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TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability.
Heimer G, Oz-Levi D, Eyal E, Edvardson S, Nissenkorn A, Ruzzo EK, Szeinberg A, Maayan C, Mai-Zahav M, Efrati O, Pras E, Reznik-Wolf H, Lancet D, Goldstein DB, Anikster Y, Shalev SA, Elpeleg O, Ben Zeev B. Heimer G, et al. Among authors: efrati o. Eur J Paediatr Neurol. 2016 Jan;20(1):69-79. doi: 10.1016/j.ejpn.2015.10.003. Epub 2015 Oct 22. Eur J Paediatr Neurol. 2016. PMID: 26542466
Liver cirrhosis and portal hypertension in cystic fibrosis.
Efrati O, Barak A, Modan-Moses D, Augarten A, Vilozni D, Katznelson D, Szeinberg A, Yahav J, Bujanover Y. Efrati O, et al. Eur J Gastroenterol Hepatol. 2003 Oct;15(10):1073-8. doi: 10.1097/00042737-200310000-00002. Eur J Gastroenterol Hepatol. 2003. PMID: 14501614
Spirometry in early childhood in cystic fibrosis patients.
Vilozni D, Bentur L, Efrati O, Minuskin T, Barak A, Szeinberg A, Blau H, Picard E, Kerem E, Yahav Y, Augarten A. Vilozni D, et al. Among authors: efrati o. Chest. 2007 Feb;131(2):356-61. doi: 10.1378/chest.06-1351. Chest. 2007. PMID: 17296633
Peak bone mass in patients with phenylketonuria.
Modan-Moses D, Vered I, Schwartz G, Anikster Y, Abraham S, Segev R, Efrati O. Modan-Moses D, et al. Among authors: efrati o. J Inherit Metab Dis. 2007 Apr;30(2):202-8. doi: 10.1007/s10545-007-0462-9. Epub 2007 Mar 8. J Inherit Metab Dis. 2007. PMID: 17347917
Exercise challenge test in 3- to 6-year-old asthmatic children.
Vilozni D, Bentur L, Efrati O, Barak A, Szeinberg A, Shoseyov D, Yahav Y, Augarten A. Vilozni D, et al. Among authors: efrati o. Chest. 2007 Aug;132(2):497-503. doi: 10.1378/chest.07-0052. Epub 2007 Jun 15. Chest. 2007. PMID: 17573494 Clinical Trial.
102 results