Literature DB >> 9925853

Moyamoya syndrome in children with Alagille syndrome: additional evidence of a vasculopathy.

A R Woolfenden1, G W Albers, G K Steinberg, J S Hahn, D C Johnston, K Farrell.   

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Year:  1999        PMID: 9925853     DOI: 10.1542/peds.103.2.505

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


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  12 in total

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Review 4.  Genetic and Proteomic Contributions to the Pathophysiology of Moyamoya Angiopathy and Related Vascular Diseases.

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5.  Occlusion of Internal Carotid Artery in Kimura's Disease.

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6.  Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension.

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7.  Multiple cerebral aneurysms and subarachnoid hemorrhage in a patient with Alagille syndrome.

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8.  Atherosclerosis causing recurrent catastrophic aortopulmonary shunt dehiscence in a patient with Alagille syndrome.

Authors:  L May; F L Hanley; A J Connolly; S Reddy
Journal:  Pediatr Cardiol       Date:  2012-08-26       Impact factor: 1.655

9.  Molecular and comparative genetics of mental retardation.

Authors:  Jennifer K Inlow; Linda L Restifo
Journal:  Genetics       Date:  2004-02       Impact factor: 4.562

Review 10.  Moyamoya disease and syndromes: from genetics to clinical management.

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