Netchine I - Search Results

1

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.

Netchine I, Sobrier ML, Krude H, Schnabel D, Maghnie M, Marcos E, Duriez B, Cacheux V, Moers Av, Goossens M, Grüters A, Amselem S. Netchine I, et al. Nat Genet. 2000 Jun;25(2):182-6. doi: 10.1038/76041. Nat Genet. 2000. PMID: 10835633

2

Pituitary stalk interruption syndrome: a clinical-biological-genetic assessment of its pathogenesis.

Pinto G, Netchine I, Sobrier ML, Brunelle F, Souberbielle JC, Brauner R. Pinto G, et al. Among authors: netchine i. J Clin Endocrinol Metab. 1997 Oct;82(10):3450-4. doi: 10.1210/jcem.82.10.4295. J Clin Endocrinol Metab. 1997. PMID: 9329385

3

Extensive phenotypic analysis of a family with growth hormone (GH) deficiency caused by a mutation in the GH-releasing hormone receptor gene.

Netchine I, Talon P, Dastot F, Vitaux F, Goossens M, Amselem S. Netchine I, et al. J Clin Endocrinol Metab. 1998 Feb;83(2):432-6. doi: 10.1210/jcem.83.2.4528. J Clin Endocrinol Metab. 1998. PMID: 9467553

4

Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency.

Duquesnoy P, Roy A, Dastot F, Ghali I, Teinturier C, Netchine I, Cacheux V, Hafez M, Salah N, Chaussain JL, Goossens M, Bougnères P, Amselem S. Duquesnoy P, et al. Among authors: netchine i. FEBS Lett. 1998 Oct 23;437(3):216-20. doi: 10.1016/s0014-5793(98)01234-4. FEBS Lett. 1998. PMID: 9824293 Free article.

5

[Molecular pathology of transcription factors implicated in the development of the anterior hypophysis].

Netchine I, Sobrier ML, Amselem S. Netchine I, et al. Arch Pediatr. 2000 May;7 Suppl 2:218s-220s. doi: 10.1016/s0929-693x(00)80044-5. Arch Pediatr. 2000. PMID: 10904717 French. No abstract available.

6

[Molecular pathology of the GHRH receptor].

Netchine I, Talon P, Amselem S. Netchine I, et al. Arch Pediatr. 2000 May;7 Suppl 2:221s-222s. doi: 10.1016/s0929-693x(00)80045-7. Arch Pediatr. 2000. PMID: 10904718 French. No abstract available.

7

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

Machinis K, Pantel J, Netchine I, Léger J, Camand OJ, Sobrier ML, Dastot-Le Moal F, Duquesnoy P, Abitbol M, Czernichow P, Amselem S. Machinis K, et al. Among authors: netchine i. Am J Hum Genet. 2001 Nov;69(5):961-8. doi: 10.1086/323764. Epub 2001 Sep 20. Am J Hum Genet. 2001. PMID: 11567216 Free PMC article.

8

Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development.

Sobrier ML, Attié-Bitach T, Netchine I, Encha-Razavi F, Vekemans M, Amselem S. Sobrier ML, et al. Among authors: netchine i. Gene Expr Patterns. 2004 Dec;5(2):279-84. doi: 10.1016/j.modgep.2004.07.003. Gene Expr Patterns. 2004. PMID: 15567726

9

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.

Sobrier ML, Netchine I, Heinrichs C, Thibaud N, Vié-Luton MP, Van Vliet G, Amselem S. Sobrier ML, et al. Among authors: netchine i. Hum Mutat. 2005 May;25(5):503. doi: 10.1002/humu.9332. Hum Mutat. 2005. PMID: 15841484

10

Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene.

Iughetti L, Sobrier ML, Predieri B, Netchine I, Carani C, Bernasconi S, Balli F, Amselem S. Iughetti L, et al. Among authors: netchine i. Clin Endocrinol (Oxf). 2008 Jul;69(1):170-2. doi: 10.1111/j.1365-2265.2007.03157.x. Epub 2008 Jul 1. Clin Endocrinol (Oxf). 2008. PMID: 18088397 No abstract available.

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