Results 161 to 170 of about 7,742,036 (343)

Evaluation of the Efficacy and Safety of Satralizumab in a Pregnant NMOSD Patient With AQP4/MOG‐IgG Dual Seropositive: A Case Report

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Neuromyelitis Optica Spectrum Disorder (NMOSD) is a chronic autoimmune neuroinflammatory disease, typically characterized by antibodies against aquaporin 4 (AQP4‐IgG) or myelin oligodendrocyte glycoprotein (MOG‐IgG). Simultaneous seropositivity for both antibodies in a single patient is exceedingly rare.
Yeting Luo, Shuhua Xie, Xianghong Liu
wiley   +1 more source

Cystoid Macular Edema as Manifestation of Smoldering Multiple Myeloma: A Case Report. [PDF]

J Vitreoretin Dis
Pandiri S, Meshkin RS, Chaaya C, Dorsey HG, Hoyek S, Zekavat SM, Patel NA.   +6 more
europepmc   +1 more source

Predicting Epileptogenic Tubers in Patients With Tuberous Sclerosis Complex Using a Fusion Model Integrating Lesion Network Mapping and Machine Learning

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Accurate localization of epileptogenic tubers (ETs) in patients with tuberous sclerosis complex (TSC) is essential but challenging, as these tubers lack distinct pathological or genetic markers to differentiate them from other cortical tubers.
Tinghong Liu, Qi Wang, Suhui Kuang, Dezhi Cao, Ping Ding, Shaohui Zhang, Haihua Wei, Zhirong Wei, Jinshan Xu, Xinyu Huang, Bing Liu, Shuli Liang   +11 more
wiley   +1 more source

Myelodysplastic Syndrome With Complex Chromosomal Karyotype Abnormalities Complicated by Multiple Intestinal Perforations: A Case Report and Literature Review. [PDF]

Case Rep Gastrointest Med
Niu ZY, Zhu MF, Tao M, Zhang C, Gu F, Li J.   +5 more
europepmc   +1 more source

Multiple Ocular Abnormalities Associated with Trisomy 4p

, 2008
Samin Hong, Sung Yong Kang, Gong Je Seong, Joo Youn Shin, Chan Yun Kim   +4 more
openalex   +2 more sources

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron, Nicholas E. Clifton, Daniel Cabezas de la Fuente, Peter Holmans, Nicholas J. Bray, Kathryn J. Peall   +5 more
wiley   +1 more source

Central neurological abnormalities and multiple chemical sensitivity caused by chronic toluene exposure [PDF]

, 2003
Yungling Leo Lee
openalex   +1 more source

Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings.

Journal of Medical Genetics, 1980
R. Bernstein, Trefor Jenkins, B. Dawson, Joan WAGNERt, Gordon Dewald, Gloria C Koo, Stephen S. Wachtel   +6 more
semanticscholar   +1 more source

An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco, Caterina Motta, Enrica Marchionni, Maria Rosaria D'Apice, Carlangelo Carrese, Giuseppe Novelli, Alessandro Martorana, Chiara Giuseppina Bonomi   +7 more
wiley   +1 more source

CerviHFENet: hybrid feature extraction-based deep learning for multi-label classification of upper cervical spine abnormalities in X-ray imaging. [PDF]

BMC Med Imaging
Wang Z, Zhang C, Zhu X, Niu K, Liu S, Wang S, Zhou X, Wang D, Xu N, He Z.   +9 more
europepmc   +1 more source