellegrino MA, Stienen GJM, Heunks LMA, Wüst RCI, Ottenheijm CAC) Am J Respir Crit Care Med 2017 Dec 15;196(12):1544-1558 PMID: 28787181 PMCID: PMC5754442 SCOPUS ID: 2-s2.0-85029879309 08/09/2017 60 Citations

Host interleukin 6 production regulates inflammation but not tryptophan metabolism in the brain during murine GVHD. (Belle L, Zhou V, Stuhr KL, Beatka M, Siebers EM, Knight JM, Lawlor MW, Weaver C, Hashizume M, Hillard CJ, Drobyski WR) JCI Insight 2017 Jul 20;2(14) PMID: 28724796 PMCID: PMC5518565 SCOPUS ID: 2-s2.0-85033974707 07/21/2017 15 Citations

Long-term effects of systemic gene therapy in a canine model of myotubular myopathy. (Elverman M, Goddard MA, Mack D, Snyder JM, Lawlor MW, Meng H, Beggs AH, Buj-Bello A, Poulard K, Marsh AP, Grange RW, Kelly VE, Childers MK) Muscle Nerve 2017 Nov;56(5):943-953 PMID: 28370029 PMCID: PMC5620115 SCOPUS ID: 2-s2.0-85019894779 04/04/2017 54 Citations

Systemic AAV8-Mediated Gene Therapy Drives Whole-Body Correction of Myotubular Myopathy in Dogs. (Mack DL, Poulard K, Goddard MA, Latournerie V, Snyder JM, Grange RW, Elverman MR, Denard J, Veron P, Buscara L, Le Bec C, Hogrel JY, Brezovec AG, Meng H, Yang L, Liu F, O'Callaghan M, Gopal N, Kelly VE, Smith BK, Strande JL, Mavilio F, Beggs AH, Mingozzi F, Lawlor MW, Buj-Bello A, Childers MK) Mol Ther 2017 Apr 05;25(4):839-854 PMID: 28237839 PMCID: PMC5383631 SCOPUS ID: 2-s2.0-85016950473 02/27/2017 101 Citations

Macrocyclic MEK1/2 inhibitor with efficacy in a mouse model of cardiomyopathy caused by lamin A/C gene mutation. (Wu W, Chordia MD, Hart BP, Kumarasinghe ES, Ji MK, Bhargava A, Lawlor MW, Shin JY, Sera F, Homma S, Muchir A, Khire UR, Worman HJ) Bioorg Med Chem 2017 Feb 01;25(3):1004-1013 PMID: 28011205 PMCID: PMC5291759 SCOPUS ID: 2-s2.0-85008155389 12/25/2016 21 Citations

Phosphatidylinositol 3-kinase inhibition restores Ca2+ release defects and prolongs survival in myotubularin-deficient mice. (Kutchukian C, Lo Scrudato M, Tourneur Y, Poulard K, Vignaud A, Berthier C, Allard B, Lawlor MW, Buj-Bello A, Jacquemond V) Proc Natl Acad Sci U S A 2016 Dec 13;113(50):14432-14437 PMID: 27911767 PMCID: PMC5167204 SCOPUS ID: 2-s2.0-85005992133 12/03/2016 36 Citations

Presentation and Diagnostic Evaluation of Mitochondrial Disease. (Dimmock DP, Lawlor MW) Pediatr Clin North Am 2017 Feb;64(1):161-171 PMID: 27894442 PMCID: PMC5130109 SCOPUS ID: 2-s2.0-84998774602 11/30/2016 21 Citations

CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies. (Alexander MS, Rozkalne A, Colletta A, Spinazzola JM, Johnson S, Rahimov F, Meng H, Lawlor MW, Estrella E, Kunkel LM, Gussoni E) Cell Stem Cell 2016 Dec 01;19(6):800-807 PMID: 27641304 PMCID: PMC5135584 SCOPUS ID: 2-s2.0-84994721676 09/20/2016 90 Citations

In Reply. (Lawlor MW) Arch Pathol Lab Med 2016 Sep;140(9):879 PMID: 27575262 SCOPUS ID: 2-s2.0-84984853585 08/31/2016

