Results 61 to 70 of about 5,851 (166)

Inborn errors of immunity in children with neuroinflammation

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Inborn errors of immunity (IEIs), an expanding group of monogenic disorders with diverse clinical manifestations, are increasingly recognized to include neuroinflammatory disease. Examples of diseases included under this umbrella are Aicardi–Goutières syndrome, deficiency of adenosine deaminase 2, familial haemophagocytic lymphohistiocytosis ...
Eppie M Yiu   +5 more
wiley   +1 more source

ULTRASONOGRAPHIC CHANGES AFTER INDIRECT REVASCULARIZATION SURGERY IN PEDIATRIC PATIENTS WITH MOYAMOYA DISEASE

open access: yes, 2017
The marked cerebral hypoperfusion of moyamoya disease (MMD) can be treated with encephaloduroarteriosynangiosis (EDAS), an indirect revascularization surgery.
Yeh, Shin-Joe;Tang, Sung-Chun;Tsai, Li-Kai;Chen, Ya-Fang;Liu, Hon-Man;Chen, Ying-An;Hsieh, Yu-Lin;Yang, Shih-Hung;Tien, Yu-Hsuan;Yang, Chi-Cheng;Kuo, Meng-Fai;Jeng, Jiann-Shing   +1 more
core   +1 more source

Enfermedad de moyamoya: a propósito de un caso

open access: yesActa Neurológica Colombiana, 2016
La enfermedad de moyamoya (EMM) es una patología crónica caracterizada por la oclusión progresiva de la vasculatura cerebral y no aterosclerótica, generando un patrón angiográfico conocido como moyamoya, que en japonés hace alusión a la apariencia en ...
Ledmar Jovanny Vargas R   +3 more
doaj   +1 more source

Acute Ischemic Stroke in Moyamoya Syndrome Associated with Thyrotoxicosis [PDF]

open access: yesJournal of Neurocritical Care, 2018
Background A few cases of moyamoya syndrome associated with thyrotoxicosis have been reported. However, studies on the association of hyperthyroidism with moyamoya syndrome are insufficient. Case Report Here we report a case of hyperthyroidism associated
Donggook Kang   +5 more
doaj   +1 more source

Bioinformatics Strategies to Identify Shared Molecular Biomarkers That Link Ischemic Stroke and Moyamoya Disease with Glioblastoma

open access: yesPharmaceutics, 2022
Expanding data suggest that glioblastoma is accountable for the growing prevalence of various forms of stroke formation, such as ischemic stroke and moyamoya disease. However, the underlying deterministic details are still unspecified.
Md Khairul Islam   +8 more
doaj   +1 more source

Perinatal complications, mode of delivery, and neurological morbidity in children with COL4A1/A2 variants

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Aim To characterize reported perinatal complications and childhood neurological diagnoses among children with COL4A1/2 variants and explore associations between mode of delivery and selected neurological outcomes. Method This was a retrospective cross‐sectional patient registry study using surveys collected through the Gould Syndrome ...
Shraddha Pandey   +3 more
wiley   +1 more source

Patient perspective on large-language model responses to questions about Moyamoya

open access: yesActa Neurochirurgica
Purpose Large Language Models (LLMs) are widely used and accessible. We investigate whether publicly available LLMs provide useful, safe, helpful and accurate information to the non-expert general community seeking answers about moyamoya. Methods ChatGPT-
Marcella R. Ruppert-Gomez   +8 more
doaj   +1 more source

Circulating choline pathway nutrients and risk of moyamoya disease

open access: yesFrontiers in Nutrition, 2022
BackgroundCirculating choline pathway nutrients play a critical role in first stroke and recurrent stroke. However, there is limited information available on the effects of choline pathway nutrients on the risk of moyamoya disease (MMD) and its subtypes.
Peicong Ge   +48 more
doaj   +1 more source

[Moyamoya disease].

open access: yesDer Radiologe, 2005
Moyamoya disease is an idiopathic progressive vasculopathy characterized by slowly progressive narrowing involving the distal internal carotid artery and the proximal circle of Willis. Collateral vessels develop to compensate for the slowly progressive stenosis.
Papanagiotou, P   +4 more
openaire   +3 more sources

Loose Anagen Hair Syndrome: A Scoping Review

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Loose anagen hair syndrome (LAHS) is a rare, non‐scarring alopecia that may occur sporadically or follow autosomal dominant inheritance. The objective of this study was to review the etiology, clinical presentation, diagnostic features (including trichoscopy, trichogram, and microscopy), natural history, and treatment outcomes of LAHS.
Romy Shenderey   +12 more
wiley   +1 more source

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