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9,190 results

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Page 1
Metabolic intermediates in lactic acidosis: compounds, samples and interpretation.
Poggi-Travert F, Martin D, Billette de Villemeur T, Bonnefont JP, Vassault A, Rabier D, Charpentier C, Kamoun P, Munnich A, Saudubray JM. Poggi-Travert F, et al. Among authors: martin d. J Inherit Metab Dis. 1996;19(4):478-88. doi: 10.1007/BF01799109. J Inherit Metab Dis. 1996. PMID: 8884572 Review.
Recognition and management of fatty acid oxidation defects: a series of 107 patients.
Saudubray JM, Martin D, de Lonlay P, Touati G, Poggi-Travert F, Bonnet D, Jouvet P, Boutron M, Slama A, Vianey-Saban C, Bonnefont JP, Rabier D, Kamoun P, Brivet M. Saudubray JM, et al. Among authors: martin d. J Inherit Metab Dis. 1999 Jun;22(4):488-502. doi: 10.1023/a:1005556207210. J Inherit Metab Dis. 1999. PMID: 10407781 Review.
Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosis.
Saudubray JM, de Lonlay P, Touati G, Martin D, Nassogne MC, Castelnau P, Sevin C, Laborde C, Baussan C, Brivet M, Vassault A, Rabier D, Bonnefont JP, Kamoun P. Saudubray JM, et al. Among authors: martin d. J Inherit Metab Dis. 2000 May;23(3):197-214. doi: 10.1023/a:1005675827612. J Inherit Metab Dis. 2000. PMID: 10863937 Review. No abstract available.
[Monoamine decarboxylase deficiency].
Billette de Villemeur T, de Lonlay P, Poggi-Travert F, Martin D, Launay JM, Munnich A, Saudubray JM. Billette de Villemeur T, et al. Among authors: martin d. Arch Pediatr. 1996;3 Suppl 1:167s-168s. doi: 10.1016/0929-693x(96)86029-5. Arch Pediatr. 1996. PMID: 8796004 French. No abstract available.
Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases.
de Lonlay P, Fournet JC, Touati G, Groos MS, Martin D, Sevin C, Delagne V, Mayaud C, Chigot V, Sempoux C, Brusset MC, Laborde K, Bellane-Chantelot C, Vassault A, Rahier J, Junien C, Brunelle F, Nihoul-Fékété C, Saudubray JM, Robert JJ. de Lonlay P, et al. Among authors: martin d. Eur J Pediatr. 2002 Jan;161(1):37-48. doi: 10.1007/s004310100847. Eur J Pediatr. 2002. PMID: 11808879 Review.
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants].
de Lonlay-Debeney P, Fournet JC, Martin D, Poggi F, Dionisi Vicci C, Spada M, Touati G, Rahier J, Brunelle F, Junien C, Robert JJ, Nihoul-Fékété C, Saudubray JM. de Lonlay-Debeney P, et al. Among authors: martin d. Arch Pediatr. 1998 Dec;5(12):1347-52. doi: 10.1016/s0929-693x(99)80055-4. Arch Pediatr. 1998. PMID: 9885743 Review. French.
Craniosynostosis and kidney malformation in a case of Hennekam syndrome.
Cormier-Daire V, Lyonnet S, Lehnert A, Martin D, Salomon R, Patey N, Broyer M, Ricour C, Munnich A. Cormier-Daire V, et al. Among authors: martin d. Am J Med Genet. 1995 May 22;57(1):66-8. doi: 10.1002/ajmg.1320570115. Am J Med Genet. 1995. PMID: 7645602
9,190 results