Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis-Reference-Cited by-同舟云学术

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Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis

Published:2007-04 Issue:2 Volume:6 Page:111-116
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Naguib Maggie L.,Schrijver Iris,Gardner Phyllis,Pique Lynn M.,Doss Samiha S.,Abu Zekry Mona A.,Aziz Mona,Nasr Samya Z.

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference34 articles.

1. Mechanisms of disease; cystic fibrosis;Row;N Engl J Med,2005

2. Comparison of the clinical manifestations of cystic fibrosis in African–Americans and Caucasians;Hamosh;J Pediatr,1998

3. Cystic fibrosis;Welsh,2001

4. Cystic Fibrosis Foundation Patient Registry 2004 Annual Data Report to the Center Directors. Bethesda, Maryland.

5. For the Cystic Fibrosis Foundation consensus panel: the diagnosis of cystic fibrosis: a consensus statement;Rosenstein;J Pediatr,1998

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1. Nationwide Survey of Cystic Fibrosis Knowledge and Resource Accessibility in Egypt;ATS Scholar;2024-08-13

2. Clinical and genetic risk factors for cystic fibrosis‐related liver disease in Egyptian CF children: A single‐center experience;Pediatric Pulmonology;2023-12

3. The Epidemiology of Cystic Fibrosis in Arab Countries: A Systematic Review;SN Comprehensive Clinical Medicine;2021-01-30

4. Clinical manifestation, laboratory findings, and outcome of children with cystic fibrosis over a 10-year period in South Iran;Egyptian Pediatric Association Gazette;2020-11-23

5. Screening for the Most Common Mutations of CFTR Gene among Egyptian Children with Difficult-to-Treat Asthma;Journal of Pediatric Genetics;2020-02-03

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