Y de Keyzer
Overview
Explore the profile of Y de Keyzer including associated specialties, affiliations and a list of published articles.
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Articles
42
Citations
425
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Recent Articles
1.
Romano S, Bajolle F, Valayannopoulos V, Lyonnet S, Colomb V, de Barace C, et al.
J Med Genet
. 2009 Apr;
46(4):287-8.
PMID: 19357119
No abstract available.
2.
Valayannopoulos V, Hubert L, Benoist J, Romano S, Arnoux J, Chretien D, et al.
J Inherit Metab Dis
. 2009 Mar;
32(2):159-62.
PMID: 19277894
An adult patient with methylmalonic aciduria due to defective cobalamin synthesis (CblA) responsive to vitamin B(12) presented suddenly with severe visual impairment ascribed to optic atrophy followed by a fatal...
3.
Damaj L, Le Lorch M, Verkarre V, Werl C, Hubert L, Nihoul-Fekete C, et al.
J Clin Endocrinol Metab
. 2008 Sep;
93(12):4941-7.
PMID: 18796520
Context: Focal forms of congenital hyperinsulinism are due to a constitutional heterozygous mutation of paternal origin in the ABCC8 gene, more often than the KCNJ11 gene, located in the 11p15.1...
4.
Cosson M, Touati G, Lacaille F, Valayannnopoulos V, Guyot C, Guest G, et al.
Mol Genet Metab
. 2008 Aug;
95(1-2):107-9.
PMID: 18676166
A boy who was diagnosed with methylmalonic aciduria (MMA) at the age of 10 days developed persistent hepatomegaly and raised transaminases from the age of 4 years. He was subsequently...
5.
Dutriez-Casteloot I, Breton C, Coupe B, Hawchar O, Enache M, Dickes-Coopman A, et al.
Horm Metab Res
. 2008 Jun;
40(4):257-61.
PMID: 18548384
Maternal undernutrition leads to intrauterine growth retardation and predisposes to the development of pathologies in adulthood. The hypothalamo-pituitary-adrenal axis is a major target of early-life programming. We showed previously that...
6.
Arnoux J, Boddaert N, Valayannopoulos V, Romano S, Bahi-Buisson N, Desguerre I, et al.
Mol Genet Metab
. 2007 Dec;
93(4):444-9.
PMID: 18093857
The congenital disorder of glycosylation type Ia (CDG-Ia) presents a broad clinical spectrum. Some patients suffer from acute vascular events (thrombosis and bleeding) and stroke-like events. No correlations have been...
7.
Mention K, Lacaille F, Valayannopoulos V, Romano S, Kuster A, Cretz M, et al.
Mol Genet Metab
. 2007 Oct;
93(1):40-3.
PMID: 17945525
We report here the 6- and 2-year follow-up of two patients diagnosed at 2 months of age with CDG-Ib who were treated with mannose, with digestive symptoms, liver involvement and...
8.
Messager M, Carriere C, Bertagna X, de Keyzer Y
Eur J Endocrinol
. 2005 Dec;
154(1):159-66.
PMID: 16382005
Objective: ACTH is frequently produced in non-pituitary tumours, leading to the ectopic-ACTH syndrome, but the molecular mechanisms of its expression remain obscure. This study was aimed at understanding the transcription...
9.
Raffin-Sanson M, de Keyzer Y, Bertagna X
Eur J Endocrinol
. 2003 Jul;
149(2):79-90.
PMID: 12887283
Proopiomelanocortin (POMC) is the polypeptide precursor of ACTH. First discovered in anterior pituitary corticotroph cells, it has more recently been revealed to have many other physiological aspects. The fine molecular...
10.
Rene P, Grino M, Viollet C, Videau C, Jullian E, Bucchini D, et al.
J Neuroendocrinol
. 2002 Sep;
14(9):737-44.
PMID: 12213135
The vasopressin V3 receptor (V3) is specifically expressed in pituitary corticotropes and mediates the stimulatory effect of vasopressin on adrenocorticotropic hormone (ACTH) release. The V3 gene is overexpressed in corticotrope...