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434 results

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Page 1
[Diagnosis of states of ketosis in pediatrics].
Ogier de Baulny H, Husson I, Castelnau P, Saudubray JM. Ogier de Baulny H, et al. Among authors: saudubray jm. Arch Pediatr. 1999;6 Suppl 2:500s-501s. doi: 10.1016/s0929-693x(99)80518-1. Arch Pediatr. 1999. PMID: 10370586 French. No abstract available.
[Protein glycosylation deficiency: clinical presentation].
Ogier de Baulny H, Poggi-Travert F, Besnard M, Saudubray JM. Ogier de Baulny H, et al. Among authors: saudubray jm. Arch Pediatr. 1996;3 Suppl 1:158s-160s. Arch Pediatr. 1996. PMID: 8796001 French. No abstract available.
Branched-chain organic acidurias.
Ogier de Baulny H, Saudubray JM. Ogier de Baulny H, et al. Among authors: saudubray jm. Semin Neonatol. 2002 Feb;7(1):65-74. doi: 10.1053/siny.2001.0087. Semin Neonatol. 2002. PMID: 12069539 Review.
[Hematologic manifestations of inborn errors of metabolism].
de Lonlay P, Fenneteau O, Touati G, Mignot C, Billette de Villemeur T, Rabier D, Blanche S, Ogier de Baulny H, Saudubray JM. de Lonlay P, et al. Among authors: saudubray jm. Arch Pediatr. 2002 Aug;9(8):822-35. doi: 10.1016/s0929-693x(02)00005-2. Arch Pediatr. 2002. PMID: 12205794 Review. French.
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. 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.
[Hereditary metabolic diseases in adults].
Saudubray JM, Nuoffer JM, de Lonlay P, Castelnau P, Touati G. Saudubray JM, et al. Rev Med Interne. 1998;19 Suppl 3:366S-375S. Rev Med Interne. 1998. PMID: 9885858 Review. French. No abstract available.
434 results