Cystic Fibrosis

Cystic Fibrosis - Heterogeneity and Personalized Treatment provides the latest research and clinical evidence for clinicians, scientists and researchers involved in the care of patients with cystic fibrosis (CF). This book outlines the burden of the CF microbiome, utilisation of CF registries to imp...

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פורמט: Online
שפה:אנגלית
יצא לאור: IntechOpen 2021
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גישה מקוונת:ONIX_20210420_9781789841466_2949
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collection Directory of Open Access Books
description Cystic Fibrosis - Heterogeneity and Personalized Treatment provides the latest research and clinical evidence for clinicians, scientists and researchers involved in the care of patients with cystic fibrosis (CF). This book outlines the burden of the CF microbiome, utilisation of CF registries to impact future care, the sequelae of hepatobiliary complication, the use of upcoming technologies to provide patient-centred care, and provides an overview of cystic fibrosis transmembrane regulator (CFTR) modulators. Looking after patients with CF is highly rewarding, allowing those of us to combine our dedication and problem-solving skills to create a personalized approach. This book is invaluable for those involved in the care of CF patients.
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institution Directory of Open Access Books
language eng
publishDate 2021
publishDateRange 2021
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publisherStr IntechOpen
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spelling doab-20.500.12854ir-675892024-03-31T22:44:29Z Cystic Fibrosis Wat, Dennis Nazareth, Dilip Respiratory medicine thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJK Dermatology Cystic Fibrosis - Heterogeneity and Personalized Treatment provides the latest research and clinical evidence for clinicians, scientists and researchers involved in the care of patients with cystic fibrosis (CF). This book outlines the burden of the CF microbiome, utilisation of CF registries to impact future care, the sequelae of hepatobiliary complication, the use of upcoming technologies to provide patient-centred care, and provides an overview of cystic fibrosis transmembrane regulator (CFTR) modulators. Looking after patients with CF is highly rewarding, allowing those of us to combine our dedication and problem-solving skills to create a personalized approach. This book is invaluable for those involved in the care of CF patients. 2021-04-20T16:19:02Z 2021-04-20T16:19:02Z 2020 book ONIX_20210420_9781789841466_2949 9781789841466 9781789841459 9781838809683 https://directory.doabooks.org/handle/20.500.12854/67589 eng image/jpeg n/a https://www.intechopen.com/books https://mts.intechopen.com/storage/books/7872/authors_book/authors_book.pdf IntechOpen IntechOpen 10.5772/intechopen.77691 10.5772/intechopen.77691 78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6 9781789841466 9781789841459 9781838809683 IntechOpen 136 open access
spellingShingle Respiratory medicine
thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJK Dermatology
Cystic Fibrosis
title Cystic Fibrosis
title_full Cystic Fibrosis
title_fullStr Cystic Fibrosis
title_full_unstemmed Cystic Fibrosis
title_short Cystic Fibrosis
title_sort cystic fibrosis
topic Respiratory medicine
thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJK Dermatology
topic_facet Respiratory medicine
thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJK Dermatology
url ONIX_20210420_9781789841466_2949