MatthewPaulWicklundMD

PubMed

• 3 citations
  Safety and efficacy of arimoclomol for inclusion body myositis: a multicentre, randomised, double-blind, placebo-controlled trial.
  Pedro M Machado, Michael P McDermott, Thomas Blaettler, Claus Sundgreen, Anthony A Amato, Emma Ciafaloni, Miriam Freimer, Summer B Gibson, Sarah M Jones, Todd D Levine...> ;The Lancet. Neurology. 2023 Oct 1
• 3 citations
  Provisional practice recommendation for the management of myopathy in VCP-associated multisystem proteinopathy.
  Bhaskar Roy, Allison Peck, Teresinha Evangelista, Gerald Pfeffer, Leo Wang, Jordi Diaz-Manera, Manisha Korb, Matthew P Wicklund, Margherita Milone, Miriam Freimer, Han...> ;Annals of Clinical and Translational Neurology. 2023 May 1
• 2 citations
  Patient Reported Quality of Life in Limb Girdle Muscular Dystrophy
  Laurel Kovalchick, Kameron Bates, Jeffrey Statland, C. Weihl, Peter B. Kang, Linda Lowes, Tahseen Mozaffar, Volker Straub, Matthew Wicklund, Chad Heatwole, Nicholas E....> ;Neuromuscular Disorders. 2021 Nov 13
• 4 citations
  Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy.
  Craig Campbell, Elaine McColl, Michael P. McDermott, William B. Martens, Michela Guglieri, Robert C. Griggs, Volker Straub, Anne-Marie Childs, Emma Ciafaloni, Perry B....> ;Neuromuscular Disorders. 2021 Jun 10
• 20 citations
  Patient Assisted Intervention for Neuropathy: Comparison of Treatment in Real Life Situations (PAIN-CONTRoLS): Bayesian Adaptive Comparative Effectiveness Randomized T...
  Richard J. Barohn, Byron J. Gajewski, Mamatha Pasnoor, Alexandra R. Brown, Laura Herbelin, Kim S. Kimminau, Dinesh Pal Mudaranthakam, Omar Jawdat, Mazen M. Dimachkie, ...> ;JAMA Neurology. 2021 Jan 1
• 11 citations
  The CINRG Becker Natural History Study: Baseline characteristics
  Paula R. Clemens, Gabriela Niizawa, Jia Feng, Julaine Florence, Andrea Smith DʼAlessandro, Lauren P. Morgenroth, Ksenija Gorni, Michela Guglieri, Anne M. Connolly, Mat...> ;Muscle & Nerve. 2020 Sep 1
• 6 citations
  Limb Girdle Muscular Dystrophies.
  Jacob Bockhorst, Matthew Wicklund> ;Neurologic Clinics. 2020 Aug 1
• Ankle bracing practices in ambulatory, corticosteroid‐naive boys with Duchenne muscular dystrophy
  Victoria Kern, Matthew Wicklund, Anne Haulman, Michael P. McDermott, William B. Martens, Robert C. Griggs, Ashutosh Kumar, Treat-Nmd> ;Muscle & Nerve. 2020 Jan 1
• 9 citations
  The Limb-Girdle Muscular Dystrophies.
  Matthew Wicklund> ;Continuum. 2019 Dec 1
• 39 citations
  Novel clinical features of glycine receptor antibody syndrome: A series of 17 cases.
  Amanda L. Piquet, Murtaza Khan, Judith E. A. Warner, Matthew Wicklund, Jeffrey Bennett, Maureen A. Leehey, Lauren Seeberger, Teri Schreiner, M. Mateo Paz Soldan, Stace...> ;Neurology(R) Neuroimmunology & Neuroinflammation. 2019 Sep 1
• Novel clinical features of glycine receptor antibody syndrome: A series of 17 cases.
  Piquet, A. L., Khan, M., Warner, J. E., Wicklund, M. P., Bennett, J. L., Leehey, M. A., Seeberger, L., Schreiner, T. L., Soldan, M. M., Clardy, S. L.> ;Neurology(R) neuroimmunology & neuroinflammation. 2019 Aug 28
• 11 citations
  Limb-girdle muscular dystrophy: A perspective from adult patients on what matters most.
  Michael Hunter, Chad Heatwole, Matthew Wicklund, Conrad C. Weihl, Tahseen Mozaffar, Jeffrey Statland, Nicholas E. Johnson> ;Muscle & Nerve. 2019 Jul 24
• 1 citations
  Development of Autoimmune Interstitial Lung Disease in a Patient with Inclusion Body Myositis.
