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Малена Коэн-Кимберкно

Отделение: Пульмонология, Педиатрия
Должность: Пульмонолог-педиатр
Языки: Английский, Иврит
Принимает: детей и взрослых
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Профессор Малена Коэн-Симберкно
Заведующая отделением детской пульмонологии и Центром лечения муковисцидоза

Профессиональная деятельность

Руководитель центра детской пульмонологии.

Научные публикации

Advances in the restoration of CFTR in children and pwCF with "mild disease"
Infection and Inflammation in the Cystic fibrosis (CF) airway
National trends in pediatric drowning - insights from the Israeli Ministry of Health registry-based cohort
Impact of COVID-19 infection on lung function and nutritional status amongst individuals with cystic fibrosis: A global cohort study
Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis with Mildly Decreased and Normal Lung Function: A Real-Life Observational Study
Long-term therapy with CFTR modulators consistently improves glucose metabolism in adolescents and adults with cystic fibrosis
Maternal and fetal outcomes in multiparous women with Cystic Fibrosis
Clinical efficacy of CFTR modulator therapy in people with cystic fibrosis carrying the I1234V mutation
Optimizing CFTR modulator therapy management for cystic fibrosis through the ReX platform
Changes in Sleep in Children and Adults with Cystic Fibrosis and Primary Ciliary Dyskinesia over Time and after CFTR Modulator Therapy
The new face of cystic fibrosis in the era of population genetic carrier screening
Ovarian reserve in women with cystic fibrosis: is this a cause of sub-fertility?
Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutation
Eradication of Nontuberculous Mycobacteria in People with Cystic Fibrosis Treated with Elexacaftor/Tezacaftor/Ivacaftor: A Multicenter Cohort Study
Pediatric respiratory admissions and related viral infections during the COVID-19 pandemic
The association between Attention-Deficit-Hyperactivity-Disorder (ADHD) symptoms and disease severity in people with Cystic Fibrosis (pwCF)
Acute pancreatitis in pancreatic-insufficient cystic fibrosis patients treated with CFTR modulators
The Impact of Highly Effective Cystic Fibrosis Transmembrane Conductance Regulator Modulators on the Health of Female Subjects With Cystic Fibrosis
Treatment effects of Elexacaftor/Tezacaftor/Ivacaftor in people with CF carrying non-F508del mutations
The clinical yield of bronchoscopy in the management of cystic fibrosis: A retrospective multicenter study
The utility of glucose area under the curve from the oral glucose tolerance test as a screening tool for cystic fibrosis-related diabetes
Targeting Persistent Biofilm Infections: Reconsidering the Topography of the Infection Site during Model Selection
Calcium carbonate mineralization is essential for biofilm formation and lung colonization
Respiratory physiotherapy in patients with cystic fibrosis and upper limb deep vein thrombosis
Lung function from school age to adulthood in primary ciliary dyskinesia
Antisense oligonucleotide splicing modulation as a novel Cystic Fibrosis therapeutic approach for the W1282X nonsense mutation
Expanding clinical phage microbiology: simulating phage inhalation for respiratory tract infections
Manual external chest compression reverses respiratory failure in children with severe air trapping
Ethical Dilemma: Elexacaftor-Tezacaftor-Ivacaftor or Lung Transplantation in Cystic Fibrosis and End-Stage Lung Disease?
Fertility and Pregnancy in Cystic Fibrosis
The Use of Infant Pulmonary Function Tests in the Diagnosis of Neuroendocrine Cell Hyperplasia of Infancy
Sleep in children with cystic fibrosis: More under the covers
Regional differences in pediatric asthma hospital admissions: National data from Israel 1996-2017
Lymphadenopathy Associated With the COVID-19 Vaccine
A Green Light for Stop Mutations
How abnormal is the normal? Clinical characteristics of CF patients with normal FEV1
Betamethasone versus dexamethasone for inpatient preschool wheezing-A case-control study
Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia
Ivacaftor in People with Cystic Fibrosis and a 3849+10kb C→T or D1152H Residual Function Mutation
Baseline Cystic fibrosis disease severity has an adverse impact on pregnancy and infant outcomes, but does not impact disease progression
