Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry
Yiallouros, Panayiotis K, Matthaiou, Andreas Î, Anagnostopoulou, Pinelopi, Kouis, Panayiotis, Libik, Malgorzata, Adamidi, Tonia, Eleftheriou, Adonis, Demetriou, Artemios, Ioannou, Phivos, Tanteles, George A, Costi, Constantina, Fanis, Pavlos, Macek, Milan, Neocleous, Vassos, Phylactou, Leonidas A
Published in Orphanet journal of rare diseases (02.10.2021)
Published in Orphanet journal of rare diseases (02.10.2021)
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Journal Article
Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis
Yiallouros, Panayiotis K, Matthaiou, Andreas Î, Anagnostopoulou, Pinelopi, Kouis, Panayiotis, Libik, Malgorzata, Adamidi, Tonia, Eleftheriou, Adonis, Demetriou, Artemios, Ioannou, Phivos, Tanteles, George A, Costi, Constantina, Fanis, Pavlos, Macek, Milan, Neocleous, Vassos, Phylactou, Leonidas A
Published in Orphanet journal of rare diseases (02.10.2021)
Published in Orphanet journal of rare diseases (02.10.2021)
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Journal Article
Clinical features of primary ciliary dyskinesia in Cyprus with emphasis on lobectomized patients
Yiallouros, Panayiotis K, Kouis, Panayiotis, Middleton, Nicos, Nearchou, Marianna, Adamidi, Tonia, Georgiou, Andreas, Eleftheriou, Adonis, Ioannou, Phivos, Hadjisavvas, Andreas, Kyriacou, Kyriacos
Published in Respiratory medicine (01.03.2015)
Published in Respiratory medicine (01.03.2015)
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