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Page 1
[Protein glycosylation deficiency: clinical presentation].
Ogier de Baulny H, Poggi-Travert F, Besnard M, Saudubray JM. Ogier de Baulny H, et al. Among authors: poggi travert f. Arch Pediatr. 1996;3 Suppl 1:158s-160s. Arch Pediatr. 1996. PMID: 8796001 French. No abstract available.
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy.
de Lonlay P, Fournet JC, Rahier J, Gross-Morand MS, Poggi-Travert F, Foussier V, Bonnefont JP, Brusset MC, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C. de Lonlay P, et al. Among authors: poggi travert f. J Clin Invest. 1997 Aug 15;100(4):802-7. doi: 10.1172/JCI119594. J Clin Invest. 1997. PMID: 9259578 Free PMC article.
Clinical features of 52 neonates with hyperinsulinism.
de Lonlay-Debeney P, Poggi-Travert F, Fournet JC, Sempoux C, Dionisi Vici C, Brunelle F, Touati G, Rahier J, Junien C, Nihoul-Fékété C, Robert JJ, Saudubray JM. de Lonlay-Debeney P, et al. Among authors: poggi travert f. N Engl J Med. 1999 Apr 15;340(15):1169-75. doi: 10.1056/NEJM199904153401505. N Engl J Med. 1999. PMID: 10202168 Free article.
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: poggi travert f. J Inherit Metab Dis. 1999 Jun;22(4):488-502. doi: 10.1023/a:1005556207210. J Inherit Metab Dis. 1999. PMID: 10407781 Review.
Clinical approach to inherited peroxisomal disorders.
Poggi-Travert F, Fournier B, Poll-The BT, Saudubray JM. Poggi-Travert F, et al. J Inherit Metab Dis. 1995;18 Suppl 1:1-18. doi: 10.1007/BF00711425. J Inherit Metab Dis. 1995. PMID: 9053544 Review.
Liver transplantation in two cases of propionic acidaemia.
Schlenzig JS, Poggi-Travert F, Laurent J, Rabier D, Jan D, Wendel U, Sewell AC, Revillon Y, Kamoun P, Saudubray JM. Schlenzig JS, et al. Among authors: poggi travert f. J Inherit Metab Dis. 1995;18(4):448-61. doi: 10.1007/BF00710056. J Inherit Metab Dis. 1995. PMID: 7494403
[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: poggi travert f. 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.
[Diagnosis of metabolic coma in children].
Poggi-Travert F, Héron B, Billette de Villemeur T, Spada M, Jouvet P, Charpentier C, Rabier D, Kamoun P, Saudubray JM. Poggi-Travert F, et al. Arch Pediatr. 1994 Sep;1(9):843-51. Arch Pediatr. 1994. PMID: 7842129 Review. French.
11 results