PMID- 17379178
OWN - NLM
STAT- MEDLINE
DCOM- 20071012
LR  - 20220408
IS  - 0003-4266 (Print)
IS  - 0003-4266 (Linking)
VI  - 68
IP  - 2-3
DP  - 2007 Jun
TI  - [A Multiple endocrine neoplasia type-1 observatory in a French-speaking area. A 
      tool from the Endocrine Tumor study Group (GTE)].
PG  - 154-9
AB  - Wermer's syndrome or Multiple Endocrine Neoplasia Type-1 (MEN1) is an autosomal 
      dominant inherited disease, related to mutations in MEN1, an approximately 10-kb 
      gene encoding menin, localized on chromosome 11q13. The Endocrine Tumor Group 
      (GTE) has set up a MEN1 observatory of 1001 regularly followed MEN1 cases. This 
      observatory aims at registering and evaluating MEN1 cases in a large cohort. Any 
      new study on a particular unexplored aspect of the disease may be proposed by a 
      physician to the GTE. This article describes the way to diagnose a new MEN1 case 
      and to register it. Procedures for participating in a new study are presented. 
      Some original results are quoted.
FAU - Goudet, P
AU  - Goudet P
AD  - Service de chirurgie viscerale et endocrinienne, hopital General, CHU de Dijon, 
      3, rue du Faubourg-Raines, BP 1519, 21033 Dijon cedex, France. 
      pierre.goudet@chu-dijon.fr
FAU - Bonithon, C
AU  - Bonithon C
FAU - Costa, A
AU  - Costa A
FAU - Cadiot, G
AU  - Cadiot G
FAU - Baudin, E
AU  - Baudin E
FAU - Murat, A
AU  - Murat A
FAU - Delemer, B
AU  - Delemer B
FAU - Tabarin, A
AU  - Tabarin A
FAU - Lecomte, P
AU  - Lecomte P
FAU - Calender, A
AU  - Calender A
CN  - Endocrine Tumor Study Group (GTE)
LA  - fre
PT  - English Abstract
PT  - Journal Article
PT  - Review
TT  - Observatoire francophone des neoplasies endocriniennes multiples de type 1. Un 
      outil du Groupe d'etude des Tumeurs Endocrines (GTE).
DEP - 20070326
PL  - France
TA  - Ann Endocrinol (Paris)
JT  - Annales d'endocrinologie
JID - 0116744
SB  - IM
MH  - Chromosomes, Human, Pair 11/genetics
MH  - Cohort Studies
MH  - France/epidemiology
MH  - Humans
MH  - Multiple Endocrine Neoplasia Type 1/*epidemiology/*genetics
MH  - Registries
RF  - 11
EDAT- 2007/03/24 09:00
MHDA- 2007/10/13 09:00
CRDT- 2007/03/24 09:00
PHST- 2006/07/22 00:00 [received]
PHST- 2006/09/19 00:00 [revised]
PHST- 2006/11/15 00:00 [accepted]
PHST- 2007/03/24 09:00 [pubmed]
PHST- 2007/10/13 09:00 [medline]
PHST- 2007/03/24 09:00 [entrez]
AID - S0003-4266(06)00007-2 [pii]
AID - 10.1016/j.ando.2006.11.003 [doi]
PST - ppublish
SO  - Ann Endocrinol (Paris). 2007 Jun;68(2-3):154-9. doi: 10.1016/j.ando.2006.11.003. 
      Epub 2007 Mar 26.