Výsledky vyhledávání - "Daphne Karfunkel-Doron"

Scopolamine Treatment and Adaptation to Airsickness

Autor: Omer Doron, Orit Samuel, Daphne Karfunkel-Doron, Dror Tal

Publikováno v: Aerospace medicine and human performance. 91(4)

BACKGROUND: Airsickness is a clinical syndrome manifesting in a variety of symptoms, particularly nausea and vomiting during flight. Studies of habituation to motion sickness in humans treated by scopolamine have produced conflicting results. The dru

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3fb2c0872e56f7f5903fa08a99e4f29
https://pubmed.ncbi.nlm.nih.gov/32493552

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Intranasal gonadotropin-releasing hormone agonist (GnRHa) for luteal-phase support following GnRHa triggering, a novel approach to avoid ovarian hyperstimulation syndrome in high responders

Autor: Nurit Carmon, Liron Sheena, Yeela Omer, Daphne Karfunkel-Doron, Yossi Mizrachi, Itai Bar-Hava, Gila Ben-David

Publikováno v: Fertility and sterility. 106(2)

Objective To study whether intranasal GnRH agonist (GnRHa) can be effectively used for luteal support in high-responder patients undergoing fresh-embryo transfer after ovulation induction with the use of GnRHa. Design Retrospective cohort study. Sett

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d94ff00cf23773ed8f5e7a26296ce61
https://pubmed.ncbi.nlm.nih.gov/27181923

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Genomic Applications in Audiological Medicine

Autor: Daphne Karfunkel-Doron, Karen B. Avraham, Zippora Brownstein

Publikováno v: Genomic Medicine: Principles and Practice

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8b447f18f27c052aa4d1edb5075766b9
https://doi.org/10.1093/med/9780199896028.003.0043

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Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing

Autor: Karen B. Avraham, Moshe Frydman, Zippora Brownstein, Anne Houdusse, Serena Sirigu, Amal Abu-Rayyan, Daphne Karfunkel-Doron, Bella Davidov, Mordechai Shohat, Moien Kanaan

Hereditary hearing loss is genetically heterogeneous, with a large number of genes and mutations contributing to this sensory, often monogenic, disease. This number, as well as large size, precludes comprehensive genetic diagnosis of all known deafne

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28098b04ed366c2f70b35183d2dfc481
https://europepmc.org/articles/PMC4023209/

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