Results 111 to 120 of about 54,758 (258)

Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro, Shiwen Koay, Gordon T. Ingle, Patricia McNamara, Laura Watson, Fion Bremner, Valeria Iodice   +6 more
wiley   +1 more source

Wilson's Disease; Clinical Presentations among Patients Attending Gastroenterology Clinic/ Baghdad Teaching Hospital

مجله كليه طب الكندي, 2013
Background:Wilson’s disease (WD) is an inherited disorder of copper metabolism that is characterized by tremendous variation in the clinical presentation.
Ahmed Kh . Mohammed, Akram Ajeel Najeeb, Wafaa Faeq Tawfeeq   +2 more
doaj  

Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study. [PDF]

Arch Iran Med, 2023
Haji Esmaeil Memar E, Heidari M, Ghabeli H, Pourbakhtyaran E, Haghighi R, Hosseiny SMM, Mamishi S, Mahmoudi S, Eshaghi H, Tavasoli AR, Mohammadi M, Shervin Badv R, Zamani G, Ghahvehchi Akbari M, Yarali B, Shirzadi R, Mohammadpour M, Yaghmaei B, Sharifzadeh Ekbatani M, Najafi Z, Ashrafi MR.   +20 more
europepmc   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

COVID-19 and neurologic manifestations: a synthesis from the child neurologist's corner. [PDF]

World J Pediatr, 2022
Valderas C, Méndez G, Echeverría A, Suarez N, Julio K, Sandoval F.   +5 more
europepmc   +1 more source

Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon, Hugues Chabriat, Dominique Hervé, Stéphanie Guey, Sophie Tezenas Du Montcel, Juliette Ortholand   +5 more
wiley   +1 more source

A case of adenosine deaminase-negative severe combined immunodeficiency with neurological abnormalities

The Turkish Journal of Pediatrics, 1995
Presented here is a 17-month-old adenosine deaminase-deficient, severe combined immunodeficient patient with chest symptoms, oral ulcer, neurologic manifestations, head lag, spasticity and developmental delay in motor functions.
I Tezcan, F Ersoy, M Cağlar, O Sanal, E Kotiloğlu, S Aysun   +5 more
doaj  

Neurologic Manifestations of the Antiphospholipid Syndrome - an Update. [PDF]

Curr Neurol Neurosci Rep, 2021
Leal Rato M, Bandeira M, Romão VC, Aguiar de Sousa D.   +3 more
europepmc   +1 more source

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li, Dong‐Lin Liang, Li‐Ping Gao, Wei‐Wei Zhang, Wei Zhou, A. Ruhan, Bing Xu, Run‐Dong Cao, Kang Xiao, Cao Chen, Qi Shi, Xiao‐Ping Dong   +11 more
wiley   +1 more source

Rise of Neurologic Manifestations During SARS-CoV-2 Omicron Wave in Children With COVID-19. [PDF]

Pediatr Infect Dis J, 2023
Dimopoulou D, Dimopoulou D, Dasoula F, Liaska M, Eleftheriou I, Maritsi D, Tsolia M, Vartzelis G.   +7 more
europepmc   +1 more source