Literature DB >> 1553246

Mitochondrial disorders in pediatrics. Clinical, biochemical, and genetic implications.

L A Clarke1.   

Abstract

Disorders secondary to mitochondrial dysfunction are likely to be common in the population. The clinical aspects of these disorders are varied and may follow nonclassic inheritance patterns. These disorders serve to illustrate the importance of the clinical history and family history in directing diagnostic approaches.

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Year:  1992        PMID: 1553246     DOI: 10.1016/s0031-3955(16)38297-9

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  4 in total

1.  Multiple presentation of mitochondrial disorders.

Authors:  A Nissenkorn; A Zeharia; D Lev; A Fatal-Valevski; V Barash; A Gutman; S Harel; T Lerman-Sagie
Journal:  Arch Dis Child       Date:  1999-09       Impact factor: 3.791

Review 2.  Familial atrioventricular septal defect: possible genetic mechanisms.

Authors:  A Kumar; C A Williams; B E Victorica
Journal:  Br Heart J       Date:  1994-01

3.  Controversies in counseling for mitochondrial conditions.

Authors:  A Kupelian; R E Falk; J Klein; P Fournier; N Fischel-Ghodsian
Journal:  J Genet Couns       Date:  1996-03       Impact factor: 2.537

4.  Clinical presentations of mitochondrial cardiomyopathies.

Authors:  D Lev; A Nissenkorn; E Leshinsky-Silver; M Sadeh; A Zeharia; B-Z Garty; L Blieden; V Barash; T Lerman-Sagie
Journal:  Pediatr Cardiol       Date:  2004-06-08       Impact factor: 1.655

  4 in total

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