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Page 1
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.
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.
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.
High prevalence of hirsutism and menstrual disorders in obese adolescent girls and adolescent girls with type 1 diabetes mellitus despite different hormonal profiles.
Samara-Boustani D, Colmenares A, Elie C, Dabbas M, Beltrand J, Caron V, Ricour C, Jacquin P, Tubiana-Rufi N, Levy-Marchal C, Delcroix C, Martin D, Benadjaoud L, Jacqz Aigrain E, Trivin C, Laborde K, Thibaud E, Robert JJ, Polak M. Samara-Boustani D, et al. Among authors: martin d. Eur J Endocrinol. 2012 Feb;166(2):307-16. doi: 10.1530/EJE-11-0670. Epub 2011 Nov 29. Eur J Endocrinol. 2012. PMID: 22127492
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.
[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.
High Prevalence of Polycystic Ovary Syndrome in Type 1 Diabetes Mellitus Adolescents: Is There a Difference Depending on the NIH and Rotterdam Criteria?
Busiah K, Colmenares A, Bidet M, Tubiana-Rufi N, Levy-Marchal C, Delcroix C, Jacquin P, Martin D, Benadjaoud L, Jacqz-Aigrain E, Laborde K, Robert JJ, Samara-Boustani D, Polak M. Busiah K, et al. Among authors: martin d. Horm Res Paediatr. 2017;87(5):333-341. doi: 10.1159/000471805. Epub 2017 Apr 24. Horm Res Paediatr. 2017. PMID: 28437788 Clinical Trial.
9,216 results