Treatment with ActRIIB-mFc Produces Myofiber Growth and Improves Lifespan in the Acta1 H40Y Murine Model of Nemaline Myopathy. (Tinklenberg J, Meng H, Yang L, Liu F, Hoffmann RG, Dasgupta M, Allen KP, Beggs AH, Hardeman EC, Pearsall RS, Fitts RH, Lawlor MW) Am J Pathol 2016 Jun;186(6):1568-81 PMID: 27102768 PMCID: PMC4901141 SCOPUS ID: 2-s2.0-84969848977 04/23/2016 23 Citations

Mechanosensory and ATP Release Deficits following Keratin14-Cre-Mediated TRPA1 Deletion Despite Absence of TRPA1 in Murine Keratinocytes. (Zappia KJ, Garrison SR, Palygin O, Weyer AD, Barabas ME, Lawlor MW, Staruschenko A, Stucky CL) PLoS One 2016;11(3):e0151602 PMID: 26978657 PMCID: PMC4792390 SCOPUS ID: 2-s2.0-84961820405 03/16/2016 24 Citations

Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Review With Cross-Species Comparisons. (Lawlor MW, Beggs AH, Buj-Bello A, Childers MK, Dowling JJ, James ES, Meng H, Moore SA, Prasad S, Schoser B, Sewry CA) J Neuropathol Exp Neurol 2016 Feb;75(2):102-10 PMID: 26823526 PMCID: PMC4765322 SCOPUS ID: 2-s2.0-84960448751 01/30/2016 59 Citations

Potentially diagnostic electron paramagnetic resonance spectra elucidate the underlying mechanism of mitochondrial dysfunction in the deoxyguanosine kinase deficient rat model of a genetic mitochondrial DNA depletion syndrome. (Bennett B, Helbling D, Meng H, Jarzembowski J, Geurts AM, Friederich MW, Van Hove JLK, Lawlor MW, Dimmock DP) Free Radic Biol Med 2016 Mar;92:141-151 PMID: 26773591 PMCID: PMC5047058 SCOPUS ID: 2-s2.0-84957568061 01/17/2016 18 Citations

Erratum to Muscle pathology, limb strength, walking gait, respiratory function and neurological impairment establish disease progression in the p.N155K canine model of X-linked myotubular myopathy [Ann Transl Med, 3, 18 (2015) 262] (Goddard MA, Mack DL, Hogrel JY, Czerniecki SM, Kelly VE, Snyder JM, Grange RW, Lawlor MW, Smith BK, Beggs AH, Childers MK) Annals of Translational Medicine January 2016;4(1) SCOPUS ID: 2-s2.0-85006220535 01/01/2016

Muscle pathology, limb strength, walking gait, respiratory function and neurological impairment establish disease progression in the p.N155K canine model of X-linked myotubular myopathy. (Goddard MA, Mack DL, Czerniecki SM, Kelly VE, Snyder JM, Grange RW, Lawlor MW, Smith BK, Beggs AH, Childers MK) Ann Transl Med 2015 Oct;3(18):262 PMID: 26605308 PMCID: PMC4630545 SCOPUS ID: 2-s2.0-85015501835 11/26/2015 13 Citations

Common Data Elements for Muscle Biopsy Reporting. (Dastgir J, Rutkowski A, Alvarez R, Cossette SA, Yan K, Hoffmann RG, Sewry C, Hayashi YK, Goebel HH, Bonnemann C, Lawlor MW) Arch Pathol Lab Med 2016 Jan;140(1):51-65 PMID: 26132600 PMCID: PMC4975562 SCOPUS ID: 2-s2.0-84954289035 07/02/2015 22 Citations

Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy. (Li F, Buck D, De Winter J, Kolb J, Meng H, Birch C, Slater R, Escobar YN, Smith JE 3rd, Yang L, Konhilas J, Lawlor MW, Ottenheijm C, Granzier HL) Hum Mol Genet 2015 Sep 15;24(18):5219-33 PMID: 26123491 PMCID: PMC4550825 SCOPUS ID: 2-s2.0-84940663695 07/01/2015 57 Citations

