Russell-Silver Dwarfism Latest Advances

Consensus on diagnosis and treatment of Silver-Russell syndrome (2025)

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: June 15, 2025

ANKS1B is a potential candidate gene for short stature and failure to thrive in children.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: May 26, 2025

A Silver-Russell syndrome family with HMGA2 gene variant

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: May 20, 2025

Genomic Insights into Short Stature in Children Born Small for Gestational Age: A Korean Multicenter Exome Study.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 01, 2025

Early Growth Hormone Treatment Enhances Growth and Nutritional Status in Silver-Russell Syndrome.

Journal: The Journal of clinical endocrinology and metabolism

Published: April 22, 2025

Functional Independence of Taiwanese Children with Silver-Russell Syndrome.

Journal: Diagnostics (Basel, Switzerland)

Published: March 22, 2025

Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell-Silver Syndrome in Infancy.

Journal: Prenatal diagnosis

Published: February 28, 2025

Correction to: "Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene".

Journal: The Journal of clinical endocrinology and metabolism

Published: December 20, 2024

Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver-Russell phenotype.

Journal: Clinical epigenetics

Published: December 19, 2024

Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: December 05, 2024

Prenatal Detection of Silver-Russell Syndrome: A First Trimester Suspicion and Diagnostic Approach.

Journal: Medicina (Kaunas, Lithuania)

Published: December 02, 2024

Intelligence, Cognition, and Psychopathology in Adults with Silver-Russell Syndrome: Overview of the Literature and Description of Three Clinical Cases.

Journal: Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists

Published: November 29, 2024

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Consensus on diagnosis and treatment of Silver-Russell syndrome (2025)

Consensus on diagnosis and treatment of Silver-Russell syndrome (2025)

ANKS1B is a potential candidate gene for short stature and failure to thrive in children.

ANKS1B is a potential candidate gene for short stature and failure to thrive in children.

A Silver-Russell syndrome family with HMGA2 gene variant

A Silver-Russell syndrome family with HMGA2 gene variant

Genomic Insights into Short Stature in Children Born Small for Gestational Age: A Korean Multicenter Exome Study.

Genomic Insights into Short Stature in Children Born Small for Gestational Age: A Korean Multicenter Exome Study.

Early Growth Hormone Treatment Enhances Growth and Nutritional Status in Silver-Russell Syndrome.

Early Growth Hormone Treatment Enhances Growth and Nutritional Status in Silver-Russell Syndrome.

Functional Independence of Taiwanese Children with Silver-Russell Syndrome.

Functional Independence of Taiwanese Children with Silver-Russell Syndrome.

Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell-Silver Syndrome in Infancy.

Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell-Silver Syndrome in Infancy.

Correction to: "Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene".

Correction to: "Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene".

Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver-Russell phenotype.

Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver-Russell phenotype.

Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study.

Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study.

Prenatal Detection of Silver-Russell Syndrome: A First Trimester Suspicion and Diagnostic Approach.

Prenatal Detection of Silver-Russell Syndrome: A First Trimester Suspicion and Diagnostic Approach.

Intelligence, Cognition, and Psychopathology in Adults with Silver-Russell Syndrome: Overview of the Literature and Description of Three Clinical Cases.

Intelligence, Cognition, and Psychopathology in Adults with Silver-Russell Syndrome: Overview of the Literature and Description of Three Clinical Cases.