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Biological attenuation of arsenic and iron in a continuous flow bioreactor treating acid mine drainage (AMD)

Water research (Oxford), 2017-10, Vol.123, p.594-606

2017

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Identification of clinical coagulase-negative staphylococci, isolated in microbiology laboratories, by matrix-assisted laser desorption/ionization-time of flight mass spectrometry and two automated systems

Clinical microbiology and infection, 2010-07, Vol.16 (7), p.998-1004

2010

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A field-pilot for passive bioremediation of As-rich acid mine drainage

Journal of environmental management, 2019-02, Vol.232, p.910-918

2019

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Diagnosis of prosthetic joint infection by beadmill processing of a periprosthetic specimen

Clinical microbiology and infection, 2011-03, Vol.17 (3), p.447-450

2011

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Guillain—Barré Syndrome following Primary Cytomegalovirus Infection: A Prospective Cohort Study

Clinical infectious diseases, 2011-04, Vol.52 (7), p.837-844

2011

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Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier

The journal of clinical endocrinology and metabolism, 2010-03, Vol.95 (3), p.1288-1300

2010

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p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2008-05, Vol.93 (5), p.1901-1908

2008

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Rapid molecular testing for Norovirus by the Xpert® Norovirus Assay improves management of nosocomial epidemics in a geriatric hospital setting

Journal of clinical virology, 2015-09, Vol.70, p.S97-S97

2015

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Clinical presentation and performance of urine dipstick for diagnosis of urinary infection in geriatric population

La revue de medecine interne, 2019-11, Vol.40 (11), p.714-721

2019

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Increased incidence of Campylobacter jejuni-associated Guillain–Barré syndromes in the Greater Paris area

Epidemiology and infection, 2014-08, Vol.142 (8), p.1609-1613

2014

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Significance of phrenic nerve electrophysiological abnormalities in Guillain-Barré syndrome

Neurology, 2005-11, Vol.65 (10), p.1646

2005

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Follow-Up of 68 Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Relevance of Genotype for Management

The journal of clinical endocrinology and metabolism, 2003-06, Vol.88 (6), p.2624-2633

2003

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Shifts in microbial diversity through land use intensity as drivers of carbon mineralization in soil

Soil biology & biochemistry, 2015-11, Vol.90, p.204-213

2015

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Echinocandins Susceptibility Patterns of 2,787 Yeast Isolates: Importance of the Thresholds for the Detection of FKS Mutations

Antimicrobial agents and chemotherapy, 2022-05, Vol.66 (5), p.e0172521-e0172521

2022

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Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease

Clinical genetics, 2009-02, Vol.75 (2), p.203-206

2009

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How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4562-4567

2000

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Guillain-Barré Syndrome and Influenza Virus Infection

Clinical infectious diseases, 2009-01, Vol.48 (1), p.48-56

2009

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Dépistage et prise en charge du déficit en 21-hydroxylase à révélation tardive chez les femmes avec hyperandrogénie

Annales d'endocrinologie, 2010-02, Vol.71 (1), p.e15-e19

2010

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Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenism

Annales d'endocrinologie, 2010-02, Vol.71 (1), p.14-18

2010

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État des lieux après inclusion de 162 patients dans le PHRC national Y-BLOC21 « évaluation de la sexualité et de la fertilité des hommes nés avec une forme classique de déficit en 21 hydroxylase

Annales d'endocrinologie, 2012-09, Vol.73 (4), p.268-268

2012

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Lasting effect of repeated application of organic waste products on microbial communities in arable soils

Applied soil ecology : a section of Agriculture, ecosystems & environment, 2018-04, Vol.125, p.278-287

2018

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Forme non classique de déficit en 21-hydroxylase : diagnostic et conseil génétique

Annales d'endocrinologie, 2014-10, Vol.75 (5), p.259-260

2014

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Adrenocortical incidentaloma with uncertain prognosis associated with an inadequately treated congenital adrenal hyperplasia

Annales d'endocrinologie, 2010-02, Vol.71 (1), p.56-59

2010

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Gene symbol: CYP21A2

Human genetics, 2007-04, Vol.121 (2), p.293-293

Tardy, Veronique T V

2007

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21-hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease

Annales d'endocrinologie, 2005-06, Vol.66 (3), p.225-232

2005

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Biological attenuation of arsenic and iron in a continuous flow bioreactor treating acid mine drainage (AMD)

Identification of clinical coagulase-negative staphylococci, isolated in microbiology laboratories, by matrix-assisted laser desorption/ionization-time of flight mass spectrometry and two automated systems

A field-pilot for passive bioremediation of As-rich acid mine drainage

Diagnosis of prosthetic joint infection by beadmill processing of a periprosthetic specimen

Guillain—Barré Syndrome following Primary Cytomegalovirus Infection: A Prospective Cohort Study

Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier

p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency

Rapid molecular testing for Norovirus by the Xpert® Norovirus Assay improves management of nosocomial epidemics in a geriatric hospital setting

Clinical presentation and performance of urine dipstick for diagnosis of urinary infection in geriatric population

Increased incidence of Campylobacter jejuni-associated Guillain–Barré syndromes in the Greater Paris area

Significance of phrenic nerve electrophysiological abnormalities in Guillain-Barré syndrome

Follow-Up of 68 Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Relevance of Genotype for Management

Shifts in microbial diversity through land use intensity as drivers of carbon mineralization in soil

Echinocandins Susceptibility Patterns of 2,787 Yeast Isolates: Importance of the Thresholds for the Detection of FKS Mutations

Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease

How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency

Guillain-Barré Syndrome and Influenza Virus Infection

Dépistage et prise en charge du déficit en 21-hydroxylase à révélation tardive chez les femmes avec hyperandrogénie

Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenism

État des lieux après inclusion de 162 patients dans le PHRC national Y-BLOC21 « évaluation de la sexualité et de la fertilité des hommes nés avec une forme classique de déficit en 21 hydroxylase

Lasting effect of repeated application of organic waste products on microbial communities in arable soils

Forme non classique de déficit en 21-hydroxylase : diagnostic et conseil génétique

Adrenocortical incidentaloma with uncertain prognosis associated with an inadequately treated congenital adrenal hyperplasia

Gene symbol: CYP21A2

21-hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease

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