Diaphragm muscle fiber weakness and ubiquitin-proteasome activation in critically ill patients. (Hooijman PE, Beishuizen A, Witt CC, de Waard MC, Girbes AR, Spoelstra-de Man AM, Niessen HW, Manders E, van Hees HW, van den Brom CE, Silderhuis V, Lawlor MW, Labeit S, Stienen GJ, Hartemink KJ, Paul MA, Heunks LM, Ottenheijm CA) Am J Respir Crit Care Med 2015 May 15;191(10):1126-38 PMID: 25760684 PMCID: PMC4451621 SCOPUS ID: 2-s2.0-84989782434 03/12/2015 175 Citations

BAG3 myofibrillar myopathy presenting with cardiomyopathy. (Konersman CG, Bordini BJ, Scharer G, Lawlor MW, Zangwill S, Southern JF, Amos L, Geddes GC, Kliegman R, Collins MP) Neuromuscul Disord 2015 May;25(5):418-22 PMID: 25728519 SCOPUS ID: 2-s2.0-84927912558 03/03/2015 68 Citations

Isolation and immortalization of patient-derived cell lines from muscle biopsy for disease modeling. (Robin JD, Wright WE, Zou Y, Cossette SC, Lawlor MW, Gussoni E) J Vis Exp 2015 Jan 18(95):52307 PMID: 25651101 PMCID: PMC4354544 SCOPUS ID: 2-s2.0-84921628370 02/05/2015 21 Citations

Whole-thorax irradiation induces hypoxic respiratory failure, pleural effusions and cardiac remodeling. (Medhora M, Gao F, Glisch C, Narayanan J, Sharma A, Harmann LM, Lawlor MW, Snyder LA, Fish BL, Down JD, Moulder JE, Strande JL, Jacobs ER) J Radiat Res 2015 Mar;56(2):248-60 PMID: 25368342 PMCID: PMC4380043 SCOPUS ID: 2-s2.0-84942308898 11/05/2014 41 Citations

Triadopathies: an emerging class of skeletal muscle diseases. (Dowling JJ, Lawlor MW, Dirksen RT) Neurotherapeutics 2014 Oct;11(4):773-85 PMID: 25168790 PMCID: PMC4391390 SCOPUS ID: 2-s2.0-84919781500 08/30/2014 61 Citations

Tissue triage and freezing for models of skeletal muscle disease. (Meng H, Janssen PM, Grange RW, Yang L, Beggs AH, Swanson LC, Cossette SA, Frase A, Childers MK, Granzier H, Gussoni E, Lawlor MW) J Vis Exp 2014 Jul 15(89) PMID: 25078247 PMCID: PMC4215994 SCOPUS ID: 2-s2.0-84904411044 08/01/2014 92 Citations

Differential muscle hypertrophy is associated with satellite cell numbers and Akt pathway activation following activin type IIB receptor inhibition in Mtm1 p.R69C mice. (Lawlor MW, Viola MG, Meng H, Edelstein RV, Liu F, Yan K, Luna EJ, Lerch-Gaggl A, Hoffmann RG, Pierson CR, Buj-Bello A, Lachey JL, Pearsall S, Yang L, Hillard CJ, Beggs AH) Am J Pathol 2014 Jun;184(6):1831-42 PMID: 24726641 PMCID: PMC4044712 SCOPUS ID: 2-s2.0-84901020192 04/15/2014 31 Citations

Gene therapy prolongs survival and restores function in murine and canine models of myotubular myopathy. (Childers MK, Joubert R, Poulard K, Moal C, Grange RW, Doering JA, Lawlor MW, Rider BE, Jamet T, Danièle N, Martin S, Rivière C, Soker T, Hammer C, Van Wittenberghe L, Lockard M, Guan X, Goddard M, Mitchell E, Barber J, Williams JK, Mack DL, Furth ME, Vignaud A, Masurier C, Mavilio F, Moullier P, Beggs AH, Buj-Bello A) Sci Transl Med 2014 Jan 22;6(220):220ra10 PMID: 24452262 PMCID: PMC4105197 SCOPUS ID: 2-s2.0-84893427190 01/24/2014 149 Citations

