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Huda Mussaffi

Showing results (41-50 of 64) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 23, 2017
Attention deficit hyperactivity disorder symptoms in patients with cystic fibrosisMalena Cohen-Cymberknoh, Tzlil Tanny, Oded Breuer, et al.
Respiration; International Review of Thoracic Diseases|May 28, 2026
Non-tuberculous mycobacteria in primary ciliary dyskinesia: a national multicenter cohort studyOphir Bar-On, Saharon Less Elazari, Haim Ben-Zvi, et al.
Human Mutation|January 19, 2016
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential DiagnosisIsrael Amirav, Julia Wallmeier, Niki T Loges, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 1, 2010
Evidence of intestinal inflammation in patients with cystic fibrosisSteven L Werlin, Ishay Benuri-Silbiger, Eitan Kerem, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 5, 2016
Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosisMalena Cohen-Cymberknoh, Noa Gilead, Silvia Gartner, et al.
Nature Genetics|March 6, 2012
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesiaHannah M Mitchison, Miriam Schmidts, Niki T Loges, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 21, 2015
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screeningPatrick Stafler, Meir Mei-Zahav, Michael Wilschanski, et al.
Blood|November 8, 2003
The mechanisms controlling NK cell autoreactivity in TAP2-deficient patientsGal Markel, Huda Mussaffi, Khoon-Lin Ling, et al.
European Journal of Immunology|July 20, 2004
Biological function of the soluble CEACAM1 protein and implications in TAP2-deficient patientsGal Markel, Hagit Achdout, Gil Katz, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 23, 2017
Attention deficit hyperactivity disorder symptoms in patients with cystic fibrosisMalena Cohen-Cymberknoh, Tzlil Tanny, Oded Breuer, et al.
Respiration; International Review of Thoracic Diseases|May 28, 2026
Non-tuberculous mycobacteria in primary ciliary dyskinesia: a national multicenter cohort studyOphir Bar-On, Saharon Less Elazari, Haim Ben-Zvi, et al.
Human Mutation|January 19, 2016
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential DiagnosisIsrael Amirav, Julia Wallmeier, Niki T Loges, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 1, 2010
Evidence of intestinal inflammation in patients with cystic fibrosisSteven L Werlin, Ishay Benuri-Silbiger, Eitan Kerem, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 5, 2016
Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosisMalena Cohen-Cymberknoh, Noa Gilead, Silvia Gartner, et al.
Nature Genetics|March 6, 2012
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesiaHannah M Mitchison, Miriam Schmidts, Niki T Loges, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 21, 2015
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screeningPatrick Stafler, Meir Mei-Zahav, Michael Wilschanski, et al.
Blood|November 8, 2003
The mechanisms controlling NK cell autoreactivity in TAP2-deficient patientsGal Markel, Huda Mussaffi, Khoon-Lin Ling, et al.
European Journal of Immunology|July 20, 2004
Biological function of the soluble CEACAM1 protein and implications in TAP2-deficient patientsGal Markel, Hagit Achdout, Gil Katz, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
Pageof 7