Results 61 to 70 of about 5,183,178 (176)
Moyamoya disease is a clinical entity characterized by progressive cerebrovascular occlusion with spontaneous development of a collateral vascular network called Moyamoya vessels. This disease mainly manifests as cerebral ischemia.
Soumya Patra +3 more
doaj +1 more source
ABSTRACT Primary cutaneous gamma‐delta T‐cell lymphoma (PCGD‐TCL) is a rare cytotoxic lymphoma with key oncogenic drivers in the JAK/STAT pathway. Also primarily involving the subcutaneous adipose tissue, subcutaneous panniculitis‐like T‐cell lymphoma (SPTCL) is more frequently encountered in scenarios of autoimmune disorders.
Bennett Christie‐Nguyen +6 more
wiley +1 more source
Current Understanding of Moyamoya Disease (MMD) and Associated Neuropsychiatric Outcomes
Alexei Antonov,1,* Anthony Terraciano,1,* Muhammed Amir Essibayi,2,3 Kainaat Javed,2 David J Altschul2,3 1Albert Einstein College of Medicine, Bronx, NY, USA; 2Department of Neurosurgery, Montefiore Medical Center, Albert Einstein College of ...
Javed K +4 more
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Atypical postoperative radiographical findings in a patient with moyamoya disease: A case report
Moyamoya disease is a chronic cerebrovascular disease characterized by spontaneous and progressive stenosis or occlusion of the internal carotid artery and its branches.
Masaki Ikegami, MD +4 more
doaj +1 more source
Inborn errors of immunity in children with neuroinflammation
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
Moyamoya disease associated with polycystic kidney disease and eosinophilic granuloma.
Moyamoya disease has been associated with renal artery stenosis, cerebral hemorrhage, and multiple cranial traumas. We report a unique case of moyamoya disease associated with polycystic kidney disease and eosinophilic granuloma. Although the etiology of
J M Massey, J B Pracyk
core +1 more source
Adult onset moyamoya disease: institutional experience.
Moyamoya disease is a progressive steno-occlusive disease of bilateral carotid forks with the formation of fine collateral vascular network and is an angiographic diagnosis. We analyzed case records of 11 patients with "adult-onset moyamoya disease." Six
KJ Harsha +9 more
core +3 more sources
Distinctive facial features in idiopathic Moyamoya disease in Caucasians: a first systematic analysis [PDF]
Background Craniofacial dysmorphic features are morphological changes of the face and skull which are associated with syndromic conditions. Moyamoya angiopathy is a rare cerebral vasculopathy that can be divided into Moyamoya syndrome, which is ...
Markus Kraemer +5 more
doaj +2 more sources
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
Diagnosis and Management of Moyamoya Disease
Moyamoya disease is an uncommon vascular disease, which causes obstruction and stenosis of arteries of the circle of Willis, and preferentially affects children and young adults. This disease is seen across the world, but is more common in East Asia.
Shinichiro Uchiyama +4 more
doaj +1 more source

