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Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates

American journal of medical genetics. Part A, 2016-03, Vol.170A (3), p.602-609

2016

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World's smallest combined en bloc liver‐pancreas transplantation

Pediatric transplantation, 2018-02, Vol.22 (1), p.n/a

2018

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The first presentation of Wolcott‐Rallison syndrome in a four‐month‐old infant with diabetic ketoacidosis (DKA) precipitating by COVID‐19: A case report

Clinical case reports, 2021-11, Vol.9 (11), p.e05096-n/a

2021

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A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes

Canadian journal of diabetes, 2018-06, Vol.42 (3), p.272-275

2018

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A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS)

American journal of medical genetics. Part A, 2012-11, Vol.158A (11), p.2788-2796

2012

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Practical management in Wolcott‐Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report

Clinical case reports, 2019-06, Vol.7 (6), p.1133-1138

2019

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Microscopic and ultrastructural features in Wolcott-Rallison syndrome, a permanent neonatal diabetes mellitus: about two autopsy cases

Pediatric diabetes, 2015-11, Vol.16 (7), p.510-520

2015

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Wolcott-Rallison syndrome, A rare paediatric case report

The international journal of frontier sciences, 2024-07, Vol.7 (1)

2024

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A busy cell—Endoplasmic reticulum stress in the pancreatic β-cell

Molecular and cellular endocrinology, 2007-10, Vol.277 (1), p.1-5

2007

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Permanent neonatal diabetes mellitus in a young Ukrainian child

Pediatric endocrinology, diabetes, and metabolism, 2016, Vol.22 (3), p.132-134

2016

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Type I interferons mediate pancreatic toxicities of PERK inhibition

Proceedings of the National Academy of Sciences - PNAS, 2015-12, Vol.112 (50), p.15420-15425

2015

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Neonatal Diabetes Mellitus: Novel Mutations

Indian journal of pediatrics, 2021-08, Vol.88 (8), p.785-792

2021

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A novel mutation in the EIF2AK3 gene with variable expressivity in two patients with Wolcott-Rallison syndrome

Clinical genetics, 2006-07, Vol.70 (1), p.34-38

2006

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Functions and pathologies of BiP and its interaction partners

Cellular and molecular life sciences : CMLS, 2009-05, Vol.66 (9), p.1556-1569

2009

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Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Annals of Pediatric Endocrinology & Metabolism, 2022, 27(3), , pp.214-222

2022

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Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience

Acta diabetologica, 2021-12, Vol.58 (12), p.1689-1700

2021

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Infantile onset diabetes mellitus and recurrent hepatic encephalopathy

Journal of Pediatric Critical Care, 2019, Vol.6 (6), p.45-46

2019

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Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database

Orphanet journal of rare diseases, 2020-04, Vol.15 (1), p.100-100, Article 100

2020

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Early Neurodegeneration in the Brain of a Child Without Functional PKR-like Endoplasmic Reticulum Kinase

Journal of neuropathology and experimental neurology, 2015-08, Vol.74 (8), p.850-857

2015

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A case report of a child with Wolcott-Rallison syndrome

Sri Lanka journal of medicine (Online), 2019-12, Vol.28 (2), p.71

2019

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The PERK Eukaryotic Initiation Factor 2α Kinase Is Required for the Development of the Skeletal System, Postnatal Growth, and the Function and Viability of the Pancreas

Molecular and Cellular Biology, 2002-06, Vol.22 (11), p.3864-3874

2002

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EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report

BMC pediatrics, 2019-03, Vol.19 (1), p.85-85, Article 85

Fatani, Tarah H

2019

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Wolcott-Rallison Syndrome, a Rare Cause of Permanent Diabetes Mellitus in Infants—Case Report

Pediatric reports, 2023-10, Vol.15 (4), p.608-616

2023

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Wolcott-Rallison syndrome in Iran: a common cause of neonatal diabetes

Journal of Pediatric Endocrinology and Metabolism, 2019-06, Vol.32 (6), p.607-613

2019

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EIF2AK3 , encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

Nature genetics, 2000-08, Vol.25 (4), p.406-409

2000

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Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates

World's smallest combined en bloc liver‐pancreas transplantation

The first presentation of Wolcott‐Rallison syndrome in a four‐month‐old infant with diabetic ketoacidosis (DKA) precipitating by COVID‐19: A case report

A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes

A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS)

Practical management in Wolcott‐Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report

Microscopic and ultrastructural features in Wolcott-Rallison syndrome, a permanent neonatal diabetes mellitus: about two autopsy cases

Wolcott-Rallison syndrome, A rare paediatric case report

A busy cell—Endoplasmic reticulum stress in the pancreatic β-cell

Permanent neonatal diabetes mellitus in a young Ukrainian child

Type I interferons mediate pancreatic toxicities of PERK inhibition

Neonatal Diabetes Mellitus: Novel Mutations

A novel mutation in the EIF2AK3 gene with variable expressivity in two patients with Wolcott-Rallison syndrome

Functions and pathologies of BiP and its interaction partners

Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience

Infantile onset diabetes mellitus and recurrent hepatic encephalopathy

Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database

Early Neurodegeneration in the Brain of a Child Without Functional PKR-like Endoplasmic Reticulum Kinase

A case report of a child with Wolcott-Rallison syndrome

The PERK Eukaryotic Initiation Factor 2α Kinase Is Required for the Development of the Skeletal System, Postnatal Growth, and the Function and Viability of the Pancreas

EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report

Wolcott-Rallison Syndrome, a Rare Cause of Permanent Diabetes Mellitus in Infants—Case Report

Wolcott-Rallison syndrome in Iran: a common cause of neonatal diabetes

EIF2AK3 , encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

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