Kolexia
Ferreux Lucile Biologie médicale
Ferreux Lucile
Biologie médicale
Hôpital Cochin
Paris, France
43 Activités
405 Followers
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{{person.topmesh1.name}} Infertilité Asthénozoospermie Infertilité masculine Syndrome de Bardet-Biedl Choristome surrénalien Endométriose Oedème Hyperplasie congénitale des surrénales Trypanosomiase

Collaborateurs

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Pocate Cheriet Khaled
Pocate Cheriet Khaled
Gpe Hosp Cochin Saint Vincent De Paul, Paris, France
Patrat Catherine
Patrat Catherine
Hôpital Cochin, Paris, France
Bourdon Mathilde
Bourdon Mathilde
Hôpital Cochin, Paris, France
Santulli Pietro
Santulli Pietro
Hôpital Cochin, Paris, France

Industries

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Ferring
9 collaboration(s)
Dernière en 2023
Merck-Serono
2 collaboration(s)
Dernière en 2023
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Dernières activités

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Endometriosis-related infertility: severe pain symptoms do not impact assisted reproductive technology outcomes.
Human reproduction (Oxford, England)   23 décembre 2023
Overview of Gene Expression Dynamics during Human Oogenesis/Folliculogenesis.
International journal of molecular sciences   19 décembre 2023
ENDOMETRIOSIS: SEVERE PAIN SYMPTOMS DO NOT IMPACT ART (ASSISTED REPRODUCTIVE TECHNOLOGY) OUTCOMES
79th Scientific Congress of the American Society for Reproductive Medicine   01 octobre 2023
O-162 Fresh or frozen Day 6 blastocyst transfer : Is there still a question?
39th Hybrid Annual Meeting of the European Society of Human Reproduction and Embryology   22 juin 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
Sperm cryopreservation in young males with congenital adrenal hyperplasia (CAH).
Clinical endocrinology   07 juillet 2022
P-554 Impact of genotype and phenotype on ICSI outcomes of cystic fibrosis (CF) men patients: a cohort study about 107 ICSI from 1999 to 2019
38th Hybrid Annual Meeting of the European Society of Human Reproduction and Embryology   29 juin 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