Should isolated Pseudo‐Bartter syndrome be considered a CFTR‐related disorder of infancy?-Reference-Cited by-同舟云学术

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Should isolated Pseudo‐Bartter syndrome be considered a CFTR‐related disorder of infancy?

Published:2019-07-21 Issue:10 Volume:54 Page:1578-1583
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol

Author:

Poli Piercarlo¹^ORCID,Rose Domenico Umberto¹,Timpano Silviana¹,Savoldi Gianfranco²,Padoan Rita¹^ORCID

Affiliation:

1. Department of PediatricsRegional support Centre for Cystic FibrosisChildren's Hospital – ASST Spedali CiviliUniversity of Brescia Brescia Italy

2. Department of PathologyLaboratory of Genetic Disorders of Childhood“A. Nocivelli” ASST Spedali Civili Brescia Italy

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.24433

Reference33 articles.

1. Cystic fibrosis

2. Macromolecular Interactions and Ion Transport in Cystic Fibrosis

3. Cystic fibrosis: current therapeutic targets and future approaches

4. Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

5. Cystic Fibrosis Mutation Database. Available at:http://www.genet.sickkids.on.ca/app

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Severe lung disease in children with cystic fibrosis missed in newborn screening;Pediatric Pulmonology;2023-10-27

2. Cystic fibrosis and CFTR-related disorder with electrolyte imbalance at diagnosis: clinical features and outcome in an Italian cohort;European Journal of Pediatrics;2023-09-19

3. Pseudo-Bartter Syndrome in Patients with Cystic Fibrosis and Clinical Features;Journal of Dr Behcet Uz Children s Hospital;2023-08-09

4. Pseudo-Bartter Syndrome in Patients with Cystic Fibrosis and Clinical Features;J DR BEHCET UZ CHILD;2023

5. ECFS standards of care on CFTR-related disorders: Updated diagnostic criteria;Journal of Cystic Fibrosis;2022-11

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