Literature DB >> 4873809

Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.

F A Hommes, H A Polman, J D Reerink.   

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Year:  1968        PMID: 4873809      PMCID: PMC2019984          DOI: 10.1136/adc.43.230.423

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


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  10 in total

1.  SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY. CASE REPORT WITH SPECIAL EMPHASIS ON ASSOCIATED PATHOLOGY OF PERIPHERAL NERVOUS SYSTEM.

Authors:  H NAMIKI
Journal:  Arch Neurol       Date:  1965-01

2.  PYRUVATE CARBOXYLASE. I. NATURE OF THE REACTION.

Authors:  M F UTTER; D B KEECH
Journal:  J Biol Chem       Date:  1963-08       Impact factor: 5.157

3.  Mammalian liver phosphoneolpyruvate carboxykinase activities.

Authors:  R C NORDLIE; H A LARDY
Journal:  J Biol Chem       Date:  1963-07       Impact factor: 5.157

4.  A disease in infants resembling chronic Wernicke's encephalopathy.

Authors:  I FEIGIN; A WOLF
Journal:  J Pediatr       Date:  1954-09       Impact factor: 4.406

5.  Subacute necrotizing encephalomyelopathy in an infant.

Authors:  D LEIGH
Journal:  J Neurol Neurosurg Psychiatry       Date:  1951-08       Impact factor: 10.154

6.  Leigh's subacute necrotizing encephalopathy: clinical and biochemical study, with special reference to therapy with lipoate.

Authors:  B E Clayton; R H Dobbs; A D Patrick
Journal:  Arch Dis Child       Date:  1967-10       Impact factor: 3.791

7.  Lactic acidosis with necrotizing encephalopathy in two sibs.

Authors:  H E Worsley; R W Brookfield; J S Elwood; R L Noble; W H Taylor
Journal:  Arch Dis Child       Date:  1965-10       Impact factor: 3.791

8.  A Wernicke-like encephalomyelopathy in children (Leigh), an inborn error of metabolism? Report of 5 cases with emphasis on its familial incidence.

Authors:  E J Ebels; E J Blokzijl; J A Troelstra
Journal:  Helv Paediatr Acta       Date:  1965-07

9.  Infantile necrotizing encephalomyelopathy (Leigh).

Authors:  J P Lakke; E J Ebels; O J ten Thye
Journal:  Arch Neurol       Date:  1967-03

10.  Effects of fatty acids, ketone bodies, lactate and pyruvate on glucose utilization by guinea-pig cerebral cortex slices.

Authors:  F S Rolleston; E A Newsholme
Journal:  Biochem J       Date:  1967-08       Impact factor: 3.857

  10 in total
  37 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.  Mitochondrial DNA 11777C>A mutation associated Leigh syndrome: case report with a review of the previously described pedigrees.

Authors:  Kinga Hadzsiev; Anita Maasz; Peter Kisfali; Endre Kalman; Eva Gomori; Endre Pal; Ervin Berenyi; Katalin Komlosi; Bela Melegh
Journal:  Neuromolecular Med       Date:  2010-05-26       Impact factor: 3.843

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.  Cytochrome c oxidase deficiency in three patients with Leigh's disease.

Authors:  M Di Rocco; E Veneselli; M O Ciccone; A Taccone; M Stroppiano; F Cottafava
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

5.  A case of pyruvate carboxylase deficiency with later prenatal diagnosis of an unaffected sibling.

Authors:  A Tsuchiyama; K Oyanagi; S Hirano; N Tachi; H Sogawa; K Wagatsuma; T Nakao; S Tsugawa; Y Kawamura
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

6.  Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuria.

Authors:  J Oizumi; K N Shaw; T A Giudici; M Carter; G N Donnell; W G Ng
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

7.  Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathy.

Authors:  B Barbiroli; R Medori; H J Tritschler; T Klopstock; P Seibel; H Reichmann; S Iotti; R Lodi; P Zaniol
Journal:  J Neurol       Date:  1995-07       Impact factor: 4.849

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.  Pyruvate carboxylase deficiency.

Authors:  K Bartlett; H K Ghneim; J H Stirk; G Dale; K G Alberti
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

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