Genetics of Familial Idiopathic Basal Ganglia Calcification (FIBGC)-Reference-Cited by-同舟云学术

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Genetics of Familial Idiopathic Basal Ganglia Calcification (FIBGC)

Published:2003 Issue: Volume: Page:443-450
ISSN:
Container-title:Genetics of Movement Disorders
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Author:

Sobrido Maria-Jesus,Geschwind Daniel H.

Publisher

Elsevier

Reference63 articles.

1. Histochemical studies on the pathogenesis of idiopathic non-arteriosclerotic cerebral calcification;Adachi;J. Neuropathol. Exp. Neurol.,1968

2. A case of Fahr's disease: clinical and CT study;Aiello;Ital. J. Neurol. Sci.,1981

3. MRI demonstration and CT correlation of the brain in patients with idiopathic intracerebral calcification;Avrahami;J. Neurol.,1994

4. Idiopathic familial cerebrovascular ferrocalcinosis (Fahr's disease) and review of differential diagnosis of intracranial calcification in children;Babbitt;Am. J. Roentg. Rad. Ther. Nucl. Med.,1969

5. Abnormal systemic metabolism of iron, porphyrin, and calcium in Fahr's disease;Beall;Ann. Neurol.,1989

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. XPR1 mutations are a rare cause of primary familial brain calcification;Journal of Neurology;2016-05-26

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