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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Pneumonia and CFTR[original query]
Spectrum of cystic fibrosis mutations in Syrian patients.
Minerva pediatrica 2015 Jun .
Jarjour R A, Al-Berrawi S, Ammar S, Majdalawi
Association of polymorphisms in genes of factors involved in regulation of splicing of cystic fibrosis transmembrane conductance regulator mRNA with acute respiratory distress syndrome in children with pneumonia.
Critical care (London, England) 2016 Sep 20 281.
Perez-Marques Francesca, Simpson Pippa, Yan Ke, Quasney Michael W, Halligan Nadine, Merchant Daniel, Dahmer Mary
Pseudo-Bartter syndrome in Chinese children with cystic fibrosis: Clinical features and genotypic findings.
Pediatric pulmonology 2020 8 55 (11): 3021-3029.
Shen Yuelin, Tang Xiaolei, Liu Jinrong, Li Huiming, Zhao Shunyi
Morbidity and mortality in carriers of the cystic fibrosis mutation CFTR Phe508del in the general population.
The European respiratory journal 2020 5 56 (3): .
Çolak Yunus, Nordestgaard Børge G, Afzal Shoa
Chronic Pancreatitis Associated With a Variant of CFTR Gene Treated With Total Pancreatectomy and Autologous Islet Cell Transplantation.
AACE clinical case reports 2023 5 9 (3): 93-96.
Shubham Agarwal, Ildiko Lingvay, Sasan Mirfakhraee, Raksha Ja
Diagnosis of cystic fibrosis: a high heterogeneity of symptoms and genotypes in a Brazil population.
BMC pediatrics 2024 7 24 (1): 422.
Daniela Gois Meneses, Fábia Regina Dos Santos, Anne Jardim Botelho, Luciana Mota Bispo, Camilla Guerra Matos, Vynicius Goltran Sobral Propheta, Alexia Ferreira Rodrigues, Géssica Uruga Oliveira, Angela Maria da Silva, Ricardo Queiroz Gurg
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