Meiner V - Search Results

1

Multi-system neurological disorder associated with a CRYAB variant.

Sadeh M, Rahat D, Meiner V, Fellig Y, Arad M, Schueler-Furman O, Hu Y, Li Y, Bönnemann CG, Lossos A. Sadeh M, et al. Among authors: meiner v. Neurogenetics. 2021 May;22(2):117-125. doi: 10.1007/s10048-021-00640-x. Epub 2021 Apr 3. Neurogenetics. 2021. PMID: 33811585

2

Early clinical heterogeneity in choreoacanthocytosis.

Lossos A, Dobson-Stone C, Monaco AP, Soffer D, Rahamim E, Newman JP, Mohiddin S, Fananapazir L, Lerer I, Linetsky E, Reches A, Argov Z, Abramsky O, Gadoth N, Sadeh M, Gomori JM, Boher M, Meiner V. Lossos A, et al. Among authors: meiner v. Arch Neurol. 2005 Apr;62(4):611-4. doi: 10.1001/archneur.62.4.611. Arch Neurol. 2005. PMID: 15824261

3

Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.

Lossos A, Stevanin G, Meiner V, Argov Z, Bouslam N, Newman JP, Gomori JM, Klebe S, Lerer I, Elleuch N, Silverstein S, Durr A, Abramsky O, Ben-Nariah Z, Brice A. Lossos A, et al. Among authors: meiner v. Arch Neurol. 2006 May;63(5):756-60. doi: 10.1001/archneur.63.5.756. Arch Neurol. 2006. PMID: 16682547

4

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families.

Elleuch N, Bouslam N, Hanein S, Lossos A, Hamri A, Klebe S, Meiner V, Birouk N, Lerer I, Grid D, Bacq D, Tazir M, Zelenika D, Argov Z, Durr A, Yahyaoui M, Benomar A, Brice A, Stevanin G. Elleuch N, et al. Among authors: meiner v. Neurogenetics. 2007 Nov;8(4):307-15. doi: 10.1007/s10048-007-0097-x. Epub 2007 Jul 28. Neurogenetics. 2007. PMID: 17661097

5

Severe infantile carnitine palmitoyltransferase II deficiency in 19-week fetal sibs.

Meir K, Fellig Y, Meiner V, Korman SH, Shaag A, Nadjari M, Soffer D, Ariel I. Meir K, et al. Among authors: meiner v. Pediatr Dev Pathol. 2009 Nov-Dec;12(6):481-6. doi: 10.2350/08-10-0548.1. Pediatr Dev Pathol. 2009. PMID: 19335026

6

MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12.

Lossos A, Oldfors A, Fellig Y, Meiner V, Argov Z, Tajsharghi H. Lossos A, et al. Among authors: meiner v. Brain. 2013 Jul;136(Pt 7):e238. doi: 10.1093/brain/aws365. Epub 2013 Feb 6. Brain. 2013. PMID: 23388406 No abstract available.

7

A novel SCARB2 mutation in progressive myoclonus epilepsy indicated by reduced β-glucocerebrosidase activity.

Zeigler M, Meiner V, Newman JP, Steiner-Birmanns B, Bargal R, Sury V, Mengistu G, Kakhlon O, Leykin I, Argov Z, Abramsky O, Lossos A. Zeigler M, et al. Among authors: meiner v. J Neurol Sci. 2014 Apr 15;339(1-2):210-3. doi: 10.1016/j.jns.2014.01.022. Epub 2014 Jan 23. J Neurol Sci. 2014. PMID: 24485911

8

Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.

Lossos A, Teltsh O, Milman T, Meiner V, Rozen R, Leclerc D, Schwahn BC, Karp N, Rosenblatt DS, Watkins D, Shaag A, Korman SH, Heyman SN, Gal A, Newman JP, Steiner-Birmanns B, Abramsky O, Kohn Y. Lossos A, et al. Among authors: meiner v. JAMA Neurol. 2014 Jul 1;71(7):901-4. doi: 10.1001/jamaneurol.2014.116. JAMA Neurol. 2014. PMID: 24797679

9

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: meiner v. J Neurol. 2014 Nov;261(11):2165-9. doi: 10.1007/s00415-014-7457-x. Epub 2014 Aug 23. J Neurol. 2014. PMID: 25149867

10

Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A gene.

Sheffer R, Bennett-Back O, Yaacov B, Edvardson S, Gomori M, Werner M, Fahham D, Anteby I, Frumkin A, Meiner V, Elpeleg O. Sheffer R, et al. Among authors: meiner v. Neurogenetics. 2015 Jan;16(1):23-6. doi: 10.1007/s10048-014-0428-7. Epub 2014 Oct 22. Neurogenetics. 2015. PMID: 25338135

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