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Pathology Features of Immune and Inflammatory Myopathies, Including a Polymyositis Pattern, Relate Strongly to Serum Autoantibodies
Pathology Features of Immune and Inflammatory Myopathies, Including a Polymyositis Pattern, Relate Strongly to Serum Autoantibodies
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Pathology Features of Immune and Inflammatory Myopathies, Including a Polymyositis Pattern, Relate Strongly to Serum Autoantibodies

Pestronk, Alan ; Choksi, Rati

Journal of neuropathology and experimental neurology, 2021-09, Vol.80 (9), p.812-820 [Periódico revisado por pares]

England: Oxford University Press

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2
Ultrasound of inherited vs. acquired demyelinating polyneuropathies
Ultrasound of inherited vs. acquired demyelinating polyneuropathies
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Ultrasound of inherited vs. acquired demyelinating polyneuropathies

Zaidman, Craig M. ; Harms, Matthew B. ; Pestronk, Alan

Journal of neurology, 2013-12, Vol.260 (12), p.3115-3121 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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3
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
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An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study

Miller, Timothy M, Dr ; Pestronk, Alan, Prof ; David, William, MD ; Rothstein, Jeffrey, Prof ; Simpson, Ericka, MD ; Appel, Stanley H, Prof ; Andres, Patricia L, MS ; Mahoney, Katy, BA ; Allred, Peggy, DPT ; Alexander, Katie, BA ; Ostrow, Lyle W, MD ; Schoenfeld, David, Prof ; Macklin, Eric A, PhD ; Norris, Daniel A, PhD ; Manousakis, Georgios, MD ; Crisp, Matthew, BS ; Smith, Richard, MD ; Bennett, C Frank, PhD ; Bishop, Kathie M, PhD ; Cudkowicz, Merit E, Prof

Lancet neurology, 2013-05, Vol.12 (5), p.435-442 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes
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Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes

Cady, Janet ; Allred, Peggy ; Bali, Taha ; Pestronk, Alan ; Goate, Alison ; Miller, Timothy M. ; Mitra, Robi D. ; Ravits, John ; Harms, Matthew B. ; Baloh, Robert H.

Annals of neurology, 2015-01, Vol.77 (1), p.100-113 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophy
Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophy
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Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophy

Griggs, Robert C ; Miller, J Phillip ; Greenberg, Cheryl R ; Fehlings, Darcy L ; Pestronk, Alan ; Mendell, Jerry R ; Moxley, Richard T ; King, Wendy ; Kissel, John T ; Cwik, Valerie ; Vanasse, Michel ; Florence, Julaine M ; Pandya, Shree ; Dubow, Jordan S ; Meyer, James M

Neurology, 2016-11, Vol.87 (20), p.2123-2131 [Periódico revisado por pares]

United States: American Academy of Neurology

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6
Altered Axonal Mitochondrial Transport in the Pathogenesis of Charcot-Marie-Tooth Disease from Mitofusin 2 Mutations
Altered Axonal Mitochondrial Transport in the Pathogenesis of Charcot-Marie-Tooth Disease from Mitofusin 2 Mutations
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Altered Axonal Mitochondrial Transport in the Pathogenesis of Charcot-Marie-Tooth Disease from Mitofusin 2 Mutations

Baloh, Robert H ; Schmidt, Robert E ; Pestronk, Alan ; Milbrandt, Jeffrey

The Journal of neuroscience, 2007-01, Vol.27 (2), p.422-430 [Periódico revisado por pares]

United States: Soc Neuroscience

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7
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms
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Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

Chung, Hyung-lok ; Wangler, Michael F. ; Marcogliese, Paul C. ; Jo, Juyeon ; Ravenscroft, Thomas A. ; Zuo, Zhongyuan ; Duraine, Lita ; Sadeghzadeh, Sina ; Li-Kroeger, David ; Schmidt, Robert E. ; Pestronk, Alan ; Rosenfeld, Jill A. ; Burrage, Lindsay ; Herndon, Mitchell J. ; Chen, Shan ; Shillington, Amelle ; Vawter-Lee, Marissa ; Hopkin, Robert ; Rodriguez-Smith, Jackeline ; Henrickson, Michael ; Lee, Brendan ; Moser, Ann B. ; Jones, Richard O. ; Watkins, Paul ; Yoo, Taekyeong ; Mar, Soe ; Choi, Murim ; Bucelli, Robert C. ; Yamamoto, Shinya ; Lee, Hyun Kyoung ; Prada, Carlos E. ; Chae, Jong-Hee ; Vogel, Tiphanie P. ; Bellen, Hugo J.

Neuron (Cambridge, Mass.), 2020-05, Vol.106 (4), p.589-606.e6 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Cryptogenic small‐fiber neuropathies: Serum autoantibody binding to trisulfated heparan disaccharide and fibroblast growth factor receptor‐3
Cryptogenic small‐fiber neuropathies: Serum autoantibody binding to trisulfated heparan disaccharide and fibroblast growth factor receptor‐3
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Cryptogenic small‐fiber neuropathies: Serum autoantibody binding to trisulfated heparan disaccharide and fibroblast growth factor receptor‐3

Levine, Todd D. ; Kafaie, Jafar ; Zeidman, Lawrence A. ; Saperstein, David S. ; Massaquoi, Reyanna ; Bland, Ruth J. ; Pestronk, Alan

Muscle & nerve, 2020-04, Vol.61 (4), p.512-515 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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9
Chronic Graft Versus Host Myopathies: Noninflammatory, Multi-Tissue Pathology With Glycosylation Disorders
Chronic Graft Versus Host Myopathies: Noninflammatory, Multi-Tissue Pathology With Glycosylation Disorders
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Chronic Graft Versus Host Myopathies: Noninflammatory, Multi-Tissue Pathology With Glycosylation Disorders

Pestronk, Alan

Journal of neuropathology and experimental neurology, 2020-01, Vol.79 (1), p.102-112 [Periódico revisado por pares]

England: Oxford University Press

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10
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy
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Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy

Harms, Matthew B. ; Sommerville, R. Brian ; Allred, Peggy ; Bell, Shaughn ; Ma, Duanduan ; Cooper, Paul ; Lopate, Glenn ; Pestronk, Alan ; Weihl, Conrad C. ; Baloh, Robert H.

Annals of neurology, 2012-03, Vol.71 (3), p.407-416 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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