Michel Dauzat

Prof. Dr. Michel Dauzat

orcid

Research Focus & Metrics

Academic Career Length

39Years (1988-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
15 May 2004 in Blood
Verified
Journal Article
Closed access
PDF file
Jean-Christophe Raymond GRISJean-Christophe Raymond GRIS
Jean-Christophe Raymond GRIS
EMEric Mercier
Eric Mercier
IQIsabelle Quéré
Isabelle Quéré
GLGéraldine Lavigne-Lissalde
Géraldine Lavigne-Lissalde
ECEva Cochery-Nouvellon
Eva Cochery-Nouvellon
PMPierre Marès
Pierre Marès
The prospective evaluation of the effect of thromboprophylaxis in women with one unexplained pregnancy loss from the 10th week of amenorrhea was performed. A total of 160 patients with heterozygous factor V Leiden mutation, prothrombin G20210A mutation, or protein S deficiency were given 5 mg folic acid daily before conception, to be continued during pregnancy, and low-dose aspirin 100 mg daily or low-molecular-weight heparin enoxaparin 40 mg was taken from the 8th week. Twenty-three of the 80 patients treated with low-dose aspirin and 69 of the 80 patients treated with enoxaparin had a healthy live birth (odds ratio [OR], 15.5; 95% confidence interval [CI], 7-34, P < .0001). Enoxaparin was superior to low-dose aspirin in each subgroup defined according to the underlying constitutional thrombophilic disorder. An associated protein Z deficiency and/or positive antiprotein Z antibodies were associated with poorer outcomes. The neonate weight was higher in the women successfully treated with enoxaparin, and neonates small for gestational age were more frequent in patients treated with low-dose aspirin. No significant side effects of the treatments could be evidenced in patients or newborns. As there is no argument to prove that low-dose aspirin may have been deleterious, these results support enoxaparin use during such at-risk pregnancies.

1 January 2011 in Genome Medicine
Verified
Journal Article
Open access
PDF file
PBPhilippe Jean Bousquet
Philippe Jean Bousquet
JAJosep M Anto
Josep M Anto
PSPeter J Sterk
Peter J Sterk
IAIan Adcock
Ian Adcock
KCKian Chung
Kian Chung
CACharles Auffray
Charles Auffray
We propose an innovative, integrated, cost-effective health system to combat major non-communicable diseases (NCDs), including cardiovascular, chronic respiratory, metabolic, rheumatologic and neurologic disorders and cancers, which together are the predominant health problem of the 21st century. This proposed holistic strategy involves comprehensive patient-centered integrated care and multi-scale, multi-modal and multi-level systems approaches to tackle NCDs as a common group of diseases. Rather than studying each disease individually, it will take into account their intertwined gene-environment, socio-economic interactions and co-morbidities that lead to individual-specific complex phenotypes. It will implement a road map for predictive, preventive, personalized and participatory (P4) medicine based on a robust and extensive knowledge management infrastructure that contains individual patient information. It will be supported by strategic partnerships involving all stakeholders, including general practitioners associated with patient-centered care. This systems medicine strategy, which will take a holistic approach to disease, is designed to allow the results to be used globally, taking into account the needs and specificities of local economies and health systems.

1 March 2008 in Journal of Thrombosis and Haemostasis
Verified
Journal Article
Closed access
PDF file
JRJ.-L. Reny
J.-L. Reny
PMP. DE Moerloose
P. DE Moerloose
MDMichel Dauzat
Michel Dauzat
PFPierre Fontana
Pierre Fontana

1 October 1998 in Hepatology
Verified
Journal Article
Open access
PDF file
PTPatrice Taourel
Patrice Taourel
PBPierre Blanc
Pierre Blanc
MDMichel Dauzat
Michel Dauzat
MCMyriam Chabre
Myriam Chabre
JPJean Pradel
Jean Pradel
JBJean-Michel Bruel
Jean-Michel Bruel
To determine the relationship between quantitative Doppler parameters of portal, hepatic, and splanchnic circulation and hepatic venous pressure gradient (HVPG), variceal size, and Child-Pugh class in patients with alcoholic cirrhosis, we studied forty patients with proved alcoholic cirrhosis who underwent Doppler ultrasonography, hepatic vein catheterization, and esophagoscopy. The following Doppler parameters were recorded: time-averaged mean blood velocity, volume flow of the main portal vein flow, and resistance index (RI) of the hepatic and of the superior mesenteric artery. Doppler findings were compared with HVPG, presence and size of esophageal varices, and Child-Pugh class. There was a significant inverse correlation between portal velocity and HVPG (r = −.69), as well as between portal vein flow and HVPG (r = −.58). No correlation was found between RI in the hepatic artery or superior mesenteric artery and HVPG. No correlation was found between portal vein measurements and presence and size of varices. Severe liver failure was associated with lower portal velocity and flow. In patients with alcoholic cirrhosis, only portal vein blood velocity and flow, but neither hepatic nor mesenteric artery RI, are correlated to the severity of portal hypertension and to the severity of liver failure.

1 March 2003 in Clinica Chimica Acta
Verified
Journal Article
Closed access
JBJ.P Bertinchant
J.P Bertinchant
APA Polge
A Polge
JJJ.M Juan
J.M Juan
MOM.C Oliva-Lauraire
M.C Oliva-Lauraire
IGI Giuliani
I Giuliani
MDMichel Dauzat
Michel Dauzat

1 October 2008 in The Journal of Physiology
Verified
Journal Article
Closed access
SNStéphane Nottin
Stéphane Nottin
GDG. Doucende
G. Doucende
ISI. Schuster‐Beck
I. Schuster‐Beck
MDMichel Dauzat
Michel Dauzat
POP. Obert
P. Obert