Results 81 to 90 of about 1,914,079 (156)
New developments in Silver-Russell syndrome and implications for clinical practice [PDF]
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
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Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?
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
Silver City Public Library Collection; no.05280
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
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Anesthesia experience in an adult Silver-Russell syndrome: a case report
Background There are no reports of anesthesia use in adult patients with Silver-Russell syndrome (SRS). Here, we report our experience with anesthesia in an adult patient with SRS complicated by chronic respiratory failure.
Akinobu Hibino +2 more
doaj +1 more source
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
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
Silver–Russell syndrome (SRS) is a representative imprinting disorder characterized by pre- and postnatal growth failure. We encountered two Japanese SRS cases with a de novo pathogenic frameshift variant of HMGA2 (NM_003483.6:c.138_141delinsCT, p ...
Kaori Yamoto +4 more
doaj +1 more source
Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation [PDF]
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
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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
Silver-Russell Syndrome: A Review
Silver-Russell syndrome (SRS) is a rare congenital imprinting disorder. The genetic findings in SRS patients are heterogeneous and often sporadic.
Bernice Sophie Spiteri +2 more
core +1 more source

