Zobrazeno 1 - 10
of 145
pro vyhledávání: '"OCYTOCINE"'
Autor:
Miermon, Camille
Breathing is a highly dynamic process that varies in frequency and amplitude. These variations are related to the emotional and cognitive state of the animal but also to the recruitment of its olfactory system for the detection of odorant molecules,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______166::cdd269a5c453f6a84ad28c31ea921868
https://theses.hal.science/tel-03909187
https://theses.hal.science/tel-03909187
Akademický článek
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Autor:
St-Onge, Sandrine
Les facteurs de transcription SIM1, OTP, POU3F2 et ARNT2 interagissent ensemble en orchestrant le développement complexe de l’hypothalamus, une région du cerveau contenant plusieurs petites populations circonscrites de neurones, dont le noyau par
Externí odkaz:
http://hdl.handle.net/1866/26208
Autor:
Maille, Julia
Publikováno v:
Médecine humaine et pathologie. 2021
Le déclenchement artificiel du travail est une pratique courante en obstétrique. Les séquences d’utilisation des dispositifs de maturation cervicales (sonde à ballonnet et tampon de prostaglandines (PGE2)) dans le cas d’un col utérin immatur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2592::ea28abfa4b5c8503fab4a6a058be95b0
https://dumas.ccsd.cnrs.fr/dumas-03219346/document
https://dumas.ccsd.cnrs.fr/dumas-03219346/document
Autor:
Royer, Juliette
Acoustic communication is crucial for social interactions. In humans, it has been suggested that abnormal processing of sensory stimuli plays an important role in social behavior of patients suffering from autism spectrum disorders (ASD), which could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______166::89baa5ff8a3cf0ddabb8e3abeefe28a7
https://theses.hal.science/tel-03767528
https://theses.hal.science/tel-03767528
Autor:
Ivezic, Pauline
Publikováno v:
Médecine humaine et pathologie. 2020
Objective: To assess the administration of oxytocin of low-risk pregnancies during labor and delivery between three distinct periods (2011, 2015, 2019). Evaluate the rate of targeted interventions of these pregnancies in spontaneous labor and determi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2592::bf7728e69a29cf887d6046f76c7ebb4c
https://dumas.ccsd.cnrs.fr/dumas-03202336
https://dumas.ccsd.cnrs.fr/dumas-03202336
Autor:
Garcette, Laura
Publikováno v:
Gynécologie et obstétrique. 2020
Introduction: suboptimal breastfeeding is a national public health problem. In fact, in France, there is a frequency of breastfeeding and a duration of execution lower than the recommendations of the World Health organization. This reality justifies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2592::d1d8f6ef901563ccf4e0b38b067c1d0a
https://dumas.ccsd.cnrs.fr/dumas-03054068
https://dumas.ccsd.cnrs.fr/dumas-03054068
Autor:
Brunet, Fanny
Publikováno v:
Médecine humaine et pathologie. 2019
What a subject perceives from his body, can be define as interoception : his learning is partly through first aid. From the relationship to oneself, to the relation to the other, what can be the links, the similarities? We make the hypothesis that th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2592::3af345b2fb8daf1c7466127c92b698b0
https://dumas.ccsd.cnrs.fr/dumas-03129800
https://dumas.ccsd.cnrs.fr/dumas-03129800
Autor:
Caccialupi Da Prato, Laura
Le Syndrome de Prader Willi (SPW) est une pathologie neurodéveloppementale d’origine génétique présentant un tableau clinique complexe et évoluant avec l’âge.Elle est caractérisée par des déficits sensori-moteurs présents dès la naissa
Externí odkaz:
http://www.theses.fr/2019AIXM0133
Autor:
Debladis, Jimmy
Publikováno v:
Neurosciences. Université Paul Sabatier-Toulouse III, 2019. Français. ⟨NNT : 2019TOU30036⟩
Prader-Willi syndrome (PWS) is a rare genetic syndrome affecting around 1 in 20,000 births in France. The two most frequent genetic origins are either a deletion in the 15q11q12 region on the paternal chromosome 15 or maternal uniparental disomy. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2592::c608db8881c568db7668981cc96f222b
https://tel.archives-ouvertes.fr/tel-02896490/file/2019TOU30036a.pdf
https://tel.archives-ouvertes.fr/tel-02896490/file/2019TOU30036a.pdf