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23篇 您的检索式：作者名="Tardy V"

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	题名	作者	年代	出处	被引量
1	Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency : identification of four novel mutations and high prevalence of Q318X mutation 显示文摘	Kharrat M Tardy V M' rad R	2004	J Clin Endocrinol Metab2004，89，1：	1
2	Guil- lain - Barr6 syndrome following primary cytomegalovirus in- fection : a prospective cohort study 显示文摘	Orikowski D Porcher R Sivadon -Tardy V	2011	Clin Infect Dis2011，52，7：	1
3	Efficiency of neonatal screening forcongenital adrenal hyperplasia due to 21-hydroxylase deficiency inchildren born in mainland France between 1996 and 2003显示文摘	Coulm B Coste J Tardy V		0，，02：	1
4	Phenotype-genotype correlations of 13 Rare CYP21A2 mutations detected in 46 patients affected with 21-Hydroxylase deficiency and in one carrier 显示文摘	Tardy V Menassa R Snlmont V	2010	J Clin Endocrinol Metab2010，95，3：	1
5	Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency显示文摘	Deneux C Tardy V Dib A		0，，：	1
6	Phenotype-geno- type correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier显示文摘	Tardy V Menassa R Sulmont V	2010	J Clin Endocrinol Metab2010，95，：	1
7	New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes 显示文摘	Moisan AM Ricketts ML Tardy V	1999	J Clin Endocrinol Metab1999，84，12：	1
8	Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier显示文摘	V Tardy R Menassa V. Sulmont A. Lienhardt-Roussie C. Lecointre R. Brauner M. David Y. Morel	2010	The Journal of Clinical Endocrinology & Metabolism2010，，3：	1
9	The Amazon bio-geochemistry applied to river basin management , part I, hydro-climatology, hydrograph separation, mass transfer balances, stable isotopes, and modeling 显示文摘	Tardy Y Bustlllo V Roquln C	2005	Applied Geochemistry2005，20，9：	1
10	Guillain - Barr6syndrome and influenza virus infection 显示文摘	Sivadon - Tardy V Orlikowski D Porcher R	2009	Clin Infect Dis2009，48，1：	1
11	Antimicrobial susceptibility of Streptococcusspecies isolated from clinical mastitis in dairy cows显示文摘	GUERIN-FAUBLEE V TARDY F BOUVERONC	2002	Int J Antimicrob Agents2002，19，3：	1
12	Efficiency of neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children born in mainland France between 1996 and 2003显示文摘	Coulm B Coste J Tardy V	2012	Arch Pediatr Adolesc Meal2012，166，2：	1
13	Detection and characteriza tionof large SERPINCI deletions in type I inherited antithrombin deficiency显示文摘	ICARD V CHEN JM TARDY B	2010	Hum genet2010，127，1：	1
14	Phenotype-genotype correlations of 13 rare CYPglA2 mutations detected in 46 patients affected with 21 hydroxylase deficiency and in one carrier显示文摘	Tardy V Menassa R Sulmont V	2010	J Clin Endocrinol Metab2010，95，12：	1
15	Efficiency of neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children born in mainland France between 1996 and 2003显示文摘	Coulm B CosteJ Tardy V	2012	Arch Pediatr Adolesc Med2012，166，2：	1
16	Antimicrobial susceptibility of Streptococcus species isolated from clinical mastitis in dairy cows显示文摘	Véronique Guérin-Faublée Florence Tardy Clarisse Bouveron Gérard Carret	2002	International Journal of Antimicrobial Agents2002，，3：	1
17	Identification of clinical coagulase negative staphylococci, isolated in microbiology laboratories, by matrix-assisted laser de- sorption/ionization-time of flight mass spectrometry and two automated systems显示文摘	Dupont C Tardy S V Bille E el al	2010	Clin Microbiol Infect2010，16，7：	1
18	Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency显示文摘	Maud Bidet Christine Bellanné-Chantelot Marie-Béatrice Galand-Portier Jean-Louis Golmard Véronique Tardy Yves Morel Séverine Clauin Christiane Coussieu Philippe Boudou Irene Mowzowicz Anne Bachelot Philippe Touraine F. Kuttenn	2010	The Journal of Clinical Endocrinology & Metabolism2010，，3：	1
19	Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21- hydroxylase deficiency显示文摘	Deneux C Tardy V Dib A	2001	J Clin Endocrinol Metab2001，86，1：	1
20	Antimicrobial susceptibility of Streptococcus species iso-lated from clinical mastitis in dairy cows 显示文摘	GUERIN-FAUBLIEE V TARDY F BOUVERON C	2002	lnt J Antimi- crob Agents2002，19，3：	1

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