Literature DB >> 3794742

Kearns-Sayre syndrome, hypoparathyroidism, and basal ganglia calcification.

A G Dewhurst, D Hall, M S Schwartz, R O McKeran.   

Abstract

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Year:  1986        PMID： 3794742      PMCID： PMC1029089          DOI： 10.1136/jnnp.49.11.1323

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  4 in total

1.  Hydrocephalus caused by increased intracranial venous pressure: a clinicopathological study.

Authors:  N P Rosman; K N Shands
Journal:  Ann Neurol       Date:  1978-05       Impact factor: 10.422

2.  Computed tomography in oculocraniosomatic disease (Kearns-Sayre syndrome).

Authors:  R S Seigel; J F Seeger; T O Gabrielsen; R J Allen
Journal:  Radiology       Date:  1979-01       Impact factor: 11.105

3.  Oculocraniosomatic neuromuscular disease with hypoparathyroidism.

Authors:  M Toppet; N Telerman-Toppet; H B Szliwowski; M Vainsel; C Coers
Journal:  Am J Dis Child       Date:  1977-04

4.  Basal ganglia calcifications on CT: relation to hypoparathyroidism.

Authors:  C Sachs; H E Sjöberg; K Ericson
Journal:  Neurology       Date:  1982-07       Impact factor: 9.910
  4 in total
  5 in total

1.  Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

Authors:  C Doriguzzi; L Palmucci; T Mongini; N Bresolin; L Bet; G Comi; R Lala
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-01       Impact factor: 10.154

2.  De Toni-Debré-Fanconi syndrome in a patient with Kearns-Sayre syndrome: a case report.

Authors:  Cristina Maria Mihai; Doina Catrinoiu; Marius Toringhibel; Ramona Mihaela Stoicescu; Anca Hancu
Journal:  J Med Case Rep       Date:  2009-11-03

3.  Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity.

Authors:  C G Bönnemann; P Meinecke; H Reich
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

Review 4.  Mitochondrial DNA mutations in renal disease: an overview.

Authors:  Larissa P Govers; Hakan R Toka; Ali Hariri; Stephen B Walsh; Detlef Bockenhauer
Journal:  Pediatr Nephrol       Date:  2020-01-10       Impact factor: 3.714

Review 5.  Endocrine disorders in mitochondrial disease.

Authors:  Andrew M Schaefer; Mark Walker; Douglass M Turnbull; Robert W Taylor
Journal:  Mol Cell Endocrinol       Date:  2013-06-13       Impact factor: 4.102
  5 in total

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