Dystrophin-deficient cardiomyocytes derived from human urine: new biologic reagents for drug discovery. (Guan X, Mack DL, Moreno CM, Strande JL, Mathieu J, Shi Y, Markert CD, Wang Z, Liu G, Lawlor MW, Moorefield EC, Jones TN, Fugate JA, Furth ME, Murry CE, Ruohola-Baker H, Zhang Y, Santana LF, Childers MK) Stem Cell Res 2014 Mar;12(2):467-80 PMID: 24434629 PMCID: PMC3966181 SCOPUS ID: 2-s2.0-84892470978 01/18/2014 118 Citations

Congenital Myopathies (Lawlor MW, Pierson CR) Pathobiology of Human Disease A Dynamic Encyclopedia of Disease Mechanisms 1 January 2014:195-209 SCOPUS ID: 2-s2.0-85043273899 01/01/2014 2 Citations

G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivo. (Wu MP, Doyle JR, Barry B, Beauvais A, Rozkalne A, Piao X, Lawlor MW, Kopin AS, Walsh CA, Gussoni E) FEBS J 2013 Dec;280(23):6097-113 PMID: 24102982 PMCID: PMC3877849 SCOPUS ID: 2-s2.0-84888297031 10/10/2013 40 Citations

Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy. (Ceyhan-Birsoy O, Agrawal PB, Hidalgo C, Schmitz-Abe K, DeChene ET, Swanson LC, Soemedi R, Vasli N, Iannaccone ST, Shieh PB, Shur N, Dennison JM, Lawlor MW, Laporte J, Markianos K, Fairbrother WG, Granzier H, Beggs AH) Neurology 2013 Oct 01;81(14):1205-14 PMID: 23975875 PMCID: PMC3795603 SCOPUS ID: 2-s2.0-84886409449 08/27/2013 192 Citations

Thin Filament Proteins: Nemaline and Related Congenital Myopathies (Lawlor MW, Beggs AH) Muscle Disease Pathology and Genetics Second Edition 8 July 2013:145-151 SCOPUS ID: 2-s2.0-85016891546 07/08/2013 2 Citations

Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy. (Ottenheijm CA, Buck D, de Winter JM, Ferrara C, Piroddi N, Tesi C, Jasper JR, Malik FI, Meng H, Stienen GJ, Beggs AH, Labeit S, Poggesi C, Lawlor MW, Granzier H) Brain 2013 Jun;136(Pt 6):1718-31 PMID: 23715096 PMCID: PMC3673460 SCOPUS ID: 2-s2.0-84878827240 05/30/2013 56 Citations

Troponin activator augments muscle force in nemaline myopathy patients with nebulin mutations. (de Winter JM, Buck D, Hidalgo C, Jasper JR, Malik FI, Clarke NF, Stienen GJ, Lawlor MW, Beggs AH, Ottenheijm CA, Granzier H) J Med Genet 2013 Jun;50(6):383-92 PMID: 23572184 PMCID: PMC3865762 SCOPUS ID: 2-s2.0-84878843972 04/11/2013 48 Citations

Selenoprotein N deficiency in mice is associated with abnormal lung development. (Moghadaszadeh B, Rider BE, Lawlor MW, Childers MK, Grange RW, Gupta K, Boukedes SS, Owen CA, Beggs AH) FASEB J 2013 Apr;27(4):1585-99 PMID: 23325319 PMCID: PMC3606527 SCOPUS ID: 2-s2.0-84875702360 01/18/2013 36 Citations

Enzyme replacement therapy rescues weakness and improves muscle pathology in mice with X-linked myotubular myopathy. (Lawlor MW, Armstrong D, Viola MG, Widrick JJ, Meng H, Grange RW, Childers MK, Hsu CP, O'Callaghan M, Pierson CR, Buj-Bello A, Beggs AH) Hum Mol Genet 2013 Apr 15;22(8):1525-38 PMID: 23307925 PMCID: PMC3605830 SCOPUS ID: 2-s2.0-84875766052 01/12/2013 69 Citations

