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Familial Sneddon's syndrome.
J Neurol. 1995 Feb;242(3):164-8. doi: 10.1007/BF00936890.
J Neurol. 1995.
PMID: 7751860
Hereditary branching enzyme dysfunction in adult polyglucosan body disease: a possible metabolic cause in two patients.
Lossos A, Barash V, Soffer D, Argov Z, Gomori M, Ben-Nariah Z, Abramsky O, Steiner I.
Lossos A, et al. Among authors: ben nariah z.
Ann Neurol. 1991 Nov;30(5):655-62. doi: 10.1002/ana.410300505.
Ann Neurol. 1991.
PMID: 1763891
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Hereditary leukoencephalopathy and palmoplantar keratoderma: a new disorder with increased skin collagen content.
Lossos A, Cooperman H, Soffer D, Ben-Nariah Z, Sagi E, Gomori M, Abramsky O, Shoshan S, Argov Z.
Lossos A, et al. Among authors: ben nariah z.
Neurology. 1995 Feb;45(2):331-7. doi: 10.1212/wnl.45.2.331.
Neurology. 1995.
PMID: 7854535
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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: ben nariah z.
Arch Neurol. 2006 May;63(5):756-60. doi: 10.1001/archneur.63.5.756.
Arch Neurol. 2006.
PMID: 16682547
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