M C Gubler
Overview
Explore the profile of M C Gubler including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
162
Citations
2633
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Guilherme R, Patrier S, Gubler M, Lemercier D, Guimiot F, Dommergues M
Placenta
. 2009 Jul;
30(8):731-4.
PMID: 19577294
We present evidence of a first-trimester discordant renin-angiotensin system (RAS) response and structural abnormalities of the kidneys in twins with twin-to-twin transfusion syndrome (TTTS). A dark red fetus and a...
2.
Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, et al.
Saudi J Kidney Dis Transpl
. 2006 Sep;
17(3):320-5.
PMID: 16970251
Alport's syndrome is a hereditary nephritis that may lead to end-stage renal disease (ESRD) in early adult life. It is a clinically and genetically heterogeneous nephropathy. Alport's syndrome is often...
3.
Ickowicz V, Eurin D, Maugey-Laulom B, Didier F, Garel C, Gubler M, et al.
Ultrasound Obstet Gynecol
. 2006 Feb;
27(3):296-300.
PMID: 16450359
Objective: To define a specific sonographic pattern for the appearance of the kidneys in fetuses affected by Meckel-Grüber syndrome (MGS). Methods: This was a retrospective analysis of 30 cases, collected...
4.
Le Caignec C, Gicquel C, Gubler M, Guyot C, You M, Laurent A, et al.
Prenat Diagn
. 2004 Apr;
24(3):165-8.
PMID: 15057946
Beckwith-Wiedemann syndrome (BWS) is an overgrowth syndrome associated with congenital malformations and tumour predisposition. BWS results from variable mutations or epigenetic modifications of imprinted genes in the 11p15 chromosomal region....
5.
Tsatsaris V, Gagnadoux M, Aubry M, Gubler M, Dumez Y, Dommergues M
BJOG
. 2002 Dec;
109(12):1388-93.
PMID: 12504976
Objective: To study perinatal and long term outcome following prenatal diagnosis of hyperechogenic kidneys. Design: Prospective observational cohort study. Setting: The Maternité Port-Royal Hôpital Cochin and at the Departments of...
6.
Levy M, Gubler M, Feingold J
Arch Pediatr
. 2001 Oct;
8(10):1086-98.
PMID: 11683102
Genes of most of the hereditary renal diseases progressing to renal insufficiency are now identified. In the first part of this paper we describe their multi-faceted genetics. Genetic heterogeneity has...
7.
Hammes A, Guo J, LUTSCH G, Leheste J, Landrock D, Ziegler U, et al.
Cell
. 2001 Aug;
106(3):319-29.
PMID: 11509181
Alternative splicing of Wt1 results in the insertion or omission of the three amino acids KTS between zinc fingers 3 and 4. In vitro experiments suggest distinct molecular functions for...
8.
Martinovic J, Benachi A, Laurent N, Daikha-Dahmane F, Gubler M
Lancet
. 2001 Aug;
358(9277):241-2.
PMID: 11480433
No abstract available.
9.
Yang Y, Zhang S, Sich M, Beziau A, van den Heuvel L, Gubler M
Pediatr Nephrol
. 2001 Jun;
16(5):429-38.
PMID: 11405118
Unlabelled: Diffuse mesangial sclerosis, isolated (IDMS) or observed in the context of Denys-Drash syndrome (DDS) due to WT1 mutation, is characterized by early onset nephrotic syndrome progressing to renal failure....
10.
Mahieu-Caputo D, Muller F, Joly D, Gubler M, Lebidois J, Fermont L, et al.
Fetal Diagn Ther
. 2001 Jun;
16(4):241-4.
PMID: 11399888
In spite of active perinatal management, twin-twin transfusion syndrome (TTTS) remains a severe disease with a high risk of neonatal mortality and morbidity. TTTS initially results from an unbalanced blood...