Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Séraphin, Nguefack"'
Autor:
Andreas Chiabi, Amandine Nadege M. Djimafo, Séraphin Nguefack, Evelyn Mah, Félicité Nguefack Dongmo, Fru Angwafo, III
Publikováno v:
Journal of Infection and Public Health, Vol 13, Iss 10, Pp 1469-1472 (2020)
Background and objective: Malaria is the most widely spread parasitic disease in the world, especially in the tropics affecting mostly children and pregnant women. In children, mostly under-fives carry the heaviest burden in terms of morbidity and mo
Externí odkaz:
https://doaj.org/article/63500ce257644e61ac5d2c65e0e5b707
Autor:
Dominique Enyama, Diomède Noukeu Njinkui, Jeanne Mayouego Kouam, Christian Eyoum, Danièle Christiane Kedy Koum, Séraphin Nguefack
Publikováno v:
The Pan African Medical Journal, Vol 39, Iss 5 (2021)
In the acute phase of the COVID-19 outbreak, focus is usually made on the fact that children are less susceptible to severe forms. However, the COVID-19 pandemic has numerous other issues in children’s health that maybe minimized in the Cameroonian
Externí odkaz:
https://doaj.org/article/a4fce42544a444ed87b1eb8e1317905a
Autor:
Karen Kengne Kamga, Nchangwi Syntia Munung, Séraphin Nguefack, Ambroise Wonkam, Jantina De Vries
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Abstract Background Fragile X Syndrome (FXS) is a neurogenetic condition that significantly impacts the lives of affected individuals and their families due to its association with intellectual disability (ID) and stigma. Method In this paper, we pre
Externí odkaz:
https://doaj.org/article/7955107e363f426c94b83b3ceb525257
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Abstract Background Most of the previous studies on Duchenne Muscular Dystrophy (DMD) were conducted in Caucasian, Asian, and Arab populations. Therefore, little is known about the features of this disease in Africans. In this study, we aimed to dete
Externí odkaz:
https://doaj.org/article/a188fa4720c845e5b4be51673534db5a
Autor:
Andreas Chiabi, Félicitée D. Nguefack, Florine Njapndounke, Marie Kobela, Kelly Kenfack, Séraphin Nguefack, Evelyn Mah, Georges Nguefack-Tsague, Fru Angwafo
Publikováno v:
BMC Pediatrics, Vol 17, Iss 1, Pp 1-7 (2017)
Abstract Background Vaccination is a major, but simple and cost effective public health intervention in the prevention of infectious diseases, especially in children. Nowadays, many children still miss scheduled vaccines in the Extended Program of Im
Externí odkaz:
https://doaj.org/article/21aff36d20c34b178f0ca9b74d83feb2
Autor:
Hubert Désiré Mbassi Awa, Rose Mbédé Nga Mvondo, Séraphin Nguefack, Charles Bengondo Messanga, Paul Olivier Koki Ndombo
Publikováno v:
The Pan African Medical Journal, Vol 32, Iss 195 (2019)
INTRODUCTION: Les maladies rares ont pour certaines des manifestations orales. Celles-ci sont souvent sous-étudiées; ce qui contribue à limiter l'offre de soins bucco-dentaires pour cette catégorie de patients. Le but est de déterminer les aspec
Externí odkaz:
https://doaj.org/article/748777cc5a234629844c9511bdcfc0aa
Autor:
Julius Dohbit Sama, Elvis Meten, Assumpta Lucienne Bella, Sylvie Kwedi Nolna, Annick Tchouamou, Séraphin Nguefack, Robinson Enow Mbu, Felicite Nguefack Dongmo, Andreas Chiabi, Evelyn Mah
Publikováno v:
Asploro Journal of Pediatrics and Child Health. 3:33-39
Introduction: Child sexual abuse is an extensive health and societal problem as even the lowest prevalence of child sexual abuse includes a huge number of victims who still need to be considered. Africa has the highest prevalence of child sexual abus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a565b5c26924052f5dfe93f7ce2eb9c9
https://doi.org/10.36502/2021/asjpch.6166
https://doi.org/10.36502/2021/asjpch.6166
Autor:
Nchangwi Syntia Munung, Ambroise Wonkam, Séraphin Nguefack, Karen Kengne Kamga, Jantina de Vries
Publikováno v:
Journal of Genetic Counseling. 30:1727-1736
Among the myriad causes of intellectual disability (ID), Fragile X Syndrome (FXS) is the leading genetic cause. Yet, little is known of how people affected by this condition make sense of it. The present study aimed to investigate the explanatory mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c718996b5418b8e79c10d4b679ca03b7
https://doi.org/10.1002/jgc4.1440
https://doi.org/10.1002/jgc4.1440
Autor:
E. Mah, Séraphin Nguefack, Félicitée Nguefack, A. Laksira, D.A. Kago Tague, Andreas Chiabi, D. Simnoue
Publikováno v:
Journal de Pédiatrie et de Puériculture. 33:77-82
Resume Introduction Une diversification inappropriee peut conduire a une malnutrition chez les enfants de 6 a 24 mois. Ce probleme crucial justifie des recherches dans la partie septentrionale du Cameroun qui est une zone tres touchee par la malnutri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e4338c58ad1114bf8a1930a7e605072
https://doi.org/10.1016/j.jpp.2019.07.006
https://doi.org/10.1016/j.jpp.2019.07.006
Autor:
Michael A. Morris, Séraphin Nguefack, Cedrik Tekendo-Ngongang, Huguette Zambo, Isabelle Moix, Stefania Gimelli, Sophie Dahoun, Frédérique Sloan-Béna, Ambroise Wonkam
Publikováno v:
Am J Med Genet A
MECP2 duplication syndrome (MDS; OMIM 300260) is an X-linked neurodevelopmental disorder, caused by nonrecurrent duplications of the Xq28 region involving the gene methyl-CpG-binding protein 2 (MECP2; OMIM 300005). The core phenotype of affected indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::499968c7c2225c007d2bd4a8f642a1e1
https://doi.org/10.1002/ajmg.a.61510
https://doi.org/10.1002/ajmg.a.61510