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Moncef Benkhalifa

Showing results (101-110 of 109) with videos related to

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Journal of Assisted Reproduction and Genetics|June 28, 2020
Pregnancy after oocyte donation in a patient with NLRP7 gene mutations and recurrent molar hydatidiform pregnanciesClaire Cozette, Florence Scheffler, Melyne Lombart, et al.
Zygote (Cambridge, England)|July 20, 2019
Endometrium immunomodulation by intrauterine insemination administration of treated peripheral blood mononuclear cell prior frozen/thawed embryos in patients with repeated implantation failureFattaneh Farifteh Nobijari, Seyedeh Soheila Arefi, Ashraf Moini, et al.
Diseases (Basel, Switzerland)|February 26, 2026
Seminal Interleukin-6 as a Biomarker of Inflammation, Oxidative Stress, and Sperm Dysfunction in Infertile MenLoïc Koumba, Mariame Kabbour, Salma Ed-Doumy, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|September 5, 2020
Can Ratios Between Prognostic Factors Predict the Clinical Pregnancy Rate in an IVF/ICSI Program with a GnRH Agonist-FSH/hMG Protocol? An Assessment of 2421 Embryo Transfers, and a Review of the LiteraturePhilippe Merviel, Michel Menard, Rosalie Cabry, et al.
Human Molecular Genetics|July 23, 2015
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish familyOzlem Okutman, Jean Muller, Yoni Baert, et al.
Journal of Clinical Medicine|November 13, 2025
Impact of Systematic Follicular Flushing on Egg Retrieval and Embryo Quality in IVF-ICSI Cycles: A Controlled Study?Modou Mamoune Mbaye, Noureddine Louanjli, Mohamed Ennaji, et al.
Toxics|March 24, 2022
Chronic Perigestational Exposure to Chlorpyrifos Induces Perturbations in Gut Bacteria and Glucose and Lipid Markers in Female Rats and Their OffspringNarimane Djekkoun, Flore Depeint, Marion Guibourdenche, et al.
Journal of Assisted Reproduction and Genetics|April 13, 2017
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish familyOzlem Okutman, Jean Muller, Valerie Skory, et al.
Human Molecular Genetics|June 2, 2012
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspotsElias Elinati, Paul Kuentz, Claire Redin, et al.
Pageof 11

Showing results (101-110 of 109) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 109 results.
Journal of Assisted Reproduction and Genetics|June 28, 2020
Pregnancy after oocyte donation in a patient with NLRP7 gene mutations and recurrent molar hydatidiform pregnanciesClaire Cozette, Florence Scheffler, Melyne Lombart, et al.
Zygote (Cambridge, England)|July 20, 2019
Endometrium immunomodulation by intrauterine insemination administration of treated peripheral blood mononuclear cell prior frozen/thawed embryos in patients with repeated implantation failureFattaneh Farifteh Nobijari, Seyedeh Soheila Arefi, Ashraf Moini, et al.
Diseases (Basel, Switzerland)|February 26, 2026
Seminal Interleukin-6 as a Biomarker of Inflammation, Oxidative Stress, and Sperm Dysfunction in Infertile MenLoïc Koumba, Mariame Kabbour, Salma Ed-Doumy, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|September 5, 2020
Can Ratios Between Prognostic Factors Predict the Clinical Pregnancy Rate in an IVF/ICSI Program with a GnRH Agonist-FSH/hMG Protocol? An Assessment of 2421 Embryo Transfers, and a Review of the LiteraturePhilippe Merviel, Michel Menard, Rosalie Cabry, et al.
Human Molecular Genetics|July 23, 2015
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish familyOzlem Okutman, Jean Muller, Yoni Baert, et al.
Journal of Clinical Medicine|November 13, 2025
Impact of Systematic Follicular Flushing on Egg Retrieval and Embryo Quality in IVF-ICSI Cycles: A Controlled Study?Modou Mamoune Mbaye, Noureddine Louanjli, Mohamed Ennaji, et al.
Toxics|March 24, 2022
Chronic Perigestational Exposure to Chlorpyrifos Induces Perturbations in Gut Bacteria and Glucose and Lipid Markers in Female Rats and Their OffspringNarimane Djekkoun, Flore Depeint, Marion Guibourdenche, et al.
Journal of Assisted Reproduction and Genetics|April 13, 2017
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish familyOzlem Okutman, Jean Muller, Valerie Skory, et al.
Human Molecular Genetics|June 2, 2012
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspotsElias Elinati, Paul Kuentz, Claire Redin, et al.
Pageof 11