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Page 1
True hermaphroditism: genetic variants and clinical management.
Hadjiathanasiou CG, Brauner R, Lortat-Jacob S, Nivot S, Jaubert F, Fellous M, Nihoul-Fékété C, Rappaport R. Hadjiathanasiou CG, et al. Among authors: nivot s. J Pediatr. 1994 Nov;125(5 Pt 1):738-44. doi: 10.1016/s0022-3476(94)70067-2. J Pediatr. 1994. PMID: 7965425 Clinical Trial.
[Clinical aspects of gonadal dysgenesis].
Mahoudeau J, Reznik Y, Nivot S. Mahoudeau J, et al. Among authors: nivot s. Bull Assoc Anat (Nancy). 1991 Mar;75(228):39-42. Bull Assoc Anat (Nancy). 1991. PMID: 1782463 Review. French.
NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects.
Roucher-Boulez F, Mallet-Motak D, Samara-Boustani D, Jilani H, Ladjouze A, Souchon PF, Simon D, Nivot S, Heinrichs C, Ronze M, Bertagna X, Groisne L, Leheup B, Naud-Saudreau C, Blondin G, Lefevre C, Lemarchand L, Morel Y. Roucher-Boulez F, et al. Among authors: nivot s. Eur J Endocrinol. 2016 Jul;175(1):73-84. doi: 10.1530/EJE-16-0056. Epub 2016 Apr 29. Eur J Endocrinol. 2016. PMID: 27129361 Free article.
Markers of recurrence and long-term morbidity in craniopharyngioma: a systematic analysis of 171 patients.
Gautier A, Godbout A, Grosheny C, Tejedor I, Coudert M, Courtillot C, Jublanc C, De Kerdanet M, Poirier JY, Riffaud L, Sainte-Rose C, Van Effenterre R, Brassier G, Bonnet F, Touraine P; Craniopharyngioma Study Group. Gautier A, et al. J Clin Endocrinol Metab. 2012 Apr;97(4):1258-67. doi: 10.1210/jc.2011-2817. Epub 2012 Feb 8. J Clin Endocrinol Metab. 2012. PMID: 22319039 Free article.
16 results