Results 81 to 90 of about 147,441 (298)
Fabre Sylvie. Enfant. In: Sorcières : les femmes vivent, n°23, 1981. Enfants. pp.
Fabre-Giacomini, Sylvie
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Fontaine Maurice. Enfant de la Lune. In: Diasporas. Histoire et sociétés, n°6, 2005. Migrations en mémoire. pp.
Fontaine, Maurice
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How to facilitate ultrasound examination of the fetal heart: the 5‐4‐3‐2‐1 method
ABSTRACT We propose a new standardized, systematic method of fetal cardiac screening, the step‐by‐step ‘5‐4‐3‐2‐1’ method. This method is based on understanding the cardiac structures through a process of navigating between the different recommended views during an abdominothoracic sweep, following a user‐friendly checklist to identify the main ...
M. Levy, B. Stos
wiley +1 more source
Introduction: The incidence of extrauterine pregnancy increases to 2â12% following in vitro fertilizationâembryo transfer. Several pathogenic theories have been suggested, including abnormal hormonal secretion or exogenous hormones administered in ...
Tariq Baghdadi +3 more
doaj +1 more source
Les instituteurs : leurs meilleures histoires drôles / Maude Enfant
Collection : Métiers pour rire !Collection : Métiers pour rire !Contient une table des matièresAvec mode texteOuvrages ...
Enfant, Maude. Auteur du texte
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Looking at Us Through Their Eyes. The Analytical Process from Ethnographic Perspectives1
Abstract This article looks at the analytical situation through the Others’ eyes—through examples from contemporary ethnographies of foreign cultures. It discusses the following issues: a) The analogy between the ontological worlds of the dead, ghosts, animals and dreams in “primitive populations” and the analytical psychological descriptions of the ...
Stefano Carta
wiley +1 more source
Abstract Purpose Inherited retinal diseases (IRDs) are a clinically and genetically heterogeneous group of disorders, with ~30% of cases remaining genetically unsolved. Complete congenital stationary night blindness (cCSNB) is a subtype of IRD, usually associated with reduced visual acuity, nystagmus and high myopia.
Filip Spanic +10 more
wiley +1 more source
Summary Germline gain‐of‐function variants in sterile alpha motif domain–containing 9‐like (SAMD9L), located on chromosome 7q, cause a multisystem disorder characterized by bone marrow failure, immunodeficiency and variable neurological involvement. Disease evolution is frequently shaped by somatic genetic rescue (SGR), most commonly through monosomy 7,
Hadjer Dellal +10 more
wiley +1 more source
Le tetanos chez le grand enfant dans un hôpital pédiatrique à Yaoundé, Cameroun
Le tétanos est évitable par la vaccination, mais peut survenir en cas d’une immunisation incomplète. Nous avons mené une étude sur les dossiers médicaux des enfants admis pour tétanos entre 2008-2009 au Centre Mère et Enfant de la Fondation Chantal BIYA ...
Mina Ntoto Njiki Kinkela +6 more
doaj +1 more source
Le cavernome porte chez l'enfant : a propos de 11 cas
Le cavernome portal est la conséquence d'une occlusion chronique, du système porte extra-hépatique formé d'un réseau de veines dont le calibre est augmenté et au sein desquelles chemine un sang portal hépatopéte.Chez l'enfant, est une cause majeure d ...
Tadmori Ilham +2 more
doaj +1 more source

