Publications by authors named "Stephane Triau"

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Toward clinical and molecular dissection of frontonasal dysplasia with facial skin polyps: From Pai syndrome to differential diagnosis through a series of 27 patients.
Daphné Lehalle, Ange-Line Bruel, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Yannis Duffourd, Stéphane Triau

Am J Med Genet A· July 2022

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Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder.
Marine Tessarech, Magali Gorce, Françoise Boussion, Jean-Philippe Bault, Stéphane Triau

Am J Med Genet A· March 2020

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The oculoauriculofrontonasal syndrome: Further clinical characterization and additional evidence suggesting a nontraditional mode of inheritance.
Daphné Lehalle, Umut Altunoglu, Ange-Line Bruel, Mirna Assoum, Yannis Duffourd, Stéphane Triau

Am J Med Genet A· December 2018

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Fatal Myopericarditis Following an Influenza A (H3N2) Infection.
Caroline Lefeuvre, Sylvie Behillil, Stéphane Triau, Antonio Monteiro-Rodrigues, François Templier

Am J Case Rep· May 2018

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Prenatal diagnosis of focal dermal hypoplasia: Report of three fetuses and review of the literature.
Laura Mary, Sophie Scheidecker, Monique Kohler, Maria-Paola Lombardi, Anne-Lise Delezoide, Stéphane Triau

Am J Med Genet A· February 2017

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Histopathology of prostate tissue after vascular-targeted photodynamic therapy for localized prostate cancer.
Caroline Eymerit-Morin, Merzouka Zidane, Souhil Lebdai, Stéphane Triau, Abdel Rahmene Azzouzi

Virchows Arch· October 2013

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Prenatal diagnosis of CHARGE syndrome by identification of a novel CHD7 mutation in a previously unaffected family.
Estelle Colin, Dominique Bonneau, Francoise Boussion, Agnès Guichet, Benoit Delorme, Stéphane Triau

Prenat Diagn· July 2012

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Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.
Olivier Gribouval, Vincent Morinière, Audrey Pawtowski, Christelle Arrondel, Satu-Leena Sallinen, Stéphane Triau

Hum Mutat· February 2012

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Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.
Louise Devisme, Céline Bouchet, Marie Gonzalès, Elisabeth Alanio, Anne Bazin, Stéphane Triau

Brain· February 2012

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An elevated level of TSH might be predictive of differentiated thyroid cancer.
Anne Dorange, Stéphane Triau, Stéphanie Mucci-Hennekinne, Alain Bizon, Sandrine Laboureau-Soares

Ann Endocrinol (Paris)· December 2011

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Increasing the number of thyroid lesions classes in microarray analysis improves the relevance of diagnostic markers.
Jean-Fred Fontaine, Delphine Mirebeau-Prunier, Mahatsangy Raharijaona, Brigitte Franc, Stephane Triau

PLoS One· October 2009

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Phenol sulfotransferase SULT1A1*2 allele and enhanced risk of upper urinary tract urothelial cell carcinoma.
Morgan Rouprêt, Géraldine Cancel-Tassin, Eva Comperat, Gaëlle Fromont, Mathilde Sibony, Stéphane Triau

Cancer Epidemiol Biomarkers Prev· November 2007

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Usefulness of repeated fine-needle cytology in the follow-up of non-operated thyroid nodules.
Frédéric Illouz, Patrice Rodien, Jean Paul Saint-André, Stéphane Triau, Sandrine Laboureau-Soares

Eur J Endocrinol· March 2007

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Duodenopancreatectomy for cystic dystrophy in heterotopic pancreas of the duodenal wall.
Patrick Pessaux, Paul Lada, Sandrine Etienne, Jean-Jacques Tuech, Emilie Lermite, Stéphane Triau

Gastroenterol Clin Biol· January 2006

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Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2.
Agnès Guichet, Stéphane Triau, Catherine Lépinard, Chantal Esculapavit, Florence Biquard

Prenat Diagn· October 2004

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