Kolexia
Dulioust Emmanuel Médecine générale
Dulioust Emmanuel
Médecine générale
Hôpital Bicêtre
Le Kremlin-Bicêtre, France
45 Activités
0 Followers
Scientifique
Digital
Production scientifique
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Expertise
Sujets de recherche
{{person.topmesh1.name}} Infertilité masculine Infertilité Asthénozoospermie Infections à VIH Tératozoospermie Dyskinésies Troubles de la motilité ciliaire Malformations multiples Syndrome de Bardet-Biedl

Collaborateurs

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Patrat Catherine
Patrat Catherine
Hôpital Cochin, Paris, France
Coutton Charles
Coutton Charles
Hôpital Nord Grenoble, La Tronche, France
Wolf Jean-Philippe
Wolf Jean-Philippe
Hôpital Cochin, Paris, France
Kherraf Zine-Eddine
Kherraf Zine-Eddine
Institut National De La Sante Et De La Recherche Medicale, Paris, France

Industries

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Merck-Serono
1 collaboration(s)
Dernière en 2022
Ferring
1 collaboration(s)
Dernière en 2021
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Dernières activités

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CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.
Clinical genetics   17 novembre 2023
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans.
iScience   10 juillet 2023
Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters.
Journal of genetics and genomics = Yi chuan xue bao   26 avril 2023
Testicular impairment in Primary Adrenal Insufficiency caused by Nicotinamide Nucleotide Transhydrogenase (NNT) deficiency - a case report: implication of oxidative stress and importance of fertility preservation.
Basic and clinical andrology   14 mars 2023
Identification of two novel point mutations in DPY19L2 leading to total globozoospermia in two unrelated patients
Abstracts from the 54th European Society of Human Genetics (ESHG) Conference   01 avril 2022
Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.
Human reproduction (Oxford, England)   02 novembre 2021
O-092 Sperm phenotype, ICSI outcome and genetic diagnosis in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum
37th Virtual Annual Meeting of the European Society of Human Reproduction and Embryology   06 août 2021
Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
Human genetics   14 juin 2021
Assisted reproductive technology outcomes in women with a chronic viral disease.
AIDS (London, England)   19 mai 2021
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
Human genetics   10 mars 2021