Results 61 to 70 of about 125,757 (235)
Variante(s) de titre : Petit almanach illustré pour ...Variante(s) de titre : Petit almanach des enfantsVariante(s) de titre : Petit almanach des enfants : organe officiel de l'Association universelle des enfants catholiques : édition françaiseAvec mode ...
Association universelle des enfants catholiques (France). Auteur du texte
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ABSTRACT Objective To describe the prenatal diagnosis, evolution, and perinatal management of kaposiform hemangioendothelioma (KHE) complicated by the Kasabach–Merritt phenomenon (KMP), and to report the first documented use of maternal sirolimus therapy (MST) in this setting. Methods We retrospectively reviewed four fetuses with a prenatal soft‐tissue
Antoine Fraissenon +11 more
wiley +1 more source
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
La compréhension de l’épidémiologie de la COVID-19 chez les enfants et les jeunes au Canada aidera à éclairer les mesures de santé publique dans les milieux où les enfants se rassemblent.
Dana Paquette +7 more
doaj +1 more source
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
INTRODUCTION: Le risque de décès serait élevé dans les unités des soins intensifs (USI) des pays en développement. Nous décrivons les décès survenus à l´Unité des Soins Intensifs du Centre Mère et Enfant de Yaoundé au Cameroun.
Félicitée Nguefack +6 more
doaj +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
In the present paper, the daily mobility of children is seen as a unique analyzer of family life styles, more especially as concerns those families that have opted to reside in the suburbs, in one of the new towns in the area of Paris .Using both ...
Sandrine Depeau
doaj

