Lombes A - Search Results

1

[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.

2

[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.

3

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

4

[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.

5

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

6

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

7

[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.

8

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.

9

[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies].

Laforêt P, Eymard B, Lombès A, Duboc D, Jehenson P, Rocchiccioli F, Chaussain M, Chateau D, Brunet P, Fardeau M. Laforêt P, et al. Among authors: lombes a. Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):458-64. Rev Neurol (Paris). 1996. PMID: 8944243 Review. French.

10

Analysis of the tissue distribution and inheritance of heteroplasmic mitochondrial DNA point mutation by denaturing gradient gel electrophoresis in MERRF syndrome.

Lombès A, Diaz C, Romero NB, Ziegler F, Fardeau M. Lombès A, et al. Neuromuscul Disord. 1992;2(5-6):323-30. doi: 10.1016/s0960-8966(06)80003-9. Neuromuscul Disord. 1992. PMID: 1300181

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

187 results

Search Page

Filters