  Christophe He, Joyce S. Lee, Carlyne D. Cool, Matthew Wicklund, Aryeh Fischer> ;The American Journal of Medicine. 2019 Jul 13
• 3 citations
  Take two: Utility of the repeat skeletal muscle biopsy
  Samah K. Aburahma, Matthew Wicklund, Dianna Quan> ;Muscle & Nerve. 2019 Jul 1
• 109 citations
  Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients.
  Babi Ramesh Reddy Nallamilli, Samya Chakravorty, Akanchha Kesari, Alice K. Tanner, Arunkanth Ankala, Thomas Schneider, Cristina da Silva, Randall Beadling, John J. Ale...> ;Annals of Clinical and Translational Neurology. 2018 Dec 1
• 17 citations
  KIF1Bβ mutations detected in hereditary neuropathy impair IGF1R transport and axon growth
  Fang Xu, Hironori Takahashi, Yosuke Tanaka, Sotaro Ichinose, Shinsuke Niwa, Matthew Wicklund, Nobutaka Hirokawa> ;The Journal of Cell Biology. 2018 Oct 1
• 3 citations
  Unique presentation of rapidly fluctuating symptoms in a child with congenital myasthenic syndrome due to RAPSN mutation.
  Ashutosh Kumar, Sheila Asghar, Robert Kavanagh, Matthew Wicklund> ;Muscle & Nerve. 2018 Sep 3
• 20 citations
  Novel valosin-containing protein mutations associated with multisystem proteinopathy.
  Ebaa Al-Obeidi, Hiroshi Yoshioka, Anita Lakatos, Lan Weiss, Marjorie R. Grafe, Johanna Palmio, Matthew Wicklund, Yadollah Harati, Molly Omizo, Bjarne Udd, Virginia Kim...> ;Neuromuscular Disorders. 2018 Jun 1
• 26 citations
  A checklist for clinical trials in rare disease: obstacles and anticipatory actions—lessons learned from the FOR-DMD trial
  Rebecca A. Crow, Kimberly A. Hart, Michael P. McDermott, Rabi Tawil, William B. Martens, Barbara E. Herr, Elaine McColl, Jennifer Wilkinson, Janbernd Kirschner, Wendy ...> ;Trials. 2018 May 10
• 6 citations
  The Effect of Propofol on Chronic Headaches in Patients Undergoing Endoscopy.
  David M. Giampetro, Victor Ruiz-Velasco, Ashlee Pruett, Matthew Wicklund, Robert Knipe> ;Pain Research & Management. 2018 Jan 21
• 55 citations
  Developing standardized corticosteroid treatment for Duchenne muscular dystrophy.
  Michela Guglieri, Kate Bushby, Michael P. McDermott, Kimberly A. Hart, Rabi Tawil, William B. Martens, Barbara E. Herr, Elaine McColl, Jennifer Wilkinson, Janbernd Kir...> ;Contemporary Clinical Trials. 2017 Jul 1
• 12 citations
  A CARASIL Patient from Americas with Novel Mutation and Atypical Features: Case Presentation and Literature Review.
  Muhammad Ibrahimi, Hiroaki Nozaki, Angelica Lee, Osamu Onodera, Raymond Reichwein, Matthew Wicklund, Mohammad El-Ghanem> ;Cerebrovascular Diseases. 2017 Jun 21
• 2 citations
  Retraction Statement. Paper ‘Low-Dose Vitamin D Prevents Muscular Atrophy and Reduces Falls and Hip Fractures in Women after Stroke: A Randomized Controlled Trial' by ...
  Oh Young Bang, Woo-Keun Seo, Ken Uchino, Dolora Wisco, Sung-Min Cho, Robert J. Marquardt, Lucy Zhang, Prateek Thatikunta, Andrew B. Buletko, Julian Hardman, Jillian Na...> ;Cerebrovascular Diseases. 2017 Jan 1
• 36 citations
  Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
  Qiang Gang, Conceição Bettencourt, Pedro Machado, Stefen Brady, Janice L. Holton, Alan M. Pittman, Deborah Hughes, Estelle Healy, M. Parton, David Hilton-Jones, Perry ...> ;Neurobiology of Aging. 2016 Nov 1
• 2 citations
  Rare disease clinical trials: Power in numbers.
