Pseudo‐Bartter syndrome in Chinese children with cystic fibrosis: Clinical features and genotypic findings-Reference-Cited by-同舟云学术

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Pseudo‐Bartter syndrome in Chinese children with cystic fibrosis: Clinical features and genotypic findings

Published:2020-08-13 Issue:11 Volume:55 Page:3021-3029
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol

Author:

Shen Yuelin¹,Tang Xiaolei¹,Liu Jinrong¹,Li Huiming¹,Zhao Shunying¹^ORCID

Affiliation:

1. Department of Respiratory Medicine, Beijing Children's Hospital, National Center for Children's Health Capital Medical University Beijing China

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.25012

Reference31 articles.

1. The implementation of standards of care in Europe: State of the art

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

3. Unique Mutations of the Cystic Fibrosis Transmembrane Conductance Regulator Gene of Three Cases of Cystic Fibrosis in Nagasaki, Japan

4. Ethnicity impacts the cystic fibrosis diagnosis: A note of caution

5. Clinical Phenotypes and Genotypic Spectrum of Cystic Fibrosis in Chinese Children

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1. Case 2: Poor Weight Gain in a 9-month-old Girl;Pediatrics in Review;2024-06-01

2. Genetic analysis and functional study of novel CFTR variants in Chinese children with cystic fibrosis;Gene;2024-05

3. Study of the Pathogenesis of CF-PBS and BS;Advances in Clinical Medicine;2024

4. Clinical characteristics and genetic mutations of 10 Chinese children with cystic fibrosis and cystic frbrosis transmembrane conductance regulator-related disorders;Chinese Medical Journal;2023-09-07

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

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