Straussberg R - Search Results

1

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: straussberg 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.

2

X-linked mental retardation with bilateral clasped thumbs: report of another affected family.

Straussberg R, Blatt I, Brand N, Kessler D, Katznelson MB, Goodman RM. Straussberg R, et al. Clin Genet. 1991 Nov;40(5):337-41. doi: 10.1111/j.1399-0004.1991.tb03105.x. Clin Genet. 1991. PMID: 1756607

3

Reversible cortical atrophy and cognitive decline induced by valproic acid.

Straussberg R, Kivity S, Weitz R, Harel L, Gadoth N. Straussberg R, et al. Eur J Paediatr Neurol. 1998;2(4):213-8. doi: 10.1016/s1090-3798(98)80022-6. Eur J Paediatr Neurol. 1998. PMID: 10726594

4

Familial infantile bilateral striatal necrosis: clinical features and response to biotin treatment.

Straussberg R, Shorer Z, Weitz R, Basel L, Kornreich L, Corie CI, Harel L, Djaldetti R, Amir J. Straussberg R, et al. Neurology. 2002 Oct 8;59(7):983-9. doi: 10.1212/wnl.59.7.983. Neurology. 2002. PMID: 12374138

5

Clinical experience with open-label topiramate use in infants younger than 2 years of age.

Watemberg N, Goldberg-Stern H, Ben-Zeev B, Berger I, Straussberg R, Kivity S, Kramer U, Brand N, Lerman-Sagie T. Watemberg N, et al. Among authors: straussberg r. J Child Neurol. 2003 Apr;18(4):258-62. doi: 10.1177/08830738030180040901. J Child Neurol. 2003. PMID: 12760428

6

Infantile bilateral striatal necrosis maps to chromosome 19q.

Basel-Vanagaite L, Straussberg R, Ovadia H, Kaplan A, Magal N, Shorer Z, Shalev H, Walsh C, Shohat M. Basel-Vanagaite L, et al. Among authors: straussberg r. Neurology. 2004 Jan 13;62(1):87-90. doi: 10.1212/01.wnl.0000101680.49036.69. Neurology. 2004. PMID: 14718703

7

An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures.

Straussberg R, Basel-Vanagaite L, Kivity S, Dabby R, Cirak S, Nurnberg P, Voit T, Mahajnah M, Inbar D, Saifi GM, Lupski JR, Delague V, Megarbane A, Richter A, Leshinsky E, Berkovic SF. Straussberg R, et al. Neurology. 2005 Jan 11;64(1):142-4. doi: 10.1212/01.WNL.0000148600.60470.E6. Neurology. 2005. PMID: 15642921

8

Familial cognitive impairment with ataxia with oculomotor apraxia.

Mahajnah M, Basel-Vanagaite L, Inbar D, Kornreich L, Weitz R, Straussberg R. Mahajnah M, et al. Among authors: straussberg r. J Child Neurol. 2005 Jun;20(6):523-5. doi: 10.1177/088307380502000610. J Child Neurol. 2005. PMID: 15996403

9

West Nile encephalitis mimicking herpes encephalitis.

Rimon A, Straussberg R, Amir J. Rimon A, et al. Among authors: straussberg r. Pediatr Neurol. 2006 Jul;35(1):62-4. doi: 10.1016/j.pediatrneurol.2005.12.010. Pediatr Neurol. 2006. PMID: 16814089

10

Familial benign neonatal sleep myoclonus.

Cohen R, Shuper A, Straussberg R. Cohen R, et al. Among authors: straussberg r. Pediatr Neurol. 2007 May;36(5):334-7. doi: 10.1016/j.pediatrneurol.2006.12.016. Pediatr Neurol. 2007. PMID: 17509467

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