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dc.contributor.editorDasí, Francisco
dc.date.accessioned2022-05-06T11:36:53Z
dc.date.available2022-05-06T11:36:53Z
dc.date.issued2022
dc.identifierONIX_20220506_9783036536699_296
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/81230
dc.description.abstractDear Colleagues, A rare disease, also known as an orphan disease, is any disease that affects a small percentage of the population. Although definitions vary from continent to continent, according to the European Union, rare diseases are those with a prevalence of less than 1 in 2000 people. Rare diseases are, in general, chronic, debilitating diseases, which in many cases threaten patients’ lives. It is estimated that 1–2 million people in the European Union are affected by a rare respiratory disease, which is a public health problem. Due to the low prevalence and severity of many of these diseases, whose symptoms often initially manifest in childhood, combined efforts are needed to improve our knowledge of the pathophysiology of these diseases that will lead to the development of new, more effective treatments. Therefore, since rare respiratory diseases represent an important field in medicine, we propose this Special Issue to promote the dissemination of the latest advances in basic and clinical research in these diseases. Prof. Dr. Francisco Dasí Guest Editor
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursingen_US
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MK Medical specialties, branches of medicine::MKG Pharmacologyen_US
dc.subject.otherstandard diagnosis
dc.subject.otherreference centres
dc.subject.otherclinical presentation
dc.subject.othercilia
dc.subject.otherprimary ciliary dyskinesia
dc.subject.otheralpha-1 antitrypsin deficiency
dc.subject.otherrare respiratory diseases
dc.subject.otherMycobacterium avium
dc.subject.otherMycobacterium intracellulare
dc.subject.othernodular bronchiectasis
dc.subject.othernon-tuberculous mycobacteria
dc.subject.otherpulmonary aspergillosis
dc.subject.otherrare pulmonary disease
dc.subject.othermiRNA expression
dc.subject.otherexhaled breath condensate
dc.subject.othersputum
dc.subject.otherseverity
dc.subject.otherpulmonary exacerbation
dc.subject.otheralpha1 antitrypsin deficiency
dc.subject.otheraugmentation therapy
dc.subject.otherreplacement therapy
dc.subject.otherrare diseases
dc.subject.othergene therapy
dc.subject.otheralpha-1-antitrypsin deficit
dc.subject.othercystic fibrosis
dc.subject.otherneonatal respiratory distress
dc.subject.otherlaterality defect
dc.subject.otherorphan diseases
dc.subject.otherPCD
dc.subject.otherimmunofluorescence
dc.subject.otherantibody
dc.subject.otherALI culture
dc.subject.otherbio-resource
dc.subject.otherprimary nasal epithelium
dc.subject.otherdiagnostics
dc.subject.otherAlpha-1 antitrypsin deficiency
dc.subject.otherliver disease
dc.subject.otherglutamate-oxaloacetate transaminase
dc.subject.otherglutamate-pyruvate transaminase
dc.subject.othergamma-glutamyl transpeptidase
dc.subject.otherresilience
dc.subject.otheractive lifestyle
dc.subject.otherstress levels
dc.subject.otherinfection control measure
dc.subject.otherself-quarantine
dc.subject.otherflow cytometry
dc.subject.othernasal epithelium
dc.subject.otheroxidative stress
dc.subject.otherreactive oxygen species
dc.subject.otherendoplasmic reticulum stress
dc.subject.otherantioxidant therapies
dc.subject.otheridiopathic pulmonary fibrosis
dc.subject.otherchronic obstructive pulmonary disease
dc.subject.otherbronchiectasis
dc.subject.otherasthma
dc.subject.otheremphysema
dc.subject.otheralpha1-antitrypsin deficiency
dc.subject.othertransient elastography
dc.subject.othern/a
dc.titleRare Respiratory Diseases: A Personal and a Public Health Problem
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-3670-5
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036536699
oapen.relation.isbn9783036536705
oapen.pages242
oapen.place.publicationBasel


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