Artikel dengan mandat akses publik - Alan PestronkPelajari lebih lanjut
Tidak tersedia di mana pun: 9
A phase I/IItrial of MYO‐029 in adult subjects with muscular dystrophy
KR Wagner, JL Fleckenstein, AA Amato, RJ Barohn, K Bushby, ...
Annals of neurology 63 (5), 561-571, 2008
Mandat: US National Institutes of Health
Peripheral nerve size in normals and patients with polyneuropathy: an ultrasound study
CM Zaidman, M Al‐Lozi, A Pestronk
Muscle & Nerve: Official Journal of the American Association of …, 2009
Mandat: US National Institutes of Health
Clinical features of late‐onset Pompe disease: A prospective cohort study
JHJ Wokke, DM Escolar, A Pestronk, KM Jaffe, GT Carter, ...
Muscle & Nerve: Official Journal of the American Association of …, 2008
Mandat: US National Institutes of Health
Nerve size in chronic inflammatory demyelinating neuropathy varies with disease activity and therapy response over time: a retrospective ultrasound study
CM Zaidman, A Pestronk
Muscle & nerve 50 (5), 733-738, 2014
Mandat: US National Institutes of Health
Calibrated quantitative ultrasound imaging of skeletal muscle using backscatter analysis
CM Zaidman, MR Holland, CC Anderson, A Pestronk
Muscle & Nerve: Official Journal of the American Association of …, 2008
Mandat: US National Institutes of Health
Cryptogenic small‐fiber neuropathies: serum autoantibody binding to trisulfated heparan disaccharide and fibroblast growth factor receptor‐3
TD Levine, J Kafaie, LA Zeidman, DS Saperstein, R Massaquoi, RJ Bland, ...
Muscle & Nerve 61 (4), 512-515, 2020
Mandat: US National Institutes of Health
Mitochondrial pathology in immune and inflammatory myopathies
AS Varadhachary, CC Weihl, A Pestronk
Current opinion in rheumatology 22 (6), 651-657, 2010
Mandat: US National Institutes of Health
Newborn brachial plexus palsy: evaluation of severity using quantitative ultrasound of muscle
CM Zaidman, MR Holland, MJ Noetzel, TS Park, A Pestronk
Muscle & Nerve 47 (2), 246-254, 2013
Mandat: US National Institutes of Health
Coenzyme Q10 deficiency in children: Frequent type 2C muscle fibers with normal morphology
RB Sommerville, CM Zaidman, A Pestronk
Muscle & nerve 48 (5), 722-726, 2013
Mandat: US National Institutes of Health
Tersedia di suatu tempat: 80
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
HJ Kim, NC Kim, YD Wang, EA Scarborough, J Moore, Z Diaz, ...
Nature 495 (7442), 467-473, 2013
Mandat: US National Institutes of Health
TDP‐43 A315T mutation in familial motor neuron disease
MA Gitcho, RH Baloh, S Chakraverty, K Mayo, JB Norton, D Levitch, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
Mandat: US National Institutes of Health
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
TM Miller, A Pestronk, W David, J Rothstein, E Simpson, SH Appel, ...
The Lancet Neurology 12 (5), 435-442, 2013
Mandat: US National Institutes of Health
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ...
Nature neuroscience 17 (5), 664-666, 2014
Mandat: US National Institutes of Health, Motor Neurone Disease Association, UK, UK …
Phase 1–2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS
T Miller, M Cudkowicz, PJ Shaw, PM Andersen, N Atassi, RC Bucelli, ...
New England Journal of Medicine 383 (2), 109-119, 2020
Mandat: National Institute for Health Research, UK
224th ENMC International Workshop:: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14–16 October 2016
Y Allenbach, AL Mammen, O Benveniste, W Stenzel, A Amato, A Aussey, ...
Neuromuscular disorders 28 (1), 87-99, 2018
Mandat: Fondazione Telethon, Italy
Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study
CM McDonald, EK Henricson, RT Abresch, T Duong, NC Joyce, F Hu, ...
The Lancet 391 (10119), 451-461, 2018
Mandat: US Department of Defense, US National Institutes of Health, US Department of …
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort
KM Flanigan, DM Dunn, A Von Niederhausern, P Soltanzadeh, ...
Human mutation 30 (12), 1657-1666, 2009
Mandat: US National Institutes of Health
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia
CC Weihl, P Temiz, SE Miller, G Watts, C Smith, M Forman, PI Hanson, ...
Journal of Neurology, Neurosurgery & Psychiatry 79 (10), 1186-1189, 2008
Mandat: US National Institutes of Health
TREM2 variant p. R47H as a risk factor for sporadic amyotrophic lateral sclerosis
J Cady, ED Koval, BA Benitez, C Zaidman, J Jockel-Balsarotti, P Allred, ...
JAMA neurology 71 (4), 449-453, 2014
Mandat: US National Institutes of Health
Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III
P Kaufmann, JLP Thompson, G Levy, R Buchsbaum, J Shefner, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
Mandat: US National Institutes of Health
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