Results
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81.
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82.
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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. [electronic resource] by
- Shoshani, T
- Augarten, A
- Gazit, E
- Bashan, N
- Yahav, Y
- Rivlin, Y
- Tal, A
- Seret, H
- Yaar, L
- Kerem, E
Producer: 19920213
In:
American journal of human genetics vol. 50
Availability: No items available.
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83.
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Efficacy of adding nebulized ipratropium bromide to nebulized albuterol therapy in acute bronchiolitis. [electronic resource] by
- Schuh, S
- Johnson, D
- Canny, G
- Reisman, J
- Shields, M
- Kovesi, T
- Kerem, E
- Bentur, L
- Levison, H
- Jaffe, D
Producer: 19921223
In:
Pediatrics vol. 90
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84.
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85.
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86.
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The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutation. [electronic resource] by
- Chiba-Falek, O
- Kerem, E
- Shoshani, T
- Aviram, M
- Augarten, A
- Bentur, L
- Tal, A
- Tullis, E
- Rahat, A
- Kerem, B
Producer: 19981231
In:
Genomics vol. 53
Availability: No items available.
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87.
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The significance of sweat Cl/Na ratio in patients with borderline sweat test. [electronic resource] by
- Augarten, A
- Hacham, S
- Kerem, E
- Sheva Kerem, B
- Szeinberg, A
- Laufer, J
- Doolman, R
- Altshuler, R
- Blau, H
- Bentur, L
Producer: 19960723
In:
Pediatric pulmonology vol. 20
Availability: No items available.
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88.
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A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian Jews. [electronic resource] by
- Shoshani, T
- Berkun, Y
- Yahav, Y
- Augarten, A
- Bashan, N
- Rivlin, Y
- Gazit, E
- Sereth, H
- Kerem, E
- Kerem, B S
Producer: 19930316
In:
Genomics vol. 15
Availability: No items available.
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89.
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Cost-benefit analysis of a national screening programme for cystic fibrosis in an Israeli population. [electronic resource] by
- Ginsberg, G
- Blau, H
- Kerem, E
- Springer, C
- Kerem, B S
- Akstein, E
- Greenberg, A
- Kolumbos, A
- Abeliovich, D
- Gazit, E
Producer: 19940601
In:
Health economics vol. 3
Availability: No items available.
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90.
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Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel. [electronic resource] by
- Kerem, E
- Kalman, Y M
- Yahav, Y
- Shoshani, T
- Abeliovich, D
- Szeinberg, A
- Rivlin, J
- Blau, H
- Tal, A
- Ben-Tur, L
Producer: 19950911
In:
Human genetics vol. 96
Availability: No items available.
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91.
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The molecular basis of partial penetrance of splicing mutations in cystic fibrosis. [electronic resource] by
- Rave-Harel, N
- Kerem, E
- Nissim-Rafinia, M
- Madjar, I
- Goshen, R
- Augarten, A
- Rahat, A
- Hurwitz, A
- Darvasi, A
- Kerem, B
Producer: 19970123
In:
American journal of human genetics vol. 60
Availability: No items available.
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92.
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Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation. [electronic resource] by
- Augarten, A
- Kerem, B S
- Yahav, Y
- Noiman, S
- Rivlin, Y
- Tal, A
- Blau, H
- Ben-Tur, L
- Szeinberg, A
- Kerem, E
Producer: 19930727
In:
Lancet (London, England) vol. 342
Availability: No items available.
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93.
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Trampoline use as physiotherapy for cystic fibrosis patients. [electronic resource] by
- Barak, A
- Wexler, I D
- Efrati, O
- Bentur, L
- Augarten, A
- Mussaffi, H
- Avital, A
- Rivlin, J
- Aviram, M
- Yahav, Y
- Kerem, E
Producer: 20050329
In:
Pediatric pulmonology vol. 39
Availability: No items available.
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94.
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Clinical and genetic risk factors for cystic fibrosis-related liver disease. [electronic resource] by
- Wilschanski, M
- Rivlin, J
- Cohen, S
- Augarten, A
- Blau, H
- Aviram, M
- Bentur, L
- Springer, C
- Vila, Y
- Branski, D
- Kerem, B
- Kerem, E
Producer: 19990205
In:
Pediatrics vol. 103
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95.
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Systemic inflammatory mediators and cystic fibrosis genotype. [electronic resource] by
- Augarten, A
- Paret, G
- Avneri, I
- Akons, H
- Aviram, M
- Bentur, L
- Blau, H
- Efrati, O
- Szeinberg, A
- Barak, A
- Kerem, E
- Yahav, J
Producer: 20050210
In:
Clinical and experimental medicine vol. 4
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96.
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Efficacy and safety of ataluren in patients with nonsense-mutation cystic fibrosis not receiving chronic inhaled aminoglycosides: The international, randomized, double-blind, placebo-controlled Ataluren Confirmatory Trial in Cystic Fibrosis (ACT CF). [electronic resource] by
- Konstan, M W
- VanDevanter, D R
- Rowe, S M
- Wilschanski, M
- Kerem, E
- Sermet-Gaudelus, I
- DiMango, E
- Melotti, P
- McIntosh, J
- De Boeck, K
Producer: 20210913
In:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society vol. 19
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97.
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Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism. [electronic resource] by
- Kerem, E
- Bistritzer, T
- Hanukoglu, A
- Hofmann, T
- Zhou, Z
- Bennett, W
- MacLaughlin, E
- Barker, P
- Nash, M
- Quittell, L
- Boucher, R
- Knowles, M R
Producer: 19990715
In:
The New England journal of medicine vol. 341
Availability: No items available.
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98.
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A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype. [electronic resource] by
- Kerem, E
- Nissim-Rafinia, M
- Argaman, Z
- Augarten, A
- Bentur, L
- Klar, A
- Yahav, Y
- Szeinberg, A
- Hiba, O
- Branski, D
- Corey, M
- Kerem, B
Producer: 19980910
In:
Pediatrics vol. 100
Availability: No items available.
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99.
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Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat tests. [electronic resource] by
- Augarten, A
- Shmilovich, H
- Doolman, R
- Aviram, M
- Akons, H
- Ben Tur, L
- Blau, H
- Kerem, E
- Rivlin, J
- Sela, B A
- Szeinberg, A
- Yahav, Y
Producer: 20001222
In:
Pediatric pulmonology vol. 30
Availability: No items available.
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100.
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Nasal potential difference measurements in patients with atypical cystic fibrosis. [electronic resource] by
- Wilschanski, M
- Famini, H
- Strauss-Liviatan, N
- Rivlin, J
- Blau, H
- Bibi, H
- Bentur, L
- Yahav, Y
- Springer, H
- Kramer, M R
- Klar, A
- Ilani, A
- Kerem, B
- Kerem, E
Producer: 20011218
In:
The European respiratory journal vol. 17
Availability: No items available.
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