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7 resultsUpdated October 25, 2026
1

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

Liver International 44(3) (2024)

Denise Aldrian; Clemens Bochdansky; Anna Maria Kavallar; Christoph Mayerhofer; Asma Deeb; Abdelhadi M. Habeb; Andrea Romera Rabasa; Anuradha Vaman Khadilkar; Ahmet Uçar; Birgit Knoppke; Dimitrios Zafeiriou; Mariarosaria Lang‐Muritano; Mohamad Saleh Miqdady; Sylvia Judmaier; Valérie A. McLin; Viktoriya Furdela; Thomas Müller; Georg Friedrich Vogel

2

A (dis)integrated stress response: Genetic diseases of eIF2α regulators

Wiley Interdisciplinary Reviews - RNA 13(3) (2021)

Alyssa M. English; Katelyn M. Green; Stephanie L. Moon

3

Genetic syndromes with diabetes: A systematic review

Obesity Reviews 22(9) (2021)

Daniel Shi; Mehras Motamed; Aurora Mejía‐Benítez; Leon Li; Ethan Lin; DALTON R. BUDHRAM; Yuvreet Kaur; David Meyre

4

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 42(3) (2017)

Farzaneh Abbasi; Maryam Habibi; Samaneh Enayati; Fatemeh Bitarafan; Maryam Razzaghy‐Azar; Aria Sotodeh; Sima Parvizi Omran; Reza Maroofian; Mahsa Mohammad Amoli

5

Anaesthesia and orphan disease

European Journal of Anaesthesiology 32(3) (2014)

A. Romera; Mónica Hervías; Maria Teresa Lopez-Gil; Itziar Tranche

6

Rare form of Permanent Neonatal Diabetes Mellitus (PNDM) due to novel mutation in EIF2AK3 gene (Wolcott—Rallison syndrome)

Problems of Endocrinology 61(6) (2015)

Yulia V. Tikhonovich; Ольга Васильевна Стотикова; П. М. Рубцов; Anatoly Nikolaevich Tiulpakov

7

Identification of Novel Mutation in EIF2AK3 Gene as a Causal Variant in a Family With Rare Disease

Journal of Medical Cases 8(3) (2017)

Raziyeh Khalesi; Masoud Garshasbi