Two siblings with familial spastic paraplegia associated with decreased levels of factor XIi
Fujii, K.; Sadoshima, S.; Kusuda, K.; Shirouzu, A.; Fujishima, M.
Rinsho Shinkeigaku 26(8): 851-855
1986
ISSN/ISBN: 0009-918X PMID: 3802679 Document Number: 271354
Document emailed within 1 workday
Related Documents
Joshita, Y.; Yamamoto, Y.; Satoh, Y.; Mizuno, Y. 1982: Two siblings of familial spastic paraplegia with retinal pigment degeneration (sine pigment) Rinsho Shinkeigaku 22(9): 789-794González-Elipe, J.; Vilanova, A.; Rapado, A.; Fernández-Criado, M.; Perianes, J. 1970: Strümpell-Lorrain's spastic paraplegia (primary lateral sclerosis, familial spastic paralysis, etc.) Revista Clinica Espanola 119(3): 233-240
Yeh, Y.C.; Mak, S.C.; Chi, C.S. 1998: Hereditary spastic paraplegia: report of two siblings Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi Zhonghua Minguo Xiao Er Ke Yi Xue Hui 39(2): 112-115
Joshita, Y.; Atsumi, T.; Miyatake, T. 1982: Two siblings with spastic paraplegia, optic atrophy and peripheral neuropathy Rinsho Shinkeigaku 22(10): 901-908
Vernea, J.; Symington, G.R. 1977: The late form of pure familial spastic paraplegia Clinical and Experimental Neurology 14: 37-41
Kolodny, E.H.; Boustany, R.M.; Rouleau, G.A.; Growden, J.H.; Martin, J.B. 1989: Familial spastic paraplegia: clinical observations and genetic studies Progress in Clinical and Biological Research 306: 205-211
Gomez Malaret, S.; Latuff, H.; Chompredepena, L. 1963: Familial Spastic Paraplegia of the type Strumpell-Lorrain in 3 Sisters Daughters of a Consanguinous Marriage Archivos de Pediatria del Uruguay 34: 673-678
Vernant, J.C. 1990: Tropical spastic paraplegia (TSP) and HTLV1 associated to paraplegia (HAP) La Revue du Praticien 40(22): 2073-2074
Fryns, J.P.; Devriendt, K.; Detroch, C.; Decock, P. 1998: Distinct familial syndrome of severe to profound mental retardation, spastic paraplegia with contrasting axial hypotonia, short stature and distinct craniofacial appearance with nasal hypoplasia Genetic Counseling 9(1): 51-54
Sato, Y.; Kaji, M.; Osame, M.; Matsuishi, T.; Itokawa, Y. 1983: Mitochondrial myopathy with increased blood lactate and pyruvate levels among siblings in familial thiamine deficiency Rinsho Shinkeigaku 23(8): 668-677
Wallace, I.D.; Cosnett, J.E. 1983: Unexplained spastic paraplegia South African Medical Journal 63(18): 689-691
Ekusheva, E.V.; Danilov, A.B. 2002: Hereditary spastic paraplegia Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 102(8): 44-52
Raggio, J.F.; Thurmon, T.F.; Anderson, E.E. 1973: X-linked hereditary spastic paraplegia Journal of the Louisiana State Medical Society: Official Organ of the Louisiana State Medical Society 125(1): 4-5
Rodríguez-Quiroga, S.A.; González-Morón, D.; Arakaki, T.; Garreto, N.él.; Kauffman, M.A. 2013: The broad phenotypic spectrum of SCA-3: hereditary spastic paraplegia Medicina 73(6): 552-554
Jain, A.P.; Gupta, P.; Nigam, S.P.; Kakrani, A.L. 1978: A study of spastic paraplegia in rural Central India Journal of Tropical Medicine and Hygiene 81(1): 9-12
Galassi, G.; Penne, A.; Colombo, A.; Forabosco, A. 1977: Complicated spastic paraplegia with sex-linked inheritance (report of a family) Acta Neurologica 32(6): 746-756
Akhmetgaleyeva, A.F.; Khidiyatova, I.M.; Saifullina, E.V.; Idrisova, R.F.; Magzhanov, R.V.; Khusnutdinova, E.K. 2016: Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia Genetika 52(6): 691-696
Uzicanin, S.; Catibusic, F.; Terzic, S.; Zubcevic, S. 2007: Familiar spastic paraplegia presenting in a boy with Klinefelter syndrome--case report Medicinski Arhiv 61(1): 52-53
Wakil, S.M.; Murad, H.N.; Baz, B.M.; Hagos, S.T.; Al-Amr, R.A.; Al-Yamani, S.A.; Al-Wadaee, S.M.; Meyer, B.F.; Bohlega, S.A. 2012: Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis Neurosciences 17(1): 48-52
Ibi, T.; Matsuoka, Y.; Sobue, I.; Matsui, T.; Tsuji, S. 1982: Adrenomyeloneuropathy. Report of two siblings and female heterozygote with spastic paraparesis Rinsho Shinkeigaku 22(11): 980-985