  Matthew Wicklund> ;Neurology. Genetics. 2016 Aug 1
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Journal Articles

• Recurrent episodes of stroke-like symptoms in a patient with Charcot-Marie-Tooth Neuropathy X type 1  
  Wu N, Said S, Sabat S, Wicklund M, Stahl MC, Case Rep Neurol, 1/1/2015
• Novel presentation of Pompe disease: inclusion-body myositis-like clinical phenotype  
  Bandyopadhyay S, Wicklund M, Specht CS, Muscle & Nerve, 1/1/2015
• SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype  
  Bugiardini E. Rivolta I, Binda A, Soriano Caminero A, Cirillo F, Cinti A, Giovannoni R, Botta A, Cardani R, Wicklund MP, Meola G, Neuromuscul Disord, 1/1/2015
• Serum metabolomic response of myasthenia gravis patient to chronic prednisone treatment  
  Sengupta M, Cheema A, Kaminski HJ, Kusner LL, Muscle Study Group, PLoS ONE, 1/1/2014
• Evidence-based guideline summary: Diagnosis and treatment of limb-girdle and distal dystrophies  
  Narayanaswami P, Weiss M, Selcen D, Raynor E, Carter G, Wicklund M, Barohn RJ, Ensrud E, Griggs RC, Gronseth G, Amato AA, Neurology, 1/1/2014
• The limb girdle muscular dystrophies  
  Wicklund MP, Kissel JT, Neurologic Clinics, 1/1/2014
• The muscular dystrophies  
  Wicklund MP, Continuum, 1/1/2013
• Phase II trial of methotrexate in myasthenia gravis  
  Pasnoor M, He J, Herbelin L, Dimachkie M, Barohn RJ, Muscle Study Group, Ann NY Acad Sci, 1/1/2012
• Amyotrophic lateral sclerosis: what role does environment play?  
  Ahmed A, Wicklund MP, Neurologic Clinics of North America, 1/1/2011
• Spinal angiography and epidural venography in juvenile muscular atrophy of the distal arm “Hirayama disease”  
  El Sheikh B, Kissel J, Christoforidis G, Wicklund M, Kehagias D, Chiocca E, Mendell J, Muscle Nerve, 1/1/2009
• Limb-girdle muscular dystrophy in the United States  
  Moore SA, Shilling CJ, Westra S, Wall C, Wicklund MP, Stolle C, Brown CA, Michele DE, Piccolo F, Winder TL, Stence A, Barresi R, King N, King W, Florence J, Campbell K..., Journal of Neuropathology & Experimental Neurology, 1/1/2006
• Amyotrophic lateral sclerosis: possible role of environmental influences  
  Wicklund MP, Neurologic Clinics of North America, 1/1/2005
• The limb girdle muscular dystrophies: years of ignorance – a decade of breakthroughs  
  Wicklund MP, Advances in Neurosciences, 1/1/2004
• The limb girdle muscular dystrophies: our ever expanding knowledge  
  Wicklund MP, Mendell JR, J Clin Neuromusc Dis, 1/1/2003
• Diagnosis and management of peripheral nerve disorders  
  Wicklund MP, Neurology, 1/1/2002
• Paraproteinemic Neuropathy  
  Wicklund MP, Kissel JT, Current Treatment Options in Neurology, 1/1/2001
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Books/Book Chapters

• 2016 Ferri's Clinical Advisor 
  Chapter: Inclusion Body Myositis 
  Wicklund MPEditors: Ferri F.Elsevier Mosby, Philadelphia, PA2015
• Horizons in Neuroscience Research 
  Chapter: Role of environmental toxins in amyotrophic lateral sclerosis (ALS) 
  Page 29 - 46Raheja D, Wicklund MEditors: Costa A and Villalba E.Nova Science Publishers2015
• 2015 Ferri's Clinical Advisor 
  Chapter: Inclusion Body Myositis 
  Wicklund MPEditors: Ferri F.Elsevier Mosby, Philadelphia, PA2015
• Encyclopedia of the Neurological Sciences 
  Chapter: Limb-Girdle Muscular Dystrophies 
  Page 890 - 896Wicklund MPEditors: Aminoff M.J. and Daroff R.B..Academic Press, Oxford, UK2014
• 2014 Ferri's Clinical Advisor 
  Chapter: Inclusion Body Myositis 
  Wicklund MPEditors: Ferri F.Elsevier Mosby, Philadelphia, PA2013
• 2013 Ferri's Clinical Advisor 
  Chapter: Inclusion Body Myositis 
  Wicklund MPEditors: Ferri F.Elsevier Mosby, Philadelphia, PA2012
