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Items: 1 to 20 of 43

1.

Temperature and nutrients as drivers of microbially mediated arsenic oxidation and removal from acid mine drainage.

Tardy V, Casiot C, Fernandez-Rojo L, Resongles E, Desoeuvre A, Joulian C, Battaglia-Brunet F, Héry M.

Appl Microbiol Biotechnol. 2018 Mar;102(5):2413-2424. doi: 10.1007/s00253-017-8716-4. Epub 2018 Jan 29.

PMID:
29380031
2.

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

Fernandez-Rojo L, Héry M, Le Pape P, Braungardt C, Desoeuvre A, Torres E, Tardy V, Resongles E, Laroche E, Delpoux S, Joulian C, Battaglia-Brunet F, Boisson J, Grapin G, Morin G, Casiot C.

Water Res. 2017 Oct 15;123:594-606. doi: 10.1016/j.watres.2017.06.059. Epub 2017 Jun 22.

PMID:
28709104
3.

Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.

Dubey S, Tardy V, Chowdhury MR, Gupta N, Jain V, Deka D, Sharma P, Morel Y, Kabra M.

Indian J Med Res. 2017 Feb;145(2):194-202. doi: 10.4103/ijmr.IJMR_329_16.

4.

Growth curves for congenital adrenal hyperplasia from a national retrospective cohort.

Bretones P, Riche B, Pichot E, David M, Roy P, Tardy V, Kassai B, Gaillard S, Bernoux D, Morel Y, Chatelain P, Nicolino M, Cornu C; French Collaborative CAH Growth Study Group.

J Pediatr Endocrinol Metab. 2016 Dec 1;29(12):1379-1388. doi: 10.1515/jpem-2016-0156.

PMID:
27852974
5.

Evolution of steroids during pregnancy: Maternal, placental and fetal synthesis.

Morel Y, Roucher F, Plotton I, Goursaud C, Tardy V, Mallet D.

Ann Endocrinol (Paris). 2016 Jun;77(2):82-9. doi: 10.1016/j.ando.2016.04.023. Epub 2016 May 4. Review.

PMID:
27155772
6.

Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus.

Birraux J, Mouafo FT, Dahoun S, Tardy V, Morel Y, Mouriquand P, Le Coultre C, Mure PY.

Afr J Paediatr Surg. 2015 Jul-Sep;12(3):177-80. doi: 10.4103/0189-6725.170191.

7.

Land Use History Shifts In Situ Fungal and Bacterial Successions following Wheat Straw Input into the Soil.

Tardy V, Chabbi A, Charrier X, de Berranger C, Reignier T, Dequiedt S, Faivre-Primot C, Terrat S, Ranjard L, Maron PA.

PLoS One. 2015 Jun 23;10(6):e0130672. doi: 10.1371/journal.pone.0130672. eCollection 2015.

8.

Secondary amenorrhoea associated with high serum 17-hydroxyprogesterone levels revealing a heterozygous CYP21A2 mutation in a woman with Addison disease.

Boscolo M, Bry-Gauillard H, Tardy V, Young J.

Clin Endocrinol (Oxf). 2015 Apr;82(4):620-2. doi: 10.1111/cen.12646. Epub 2014 Dec 11. No abstract available.

PMID:
25353971
9.

Stability of soil microbial structure and activity depends on microbial diversity.

Tardy V, Mathieu O, Lévêque J, Terrat S, Chabbi A, Lemanceau P, Ranjard L, Maron PA.

Environ Microbiol Rep. 2014 Apr;6(2):173-83. doi: 10.1111/1758-2229.12126. Epub 2013 Dec 2.

PMID:
24596291
10.

Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: multicenter study of 45 French male patients.

Pierre P, Despert F, Tranquart F, Coutant R, Tardy V, Kerlan V, Sonnet E, Baron S, Lorcy Y, Emy P, Delavierre D, Monceaux F, Morel Y, Lecomte P.

Ann Endocrinol (Paris). 2012 Dec;73(6):515-22. doi: 10.1016/j.ando.2012.09.005. Epub 2012 Nov 3.

PMID:
23131470
11.

Efficiency of neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children born in mainland France between 1996 and 2003.

Coulm B, Coste J, Tardy V, Ecosse E, Roussey M, Morel Y, Carel JC; DHCSF Study Group.

Arch Pediatr Adolesc Med. 2012 Feb;166(2):113-20. doi: 10.1001/archpediatrics.2011.774.

12.

Methanobacterium lacus sp. nov., isolated from the profundal sediment of a freshwater meromictic lake.

Borrel G, Joblin K, Guedon A, Colombet J, Tardy V, Lehours AC, Fonty G.

Int J Syst Evol Microbiol. 2012 Jul;62(Pt 7):1625-9. doi: 10.1099/ijs.0.034538-0. Epub 2011 Sep 2.

PMID:
21890730
13.

Molecular defects of the CYP21A2 gene in Greek-Cypriot patients with congenital adrenal hyperplasia.

Skordis N, Kyriakou A, Tardy V, Ioannou YS, Varvaresou A, Dracopoulou-Vabouli M, Patsalis PC, Shammas C, Neocleous V, Phylactou LA.

Horm Res Paediatr. 2011;75(3):180-6. doi: 10.1159/000320040. Epub 2010 Sep 14.

PMID:
20838032
14.

Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.

Tardy V, Menassa R, Sulmont V, Lienhardt-Roussie A, Lecointre C, Brauner R, David M, Morel Y.

J Clin Endocrinol Metab. 2010 Mar;95(3):1288-300. doi: 10.1210/jc.2009-1202. Epub 2010 Jan 15.

PMID:
20080860
15.

Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Bidet M, Bellanné-Chantelot C, Galand-Portier MB, Golmard JL, Tardy V, Morel Y, Clauin S, Coussieu C, Boudou P, Mowzowicz I, Bachelot A, Touraine P, Kuttenn F.

J Clin Endocrinol Metab. 2010 Mar;95(3):1182-90. doi: 10.1210/jc.2009-1383. Epub 2010 Jan 15.

PMID:
20080854
16.

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

Young J, Tardy V, de la Perrière AB, Bachelot A, Morel Y; French Society of Endocrinology.

Ann Endocrinol (Paris). 2010 Feb;71(1):14-8. doi: 10.1016/j.ando.2009.12.009. Epub 2010 Jan 12. Review.

PMID:
20070950
17.

Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers.

Paris F, Tardy V, Chalançon A, Picot MC, Morel Y, Sultan C.

Gynecol Endocrinol. 2010 May;26(5):319-24. doi: 10.3109/09513590903511505.

PMID:
20059433
18.

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

Chevalier N, Carrier P, Piche M, Chevallier A, Wagner K, Tardy V, Benchimol D, Fénichel P.

Ann Endocrinol (Paris). 2010 Feb;71(1):56-9. doi: 10.1016/j.ando.2009.10.001. Epub 2009 Nov 25.

PMID:
19942208
19.

Precocious pubarche: distinguishing late-onset congenital adrenal hyperplasia from premature adrenarche.

Armengaud JB, Charkaluk ML, Trivin C, Tardy V, Bréart G, Brauner R, Chalumeau M.

J Clin Endocrinol Metab. 2009 Aug;94(8):2835-40. doi: 10.1210/jc.2009-0314. Epub 2009 May 19.

PMID:
19454583
20.

Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia.

Cavarzere P, Samara-Boustani D, Flechtner I, Dechaux M, Elie C, Tardy V, Morel Y, Polak M.

Eur J Endocrinol. 2009 Aug;161(2):285-92. doi: 10.1530/EJE-09-0145. Epub 2009 May 18.

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