关注
Jennifer Orthmann-Murphy
Jennifer Orthmann-Murphy
在 pennmedicine.upenn.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex
EG Hughes, JL Orthmann-Murphy, AJ Langseth, DE Bergles
Nature neuroscience 21 (5), 696-706, 2018
4992018
Gap junctions couple astrocytes and oligodendrocytes
JL Orthmann-Murphy, CK Abrams, SS Scherer
Journal of Molecular Neuroscience 35, 101-116, 2008
2592008
Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins
JL Orthmann-Murphy, M Freidin, E Fischer, SS Scherer, CK Abrams
Journal of Neuroscience 27 (51), 13949-13957, 2007
2102007
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations
JL Orthmann-Murphy, E Salsano, CK Abrams, A Bizzi, G Uziel, ...
Brain 132 (2), 426-438, 2009
1712009
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus–Merzbacher-like disease
JL Orthmann-Murphy, AD Enriquez, CK Abrams, SS Scherer
Molecular and Cellular Neuroscience 34 (4), 629-641, 2007
1252007
Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone‐induced demyelination
EG Baxi, J DeBruin, J Jin, HJ Strasburger, MD Smith, ...
Glia 65 (12), 2087-2098, 2017
1002017
Remyelination alters the pattern of myelin in the cerebral cortex
J Orthmann-Murphy, CL Call, GC Molina-Castro, YC Hsieh, MN Rasband, ...
Elife 9, e56621, 2020
952020
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia: review of clinical manifestations as foundations for therapeutic development
S Papapetropoulos, A Pontius, E Finger, V Karrenbauer, DS Lynch, ...
Frontiers in neurology 12, 788168, 2022
452022
Gap junction disorders of myelinating cells
KA Kleopa, J Orthmann-Murphy, I Sargiannidou
Reviews in the Neurosciences 21 (5), 397-419, 2010
282010
Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource
RL Koch, C Soler-Alfonso, BT Kiely, A Asai, AL Smith, DS Bali, PB Kang, ...
Molecular genetics and metabolism 138 (3), 107525, 2023
202023
Temporal trends and yield of clinical diagnostic genetic testing in adult neurology
MH Guo, TM Bardakjian, MR Brzozowski, SS Scherer, C Quinn, L Elman, ...
American Journal of Medical Genetics Part A 185 (10), 2922-2928, 2021
182021
Therapeutic application of monoclonal antibodies in multiple sclerosis
JL Orthmann‐Murphy, PA Calabresi
Clinical Pharmacology & Therapeutics 101 (1), 52-64, 2017
172017
Motor learning and physical exercise in adaptive myelination and remyelination
MS Bloom, J Orthmann-Murphy, JB Grinspan
ASN neuro 14, 17590914221097510, 2022
142022
The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population
W Mu, N Schiess, JL Orthmann-Murphy, AW El-Hattab
Journal of Neurogenetics 33 (1), 21-26, 2019
142019
Novel mutation in the KCNJ10 gene in three siblings with seizures, ataxia and no electrolyte abnormalities
MA Al Dhaibani, AW El-Hattab, KB Holroyd, J Orthmann-Murphy, ...
Journal of neurogenetics 32 (1), 1-5, 2018
142018
Pelizaeus-Merzbacher-like disease 1
N Nahhas, A Conant, J Orthmann-Murphy, A Vanderver, G Hobson
122019
Clinical reasoning: a 70-year-old woman with acute-onset weakness and progressive hemiataxia
KC Schreck, JL Orthmann-Murphy, SD Newsome
Neurology 87 (22), e264-e268, 2016
62016
Disparities in genetic testing for neurologic disorders
A Baldwin, J Copeland, M Azage, L Dratch, K Johnson, RA Paul, ...
Neurology 102 (6), e209161, 2024
52024
Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States
LA Adang, JL Bonkowsky, JJ Boelens, E Mallack, R Ahrens-Nicklas, ...
Cytotherapy 26 (7), 739-748, 2024
42024
Genetic testing in adults with neurologic disorders: Indications, approach, and clinical impacts
L Dratch, M Azage, A Baldwin, K Johnson, RA Paul, TM Bardakjian, ...
Journal of neurology 271 (2), 733-747, 2024
42024
系统目前无法执行此操作,请稍后再试。
文章 1–20