Severe hyperhomocysteinemia manifesting as moyamoya vasculopathy and Henoch-Schonlein purpura
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Reference7 articles.
1. Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial Disease
2. Nephrotic syndrome and thrombotic microangiopathy caused by cobalamin C deficiency;Koenig;Pediatr Nephrol,2015
3. Moyamoya syndrome associated with Henoch-Schönlein purpura;Shiari;Iran J Child Neurol,2016
4. Quasi-Moyamoya disease and heterozygosity for homocystinuria in a five-year-old girl;van Diemen-Steenvoorde;Neuropediatrics,1990
5. A case of homocystinuria misdiagnosed as moyamoya disease: a case report;Erol;Iran Red Crescent Med J,2016
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2. Risk factors of renal trauma in children with severe Henoch-Schonlein purpura and effect of mycophenolate mofetil on pediatric renal function;Translational Pediatrics;2021-12
3. Western Moyamoya Phenotype: A Scoping Review;Cureus;2021-11-22
4. Author response: Severe hyperhomocysteinemia manifesting as moyamoya vasculopathy and Henoch-Schonlein purpura;Neurology;2019-06-03
5. Reader response: Severe hyperhomocysteinemia manifesting as moyamoya vasculopathy and Henoch-Schonlein purpura;Neurology;2019-06-03
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