Phenotypic and molecular characteristics of CF patients carrying the I1234V mutation
Cystic fibrosis in low and middle-income countries (LMIC): A view from four different regions of the world
The Long-Term Effect of a Quality Improvement Intervention in the Management of Bronchiolitis
Hydrocarbon Intoxication in Children: Clinical and Sociodemographic Characteristics
Sleep disorders in cystic fibrosis: A systematic review and meta-analysis
Sleep disorders in patients with primary ciliary dyskinesia, cystic fibrosis with and without pancreatic insufficiency
Giant lung cysts following necrotizing pneumonia: Resolution with conservative treatment
Failure to conceive in women with CF is associated with pancreatic insufficiency and advancing age
Increasing Vitamin D Serum Levels Is Associated With Reduced Pulmonary Exacerbations in Patients With Cystic Fibrosis
Primary sclerosing cholangitis is associated with abnormalities in CFTR
A quality improvement intervention to reduce emergency department radiography for bronchiolitis
Attention deficit hyperactivity disorder symptoms in patients with cystic fibrosis
Clinical impact of Pseudomonas aeruginosa colonization in patients with Primary Ciliary Dyskinesia
Ivacaftor for the p.Ser549Arg (S549R) gating mutation - The Israeli experience
Predictors of Prolonged Hospitalizations in Pediatric Complicated Pneumonia
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening
Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practices
Comparison of Nasal Potential Difference and Intestinal Current Measurements as Surrogate Markers for CFTR Function
Complicated community acquired pneumonia in childhood: Different types, clinical course, and outcome
Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosis
Treatment of cystic fibrosis in low-income countries
Hepatopulmonary Syndrome in Patients With Cystic Fibrosis and Liver Disease
Disparities in Cystic Fibrosis Care and Outcome: Socioeconomic Status and Beyond
Ataluren for the treatment of cystic fibrosis
Reversible airway obstruction in cystic fibrosis: Common, but not associated with characteristics of asthma
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis
Adherence pattern to study drugs in clinical trials by patients with cystic fibrosis
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screening
Association of chronic Candida albicans respiratory infection with a more severe lung disease in patients with cystic fibrosis
A reach-out system for video microscopy analysis of ciliary motions aiding PCD diagnosis
Antibiotic treatment for children hospitalized with community-acquired pneumonia after oral therapy
Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis
Continuous intravenous β-lactam antibiotics in cystic fibrosis patients with severe drug hypersensitivity
Differences in disease expression between primary ciliary dyskinesia and cystic fibrosis with and without pancreatic insufficiency
CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia
Airway inflammation in cystic fibrosis: molecular mechanisms and clinical implications
Mitochondrial OXPHOS function is unaffected by chronic azithromycin treatment
LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects
Differences in the pattern of structural abnormalities on CT scan in patients with cystic fibrosis and pancreatic sufficiency or insufficiency
Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis
Antibiotic treatment of children with community-acquired pneumonia: comparison of penicillin or ampicillin versus cefuroxime
Concomitant cystic fibrosis and coeliac disease: reminder of an important clinical lesson
Could you please pass the salt?
Managing cystic fibrosis: strategies that increase life expectancy and improve quality of life
Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis
Late-onset central hypoventilation presenting as extubation failure
18F-fluorodeoxyglucose-PET/CT imaging of lungs in patients with cystic fibrosis
Meconium ileus in patients with cystic fibrosis is not a risk factor for clinical deterioration and survival: the Israeli Multicenter Study
Intravenous monthly pulse methylprednisolone treatment for ABPA in patients with cystic fibrosis
Primary ciliary dyskinesia: prospects for new therapies, building on the experience in cystic fibrosis
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