Results 121 to 130 of about 299,585 (267)

Adolescent-specific adaptations to caregiving unpredictability: A longitudinal examination of cognitive flexibility. [PDF]

Dev Psychol
Niemiec E, Fields A, Vannucci A, Abramson L, Bloom PA, Camacho NL, Choy T, Durazi A, Gibson L, Hadis SS, Harmon C, Heleniak C, Umbach R, VanTieghem M, Dozier M, Milham MP, Tottenham N.   +16 more
europepmc   +1 more source

Sleeping through the ages: Developmental trajectories of actigraphy-derived sleep-wake patterns across adolescence and emerging adulthood. [PDF]

Dev Psychol
Thompson MJ, Altinoz ZS, Ehrhardt AD, Hinnant JB, Erath SA, Buckhalt JA, El-Sheikh M.   +6 more
europepmc   +1 more source

Parenting Adolescents

, 2019
Soenens, Bart, Vansteenkiste, Maarten, Beyers, Wim   +2 more
openaire   +2 more sources

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

Aggressiveness that makes one grow: a destructive or vital force in adolescence? Reflections and working hypotheses. [PDF]

Front Behav Neurosci
Demaria F, Pontillo M, Di Vincenzo C, Vicari S.   +3 more
europepmc   +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

Uncovering trajectories of personality functioning in adolescence and their associations with baseline psychopathology. [PDF]

Front Psychiatry
Gaudiešiūtė E, Sharp C, Skabeikytė-Norkienė G, Barkauskienė R.   +3 more
europepmc   +1 more source

Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan, Sophia C. Pasia, Emmanouil Rampakakis, Reggie Hamdy, Frank Rauch, Lauren C. Hyer, Joel Lerman, Haluk Altiok, Krister Freese, Cary Mielke, Sarah B. Nossov, Philip F. Giampietro, Thania Ordaz‐Robles, Noémi Dahan‐Oliel   +13 more
wiley   +1 more source

Time-varying associations among maternal and paternal warmth, sibling intimacy, and youth familism values among U.S. Mexican-origin youth. [PDF]

Cultur Divers Ethnic Minor Psychol
Son D, Updegraff KA, Cahill KM, Almeida LM, Umaña-Taylor AJ.   +4 more
europepmc   +1 more source

Brugada Syndrome: New Implications for Heterozygous Carriers of the Pathogenic SCN5A c.689T>C(p.Ile230Thr) Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in the SCN5A gene and its subunits have been identified in individuals with Brugada Syndrome. One such SCN5A variant, c.689T>C(p.Ile230Thr), was previously reported as disease‐causing only in homozygous individuals, with heterozygous carriers being unaffected.
Shayla Shojaat, Benjamin Hale, Taylor Warner   +2 more
wiley   +1 more source