Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Eitan, Kerem"'
Publikováno v:
Paediatric Respiratory Reviews. 30:65-71
Interstitial lung diseases in children (chILD) are rare and diverse. The current classifications include a group of early onset chILD specific to infancy, namely neuro-endocrine cell hyperplasia of infancy (NEHI), pulmonary interstitial glycogenosis
Autor:
David Shoseyov, Malena Cohen-Cymberknoh, Polina Stepensky, Eitan Kerem, Klaus Warnatz, Oded Breuer, Baerbel Keller, Susanne Unger, Hagit Daum
Publikováno v:
Respiratory Medicine. 126:39-45
Background In a substantial number of patients with non-cystic fibrosis (CF) bronchiectasis an etiology cannot be found. Various complex immunodeficiency syndromes account for a significant portion of these patients but the mechanism elucidating the
Autor:
Eitan Kerem, David Shoseyov, Alex Gileles-Hillel, M. Mei-Zahav, Joel Reiter, R. Tzabari, Malena Cohen-Cymberknoh, P. Stafler, L. Yochi
Publikováno v:
A53. CLINICAL STUDIES IN NEONATAL AND PEDIATRIC LUNG DISEASE AND CYSTIC FIBROSIS.
Autor:
David Shoseyov, Mareike Price, Elie Picard, Nurith Hiller, Galit Livnat, Angelo Barbato, Deborah Snijders, Nir Weigert, Ugo Pradal, Huda Mussaffi, Mirella Collura, Michal Gur, Natalia Simanovsky, Kris De Boeck, Malena Cohen-Cymberknoh, Israel Amirav, Michal Shteinberg, Micha Aviram, Lea Bentur, Alex Gileles-Hillel, Hannah Blau, Joseph Rivlin, Eitan Kerem, Mieke Boon, Oded Breuer
Publikováno v:
Respiratory medicine. 131
Background Airway infections in Primary Ciliary Dyskinesia (PCD) are caused by different microorganisms, including pseudomonas aeruginosa (PA). The aim of this study was to investigate the association of PA colonization and the progression of lung di
Publikováno v:
Neuromuscular disorders : NMD. 27(10)
A 7-week-old infant presented with persistent noisy breathing and aspirations during swallowing. Neurological examination and brain MRI were normal. His 12-year-old brother underwent pneumonectomy at the age of 10 years due to recurrent aspirations l
Autor:
Natalia Simanovsky, David Shoseyov, Alex Gileles Hillel, Malena Cohen-Cymberknoh, Nurith Hiller, Eitan Kerem
Publikováno v:
Chest. 145:738-744
Background Impaired mucociliary clearance causes pulmonary disease in primary ciliary dyskinesia (PCD) and contributes to cystic fibrosis (CF) lung disease. Although the sinopulmonary disease is similar, morbidity and mortality are different. Both pa
Autor:
Micha Aviram, Malena Cohen-Cymberknoh, Eran Israeli, Yasmin Yaakov, Edna Schachar, David Shoseyov, Joseph Rivlin, Michael Wilschanski, Eitan Kerem, Lea Bentur, Elie Picard, Eyal Shteyer
Publikováno v:
Pediatric Pulmonology. 48:229-235
The sweat test and nasal potential difference measurement are now established tools in the diagnostic work up of cystic fibrosis (CF). Intestinal current measurement (ICM) is under consideration as an aid in the diagnosis of CF especially in young ch
Autor:
Daniela, Rauch, Martin, Wetzke, Simone, Reu, Waltraud, Wesselak, Andrea, Schams, Meike, Hengst, Birgit, Kammer, Julia, Ley-Zaporozhan, Matthias, Kappler, Marijke, Proesmans, Joanna, Lange, Amparo, Escribano, Eitan, Kerem, Frank, Ahrens, Frank, Brasch, Nicolaus, Schwerk, Matthias, Griese, B, Niggemann
Publikováno v:
American journal of respiratory and critical care medicine. 193(4)
Persistent tachypnea of infancy (PTI) is a specific clinical entity of undefined etiology comprising the two diseases neuroendocrine cell hyperplasia of infancy (NEHI) and pulmonary interstitial glycogenosis. The outcome of typical NEHI is favorable.
Autor:
Moshe Santo, Yaakov Yahav, Samuel N. Adler, Eyal Shteyer, Michael Wilschanski, Ian O. Ellis, Efrat Broide, Idit Segal, Yasmin Yaakov, Aaron Lerner, Aharon Klar, Roger Mountford, Hannah Blau, Eitan Kerem, Micha Aviram
Publikováno v:
Journal of Clinical Gastroenterology. 42:810-814
GOALS: To understand the relationship between acute recurrent pancreatitis and cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction. BACKGROUND: An emerging number of patients present with a nonclassic phenotype of cystic fibrosis (
Autor:
A. Augarten, Y. Yahav, L. Ben Tur, Hannah Blau, Amir Szeinberg, A. Diver-Habber, H. Berman, Hannah Akons, D. Katznelson, Joseph Rivlin, Eitan Kerem, Micha Aviram, L. Theodor, Gideon Paret, Batsheva Kerem
Publikováno v:
Clinical and Experimental Medicine. 3:119-123
Patients with normal or borderline sweat tests present a diagnostic challenge. In spite of the availability of genetic analysis and measurement of nasal potential difference, there is still uncertainty in diagnosing cystic fibrosis in some patients.