Results 231 to 240 of about 2,413,929 (366)

Interaction of FXTAS Family History and College Degree Attainment Predicts Trajectories of Cognitive and Motor Symptoms in FMR1 Premutation Carrier Women

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT The present longitudinal study focuses on FMR1 premutation carrier women during midlife and early old age (n = 115). Bringing together the genetic risk factor of a family history of FXTAS and the environmental protective factor of higher education, the goal of the study was to determine how these factors potentially interact to predict self ...
Jinkuk Hong, Leann Smith DaWalt, Jessica Klusek, Elizabeth M. Berry‐Kravis, Marsha Mailick   +4 more
wiley   +1 more source

Global folate deficiency among adolescent girls: A systematic review and meta-analysis. [PDF]

PLoS One
Aweke MN, Alhur AA, Baykemagn ND, Lakew G, Gebretsadkan BT, Alemu GG, Bazezew AM, Yirsaw AN, Wondie WT, Mengistie BA.   +9 more
europepmc   +1 more source

PEER EDUCATION MODEL FOR FAMILY LIFE PREPARATION IN FEMALE ADOLESCENTS OF ISLAMIC BOARDING SCHOOLS

Azizatul Hamidiyah, Sandra Fikawati, Ahmad Syafiq, I Nahe’, Sabarinah Prasetyo, Waryono Waryono, Eko Setiawan, National Population and Family Planning Agency, Indonesia, D Anshari   +8 more
openalex   +1 more source

Geographic inequities in human papillomavirus vaccine non-uptake and its determinants among adolescent girls in Ethiopia: Evidence from the National Immunization Survey. [PDF]

PLoS One
Assefa KT, Worku AG, Muche AA, Geremew BM, Woldetsadik MA, Alemu K.   +5 more
europepmc   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Who plays a more crucial role in adolescent well-being: Interactions with parents or peers? An investigation of adolescents aged 10 to 18 years. [PDF]

Appl Psychol Health Well Being
Ding R, Xia A, Pan J, Zhang P, Liu T.
europepmc   +1 more source

New Instrument of Adolescents’ Peer Interaction Research

, 2015
K.N. Polivanova
openalex   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Modern contraceptive use after sexual debut among Ghanaian adolescent girls (15-19 years): a secondary analysis of the 2022 Demographic and Health Survey. [PDF]

Contracept Reprod Med
Henry M, Debuo Der A, Atongo FA, Oloo B, Brifo H, Tsekpetse P.   +5 more
europepmc   +1 more source

First National Expanded Genomic Newborn Screening Program in Qatar; A Pilot Study, Doha‐Heidelberg Collaboration

American Journal of Medical Genetics Part A, EarlyView.
Reem Alsulaiman, Sarah Okashah, Radja Messai Badji, Fatemeh Abbaszadeh, Yaser Alsarraj, Rehab Ali Abdulrahman, Noora Shahbeck, Thalib Moideen, Reema El Hassan, Fatima Al‐Hamaydeh, Einas Alkuwari, Said Ismail, Hilal Al‐ Rifai, Ghassan Abdoh, Christian P. Schaaf, Georg Hoffmann, Saad Al‐Kaabi, Wadha Al‐Muftah, Tawfeg Ben‐Omran   +18 more
wiley   +1 more source