Lombes A - Search Results

1

Clinical approach to inherited metabolic diseases in the neonatal period: a 20-year survey.

Saudubray JM, Ogier H, Bonnefont JP, Munnich A, Lombes A, Hervé F, Mitchel G, Thé BP, Specola N, Parvy P, et al. Saudubray JM, et al. Among authors: lombes a. J Inherit Metab Dis. 1989;12 Suppl 1:25-41. doi: 10.1007/BF01799284. J Inherit Metab Dis. 1989. PMID: 2509810

2

[Clinical approach to hereditary metabolic disorders in neonates. Review of 20 years' experience].

Saudubray JM, Ogier H, Bonnefont JP, Munich A, Lombes A, Hervé F, Mitchel G, Poll The B, Specola N, Parvy B, et al. Saudubray JM, et al. Among authors: lombes a. Cesk Pediatr. 1990 Jan;45(1):1-6. Cesk Pediatr. 1990. PMID: 2393916 Czech.

3

Hyperketotic states due to inherited defects of ketolysis.

Saudubray JM, Specola N, Middleton B, Lombes A, Bonnefont JP, Jakobs C, Vassault A, Charpentier C, Day R. Saudubray JM, et al. Among authors: lombes a. Enzyme. 1987;38(1-4):80-90. doi: 10.1159/000469194. Enzyme. 1987. PMID: 2894307 Review.

4

[Research methods in metabolic myopathies in children].

Lombes A, Ogier H, Bonnefont JP, Munnich A, Saudubray JM. Lombes A, et al. Ann Med Interne (Paris). 1987;138(6):441-3. Ann Med Interne (Paris). 1987. PMID: 3324848 Review. French. No abstract available.

5

The fasting test in paediatrics: application to the diagnosis of pathological hypo- and hyperketotic states.

Bonnefont JP, Specola NB, Vassault A, Lombes A, Ogier H, de Klerk JB, Munnich A, Coude M, Paturneau-Jouas M, Saudubray JM. Bonnefont JP, et al. Among authors: lombes a. Eur J Pediatr. 1990 Dec;150(2):80-5. doi: 10.1007/BF02072043. Eur J Pediatr. 1990. PMID: 2279514

6

[Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset].

Saudubray JM, Lyonnet S, Lombes A, Hervé F, Bonnefont JP, Munnich A, Ogier H. Saudubray JM, et al. Among authors: lombes a. J Genet Hum. 1989 Dec;37(4-5):299-310. J Genet Hum. 1989. PMID: 2635710 French. No abstract available.

7

[Apparently idiopathic primary myocardiopathies in children. The role of metabolic etiology].

Lombes A, Hervé F, Ogier H, Pellet A, Sidi D, Villain E, Kachaner J, Charpentier C, Paturneau-Jouas M, Fardeau M, et al. Lombes A, et al. Arch Fr Pediatr. 1987 Oct;44(8):569-78. Arch Fr Pediatr. 1987. PMID: 3442458 French.

8

A new case of methylmalonic aciduria with unexplained negative urinary methylmalonic colorimetric test.

Charpentier C, Coude M, Perignon JL, Lombes A, Saudubray JM, Divry P. Charpentier C, et al. Among authors: lombes a. J Inherit Metab Dis. 1986;9(4):408-9. doi: 10.1007/BF01800500. J Inherit Metab Dis. 1986. PMID: 3104683 No abstract available.

9

[Clinical variability and diagnosis steps in childhood mitochondrial disease].

Mercier S, Josselin de Wasch M, Labarthe F, Jardel C, Lombès A, Munnich A, Toutain A, Nivet H, Saliba E, Chantepie A, Castelnau P. Mercier S, et al. Among authors: lombes a. Arch Pediatr. 2009 Apr;16(4):322-30. doi: 10.1016/j.arcped.2008.12.024. Epub 2009 Feb 23. Arch Pediatr. 2009. PMID: 19233626 French.

10

de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency.

Ogier H, Lombes A, Scholte HR, Poll-The BT, Fardeau M, Alcardi J, Vignes B, Niaudet P, Saudubray JM. Ogier H, et al. Among authors: lombes a. J Pediatr. 1988 May;112(5):734-9. doi: 10.1016/s0022-3476(88)80690-5. J Pediatr. 1988. PMID: 2834526

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