Results 101 to 110 of about 4,251 (209)

Daughter vs. daughter‐in‐law: Kinship roles and women's time use in India

open access: yesDevelopment Policy Review, Volume 44, Issue 6, November 2026.
Abstract Motivation Women's labour force participation in India remains low despite improvements in education and economic conditions. Household organization and kinship relations may shape women's opportunities for paid work by influencing how unpaid work is allocated among women within the same family.
Tanu Gupta, Digvijay S. Negi
wiley   +1 more source

Marble Under a Strange Spell: St. John Rivers’ “Long-Cherished Scheme” to Wed Jane Eyre

open access: yesJournal of Popular Romance Studies, 2017
For most readers, the third volume of Charlotte Brontë’s Jane Eyre is the least gratifying of this great literary achievement of the Victorian era. Thornfield Hall and its passionate proprietor Edward Rochester are distant memories to “Jane Elliott” as ...
Michelle Thurlow
doaj  

Depression Beyond the 6‐Month Postpartum Period: A Mixed‐Method Study Among Women in Nepal

open access: yesJournal of Advanced Nursing, Volume 82, Issue 11, Page 10029-10042, November 2026.
ABSTRACT Aim This study aimed to comprehensively examine social and clinical factors contributing to postpartum depression among women in Nepal and identify their perspectives/experiences regarding postpartum mental health. Design and Methods The explanatory sequential mixed‐method study was conducted in two phases. In the quantitative phase, data were
Sangita Pudasainee‐Kapri   +7 more
wiley   +1 more source

Board Gender Diversity and Firm Financial Performance: Exploring the role of Directors’ Family Affiliations

open access: yesJournal of Management Studies, Volume 63, Issue 7, Page 4151-4183, November 2026.
Abstract Recent studies acknowledge that the contribution of female directors at the board may not be uniform but instead varies depending on their individual characteristics and board context. In this study we focus on a pivotal yet insufficiently explored facet of female directors – their affiliation with the business owning family – and assess its ...
Yuliya Ponomareva   +3 more
wiley   +1 more source

Prevalence of Rare Diseases in Consanguineous Marriages: A Case of Ullrich Muscular Dystrophy in a Resource‐Limited Setting

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
Ullrich Muscular Dystrophy in Consanguineous Marriage. ABSTRACT In regions with high consanguinity, rare recessive disorders like Ullrich congenital muscular dystrophy (UCMD) may present at birth with hypotonia and respiratory distress. To enhance quality of life and prevent recurrence in future pregnancies, early recognition, genetic counseling, and ...
Kanza Farhan   +5 more
wiley   +1 more source

Bardet–Biedl Syndrome Presenting With Acute Kidney Injury Revealing Previously Undiagnosed Advanced Chronic Kidney Disease in a Young Adult: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Bardet–Biedl syndrome (BBS) is an autosomal recessive disorder characterized by obesity, rod‐cone dystrophy, polydactyly, developmental delay, renal dysfunction, and genitourinary abnormalities. We report the case of a 27‐year‐old female with previously undiagnosed BBS who presented with acute kidney injury precipitated by acute ...
Aqeel Abbas   +8 more
wiley   +1 more source

PERRAULT'S SYNDROME: A CLINICAL AND GENETIC INVESTIGATION OF THREE SISTERS

open access: yesActa Medica Iranica, 1999
Perrault's syndrome (P.S.) is rare. The combination of gonadal dysgenesis and hearing loss was accompanied by 46,XXkaryotype in three sisters with parental consanguineous marriage.
P. Mehdipour   +2 more
doaj  

Unclassified COL6A1 Variant in a Child With Congenital Hypotonia: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT We report a 3‐year‐old male with congenital hypotonia, proximal contractures, and distal hyperlaxity. Exome sequencing identified a novel homozygous COL6A1 variant (c.2821C>T), classified as a variant of uncertain significance. The distinct phenotype strongly supports Ullrich congenital muscular dystrophy, expanding the gene's mutational ...
Khadeeja Nofal   +5 more
wiley   +1 more source

The Case for Banning Cousin Marriage

open access: yesOxford Journal of Law and Religion
Abstract This article presents the universal case for banning cousin marriage regardless of jurisdiction or culture. It is intended both as a resource—the relevant facts and opposing arguments will be set out plainly for reference purposes—and a legal argument which seeks to demonstrate that the weight of evidence concerning this poorly ...
openaire   +1 more source

Remembering Interracial Intimacies: South Asian Perspectives on Black/Brown Sex and Romance in Colonial East Africa

open access: yesGender &History, Volume 38, Issue 3, Page 833-845, October 2026.
ABSTRACT Bringing together historical evidence, postcolonial fiction and memory work, this study recovers South Asian cultural attitudes towards interracial heterosexual romance from the margins of East African history. It asks why Black/brown intimacy was treated as taboo and denied legitimacy within South Asian diasporic communities in British‐ruled ...
Carissa Chew
wiley   +1 more source

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