Hereditary spastic paraplegia


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Claus D, Waddy HM, Harding AE (1990) Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study. Ann Neurol 28:43-9.

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Fink JK, Sharp G, Lange B, Wu CB, Haley T, Otterud B, Peacock M, Leppert M (1995a) Autosomal dominant hereditary spastic paraparesis, type I: clinical and genetic analysis of a large North American family. Neurology 45:325-31.

Fink JK, Wu CB, Jones SM, Sharp GB, Lange BM, Lesicki A, Reinglass T, Varvil T, Otterud B, Leppert M (1995b) Familial spastic paraplegia: tight linkage to chromosome 15q. Am J Hum Genet 56:188-92.

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Fink JK (1997) Advances in hereditary spastic paraplegia. Current Opinion in Neurology 10:313-8.

Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G (1995) Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity. Am J Hum Genet 56:183-7.

Harding AE (1981) Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families. J Neurol Neurosurg Psychiatry 44:871-83.

Harding AE (1993) Hereditary spastic paraplegias. Semin Neurol 13:333-6.

Hazan J, Fontaine B, Bruyn RPM, Lamy C, Van deutekom JCT, Rime CS, Durr A, Melki J, Lyoncaen O, Agid Y, Munnich A, Padberg GW, Derecondo J, Frants RR, Brice A, Weissenbach J (1994) Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p. Hum Mol Genet 3:1569-73.

Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J (1993) Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Nat Genet 5:163-7.

Hentati A, Pericack-Vance MA, Hung W-Y, et al. Linkage of the "pure" recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. [Abstract] Hum Genet 1993;53:1013

Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung W, Boustany RM, Bohlega S, Iqbal Z, Huether CA, Ben Hamida M, Siddique T (1994) Linkage of the late onset automal dominant familial spastic paraplegia to chromosome 2p markers. Hum Molec Genet 3:1867-71.

Holmes G, Shaywitz B (1977) Strumpell's pure familial spastic paraplegia: case study and review of the literature. J Neurol Neurosurg Psychiatry 40:1003-8.

Kenwrick S, Ionasescu V, Ionasescu G, Searby C, King A, Dubowitz M, Davies KE (1986) Linkage studies of X-linked recessive spastic paraplegia using DNA probes. Hum Genet 73:264-6.

Keppen L, Leppert M, O'Connell P (1987) Etiological heterogeneity in X-linked spastic paraplegia. Am J Hum Genet 41:933-43.

Kobayashi H, Hoffman EP, Marks HG (1994) The rumpshaker mutation in spastic paraplegia. Nature Genet 7:351-2.

Lennon F, Gaskell PC, Woopert C, Aulsworth AS, Malin D, Warner C, Farell CD, Albright SG, Vance JM, Pericak-Vance MA (1995) Linkage and heterogeneity in hereditary spastic paraparesis. Am J Hum Genet (suppl) 1995:(in press)

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Nielsen, Koefoed P, Abell K, et. al. CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24. Hum Molec Genet 1997;6:1811-1816,

Opjordsmoen S, Nyberg-Hansen R (1980) Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia. Acta Neurol Scand 61:35-41.

Pelosi L, Lanzillo B, Perretti A (1991) Motor and somatosensory evoked potentials in hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 54:1099-102.

Philipp E (1949) Hereditary (familial) spastic paraplegia: report of six cases in one family. New Zeal Med J 48:22-5.

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Polo JM, Calleja J, Combarris O, Berciano J (1993) Hereditary "pure" spastic paraplegia: a study of nine families. J Neurol Neurosurg Psychiatry 56:175-81.

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Rhein J (1914) Family spastic paralysis. J Nerv Ment Dis 44:115-44.

Roe P (1963) Hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 26:516-9.

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Schady W, Dick JP, Sheard A, Crampton S (1991) Central motor conduction studies in hereditary spastic paraplegia. J Neurol Neurosurg Psychiatry 54:775-9.

Schady W, Scheard A (1990) A qualitative study of sensory functions in hereditary spastic paraplegia. Brain 113:709-20.

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Zastz M, Penha-Serrano C, Otto PA (1976) X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg. J Med Genet 13:217-22.

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