Results 191 to 200 of about 9,406,168 (354)

Misdiagnosis of Susac syndrome as demyelinating disease and primary angiitis of the central nervous system: A case report. [PDF]

Front Neurol, 2022
Wu G, Jiang W, Li Z, Huang D, Wu L.
europepmc   +1 more source

Broadening the Clinical Spectrum of Axonal Hereditary Neuropathies: A Comparative Case Study on DNAJB2‐ and HINT1‐Related Disease

Journal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.
ABSTRACT Background and Aims Differentiating hereditary axonal polyneuropathies caused by distinct gene variants remains a clinical challenge. This comparative case study of DNAJB2‐ and HINT1‐related neuropathies aimed to broaden the phenotypic spectrum associated with these genes and to explore non‐motor symptoms and quality of life (QoL) in affected ...
Bogdan Bjelica, Corinna Hendrich, Sandra von Hardenberg, Milica Vukojevic, Sonja Körner, Thomas Gschwendtberger, Aiden Haghikia, Stojan Peric, Susanne Petri   +8 more
wiley   +1 more source

Congestive myelopathy due to spinal dural arteriovenous fistula mimicking CNS demyelinating disease. [PDF]

J Cerebrovasc Endovasc Neurosurg, 2022
Kim N, Kim H, Kim H, Park J.
europepmc   +1 more source

Prolactin Receptor Deficiency Promotes Hypomyelination in White Matter Tracts During Postnatal Central Nervous System Maturation in Mice

Glia, Volume 74, Issue 2, February 2026.
Prolactin action is essential for proper myelination of white matter tracts during neonatal and prepubertal stages in mice. Lack of prolactin receptor (Prlr−/−) signaling leads to hypomyelination and impaired locomotor function. ABSTRACT A large wave of myelination in the central nervous system (CNS) of mammals occurs during postnatal development ...
Ana L. Ocampo‐Ruiz, José L. Dena‐Beltrán, Marco A. Dimas‐Rufino, Ximena Castillo, Dina I. Vazquez‐Carrillo, Andrea Silos‐Guajardo, Xarubet Ruiz‐Herrera, Edith Garay, Gonzalo Martínez de la Escalera, Carmen Clapp, Rogelio O. Arellano, Abraham J. Cisneros‐Mejorado, Yazmín Macotela   +12 more
wiley   +1 more source

Family Game Show-style Didactic for Teaching Nervous System Disorders during Emergency Medicine Training [PDF]

, 2020
Boysen Osborn, Megan, Brinley Rajagopal, Alaina, Sudario, Gabriel, Weiland, David   +3 more
core  

More on differential diagnosis of demyelinating and hereditary diseases

, 2020
А. С. Агафьина, А.Ю. Рудник, М.А. Федяков, О.С. Глотов, Т.Н. Кашко, Д.Г. Короткова, Galina Buyanova   +6 more
openalex   +1 more source

Chronic inflammatory demyelinating polyneuropathy as an autoimmune disease.

Journal of Autoimmunity, 2019
Yhojan Rodríguez, Nikhil Vatti, C. Ramírez-Santana, Christopher Chang, Oscar Mancera-Páez, M. Gershwin, J. Anaya   +6 more
semanticscholar   +1 more source

Aberrant Molecular Myelin Architecture in Charcot–Marie–Tooth Disease Type 1A and Hereditary Neuropathy With Liability to Pressure Palsies

Glia, Volume 74, Issue 2, February 2026.
PMP22 copy number variation disrupts myelin architecture at SLIs and Nodes of Ranvier. Adherens junction and axoglial domain defects are often more severe in CMT1A than HNPP. Findings support PMP22 functioning as a structural organizer of myelin. ABSTRACT Charcot–Marie–Tooth Disease Type 1A (CMT1A) and Hereditary Neuropathy with Liability to Pressure ...
Kathryn R. Moss, Marvis A. Arowolo, Dave R. Gutierrez, Ahmet Höke   +3 more
wiley   +1 more source

Demyelinating Disease of the Central Nervous System Concurrent With COVID-19. [PDF]

Cureus, 2021
Karsidag S, Sahin S, Ates MF, Cinar N, Kendirli S.   +4 more
europepmc   +1 more source

Selective Accumulation of Pro-Inflammatory T Cells in the Intestine Contributes to the Resistance to Autoimmune Demyelinating Disease

, 2014
Kerstin Berer, Marina Boziki, Gurumoorthy Krishnamoorthy   +2 more
openalex   +2 more sources