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Nasal potential difference measurements in patients with atypical cystic fibrosis

The European respiratory journal, 2001-06, Vol.17 (6), p.1208-1215

2001

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Multicenter cross-sectional study of nontuberculous mycobacterial infections among cystic fibrosis patients, Israel

Emerging infectious diseases, 2008-03, Vol.14 (3), p.378-384

2008

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Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations

The New England journal of medicine, 2003-10, Vol.349 (15), p.1433-1441

2003

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Congenital bilateral absence of vas deferens in the absence of cystic fibrosis

The Lancet (British edition), 1994-11, Vol.344 (8935), p.1473-1474

1994

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Nasal potential difference in non classic cystic fibrosis – long term follow up

Journal of cystic fibrosis, 2008-06, Vol.7, p.S10-S10

2008

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Short term improvement of pulmonary function tests following airway clearance using the TRI-GYM™ breathing exercisers

Journal of cystic fibrosis, 2008-06, Vol.7, p.S74-S74

2008

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Physician-Patient Communication Course: When the Inauguration of a New Israeli Medical School Coincided with COVID-19 Pandemic

Advances in medical education and practice, 2023-01, Vol.14, p.1013-1024

2023

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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

American journal of human genetics, 1992-01, Vol.50 (1), p.222-228

1992

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Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation

The Lancet (British edition), 1993-07, Vol.342 (8862), p.25-26

1993

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The Role of Computer Games in Measuring Spirometry in Healthy and “Asthmatic” Preschool Children

Chest, 2005-09, Vol.128 (3), p.1146-1155

2005

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Invasive mechanical ventilation: risk factor for death in patients with cystic fibrosis admitted to intensive care unit – Outcome and prolonged follow up

Journal of cystic fibrosis, 2008-06, Vol.7, p.S68-S68

2008

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Trampoline use as physiotherapy for cystic fibrosis patients

Pediatric pulmonology, 2005-01, Vol.39 (1), p.70-73

2005

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Long Term Nutritional Rehabilitation by Gastrostomy in Israeli Patients with Cystic Fibrosis: Clinical Outcome in Advanced Pulmonary Disease

Journal of pediatric gastroenterology and nutrition, 2006-02, Vol.42 (2), p.222-228

2006

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A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype

Pediatrics (Evanston), 1997-09, Vol.100 (3), p.E5-e5

1997

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Oligohydrosis and Hyperthermia: Pilot Study of a Novel Topiramate Adverse Effect

Journal of child neurology, 2003-04, Vol.18 (4), p.254-257

2003

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Nasal potential difference in non-classic cystic fibrosis-long term follow up

Pediatric pulmonology, 2008-06, Vol.43 (6), p.545-549

2008

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Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests

Clinical and experimental medicine, 2003-09, Vol.3 (2), p.119-123

2003

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The critical first six months in cystic fibrosis: A syndrome of severe bronchiolitis

Pediatric pulmonology, 1997-08, Vol.24 (2), p.134-136

1997

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Nephrotic syndrome and fibrillary glomerulonephritis

Journal of internal medicine, 1997-07, Vol.242 (1), p.83-86

1997

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Effect of low altitude at the Dead Sea on exercise capacity and cardiopulmonary response to exercise in cystic fibrosis patients with moderate to severe lung disease

Pediatric pulmonology, 2006-03, Vol.41 (3), p.234-241

2006

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Similar levels of mRNA from the W1282X and the ΔF508 cystic fibrosis alleles, in nasal epithelial cells

The Journal of clinical investigation, 1994-04, Vol.93 (4), p.1502-1507

1994

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Correlation between genotype and phenotype in patients with cystic fibrosis

The New England journal of medicine, 1994-03, Vol.330 (12), p.866-866

1994

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D‐Lactic acidosis: a treatable encephalopathy in pediatric patients

Acta Paediatrica, 1993-01, Vol.82 (1), p.119-121

1993

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Familial concordance of phenotype and microbial variation among siblings with CF

Pediatric pulmonology, 2004-10, Vol.38 (4), p.292-297

2004

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Variables affecting outcome from severe brain injury in children

Intensive care medicine, 1988-01, Vol.14 (4), p.417-421

1988

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Nasal potential difference measurements in patients with atypical cystic fibrosis

Multicenter cross-sectional study of nontuberculous mycobacterial infections among cystic fibrosis patients, Israel

Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations

Congenital bilateral absence of vas deferens in the absence of cystic fibrosis

Nasal potential difference in non classic cystic fibrosis – long term follow up

Short term improvement of pulmonary function tests following airway clearance using the TRI-GYM™ breathing exercisers

Physician-Patient Communication Course: When the Inauguration of a New Israeli Medical School Coincided with COVID-19 Pandemic

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation

The Role of Computer Games in Measuring Spirometry in Healthy and “Asthmatic” Preschool Children

Invasive mechanical ventilation: risk factor for death in patients with cystic fibrosis admitted to intensive care unit – Outcome and prolonged follow up

Trampoline use as physiotherapy for cystic fibrosis patients

Long Term Nutritional Rehabilitation by Gastrostomy in Israeli Patients with Cystic Fibrosis: Clinical Outcome in Advanced Pulmonary Disease

A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype

Oligohydrosis and Hyperthermia: Pilot Study of a Novel Topiramate Adverse Effect

Nasal potential difference in non-classic cystic fibrosis-long term follow up

Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests

The critical first six months in cystic fibrosis: A syndrome of severe bronchiolitis

Nephrotic syndrome and fibrillary glomerulonephritis

Effect of low altitude at the Dead Sea on exercise capacity and cardiopulmonary response to exercise in cystic fibrosis patients with moderate to severe lung disease

Similar levels of mRNA from the W1282X and the ΔF508 cystic fibrosis alleles, in nasal epithelial cells

Correlation between genotype and phenotype in patients with cystic fibrosis

D‐Lactic acidosis: a treatable encephalopathy in pediatric patients

Familial concordance of phenotype and microbial variation among siblings with CF

Variables affecting outcome from severe brain injury in children

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