Wolcott Rallison Syndrome Latest Advances

Characterization of monogenic diabetes among Sudanese children: a multi-center experience from a population with high consanguinity.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: June 04, 2025

A Novel EIF2AK3 Variant Causing Wolcott-Rallison Syndrome With Early Neonatal Diabetic Ketoacidosis as Initial Presentation: A Case Report.

Journal: Clinical case reports

Published: May 29, 2025

Using SARS-CoV-2-Positive Donors Under 1 Year of Age: A Case Series of Successful Combined Liver-Pancreas and Isolated Liver Pediatric Transplantation.

Journal: Pediatric transplantation

Published: May 09, 2025

Wolcott-Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: April 20, 2025

Wolcott-Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure - a case report.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: March 02, 2025

Wolcott-Rallison syndrome - crosstalk between PERK- EIF2A and type II interferon signaling.

Journal: European journal of medical genetics

Published: December 26, 2024

Cervical spinal decompression and fusion in the setting of Wolcott-Rallison Syndrome: a rare pediatric indication and its surgical considerations.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: October 20, 2024

PERK inhibition with GSK2606414 in zebrafish evokes developmental defects consistent with Wolcott-Rallison syndrome phenotypes.

Journal: bioRxiv : the preprint server for biology

Published: April 25, 2024

Recurrent Liver Failure Due to Wolcott Rallison Syndrome.

Journal: Indian journal of pediatrics

Published: March 31, 2024

Ethnic variation and structure-function analysis of tauopathy-associated PERK alleles.

Journal: medRxiv : the preprint server for health sciences

Published: March 18, 2024

Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study.

Journal: Liver international : official journal of the International Association for the Study of the Liver

Published: November 16, 2023

Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan.

Journal: Pediatric diabetes

Published: November 13, 2023

Wolcott Rallison Syndrome Latest Advances

Find the Latest Research About Wolcott Rallison Syndrome

Characterization of monogenic diabetes among Sudanese children: a multi-center experience from a population with high consanguinity.

Characterization of monogenic diabetes among Sudanese children: a multi-center experience from a population with high consanguinity.

A Novel EIF2AK3 Variant Causing Wolcott-Rallison Syndrome With Early Neonatal Diabetic Ketoacidosis as Initial Presentation: A Case Report.

A Novel EIF2AK3 Variant Causing Wolcott-Rallison Syndrome With Early Neonatal Diabetic Ketoacidosis as Initial Presentation: A Case Report.

Using SARS-CoV-2-Positive Donors Under 1 Year of Age: A Case Series of Successful Combined Liver-Pancreas and Isolated Liver Pediatric Transplantation.

Using SARS-CoV-2-Positive Donors Under 1 Year of Age: A Case Series of Successful Combined Liver-Pancreas and Isolated Liver Pediatric Transplantation.

Wolcott-Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene.

Wolcott-Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene.

Wolcott-Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure - a case report.

Wolcott-Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure - a case report.

Wolcott-Rallison syndrome - crosstalk between PERK- EIF2A and type II interferon signaling.

Wolcott-Rallison syndrome - crosstalk between PERK- EIF2A and type II interferon signaling.

Cervical spinal decompression and fusion in the setting of Wolcott-Rallison Syndrome: a rare pediatric indication and its surgical considerations.

Cervical spinal decompression and fusion in the setting of Wolcott-Rallison Syndrome: a rare pediatric indication and its surgical considerations.

PERK inhibition with GSK2606414 in zebrafish evokes developmental defects consistent with Wolcott-Rallison syndrome phenotypes.

PERK inhibition with GSK2606414 in zebrafish evokes developmental defects consistent with Wolcott-Rallison syndrome phenotypes.

Recurrent Liver Failure Due to Wolcott Rallison Syndrome.

Recurrent Liver Failure Due to Wolcott Rallison Syndrome.

Ethnic variation and structure-function analysis of tauopathy-associated PERK alleles.

Ethnic variation and structure-function analysis of tauopathy-associated PERK alleles.

Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study.

Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study.

Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan.

Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan.