Mory A - Search Results

1

A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema.

Melikhan-Revzin S, Kurolap A, Dagan E, Mory A, Gershoni-Baruch R. Melikhan-Revzin S, et al. Among authors: mory a. Lymphat Res Biol. 2015 Jun;13(2):107-11. doi: 10.1089/lrb.2014.0044. Epub 2015 Jun 2. Lymphat Res Biol. 2015. PMID: 26091405

2

Leukocyte adhesion deficiency type II: long-term follow-up and review of the literature.

Gazit Y, Mory A, Etzioni A, Frydman M, Scheuerman O, Gershoni-Baruch R, Garty BZ. Gazit Y, et al. Among authors: mory a. J Clin Immunol. 2010 Mar;30(2):308-13. doi: 10.1007/s10875-009-9354-0. Epub 2010 Jan 23. J Clin Immunol. 2010. PMID: 20099014 Review.

3

The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers.

Inzelberg R, Cohen OS, Aharon-Peretz J, Schlesinger I, Gershoni-Baruch R, Djaldetti R, Nitsan Z, Ephraty L, Tunkel O, Kozlova E, Inzelberg L, Kaplan N, Fixler Mehr T, Mory A, Dagan E, Schechtman E, Friedman E, Hassin-Baer S. Inzelberg R, et al. Among authors: mory a. Neurology. 2012 Mar 13;78(11):781-6. doi: 10.1212/WNL.0b013e318249f673. Epub 2012 Feb 8. Neurology. 2012. PMID: 22323743

4

A nonsense mutation in the human homolog of Drosophila rogdi causes Kohlschutter-Tonz syndrome.

Mory A, Dagan E, Illi B, Duquesnoy P, Mordechai S, Shahor I, Romani S, Hawash-Moustafa N, Mandel H, Valente EM, Amselem S, Gershoni-Baruch R. Mory A, et al. Am J Hum Genet. 2012 Apr 6;90(4):708-14. doi: 10.1016/j.ajhg.2012.03.005. Am J Hum Genet. 2012. PMID: 22482807 Free PMC article.

5

Duplication in CHIT1 gene and the risk for Aspergillus lung disease in CF patients.

Livnat G, Bar-Yoseph R, Mory A, Dagan E, Elias N, Gershoni R, Bentur L. Livnat G, et al. Among authors: mory a. Pediatr Pulmonol. 2014 Jan;49(1):21-7. doi: 10.1002/ppul.22749. Epub 2013 Jan 28. Pediatr Pulmonol. 2014. PMID: 23359515

6

A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred.

Mory A, Ruiz FX, Dagan E, Yakovtseva EA, Kurolap A, Parés X, Farrés J, Gershoni-Baruch R. Mory A, et al. Eur J Hum Genet. 2014 Mar;22(3):419-22. doi: 10.1038/ejhg.2013.157. Epub 2013 Jul 24. Eur J Hum Genet. 2014. PMID: 23881059 Free PMC article.

7

BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control study.

Dagan E, Cohen Y, Mory A, Adir V, Borochowitz Z, Raanani H, Kurolap A, Melikhan-Revzin S, Meirow D, Gershoni-Baruch R. Dagan E, et al. Among authors: mory a. Eur J Hum Genet. 2014 Feb;22(2):277-9. doi: 10.1038/ejhg.2013.281. Epub 2013 Nov 27. Eur J Hum Genet. 2014. PMID: 24281364 Free PMC article.

8

Kohlschutter-Tonz syndrome: clinical and genetic insights gained from 16 cases deriving from a close-knit village in Northern Israel.

Mory A, Dagan E, Shahor I, Mandel H, Illi B, Zolotushko J, Kurolap A, Chechik E, Valente EM, Amselem S, Gershoni-Baruch R. Mory A, et al. Pediatr Neurol. 2014 Apr;50(4):421-6. doi: 10.1016/j.pediatrneurol.2014.01.006. Epub 2014 Jan 7. Pediatr Neurol. 2014. PMID: 24630287

9

The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews.

Dagan E, Schlesinger I, Ayoub M, Mory A, Nassar M, Kurolap A, Peretz-Aharon J, Gershoni-Baruch R. Dagan E, et al. Among authors: mory a. Parkinsonism Relat Disord. 2015 Sep;21(9):1067-71. doi: 10.1016/j.parkreldis.2015.06.016. Epub 2015 Jun 19. Parkinsonism Relat Disord. 2015. PMID: 26169695

10

SMPD1 mutations and Parkinson disease.

Dagan E, Adir V, Schlesinger I, Borochowitz Z, Ayoub M, Mory A, Nassar M, Kurolap A, Aharon-Peretz J, Gershoni-Baruch R. Dagan E, et al. Among authors: mory a. Parkinsonism Relat Disord. 2015 Oct;21(10):1296-7. doi: 10.1016/j.parkreldis.2015.08.019. Epub 2015 Aug 20. Parkinsonism Relat Disord. 2015. PMID: 26318962 No abstract available.

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