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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
1998 3
2000 1
2001 2
2002 2
2003 1
2004 1
2005 1
2006 2
2008 1
2009 1
2010 1
2016 1
2017 1
2018 2
2019 1
2020 3
2022 0
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24 results
Results by year
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Page 1
ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia.
Bouwkamp CG, Afawi Z, Fattal-Valevski A, Krabbendam IE, Rivetti S, Masalha R, Quadri M, Breedveld GJ, Mandel H, Tailakh MA, Beverloo HB, Stevanin G, Brice A, van IJcken WFJ, Vernooij MW, Dolga AM, de Vrij FMS, Bonifati V, Kushner SA. Bouwkamp CG, et al. Among authors: masalha r. Neurol Genet. 2018 Mar 21;4(2):e223. doi: 10.1212/NXG.0000000000000223. eCollection 2018 Apr. Neurol Genet. 2018. PMID: 29577077 Free PMC article.
Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.
Afawi Z, Oliver KL, Kivity S, Mazarib A, Blatt I, Neufeld MY, Helbig KL, Goldberg-Stern H, Misk AJ, Straussberg R, Walid S, Mahajnah M, Lerman-Sagie T, Ben-Zeev B, Kahana E, Masalha R, Kramer U, Ekstein D, Shorer Z, Wallace RH, Mangelsdorf M, MacPherson JN, Carvill GL, Mefford HC, Jackson GD, Scheffer IE, Bahlo M, Gecz J, Heron SE, Corbett M, Mulley JC, Dibbens LM, Korczyn AD, Berkovic SF. Afawi Z, et al. Among authors: masalha r. Neurology. 2016 Feb 23;86(8):713-22. doi: 10.1212/WNL.0000000000002404. Epub 2016 Jan 22. Neurology. 2016. PMID: 26802095 Free PMC article.
Brachioradial pruritus: a symptom of neuropathy.
Cohen AD, Masalha R, Medvedovsky E, Vardy DA. Cohen AD, et al. Among authors: masalha r. J Am Acad Dermatol. 2003 Jun;48(6):825-8. doi: 10.1067/mjd.2003.494. J Am Acad Dermatol. 2003. PMID: 12789170
24 results