• Conn’s Current Therapy 2002 
  Chapter: Peripheral Neuropathy 
  Page 958 - 966Wicklund MP and Mendell JREditors: Rakel RE, Bope ET.W. B. Saunders, Philadelphia, PA2012
• Neuromuscular Disorders 
  Chapter: Approach to Diseases of Muscle 
  Page 9 - 14Wicklund MPEditors: Tawil R & Venance S.Wiley-Blackwell, Oxford, UK2011
• 2012 Ferri's Clinical Advisor 
  Chapter: Inclusion Body Myositis 
  Wicklund MPEditors: Ferri F.Elsevier Mosby, Philadelphia, PA2011
• The 5-Minute Neurology Consult 
  Chapter: Metabolic Myopathies 
  Wicklund, MPEditors: Lynn J, Rae-Grant A, Newton H.Lippincott, Williams & Wilkins, Philadelphia, PA2004
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Abstracts/Posters

• Phase II trial of methotrexate in myasthenia gravis
  Pasnoor M, Herbelin L, He J, Dimatchkie M, Nations S, Bril V, Wang A, Kissel J, Burns T, Saperstein D, Rosenfeld J, Shaibani A, Jackson C, Swenson A, Howard J, Goyal N..., Muscle Nerve, 1/1/2014
• Novel mutation causes refractory sensorimotor axonal polyneuropathy with cranial nerve involvement
  Velazquez Y, Kaur D, Wicklund M, Muscle Nerve, 1/1/2014
• Correlation between neuromuscular physical examination and electrodiagnostic studies results
  Velazquez Y, Cochran A, Wicklund M, Muscle Nerve, 1/1/2014
• Phase II trial of methotrexate in myasthenia gravis
  Pasnoor M, Herbelin L, He Q, Dimachkie M, Nations S, Bril V, Wang A, Kissel J, Burns T, Saperstein D, Rosenfeld J, Shaibani A, Jackson C, Swenson A, Howard J, Goyal N,..., Neurology, 1/1/2014
• Patient presenting with paresthesias and hemi-diaphragmatic paralysis
  Kaur D, Velazquez Y, Scollard D, Specht C, Wicklund M, J Clin Neuromusc Dis, 1/1/2014
• Sodium channel gene mutation: a possible role in myotonic dystrophy type 2 with severe myotonia
  Bugiardini E, Soriano Caminero A, Cardani R, Valaperta R, Wicklund MP, Meola G, International Myotonic Dystrophy Consortium (IDMC-9) Meeting, San Sebastian, Basque Country, Spain, 1/1/2013
• Myotonic Dystrophy Type 2 and Sodium Channel Gene Mutation: a case with Early and Severe Myotonia
  Bugiardini E, Soriano Caminero A, Cardani R, Valaperta R, Wicklund MP, Meola G, Muscle Study Group (MSG) Meeting, Oxford, England, 1/1/2013
• Chloride and sodium channel genes as modifying factor in juvenile myotonic dystrophy type 2
  Bugiardini E, Soriano Caminero A, Cardani R, Botta A, Wicklund M, Meola G, Italian Society of Myology Meeting, 1/1/2013
• Relative prevalence of limb girdle muscular dystrophies in the United States population
  Wicklund M, DiVincenzo C, Liaquat K, Karbassi I, Neurology, 1/1/2013
• Osteoporosis in neuromuscular medicine
  Soriano-Caminero A, Wicklund M, Mozaffar T, Goyal N, J Clin Neuromusc Dis, 1/1/2013
• Double trouble
  Soriano-Caminero A, Wicklund M, Baccon J, J Clin Neuromusc Dis, 1/1/2013
• In-frame mutation in the WW-CR dystrophin domain: a case with DMD phenotype and relatively preserved dystrophin expression
  Raheja D, Housman C, Giordano A, Wicklund M, Specht C, J Neuropathol Exp Neurol, 1/1/2012
• Parkinsonism and dermatomyositis: a rare presentation
  Raheja D, Specht C, Wicklund M, Ahmed A, J Clin Neuromuscul Dis, 1/1/2012
• Progressive weakness, wasting and white matter disease
  Wicklund M, J Clin Neuromuscul Dis, 1/1/2011
• Inclusion body myositis: evaluation of 116 cases
  Wicklund M, Arnold D, Kissel J, Neurology, 1/1/2010
• Hereditary neuropathy with pressure palsies: analysis of 24 de novo, unrelated cases
  Scheiner C, Amato A, Wicklund M, Neurology, 1/1/2010
• Sprained ankles, abdominal laxity, progressive weakness and a “funny” walk in a 48 year old male
  Wicklund M, Heller S, Sumner N, J Clin Neuromusc Dis, 1/1/2010
