Search Results - "Yahav, Y"
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Nasal potential difference measurements in patients with atypical cystic fibrosis
Published in The European respiratory journal (01-06-2001)“…The diagnosis of cystic fibrosis (CF) is based on characteristic clinical and laboratory findings. However, a subgroup of patients present with an atypical…”
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Congenital bilateral absence of vas deferens in the absence of cystic fibrosis
Published in The Lancet (British edition) (26-11-1994)“…The high frequency of mutations in the cystic fibrosis gene in patients with congenital bilateral absence of vas deferens (CBAVD) has raised the question…”
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Nasal potential difference in non classic cystic fibrosis – long term follow up
Published in Journal of cystic fibrosis (01-06-2008)Get full text
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Short term improvement of pulmonary function tests following airway clearance using the TRI-GYM™ breathing exercisers
Published in Journal of cystic fibrosis (01-06-2008)Get full text
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Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease
Published in American journal of human genetics (01-01-1992)“…Only about 30% of the cystic fibrosis chromosomes in the Israeli cystic fibrosis patient populations carry the major CF mutation (delta F508). Since different…”
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Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation
Published in The Lancet (British edition) (03-07-1993)“…Different mutations in the cystic fibrosis (CF) gene appear to contribute to heterogeneity of the CF phenotype. We investigated 15 patients with CF who have…”
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Trampoline use as physiotherapy for cystic fibrosis patients
Published in Pediatric pulmonology (01-01-2005)“…Physicians and physiotherapists who care for CF patients have recommended the use of trampolines as a physiotherapeutic tool for enhancing cardiopulmonary…”
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Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations
Published in The New England journal of medicine (09-10-2003)“…A small fraction of patients with cystic fibrosis have a genetic defect that introduces a premature stop codon into the CFTR gene; this results in a truncated…”
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Multicenter cross-sectional study of nontuberculous mycobacterial infections among cystic fibrosis patients, Israel
Published in Emerging infectious diseases (01-03-2008)“…This 2-year cross-sectional evaluation of nontuberculous mycobacterial (NTM) infections involved all Israeli medical centers that treat cystic fibrosis…”
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Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests
Published in Clinical and experimental medicine (01-09-2003)“…Patients with normal or borderline sweat tests present a diagnostic challenge. In spite of the availability of genetic analysis and measurement of nasal…”
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The critical first six months in cystic fibrosis: A syndrome of severe bronchiolitis
Published in Pediatric pulmonology (01-08-1997)“…The syndrome of infantile bronchiolitis in cystic fibrosis (CF) carries a high mortality. Fifteen cases of CF encountered over the past 19 years with severe…”
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A Missense Cystic Fibrosis Transmembrane Conductance Regulator Mutation With Variable Phenotype
Published in Pediatrics (Evanston) (01-09-1997)“…Cystic fibrosis (CF) has variable clinical presentation. Disease severity is partially associated with the type of mutation. The aim of this study was to…”
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Nephrotic syndrome and fibrillary glomerulonephritis
Published in Journal of internal medicine (01-07-1997)“…Laufer J, Augarten A, Szeinberg A, Rapoport J, Katzenelson D, Yahav Y (The Chaim Sheba Medical Center, Tel Hashomer, Affiliated to the Sackler School of…”
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Physician-Patient Communication Course: When the Inauguration of a New Israeli Medical School Coincided with COVID-19 Pandemic
Published in Advances in medical education and practice (01-01-2023)“…Purpose: The curriculum of the Adelson School of Medicine at Ariel University, the newly established sixth medical school in Israel, includes a simulation…”
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Correlation between genotype and phenotype in patients with cystic fibrosis
Published in The New England journal of medicine (24-03-1994)Get full text
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Similar levels of mRNA from the W1282X and the ΔF508 cystic fibrosis alleles, in nasal epithelial cells
Published in The Journal of clinical investigation (01-04-1994)“…The effect of nonsense mutations on mRNA levels is variable. The levels of some mRNAs are not affected and truncated proteins are produced, while the levels of…”
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D-lactic acidosis: a treatable encephalopathy in pediatric patients
Published in Acta pædiatrica (Oslo) (01-01-1993)“…A 20-month old infant, who had short bowel syndrome following extensive surgery for a mid gut volvulus, developed hyperchloremic acidosis, with a large anion…”
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The role of computer games in measuring spirometry in healthy and "asthmatic" preschool children
Published in Chest (01-09-2005)“…To explore the role of respiratory interactive computer games in teaching spirometry to preschool children, and to examine whether the spirometry data achieved…”
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Variables affecting outcome from severe brain injury in children
Published in Intensive care medicine (01-01-1988)“…This study evaluates the outcome of 56 severely brain injured children (mean age 6.2 +/- 2.1 years) and relates the Initial Glasgow Coma Scale (IGCS), initial…”
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