Search Results - "Gianni Mastella"
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Sweat testing: can the conductivity analysis take the place of the classic Gibson and Cooke technique?
Published in Jornal de pediatria (01-03-2010)Get full text
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Allergic Bronchopulmonary Aspergillosis in Cystic Fibrosis—State of the Art: Cystic Fibrosis Foundation Consensus Conference
Published in Clinical infectious diseases (01-10-2003)“…Because of the difficulties of recognizing allergic bronchopulmonary aspergillosis (ABPA) in the context of cystic fibrosis (because of overlapping clinical,…”
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An overview of international literature from cystic fibrosis registries. Part 3. Disease incidence, genotype/phenotype correlation, microbiology, pregnancy, clinical complications, lung transplantation, and miscellanea
Published in Journal of cystic fibrosis (01-03-2011)“…Abstract This is the third article related to a review of the literature based on data from national cystic fibrosis (CF) patient registries up to June 2008…”
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Update of literature from cystic fibrosis registries 2012–2015. Part 6: Epidemiology, nutrition and complications
Published in Pediatric pulmonology (01-03-2017)“…Summary Patient registries provide useful information to afford more knowledge on rare diseases like Cystic Fibrosis (CF). Twenty‐two studies originating from…”
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An overview of international literature from cystic fibrosis registries. Part 5: Update 2012-2015 on lung disease
Published in Pediatric pulmonology (01-11-2016)“…Summary Patient registry data is a tool for defining the clinical course and risk factors in patients with less common diseases like Cystic Fibrosis. Forty‐one…”
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Gerd Döring
Published in The international journal of biochemistry & cell biology (01-07-2014)Get full text
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Effect of different inspiratory maneuvers on FEV1 in patients with cystic fibrosis
Published in Chest (01-09-1996)“…The time course of inspiration has been shown to have a significant influence on the subsequent maximal expiratory flows and timed forced expiratory volumes in…”
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An overview of international literature from cystic fibrosis registries. Part 4: Update 2011
Published in Journal of cystic fibrosis (01-12-2012)“…Abstract A total of 53 national cystic fibrosis (CF) patient registry studies published between July 2008 and November 2011 have been reviewed, focusing on the…”
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Obituary: Gerd Döring
Published in The international journal of biochemistry & cell biology (01-07-2014)Get full text
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An overview of international literature from cystic fibrosis registries 2. Neonatal screening and nutrition/growth
Published in Journal of cystic fibrosis (01-03-2010)“…This is the second article related to a review of the literature based on data from national cystic fibrosis (CF) registries up to June 2008 and covering a…”
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Teste do suor: a análise de condutividade pode tomar o lugar do método clássico de Gibson e Cooke?
Published in Jornal de pediatria (01-04-2010)Get full text
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Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings
Published in The Journal of clinical investigation (01-12-2001)“…To investigate the impact of chloride (Cl(-)) permeability, mediated by residual activity of the cystic fibrosis transmembrane conductance regulator (CFTR) or…”
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An overview of international literature from cystic fibrosis registries
Published in Journal of cystic fibrosis (01-03-2010)“…Abstract Background This is the second article related to a review of the literature based on data from national cystic fibrosis (CF) registries up to June…”
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Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis
Published in Human mutation (01-08-2001)“…Many Cystic Fibrosis (CF) carriers have been detected testing some subjects with chronic pancreatititis for a limited number of mutations. The aim of this…”
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Shwachman's Syndrome: Pathomorphosis and Long-term Outcome
Published in Journal of pediatric gastroenterology and nutrition (01-09-1999)“…BACKGROUND:Shwachman's syndrome is the second most common cause of inherited/congenital pancreatic insufficiency after cystic fibrosis. The main associated…”
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Nasal potential difference in congenital bilateral absence of the vas deferens
Published in American journal of respiratory and critical care medicine (01-09-1998)“…Congenital bilateral absence of the vas deferens (CBAVD) is supposed to be due to defective activity of the cystic fibrosis (CF) transmembrane conductance…”
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International practice patterns by age and severity of lung disease in cystic fibrosis: Data from the epidemiologic registry of cystic fibrosis (ERCF)
Published in Pediatric pulmonology (01-08-1997)“…The Epidemiologic Registry of Cystic Fibrosis provides clinical profiles for more than 6,800 patients and descriptions of practice patterns across eight…”
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Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test
Published in Journal of medical genetics (01-03-2001)“…A DNA polymorphic sequence of five thymines in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which is very commonly involved…”
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