Results 71 to 80 of about 1,914,079 (159)

Beyond snapshots: A systematic review of dyadic and triadic parent–adolescent ecological momentary assessment studies across diverse and general populations

open access: yesJournal of Research on Adolescence, Volume 36, Issue 3, September 2026.
Abstract The last decade has seen a surge in studies using Ecological Momentary Assessment (EMA), where participants complete brief daily questionnaires to capture real‐time experiences. While widely used to study adolescents' social–emotional processes, EMA that simultaneously assesses adolescents and their parents (i.e., dyadic and triadic designs ...
Reuma Gadassi‐Polack   +2 more
wiley   +1 more source

Silver-Russell syndrome as a cause for early intrauterine growth restriction

open access: yes, 2005
The diagnosis of Silver-Russell syndrome is based on the characteristic growth restriction and the presence of typical dysmorphic features. We present the prenatal and postnatal findings of a case that was treated at our perinatal center.
Kai Dittmann   +5 more
core   +1 more source

Russell Silver syndrome: a perspective on growth and the influence of growth hormone therapy

open access: yesIndian Journal of Endocrinology and Metabolism, 2012
A 6 years male child was referred to our Endocrinology clinic with complaints of failure to thrive and he displayed the characteristic features of Russell Silver Syndrome which included short stature, relative macrocephaly, triangular facies and ...
J V Mascarenhas, Vageesh S Ayyar
doaj   +1 more source

증례 보고 : Russell-Silver Syndrome

open access: yes, 2002
Russell-Silver syndrome is a type of intrauterine growth retardation, characterized by short stature noted at birth, hemiatrophy or asymmetry, variation in sexual development and other abnormalities, including cafe-aulait pigmentation and clinodactyly ...
장기택, 이진, 김종철
core  

Silver-russell syndrome: A case report

open access: yes, 2012
Silver-Russell sendromu, intrauterin ve postnatal büyüme geriliği, relatif makrosefali, üçgen yüz, vücut asimetrisi ve el 5. parmakta klinodaktili özelliklerinin görüldüğü bir genetik hastalıktır.
Filiz Hazan   +4 more
core  

The Case of Dilated Cardiomiopathy, the Girl of Three Years from the Silver-Rassel Syndrom

open access: yesМедицинский вестник Юга России, 2012
Dilated cardiomyopathy is a serious disabling disease with unclear etiology. In some cases, its occurrence is associated with genetic mutations. In this context the case of dilated cardiomyopathy of the three years old girl from the Silver-Russell ...
A. A. Lebedenko   +5 more
doaj  

Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome.

open access: yesPLoS ONE, 2013
BackgroundRecent studies have revealed relative frequency and characteristic phenotype of two major causative factors for Silver-Russell syndrome (SRS), i.e. epimutation of the H19-differentially methylated region (DMR) and uniparental maternal disomy 7 (
Tomoko Fuke   +17 more
doaj   +1 more source

A rare case of Silver-Russell syndrome associated with growth hormone deficiency and urogenital abnormalities

open access: yesIndian Journal of Endocrinology and Metabolism, 2012
Introduction: Silver-Russell syndrome (SRS) is a very rare genetic disorder. This is usually characterized by asymmetry in the size of the two halves or other parts of the body.
Namburi Rajendra Prasad   +4 more
doaj   +1 more source

Silver-Russell Syndrome Synonym: Russell-Silver Syndrome

open access: yes, 2019
International audienceClinical characteristics Silver-Russell Syndrome (SRS) is typically characterized by asymmetric gestational growth restriction resulting in affected individuals being born small for gestational age, with relative macrocephaly at ...
Saal, Howard, M   +2 more
core   +1 more source

Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome.

open access: yes, 2016
Russell-Silver syndrome is a heterogeneous disorder characterized by intrauterine growth retardation, postnatal growth deficiency, characteristic facial appearance, and other variable features.
Stavropoulos, Dimitri J   +21 more
core   +1 more source

Home - About - Disclaimer - Privacy