Literature DB >> 5034864

Pathogenesis of Leigh's encephalomyelopathy.

T T Tang, T A Good, P R Dyken, S D Johnsen, S R McCreadie, S T Sy, H A Lardy, F B Rudolph.   

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Year:  1972        PMID： 5034864     DOI： 10.1016/s0022-3476(72)80428-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  13 in total

1.  Leigh's disease: significance of the biochemical changes in brain.

Authors:  J V Murphy; L Craig
Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-11       Impact factor: 10.154

2.  Pyruvate carboxylase defect: metabolic studies on cultured skin fibroblasts.

Authors:  J Oizumi; W G Ng; G N Donnell
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.

Authors:  K Tada; G Takada; K Omura; Y Itokawa
Journal:  Eur J Pediatr       Date:  1978-01-17       Impact factor: 3.183

4.  Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.

Authors:  S Miyabayashi; T Ito; K Narisawa; K Iinuma; K Tada
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

5.  Hepatic glycogen synthetase deficiency.

Authors: 
Journal:  Arch Dis Child       Date:  1973-02       Impact factor: 3.791

Review 6.  The biotin-dependent carboxylase deficiencies.

Authors:  B Wolf; G L Feldman
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

7.  Biotinidase deficiency: a survey of 10 cases.

Authors:  H J Wastell; K Bartlett; G Dale; A Shein
Journal:  Arch Dis Child       Date:  1988-10       Impact factor: 3.791

8.  Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.

Authors:  P M van Erven; F J Gabreëls; W Ruitenbeek; W O Renier; K J Lamers; J L Sloof
Journal:  J Neurol       Date:  1987-05       Impact factor: 4.849

9.  Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid.

Authors:  H Maesaka; K Komiya; K Misugi; K Tada
Journal:  Eur J Pediatr       Date:  1976-05-04       Impact factor: 3.183

10.  Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosis.

Authors:  A Oldfors; M Tulinius; E Holme; H Kalimo; B Kristiansson; B O Eriksson
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088
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