Results 81 to 90 of about 10,054 (226)

“A Person's God Should Look Like Them”: African Traditional Religions Among Black Queer Millennials and Gen Z Americans

open access: yesJournal for the Scientific Study of Religion, EarlyView.
ABSTRACT How are young Black Americans practicing spirituality contemporarily? Today younger generations of Black Americans are more likely than older Black Americans to identify as religiously unaffiliated or as practicing a non‐Christian faith. Drawing on 109 interviews with Black Millennial and Gen Z Americans, I examine how some of these younger ...
Terrell J. A. Winder
wiley   +1 more source

Femmes et représentations du féminin au cœur de la littérature française et de l’Histoire [PDF]

open access: yesÇédille: Revista de Estudios Franceses, 2019
À propos de l’ouvrage dirigé par Mercè Boixareu, Figures féminines de l’histoire occidentale dans la littérature française, édité par Esther Juan-Oliva et Ángela M. Romera-Pintor, avec Préface de Michelle Perrot (Paris, Honoré Champion, 2016, 484 p. ISBN
Nieves Ibeas-Vuelta
doaj  

The (trans)national Russian religious imagination in exile: Iulia de Beausobre (1893‐1977)

open access: yesModern Theology, EarlyView.
Abstract The article offers a case study of how Russian Orthodox who migrated from the Soviet Union after the Bolshevik Revolution of 1917 reimagined their religious identity and their church in a transnational setting. Iulia de Beausobre (1893‐1977) was a Russian aristocrat who fell victim to the Stalinist purges but survived the Soviet prison system ...
Ruth Coates
wiley   +1 more source

Une traductrice spécialisée au XIXe siècle : María Antonia Gutiérrez Bueno y Ahoiz et la maladie du « choléra-morbus » [PDF]

open access: yesSynergies Espagne, 2019
Au XIXe siècle, période historique d’avancées scientifiques ayant fait suite aux Lumières, les Sciences et les Lettres étaient des métiers réservés au genre masculin ; la traduction spécialisée n’y fit pas exception.
Sandra Pérez Ramos
doaj  

Social Inequalities in Infant Mortality Related to Congenital Anomalies: A Population‐Based Register Study

open access: yesPaediatric and Perinatal Epidemiology, EarlyView.
ABSTRACT Background Infant mortality has recently increased in France, especially in deprived areas. Congenital anomalies (CA) are a major cause of infant mortality and could contribute to these trends. Objectives This study aimed to investigate socio‐spatial inequalities in infant mortality associated with CA.
Bermet Amirova   +6 more
wiley   +1 more source

Political Gender Stereotypes in Parallel: Are Elites or Citizens More Prejudiced?

open access: yesSwiss Political Science Review, EarlyView.
Abstract Research shows that many voters ascribe stereotypical traits and issue competences to male and female politicians – such as viewing women as more compassionate and honest, and men as more competent and decisive – and use these perceptions when evaluating candidates.
Nathalie Giger, Anke Tresch
wiley   +1 more source

Transgresiones corporales y metamorfosis queer de dos santas vivas: Juana de la Cruz y Luisa Benítez. Cuerpo, género y ambigüedad

open access: yesE-Spania
Dans cette recherche, nous abordons les transgressions de genre de deux femmes considérées, à leur époque et dans leur contexte, comme des saintes vivantes : Sœur Juana de la Cruz et Luisa Benítez.
Margarita Paz Torres
doaj   +1 more source

Theatres of Indirectness: Passive Aggression and Failure

open access: yes
Critical Quarterly, EarlyView.
Sara Crangle, Sam Ladkin
wiley   +1 more source

Maternal–fetal platelet alloimmunization: Identification of risk factors for severe neonatal thrombocytopenia

open access: yesTransfusion, EarlyView.
Abstract Background Feto‐maternal platelet alloimmunization (FNAIT) is a rare condition (1 in 1500 live pregnancies), most commonly diagnosed based on clinical neonatal hemorrhagic manifestations, which can vary in severity. The aim of our study was to identify risk factors for severe fetal/neonatal thrombocytopenia in cases of FNAIT.
Elise Deroubaix   +7 more
wiley   +1 more source

Clinical outcomes of exclusive enzyme therapy (laronidase) in a cohort of patients with mucopolysaccharidosis type I

open access: yesOrphanet Journal of Rare Diseases
Background Mucopolysaccharidosis type I (MPS I), is an autosomal recessive disorder caused by a deficiency in the enzyme α-L-iduronidase (IDUA), leading to the accumulation of glycosaminoglycans (GAGs) in tissues.
Nathalie Guffon   +6 more
doaj   +1 more source

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