Results 81 to 90 of about 1,914,079 (159)

SILVER-RUSSELL SYNDROME IN COMBINATION WITH INFANTILE CEREBRAL PALSY: CLINICAL OBSERVATION

open access: yesМедицина в Кузбассе
A case of combination a rare genetic pathology – Silver-Russell syndrome – with cerebral palsy in three-year-old child is described. The cause of this syndrome is loss of chromosome’s 11p15 (11p15LOM) methylation, maternal uni-parental disomy of ...
Нина Геннадьевна Коновалова   +3 more
doaj  

New developments in Silver-Russell syndrome and implications for clinical practice [PDF]

open access: yes, 2016
Silver-Russell syndrome is a clinically and genetically heterogeneous disorder, characterized by prenatal and postnatal growth restriction, relative macrocephaly, body asymmetry and characteristic facial features.
Ishida, M
core  

Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?

open access: yesClinical Epigenetics, 2018
Background Loss of paternal methylation (LOM) of the H19/IGF2 intergenic differentially methylated region (H19/IGF2:IG-DMR) causes alteration of H19/IGF2 imprinting and Silver-Russell syndrome (SRS).
Angela Sparago   +2 more
doaj   +1 more source

Limb lengthening in children with Russell–Silver syndrome: A comparison to other etiologies

open access: yesJournal of Children's Orthopaedics, 2013
Introduction/background Russell–Silver syndrome (RSS) is the combination of intrauterine growth retardation, difficulty feeding, and postnatal growth retardation. Leg length discrepancy (LLD) is one of four major diagnostic criteria of RSS and is present
V. Goldman   +4 more
doaj   +1 more source

Silver City Public Library Collection; no.05280

open access: yes, 1910
Sepia image of Hanover- a small mining town situated in a valley at the foot of an arid scrub covered mountainous terrain outside of Silver City. Stamped on the lower left corner of the original negative; ""Hermosa Copper Co."" Stamped on the lower right
unknown
core  

Abstracts

open access: yesMolecular Oncology, Volume 20, Issue S1, Page 1-692, August 2026.
Abstracts submitted to the ‘EACR 2026 Congress: Innovative Cancer Science’, from 08–11 June 2026 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley   +1 more source

Adolescent growth and pubertal progression in the Silver-Russell syndrome

open access: yes, 1988
The pattern of growth and development of 18 adolescent children with the Silver-Russell syndrome was studied. Mature height was about -3.6 standard deviation scores in both sexes.
Davies, P.S.W.   +5 more
core   +1 more source

Molecular characterization of imprinting disorders: Beckwith–Wiedemann, Silver–Russell, and Prader-Willi syndromes in Egyptian patients

open access: yesBMC Pediatrics
Background Imprinted genes, characterized by monoallelic expressions (either maternal or paternal), they are crucial for normal growth and development. Disruption of their monoallelic expressions leads to imprinting disorders (ImpDis).
Amal M. Mohamed   +11 more
doaj   +1 more source

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation [PDF]

open access: yes, 2017
Maternal uniparental disomy for the entire chromosome 7 has so far been reported in three patients with intrauterine and postnatal growth retardation. Two were detected because they were homozygous for a cystic fibrosis mutation for which only the mother
Ilyina, Helena   +12 more
core  

The Streams of Little Silver

open access: yes, 1995
This pamphlet provides information to help the residents of Little Silver protect local waterways from pollution.Prepared with a grant from the New Jersey Department of Environmental Protection, Office of Environmental Services.Purpose: To help the ...

core   +1 more source

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