I. Sarouk

发表

Acute meningitis among infants and toddlers with febrile seizures: time for a reappraisal of the value of a lumbar puncture.

N. Watemberg, I. Sarouk, P. Fainmesser, 2012, The Israel Medical Association journal : IMAJ.

FVC deterioration, airway obstruction determination, and life span in Ataxia telangiectasia.

D. Vilozni, I. Sarouk, O. Efrati, 2015, Respiratory medicine.

The Value of Measuring Inspiratory Capacity in Subjects With Cystic Fibrosis

D. Vilozni, I. Sarouk, O. Efrati, 2018, Respiratory Care.

Consequences of Expiratory Flow Limitation at Rest in Subjects with Cystic Fibrosis.

D. Vilozni, I. Sarouk, M. Segel, 2016, Annals of the American Thoracic Society.

Tracheomegalia in CF: Alarms in Spirometry Performance

D. Vilozni, I. Sarouk, O. Efrati, 2019 .

Endocrine abnormalities in ataxia telangiectasia: findings from a national cohort

A. Lahad, Y. Levy-Shraga, D. Modan-Moses, 2016, Pediatric Research.

Cough Characteristics and FVC Maneuver in Cystic Fibrosis

D. Vilozni, I. Sarouk, O. Efrati, 2014, Respiratory Care.

Resting Energy Expenditure in Patients With Familial Dysautonomia: A Preliminary Study

D. Vilozni, A. Lahad, L. Norcliffe-Kaufmann, 2019, Journal of pediatric gastroenterology and nutrition.

Elevated IgM levels as a marker for a unique phenotype in patients with Ataxia telangiectasia

A. Lahad, B. Weiss, R. Somech, 2018, BMC Pediatrics.

Failure to conceive in women with CF is associated with pancreatic insufficiency and advancing age.

E. Picard, H. Mussaffi, H. Blau, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosis

K. De Boeck, L. Bentur, I. Sarouk, 2018, Journal of asthma and allergy.

Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis

C. Verfaillie, M. Ferrante, A. Ramalho, 2020, European Respiratory Journal.

Several siblings with Cystic Fibrosis as a risk factor for poor outcome.

D. Vilozni, I. Sarouk, O. Efrati, 2015, Respiratory medicine.

Nutritional Status in Childhood as a Prognostic Factor in Patients with Cystic Fibrosis

D. Vilozni, N. Nathan, I. Sarouk, 2019, Lung.

Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two Siblings

Y. Anikster, I. Sarouk, S. Barak, 2020, Diagnostics.

The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers.

E. Friedman, E. Pras, Y. Laitman, 2016, Cancer genetics.

P217 Cystic fibrosis with pancreatic insufficiency is associated with a high incidence of subfertility in women

E. Picard, H. Mussaffi, H. Blau, 2018, Journal of Cystic Fibrosis.

Spontaneous pneumothorax—When do we need to intervene?

D. Vilozni, I. Sarouk, O. Efrati, 2021, The clinical respiratory journal.

Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening

E. Picard, H. Mussaffi, D. Prais, 2017, Molecular genetics & genomic medicine.

Tracheal diverticula in cystic fibrosis-A potentially important underreported finding on chest CT.

I. Sarouk, O. Efrati, G. Gayer, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Phenotypic and molecular characteristics of CF patients carrying the I1234V mutation.

H. Senderowitz, N. Khazanov, I. Sarouk, 2020, Respiratory medicine.

Ivacaftor for the p.Ser549Arg (S549R) gating mutation - The Israeli experience.

H. Blau, D. Vilozni, E. Kerem, 2017, Respiratory medicine.

Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis.

D. Vilozni, J. Rivlin, D. Shoseyov, 2015, World journal of gastroenterology.

Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis Observational Study

D. Vilozni, J. Rivlin, D. Shoseyov, 2015 .

Secondary enuresis and urological manifestations in children with ataxia telangiectasia.

T. Erlich, G. Heimer, I. Sarouk, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Liver Disease in Pediatric Patients With Ataxia Telangiectasia: A Novel Report

A. Lahad, B. Weiss, R. Somech, 2016, Journal of pediatric gastroenterology and nutrition.

Glucose intolerance in cystic fibrosis as a determinant of pulmonary function and clinical status.

D. Vilozni, R. Hemi, H. Kanety, 2015, Diabetes research and clinical practice.

Progressive flow-to-volume dysanapsis in cystic fibrosis: a predictor for lung transplantation?

D. Vilozni, I. Sarouk, O. Efrati, 2012, American journal of respiratory and critical care medicine.

Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutation.

B. Kerem, E. Kerem, F. Ratjen, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

133 Clinical response to elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with the N1303K and non-modulator responsive mutation

E. Kerem, J. Reiter, I. Sarouk, 2022, Journal of Cystic Fibrosis.

Cough ability measurements and recurrent respiratory symptoms in individuals with Ataxia Telangiectasia

D. Vilozni, I. Sarouk, O. Efrati, 2016, The Journal of asthma : official journal of the Association for the Care of Asthma.

The Short-Term Effect of Breathing Tasks Via an Incentive Spirometer on Lung Function Compared With Autogenic Drainage in Subjects With Cystic Fibrosis

D. Vilozni, I. Sarouk, O. Efrati, 2015, Respiratory Care.

FVC deterioration, airway obstruction determination, and life span in Ataxia telangiectasia.

D. Vilozni, I. Sarouk, O. Efrati, 2015, Respiratory medicine.

Several siblings with Cystic Fibrosis as a risk factor for poor outcome.

D. Vilozni, I. Sarouk, O. Efrati, 2015, Respiratory medicine.