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Literature DB >> 17264596

Wolcott-Rallison syndrome: clinical, radiological and histological findings in a Saudi child.

B Bin-Abbas¹, S Shabib, B Hainau, A Al-Ashwal.

Abstract

Entities: Disease Species

Year: 2001 PMID： 17264596 DOI： 10.5144/0256-4947.2001.73

Source DB: PubMed Journal: Ann Saudi Med ISSN： 0256-4947 Impact factor: 1.526

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Cited

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7 in total

1. Neonatal diabetes mellitus with recurrent hepatitis.

Authors: N Suresh; R Ganesh; T Eswararaja; T Vasanthi; Janani Sankar; Malathi Sathiasekaran
Journal: Indian J Pediatr Date: 2006-05 Impact factor: 1.967

2. Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene.

Authors: Ercan Mihci; Doğa Türkkahraman; Sian Ellard; Sema Akçurin; Iffet Bircan
Journal: J Clin Res Pediatr Endocrinol Date: 2012-06

3. Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohort.

Authors: Abdelhadi M Habeb; Asma Deeb; Matthew Johnson; Mohammed Abdullah; Majidah Abdulrasoul; Hussain Al-Awneh; Mohammed S F Al-Maghamsi; Fathiya Al-Murshedi; Ramlah Al-Saif; Siham Al-Sinani; Dina Ramadan; Hala Tfayli; Sarah E Flanagan; Sian Ellard
Journal: Horm Res Paediatr Date: 2015-02-05 Impact factor: 2.852

7. Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.

Authors: Babak Behnam; Marjan Shakiba; Ali Ahani; Maryam Razzaghy Azar
Journal: Hepat Mon Date: 2013-06-09 Impact factor: 0.660

7 in total

Wolcott-Rallison syndrome: clinical, radiological and histological findings in a Saudi child.

1. Neonatal diabetes mellitus with recurrent hepatitis.

2. Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene.

3. Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohort.

Review 4. Wolcott-Rallison syndrome in a Bedouin boy.

5. Re: EIF2AK3 mutations in patients with Wolcott-Rallison syndrome.

Review 6. Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.

7. Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.