Large duplication in MTM1 associated with myotubular myopathy. (Amburgey K, Lawlor MW, Del Gaudio D, Cheng YW, Fitzpatrick C, Minor A, Li X, Aughton D, Das S, Beggs AH, Dowling JJ) Neuromuscul Disord 2013 Mar;23(3):214-8 PMID: 23273872 PMCID: PMC3594803 SCOPUS ID: 2-s2.0-85027946146 01/01/2013 10 Citations

Myotubularin-deficient myoblasts display increased apoptosis, delayed proliferation, and poor cell engraftment. (Lawlor MW, Alexander MS, Viola MG, Meng H, Joubert R, Gupta V, Motohashi N, Manfready RA, Hsu CP, Huang P, Buj-Bello A, Kunkel LM, Beggs AH, Gussoni E) Am J Pathol 2012 Sep;181(3):961-8 PMID: 22841819 PMCID: PMC3432426 SCOPUS ID: 2-s2.0-84865267643 07/31/2012 35 Citations

Oxygen gas-filled microparticles provide intravenous oxygen delivery. (Kheir JN, Scharp LA, Borden MA, Swanson EJ, Loxley A, Reese JH, Black KJ, Velazquez LA, Thomson LM, Walsh BK, Mullen KE, Graham DA, Lawlor MW, Brugnara C, Bell DC, McGowan FX Jr) Sci Transl Med 2012 Jun 27;4(140):140ra88 PMID: 22745438 SCOPUS ID: 2-s2.0-84863227471 06/30/2012 109 Citations

Thermoresponsive nanogels for prolonged duration local anesthesia. (Hoare T, Young S, Lawlor MW, Kohane DS) Acta Biomater 2012 Oct;8(10):3596-605 PMID: 22732383 PMCID: PMC3429626 SCOPUS ID: 2-s2.0-84865484651 06/27/2012 66 Citations

Toxicogenomic analysis of a sustained release local anesthetic delivery system. (Shichor I, Shomron N, Lawlor MW, Bae SA, Zoldan J, Langer R, Kohane DS) Biomaterials 2012 May;33(13):3586-93 PMID: 22341215 PMCID: PMC3288387 SCOPUS ID: 2-s2.0-84857441486 02/22/2012 11 Citations

Nanogel scavengers for drugs: local anesthetic uptake by thermoresponsive nanogels. (Hoare T, Sivakumaran D, Stefanescu CF, Lawlor MW, Kohane DS) Acta Biomater 2012 Apr;8(4):1450-8 PMID: 22244983 PMCID: PMC3289739 SCOPUS ID: 2-s2.0-84857781615 01/17/2012 31 Citations

Erratum: Elasticity and safety of alkoxyethyl cyanoacrylate tissue adhesives (Acta Biomaterialia (2011) 7 (3150-3157)) (Mizrahi B, Stefanescu CF, Yang C, Lawlor MW, Ko D, Langer R, Kohane DS) Acta Biomaterialia January 2012;8(1):458 SCOPUS ID: 2-s2.0-84855917457 01/01/2012 3 Citations

Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype. (Pierson CR, Dulin-Smith AN, Durban AN, Marshall ML, Marshall JT, Snyder AD, Naiyer N, Gladman JT, Chandler DS, Lawlor MW, Buj-Bello A, Dowling JJ, Beggs AH) Hum Mol Genet 2012 Feb 15;21(4):811-25 PMID: 22068590 PMCID: PMC3263994 SCOPUS ID: 2-s2.0-84856350401 11/10/2011 54 Citations

An in vivo rodent model of contraction-induced injury in the quadriceps muscle. (Pratt SJP, Lawlor MW, Shah SB, Lovering RM) Injury 2012 Jun;43(6):788-93 PMID: 22001505 PMCID: PMC3310278 SCOPUS ID: 2-s2.0-84860740259 10/18/2011 21 Citations

Polydopamine coatings enhance biointegration of a model polymeric implant (Jeong KJ, Wang L, Stefanescu CF, Lawlor MW, Polat J, Dohlman CH, Langer RS, Kohane DS) Soft Matter 21 September 2011;7(18):8305-8312 SCOPUS ID: 2-s2.0-80052529624 09/21/2011 46 Citations

