Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Brice Poreau"'
Autor:
Brice Poreau
Publikováno v:
Revue Médecine et Philosophie, Vol 1, Iss 1 (2019)
L’objectif de cet article est de montrer la construction de normes des troubles du spectre de l’autisme faisant suite à l’observation de Kanner en 1943 et d’évoquer les limites de ces normes en utilisant les travaux sur le normal et le pa
Externí odkaz:
https://doaj.org/article/850f67faf2554540a69182157ac5ce15
Autor:
Brice Poreau
Publikováno v:
The Pan African Medical Journal, Vol 29, Iss 146 (2018)
Prenatal diagnosis, care and management are involved in mortality and morbidity of every country. A high prevalence is estimated in Africa. We use bibliometrics and mapping tools to explore the area studies and countries involved in scientific resear
Externí odkaz:
https://doaj.org/article/d678ea49ea5044208291b83eb9753fd1
Autor:
Brice POREAU
Publikováno v:
Iranian Journal of Public Health, Vol 46, Iss 3 (2017)
Background: Due to embargoes and sanctions from 1979 until 2015, impact on scientific research in Iran may be critical. Public health is the main example of this burning point. In this paper, the aim was to map the scientific research in public healt
Externí odkaz:
https://doaj.org/article/221cc02780a748d0b96f0ef75036626a
Autor:
Brice Poreau
Publikováno v:
The Pan African Medical Journal, Vol 23, Iss 220 (2016)
INTRODUCTION: neurodegenerative disorders are involved in mortality and morbidity of every country. A high prevalence is estimated in Africa. Neurodegenerative disorders are defined by a progressive or self-limiting alteration of neurons implied in s
Externí odkaz:
https://doaj.org/article/6e729a93fe8f4494bb170f7a93347ca6
Autor:
Mathilde Chivet, Maximilian McCluskey, Anne Sophie Nicot, Julie Brocard, Mathilde Beaufils, Diane Giovannini, Benoit Giannesini, Brice Poreau, Jacques Brocard, Sandrine Humbert, Frédéric Saudou, Julien Fauré, Isabelle Marty
Publikováno v:
Journal of General Physiology. 155
The expression of the Huntingtin protein, well known for its involvement in the neurodegenerative Huntington’s disease, has been confirmed in skeletal muscle. The impact of HTT deficiency was studied in human skeletal muscle cell lines and in a mou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c231337ed4e85c94b483438d2d1d23a
https://doi.org/10.1085/jgp.202213103
https://doi.org/10.1085/jgp.202213103
Autor:
Anouk Emadali, Pierre-Simon Jouk, Loris Delrieu, Brice Poreau, Hervé Sartelet, Alexia Apostolou, Julien Thévenon, Guillaume Lallemand
Publikováno v:
Pathobiology. 87:302-310
Multicystic renal dysplasia is a congenital cystic anomaly of the kidney caused by abnormal metanephric differentiation with immature tubules. It is surrounded by mesenchymal collars and islands of immature mesenchyma present between the cysts. The P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01f4f7b48e9f72fc44be380bec395f83
https://doi.org/10.1159/000509152
https://doi.org/10.1159/000509152
Publikováno v:
Transfusion Clinique et Biologique. 29:337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1b4639ad9fd13aa967ca55d2a0ee40a
https://doi.org/10.1016/j.tracli.2022.08.018
https://doi.org/10.1016/j.tracli.2022.08.018
Autor:
Renaud Touraine, Véronique Adouard, Pierre-Simon Jouk, Véronique Satre, Radu Harbuz, Claire Vettier, Claire Barro, Charles Coutton, Francis Ramond, Julien Thevenon, Brice Poreau, Klaus Dieterich
Publikováno v:
American Journal of Medical Genetics Part A. 179:650-654
The AMME syndrome defined as the combination of Alport syndrome, intellectual disability, midface hypoplasia, and elliptocytosis (AMME) is known to be a contiguous gene syndrome associated with microdeletions in the region Xq22.3q23. Recently, using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84530a318dc449d13a19b48b014a44c8
https://doi.org/10.1002/ajmg.a.61057
https://doi.org/10.1002/ajmg.a.61057
Autor:
Brice Poreau
Publikováno v:
Médecine et philosophie
Médecine et philosophie, Association Médecine et philosophie, 2020
Médecine et philosophie, 2020
Médecine et philosophie, Association Médecine et philosophie, 2020
Médecine et philosophie, 2020
L’utilisation de l’intelligence artificielle dans le domaine de la santé pose la question des limites de celle-ci : jusqu’où devons-nous employer l’intelligence artificielle, la médecine pourrait-elle être déshumanisée et perdre son sen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1554a8584cc362476c5dfa7c23a7213
https://shs.hal.science/halshs-03119592
https://shs.hal.science/halshs-03119592
Autor:
Aurélien Courvoisier, Marco Bigoni, Marco Turati, Lilia Brahim, Brice Poreau, Giovanni Zatti, Andrea Cossio, Julien Thevenon
KBG Syndrome is a rare syndrome characterized by facial and hand anomalies, postnatal short stature, delayed bone age, intellectual disability and macrodontia. A key role of mutations in ANRKD11 gene was observed not only in central nervous system bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae63b416f43c2f523dc28cdca0d8db82
http://hdl.handle.net/10281/300335
http://hdl.handle.net/10281/300335