Results 211 to 220 of about 51,586 (301)

Glanzmann Thrombasthenia in a 14-Month-Old Infant: A Rare Platelet Function Disorder Presenting With Persistent Mucocutaneous Bleeding. [PDF]

Cureus
Chemlal I, Tkak H, Azizi M, Ghanam A.
europepmc   +1 more source

Listening to Children's Need to Matter in Skipped Generation Migrant Households: A Study in Rural Hunan, China

Child &Family Social Work, EarlyView.
ABSTRACT This article explores the experiences of children who live in skipped generation households because of parental migration. Drawing on our matched interviews with 34 children and 20 grandparents from 19 skipped generation households in rural Hunan, central China, we examine what the children wanted significant adults to know about their care ...
Rachel Murphy, Li Mi, Xiaoyan Huang
wiley   +1 more source

Association between tobacco-related social environment and e-cigarette use among young adults in northern Vietnam: A cross-sectional study with latent class analysis. [PDF]

Tob Induc Dis
Vu MC, Isaranuwatchai W, Chotipanvithayakul R, Wichaidit W.   +3 more
europepmc   +1 more source

Who Is a Sibling? Social Work Professionals' Views on Definitions of Siblinghood in Foster Care in England

Child &Family Social Work, EarlyView.
ABSTRACT When children are placed in foster care, social work professionals decide whether they should and can be placed with their siblings. In England, this has become an important discussion within social work, as research has highlighted both the value of sibling co‐placement and the extent to which it often does not happen.
Florie J. E. Schmits, Esther Dermott
wiley   +1 more source

Nathalie Heinich, La Fabrique du patrimoine. De la cathédrale à la petite cuillère

Mondes du Tourisme, 2010
Saskia Cousin
doaj  

Lynch syndrome with <i>MLH1</i> germline variant in an extended family: a case report. [PDF]

Open Life Sci
Duan Z, Hu C, Cao T, Chen C, Li Y.
europepmc   +1 more source

Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature

Clinical Genetics, EarlyView.
Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi, Abdul A. Peer‐Zada, Abeer S. Alaqidi, Corinne Collet, Capucine Coulon, Aziza Mushiba, Florence Petit   +6 more
wiley   +1 more source

Racial Disparities in Psychoneurological Symptoms and Health-Promoting Behaviors Among Breast Cancer Survivors: A Two-Year Longitudinal Study. [PDF]

Oncol Nurs Forum
Yang GS, Graziano TA, Li A, Oppong AF, Cousin L, Lynch Kelly D, Starkweather A, Lyon DE.   +7 more
europepmc   +1 more source

Positive and Negative Experiences of Caring Among Adolescent Young Carers

Children &Society, EarlyView.
ABSTRACT Research has highlighted that adolescent young carers (AYCs) are in a vulnerable position due to their caring responsibilities being combined with the challenges of adolescence. However, caring among adolescents does not have to be a solely negative experience and positive experiences of caring can co‐exist.
Miriam Svensson, Kevin J. McKee, Francesco Barbabella, Lennart Magnusson, Rosita Brolin, Elizabeth Hanson   +5 more
wiley   +1 more source

Clinical and molecular characteristics of fructose 1, 6 bisphosphatase deficiency in 6 Egyptian patients and two common variants. [PDF]

Orphanet J Rare Dis
Elsayed SM, Mahmoud RG, Fereig YA.
europepmc   +1 more source