Novel mutations in NEB cause abnormal nebulin expression and markedly impaired muscle force generation in severe nemaline myopathy. (Lawlor MW, Ottenheijm CA, Lehtokari VL, Cho K, Pelin K, Wallgren-Pettersson C, Granzier H, Beggs AH) Skelet Muscle 2011 Jun 20;1(1):23 PMID: 21798101 PMCID: PMC3156646 SCOPUS ID: 2-s2.0-84861231735 07/30/2011 57 Citations

Elasticity and safety of alkoxyethyl cyanoacrylate tissue adhesives. (Mizrahi B, Stefanescu CF, Yang C, Lawlor MW, Ko D, Langer R, Kohane DS) Acta Biomater 2011 Aug;7(8):3150-7 PMID: 21569875 PMCID: PMC4059060 SCOPUS ID: 2-s2.0-79959844652 05/17/2011 90 Citations

Erratum: Prolonged duration local anesthesia with minimal toxicity (Proceedings of the National Academy of Sciences of the United States of America (2009) 106, 17, (7125-7130) DOI: 10.1073/pnas.0900598106) (Epstein-Barash H, Shichor I, Kwon AH, Hall S, Lawlor MW, Langer R, Kohane DS) Proceedings of the National Academy of Sciences of the United States of America 8 March 2011;108(10):4264 SCOPUS ID: 2-s2.0-79952747712 03/08/2011

Changes in cross-bridge cycling underlie muscle weakness in patients with tropomyosin 3-based myopathy. (Ottenheijm CA, Lawlor MW, Stienen GJ, Granzier H, Beggs AH) Hum Mol Genet 2011 May 15;20(10):2015-25 PMID: 21357678 PMCID: PMC3080611 SCOPUS ID: 2-s2.0-79955371742 03/02/2011 59 Citations

Inhibition of activin receptor type IIB increases strength and lifespan in myotubularin-deficient mice. (Lawlor MW, Read BP, Edelstein R, Yang N, Pierson CR, Stein MJ, Wermer-Colan A, Buj-Bello A, Lachey JL, Seehra JS, Beggs AH) Am J Pathol 2011 Feb;178(2):784-93 PMID: 21281811 PMCID: PMC3069865 SCOPUS ID: 2-s2.0-79951842509 02/02/2011 56 Citations

Inhibition of activin receptor type IIB increases strength and lifespan in myotubularin-deficient mice (The American Journal of Pathology (2011) 178 (784-793)) (Lawlor MW, Read BP, Edelstein R, Yang N, Pierson CR, Stein MJ, Wermer-Colan A, Buj-Bello A, Lachey JL, Seehra JS, Beggs AH) American Journal of Pathology March 2011;178(3):1406 SCOPUS ID: 2-s2.0-79952741382 01/01/2011

Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene. (Zhou Y, Cheunsuchon P, Nakayama Y, Lawlor MW, Zhong Y, Rice KA, Zhang L, Zhang X, Gordon FE, Lidov HG, Bronson RT, Klibanski A) Development 2010 Aug;137(16):2643-52 PMID: 20610486 PMCID: PMC2910384 SCOPUS ID: 2-s2.0-77955744813 07/09/2010 130 Citations

Functional muscle analysis of the Tcap knockout mouse. (Markert CD, Meaney MP, Voelker KA, Grange RW, Dalley HW, Cann JK, Ahmed M, Bishwokarma B, Walker SJ, Yu SX, Brown M, Lawlor MW, Beggs AH, Childers MK) Hum Mol Genet 2010 Jun 01;19(11):2268-83 PMID: 20233748 PMCID: PMC2865379 SCOPUS ID: 2-s2.0-77953511024 03/18/2010 43 Citations

Neuropathology of a fatal case of posterior reversible encephalopathy syndrome. (Kheir JN, Lawlor MW, Ahn ES, Lehmann L, Riviello JJ, Silvera VM, McManus M, Folkerth RD) Pediatr Dev Pathol 2010;13(5):397-403 PMID: 20158377 SCOPUS ID: 2-s2.0-79952197856 02/18/2010 23 Citations

Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion. (Lawlor MW, Dechene ET, Roumm E, Geggel AS, Moghadaszadeh B, Beggs AH) Hum Mutat 2010 Feb;31(2):176-83 PMID: 19953533 PMCID: PMC2815199 SCOPUS ID: 2-s2.0-75149179143 12/03/2009 81 Citations

Prolonged duration local anesthesia with minimal toxicity. (Epstein-Barash H, Shichor I, Kwon AH, Hall S, Lawlor MW, Langer R, Kohane DS) Proc Natl Acad Sci U S A 2009 Apr 28;106(17):7125-30 PMID: 19365067 PMCID: PMC2678453 SCOPUS ID: 2-s2.0-66349108420 04/15/2009 144 Citations

Effect of chemical permeation enhancers on nerve blockade. (Simons EJ, Bellas E, Lawlor MW, Kohane DS) Mol Pharm 2009;6(1):265-73 PMID: 19105721 PMCID: PMC2646764 SCOPUS ID: 2-s2.0-62649146532 12/25/2008 44 Citations

Three-dimensional conductive constructs for nerve regeneration. (George PM, Saigal R, Lawlor MW, Moore MJ, LaVan DA, Marini RP, Selig M, Makhni M, Burdick JA, Langer R, Kohane DS) J Biomed Mater Res A 2009 Nov;91(2):519-27 PMID: 18985787 SCOPUS ID: 2-s2.0-70349445295 11/06/2008 46 Citations

Malignant solitary fibrous tumour of the meninges with marked amianthoid fibre deposition. (Lawlor MW, Nielsen GP, Louis DN) Neuropathol Appl Neurobiol 2008 Oct;34(5):569-72 PMID: 18298634 SCOPUS ID: 2-s2.0-52949123647 02/27/2008 7 Citations

Anti-neurofilament antibodies in neuropathy with monoclonal gammopathy of undetermined significance produce experimental motor nerve conduction block. (Stubbs EB Jr, Lawlor MW, Richards MP, Siddiqui K, Fisher MA, Bhoopalam N, Siegel GJ) Acta Neuropathol 2003 Feb;105(2):109-16 PMID: 12536221 SCOPUS ID: 2-s2.0-0037313279 01/22/2003 20 Citations

Antibodies to L-periaxin in sera of patients with peripheral neuropathy produce experimental sensory nerve conduction deficits. (Lawlor MW, Richards MP, De Vries GH, Fisher MA, Stubbs EB Jr) J Neurochem 2002 Nov;83(3):592-600 PMID: 12390521 SCOPUS ID: 2-s2.0-0036829266 10/23/2002 13 Citations

Sensory nerve conduction deficit in experimental monoclonal gammopathy of undetermined significance (MGUS) neuropathy. (Lawlor MW, Richards MP, Fisher MA, Stubbs EB Jr) Muscle Nerve 2001 Jun;24(6):809-16 PMID: 11360265 SCOPUS ID: 2-s2.0-0035008590 05/22/2001 9 Citations

Assessment of serum-mediated neurotoxicity in Navajo neuropathy. (Lawlor MW, Holve S, Stubbs EB Jr) Electromyogr Clin Neurophysiol 2000 Jun;40(4):211-4 PMID: 10907598 SCOPUS ID: 2-s2.0-0033932019 07/25/2000 4 Citations

Last update: 01/08/2025

© 2026 Clinical & Translational Science Institute
Medical College of Wisconsin
8701 Watertown Plank Road
Milwaukee, WI 53223

Publication and ontology data from NCBI | Disclaimer and Copyright

This site is a collaborative effort of the Medical College of Wisconsin and the Clinical and Translational Science Institute (CTSI), part of the Clinical and Translational Science Award program funded by the National Center for Advancing Translational Sciences (Grant Number 2UL1TR001436) at the National Institutes of Health (NIH).

Profiles for MCW, MU, MSOE, UWM, BCW, CW, Froedtert, and VA Faculty

Michael W. Lawlor PhD, MD

Adjunct Professor

Publications (107)