Scheie Syndrome Diagnosed After Cerebral Infarction-Reference-Cited by-同舟云学术

Scheie Syndrome Diagnosed After Cerebral Infarction

Published:2012-05 Issue:4 Volume:21 Page:330-332
ISSN:1052-3057
Container-title:Journal of Stroke and Cerebrovascular Diseases
language:en
Short-container-title:Journal of Stroke and Cerebrovascular Diseases

Author:

Fujii Daiki,Manabe Yasuhiro,Tanaka Tomotaka,Kono Syoichiro,Sakai Yasuko,Narai Hisashi,Omori Nobuhiko,Furujyo Mahoko,Abe Koji

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Rehabilitation,Surgery

Reference8 articles.

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2. Guidelines for the management of mucopolysaccharidosis type I;Martins;J Pediatr,2009

3. Attenuated type I mucopolysaccharidosis in the different diagnosis of juvenile idiopathic arthritis: A series of 13 patients with Scheie syndrome;Climaz;Clin Exp Rheumatol,2006

4. Legg-Perthes disease-like joint involvement and diagnosis delay in Scheie syndrome: A case report;Melikoglu;Clin Rheumatol,2007

5. Neurological findings in Hunter disease: Pathology and possible therapeutic effects reviewed;Al Sawaf;J Inherit Metab Dis,2008

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1. Clinical and neuroimaging review of monogenic cerebral small vessel disease from the prenatal to adolescent developmental stage;Japanese Journal of Radiology;2023-10-17

2. Case Report: Cerebral Revascularization in a Child With Mucopolysaccharidosis Type I;Frontiers in Pediatrics;2021-06-10

3. Acute Arterial Ischemic Stroke in a Treated Child with Hunter's Syndrome: A Case Report and Review of the Literature;Journal of Pediatric Neurology;2021-01-13

4. Cardiac rhythm abnormalities - An underestimated cardiovascular risk in adult patients with Mucopolysaccharidoses;Molecular Genetics and Metabolism;2020-06

5. Agreement between the results of meta-analyses from case reports and from clinical studies regarding the efficacy of laronidase therapy in patients with mucopolysaccharidosis type I who initiated enzyme replacement therapy in adult age: An example of case reports meta-analyses as an useful tool for evidence-based medicine in rare diseases;Molecular Genetics and Metabolism;2018-02