Lossos A - Search Results

1

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family.

Lossos A, Reches A, Gal A, Newman JP, Soffer D, Gomori JM, Boher M, Ekstein D, Biran I, Meiner Z, Abramsky O, Rosenmann H. Lossos A, et al. J Neurol. 2003 Jun;250(6):733-40. doi: 10.1007/s00415-003-1074-4. J Neurol. 2003. PMID: 12796837

2

Phenotypic variability among adult siblings with Sjögren-Larsson syndrome.

Lossos A, Khoury M, Rizzo WB, Gomori JM, Banin E, Zlotogorski A, Jaber S, Abramsky O, Argov Z, Rosenmann H. Lossos A, et al. Arch Neurol. 2006 Feb;63(2):278-80. doi: 10.1001/archneur.63.2.278. Arch Neurol. 2006. PMID: 16476818 Free PMC article.

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. Arch Neurol. 2006 May;63(5):756-60. doi: 10.1001/archneur.63.5.756. Arch Neurol. 2006. PMID: 16682547

4

A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12.

Lossos A, Baala L, Soffer D, Averbuch-Heller L, Dotan S, Munnich A, Lyonnet S, Gomori JM, Genem A, Neufeld M, Abramsky O, Zlotogora J, Argov Z. Lossos A, et al. Brain. 2005 Jan;128(Pt 1):42-51. doi: 10.1093/brain/awh338. Epub 2004 Nov 17. Brain. 2005. PMID: 15548556

5

Extended phenotype in the transthyretin Tyr77 familial amyloid polyneuropathy.

Lossos A, Soffer D, Steiner-Birmanns B, Hassin-Baer S, Sadeh M, Sagi M, Linetski E, Abramsky O, Argov Z, Rosenmann H. Lossos A, et al. Eur Neurol. 2005;53(2):55-9. doi: 10.1159/000084299. Epub 2005 Mar 7. Eur Neurol. 2005. PMID: 15753613

6

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. Arch Neurol. 2005 Apr;62(4):611-4. doi: 10.1001/archneur.62.4.611. Arch Neurol. 2005. PMID: 15824261

7

Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme gene.

Lossos A, Meiner Z, Barash V, Soffer D, Schlesinger I, Abramsky O, Argov Z, Shpitzen S, Meiner V. Lossos A, et al. Ann Neurol. 1998 Dec;44(6):867-72. doi: 10.1002/ana.410440604. Ann Neurol. 1998. PMID: 9851430

8

Intrafamilial heterogeneity of movement disorders: report of three cases in one family.

Lossos A, Cohen O, Meiner V, Blumenfeld A, Reches A. Lossos A, et al. J Neurol. 1997 Jul;244(7):426-30. doi: 10.1007/s004150050116. J Neurol. 1997. PMID: 9266460

9

Leukoencephalopathy with neuroaxonal spheroids presenting as frontotemporal dementia.

Levin N, Soffer D, Biran I, Gomori JM, Bocher M, Blumen SC, Abramsky O, Segal R, Lossos A. Levin N, et al. Among authors: lossos a. Isr Med Assoc J. 2008 May;10(5):386-7. Isr Med Assoc J. 2008. PMID: 18605367 No abstract available.

10

Lipoid proteinosis with bilateral amygdalae calcifications, headache, and cognitive impairments.

Arkadir D, Lerer I, Klapholz L, Halpert M, Newman JP, Gomori JM, Lossos A. Arkadir D, et al. Among authors: lossos a. Neurology. 2013 Jul 16;81(3):303-4. doi: 10.1212/WNL.0b013e31829bfe1c. Neurology. 2013. PMID: 23858412 No abstract available.

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