Straussberg R - Search Results

1

Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia.

Halevy A, Lerer I, Cohen R, Kornreich L, Shuper A, Gamliel M, Zimerman BE, Korabi I, Meiner V, Straussberg R, Lossos A. Halevy A, et al. Among authors: straussberg r. J Neurol. 2014 Nov;261(11):2165-9. doi: 10.1007/s00415-014-7457-x. Epub 2014 Aug 23. J Neurol. 2014. PMID: 25149867

2

Autosomal recessive microcephaly with neonatal myoclonic seizures: clinical and MRI findings.

Straussberg R, Kornreich L, Harel L, Varsano I. Straussberg R, et al. Am J Med Genet. 1998 Nov 2;80(2):136-9. doi: 10.1002/(sici)1096-8628(19981102)80:2<136::aid-ajmg9>3.0.co;2-5. Am J Med Genet. 1998. PMID: 9805130

3

A novel mutation of late-onset very-long-chain acyl-CoA dehydrogenase deficiency.

Straussberg R, Strauss AW. Straussberg R, et al. Pediatr Neurol. 2002 Aug;27(2):136-7. doi: 10.1016/s0887-8994(02)00404-6. Pediatr Neurol. 2002. PMID: 12213615

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

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

6

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

7

Thiamine deficiency in infants: MR findings in the brain.

Kornreich L, Bron-Harlev E, Hoffmann C, Schwarz M, Konen O, Schoenfeld T, Straussberg R, Nahum E, Ibrahim AK, Eshel G, Horev G. Kornreich L, et al. Among authors: straussberg r. AJNR Am J Neuroradiol. 2005 Aug;26(7):1668-74. AJNR Am J Neuroradiol. 2005. PMID: 16091511 Free PMC article.

8

Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.

Basel-Vanagaite L, Muncher L, Straussberg R, Pasmanik-Chor M, Yahav M, Rainshtein L, Walsh CA, Magal N, Taub E, Drasinover V, Shalev H, Attia R, Rechavi G, Simon AJ, Shohat M. Basel-Vanagaite L, et al. Among authors: straussberg r. Ann Neurol. 2006 Aug;60(2):214-22. doi: 10.1002/ana.20902. Ann Neurol. 2006. PMID: 16786527

9

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

10

Acute infantile bilateral striatal necrosis: single-photon emission computed tomography (SPECT) imaging and review.

Zevit N, Steinmetz A, Kornreich L, Straussberg R. Zevit N, et al. Among authors: straussberg r. J Child Neurol. 2007 Oct;22(10):1222-6. doi: 10.1177/0883073807304194. J Child Neurol. 2007. PMID: 17940250

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