Syndrome Fahr: Neurologic manifestation of endocrine disease
Author:
Publisher
Centre for Evaluation in Education and Science (CEON/CEES)
Subject
General Medicine
Link
https://scindeks-clanci.ceon.rs/data/pdf/1821-1925/2020/1821-19252077057M.pdf
Reference46 articles.
1. Manyam BV, Walters AS, Narla KR. Bilateral striopallidodentate calcinosis: clinical characteristics of patients seen in a registry. Movement disorders: official journal of the Movement Disorder Society 2001; 16(2): 258-264;
2. Moskowitz MA, Winickoff RN, Heinz ER. Familial calcification of the basal ganglions: a metabolic and genetic study. N Engl J Med 1971. 285(2): 72-77;
3. Ellie E, Julien J, Ferrer X. Familial idiopathic striopallidodentate calcifications. Neurology 1989, 39(3): 381-385;
4. Manyam BV. What is and what is not 'Fahr's disease'. Parkinsonism Relat Disord 2005. 11(2): 73-80;
5. Yamada N, Hayashi T. Asymptomatic familial basal ganglia calcification with autosomal dominant inheritance: a family report. No to hattatsu Brain and development 2000; 32(6): 515-519;
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