• Scapuloperoneal weakness with wasting of the muscles of the scapula
  Baugh L, Wicklund M, J Clin Neuromusc Dis, 1/1/2009
• Spinal angiography reveals functional venous engorgement in Hirayama’s syndrome
  El Sheikh B, Wicklund M, Christoforidis G, Kissel J, Mendell J, Neurology, 1/1/2006
• Limb-girdle muscular dystrophy in the USA: distribution of immunophenotypes and genotypes from an ongoing multi-center collaborative study
  Moore SA, Shilling CJ, Westra S, Wicklund MP, Brown CA, Michele DE, Stolle C, Campbell KP, Fenichel GM, Griggs RC, Kissel JT, Mathews KD, Pestronk A, Wall C, Mendell JR, Journal of Neuropathology and Experimental Neurology, 1/1/2004
• Establishing the prevalence of LGMD genotypes in North America: An ongoing multi-center collaborative study
  Shilling CJ, Wicklund MP, Moore SA, et al, Neurology, 1/1/2004
• Progressive upper extremity weakness in a 16-year-old boy
  Wicklund MP, Kehagias DT, Christophoridis GA, Mendell JR, J Child Neurology, 1/1/2004
• Histological-based diagnosis expands the phenotypic boundaries in inclusion body myositis
  Wicklund MP, Mendell JR, Kissel JT, 1st Annual 59th MDW Research Appreciation Day, 1/15/2003
• Distal muscular dystrophy affecting the calves with onset after age 30: not due to dysferlinopathy
  Katz J, Barohn R, Rando T, Jackson C, Wicklund M, Saperstein D, Amato A, Neurology, 1/1/2003
• Addressing the risk factors post-stroke: How good are we really?
  Vogt M, Wicklund MP, SAFP meeting, 1/1/2003
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Lectures

• Diagnosis of Genetic Muscle Diseases in 2015 – A Net More Likely Will Yield a Diagnosis 
  1/26/2015
• Limb Girdle Muscular Dystrophies 
  Columbus, OH - 1/25/2015
• Dyferlinopathies: LGMD2B, Miyoshi & Others 
  Dallas, TX - 1/24/2015
• Muscle Disease Made Ridiculously Simple 
  State College, PA - 1/16/2015
• Weakness, Multiple Sclerosis and Zebrafish 
  Hershey, PA - 1/11/2015
• Muscular Dystrophies 
  Augusta, GA - 1/11/2015
• Late-Onset Pompe Disease – Diagnosis and Management of Asymptomatic/Oligosymptomatic Cases 
  Boston, MA - 1/21/2014
• LGMDs – Navigating the Diagnostic Odyssey 
  Chicago, IL - 1/19/2014
• Diagnosis & Treatment of Neuromuscular Disorders – Or, I’m weak and I don’t know why 
  Harrisburg, PA - 1/9/2014
• Practical Treatments for Common Neuromuscular Disorders 
  State College, PA - 1/27/2013
• Neuromuscular Division Research Update 
  Hershey, PA - 1/22/2013
• Progressive Weakness, Wasting and White Matter Disease 
  Dallas, TX - 1/17/2011
• Updates in Neuromuscular Medicine: the Top Ten for 2011 
  Hershey, PA - 1/16/2011
• Muscular Weakness: Cases and Concepts 
  Harrisburg, PA - 1/13/2011
• Sprained Ankles, a Funny Walk, Abdominal Laxity, and Progressive Weakness in a 48 Year Old Male 
  Dallas, TX - 1/25/2010
• Neurology Review 
  San Antonio, TX - 1/10/2010
• Updates in Neuromuscular Medicine – The ‘Top Ten’ for 2010 
  San Antonio, TX - 1/5/2010
• The Limb Girdle Muscular Dystrophies – An Ongoing Explosion of Knowledge! 
  Chicago, IL - 1/14/2008
• The Heart of the Matter – Cardiomyopathies and Cardiac Involvement in Skeletal Muscle Disease 
  Boston, MA - 1/5/2007
• The Limb Girdle Muscular Dystrophies – An Explosion of Knowledge over 15 Years! 
  San Diego, CA - 1/2/2006
• Limb Girdle Muscular Dystrophies – Not So Uncommon Anymore 
  San Antonio, TX - 1/22/2005
• Neuromuscular Cases: Unusual yet not Uncommon 
  Austin, TX - 1/12/2005
• Progressive Upper Extremity Weakness in a 16-Year-Old Boy 
  Dallas, TX - 1/27/2004
• Topics in Muscle Disease 
  Fort Sam Houston, TX - 1/23/2004
• Diagnosis of Muscle Disease 
  San Francisco, CA - 1/1/2004
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