Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Recessive isolated growth hormone deficiency and mutations in the ghrelin receptor.
J Clin Endocrinol Metab. 2009 Nov;94(11):4334-41. doi: 10.1210/jc.2009-1327. Epub 2009 Sep 29.
J Clin Endocrinol Metab. 2009.
PMID: 19789204
Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature.
Pantel J, Legendre M, Cabrol S, Hilal L, Hajaji Y, Morisset S, Nivot S, Vie-Luton MP, Grouselle D, de Kerdanet M, Kadiri A, Epelbaum J, Le Bouc Y, Amselem S.
Pantel J, et al. Among authors: vie luton mp.
J Clin Invest. 2006 Mar;116(3):760-8. doi: 10.1172/JCI25303.
J Clin Invest. 2006.
PMID: 16511605
Free PMC article.
Item in Clipboard
Symptomatic heterozygotes and prenatal diagnoses in a nonconsanguineous family with syndromic combined pituitary hormone deficiency resulting from two novel LHX3 mutations.
Sobrier ML, Brachet C, Vié-Luton MP, Perez C, Copin B, Legendre M, Heinrichs C, Amselem S.
Sobrier ML, et al. Among authors: vie luton mp.
J Clin Endocrinol Metab. 2012 Mar;97(3):E503-9. doi: 10.1210/jc.2011-2095. Epub 2012 Jan 11.
J Clin Endocrinol Metab. 2012.
PMID: 22238406
Item in Clipboard
Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism.
Fritez N, Sobrier ML, Iraqi H, Vié-Luton MP, Netchine I, El Annas A, Pantel J, Collot N, Rose S, Piterboth W, Legendre M, Chraibi A, Amselem S, Kadiri A, Hilal L.
Fritez N, et al. Among authors: vie luton mp.
Clin Endocrinol (Oxf). 2015 Jun;82(6):876-84. doi: 10.1111/cen.12706. Epub 2015 Feb 6.
Clin Endocrinol (Oxf). 2015.
PMID: 25557026
Item in Clipboard
Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities.
Sobrier ML, Maghnie M, Vié-Luton MP, Secco A, di Iorgi N, Lorini R, Amselem S.
Sobrier ML, et al. Among authors: vie luton mp.
J Clin Endocrinol Metab. 2006 Nov;91(11):4528-36. doi: 10.1210/jc.2006-0426. Epub 2006 Aug 29.
J Clin Endocrinol Metab. 2006.
PMID: 16940453
Item in Clipboard
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: vie luton mp.
Hum Mutat. 2005 May;25(5):503. doi: 10.1002/humu.9332.
Hum Mutat. 2005.
PMID: 15841484
Item in Clipboard
Unusual phenotypic features in a patient with a novel splice mutation in the GHRHR gene.
Hilal L, Hajaji Y, Vie-Luton MP, Ajaltouni Z, Benazzouz B, Chana M, Chraïbi A, Kadiri A, Amselem S, Sobrier ML.
Hilal L, et al. Among authors: vie luton mp.
Mol Med. 2008 May-Jun;14(5-6):286-92. doi: 10.2119/2007-00128.Hilal.
Mol Med. 2008.
PMID: 18297129
Free PMC article.
Item in Clipboard
Cite
Cite