scholarly journals Asp192Val, A novel mutation in 2 Omani Siblings with Cystic fibrosis: A case report and review of literature

2021 ◽  
pp. 1-4
Keyword(s):  
Cystic Fibrosis ◽  
Case Report ◽  
Novel Mutation ◽  
Review Of Literature

scholarly journals A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature

2015 ◽  
Vol 30 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Aisha Al-Sinani ◽  
Waad-Allah Mula-Abed ◽  
Manal Al-Kindi ◽  
Ghariba Al-Kusaibi ◽  
Hanan Al-Azkawi ◽  
...  
Keyword(s):  
Case Report ◽  
Novel Mutation ◽  
Hydroxysteroid Dehydrogenase ◽  
Review Of Literature ◽  
First Case ◽  
Type 3

First recovery ofRasamsonia argillaceaspecies complex isolated in adolescent patient with cystic fibrosis in Slovenia - case report and review of literature

Mycoses ◽  
2015 ◽  
Vol 58 (8) ◽  
pp. 506-510 ◽  
Author(s):  
Tadeja Matos ◽  
Tjaša Cerar ◽  
Marina Praprotnik ◽  
Uroš Krivec ◽  
Mateja Pirš
Keyword(s):  
Cystic Fibrosis ◽  
Case Report ◽  
Adolescent Patient ◽  
Review Of Literature

Fatal DisseminatedAspergillus PenicillioidesInfection in a 3-Month-Old Infant with Suspected Cystic Fibrosis: Autopsy Case Report with Review of Literature

2015 ◽  
Vol 19 (6) ◽  
pp. 506-511 ◽  
Author(s):  
Kirti Gupta ◽  
Parikshaa Gupta ◽  
Joseph L Mathew ◽  
Arun Bansal ◽  
Gangandeep Singh ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Case Report ◽  
Autopsy Case ◽  
Review Of Literature

A Novel Mutation in Cystic Fibrosis Presenting as Pseudo Bartter Syndrome: A Case Report

2021 ◽  
Author(s):  
Seema Shah ◽  
Sunil Jondhale ◽  
Manas Ranjan Sahoo ◽  
Tushar Jagzape ◽  
Swasti Keshri ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Case Report ◽  
Novel Mutation ◽  
Bartter Syndrome
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