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Journal Abstract Search

126 related items for PubMed ID: 3587641

  • 21. Hereditary spastic paraplegia: a clinical and genetic study of cases in the north-east of England.
    Livingstone IR, Roberts DF.
    J Genet Hum; 1983 Dec; 31(4):295-305. PubMed ID: 6582228
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  • 23. Familial spastic paraplegia-clinical and pathologic studies in a large kindred.
    Sack GH, Huether CA, Garg N.
    Johns Hopkins Med J; 1978 Oct; 143(4):117-21. PubMed ID: 703033
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  • 24. Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
    Fink JK, Wu CT, Jones SM, Sharp GB, Lange BM, Lesicki A, Reinglass T, Varvil T, Otterud B, Leppert M.
    Am J Hum Genet; 1995 Jan; 56(1):188-92. PubMed ID: 7825577
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  • 26. Familial spastic paraplegia: a clinical and electrodiagnostic evaluation.
    Owens LA, Peterson CR, Burdick AB.
    Arch Phys Med Rehabil; 1982 Aug; 63(8):357-61. PubMed ID: 7115028
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  • 27. Manifesting heterozygosity in sex-linked spastic paraplegia?
    Young ID, Pye IF, Moore JR.
    J Neurol Neurosurg Psychiatry; 1984 Mar; 47(3):311-3. PubMed ID: 6707681
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  • 28. Familial spastic paraplegia, mental retardation, and precocious puberty.
    Raphaelson MI, Stevens JC, Elders J, Comite F, Theodore WH.
    Arch Neurol; 1983 Dec; 40(13):809-10. PubMed ID: 6639408
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  • 29. A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3.
    Muglia M, Magariello A, Nicoletti G, Patitucci A, Gabriele AL, Conforti FL, Mazzei R, Caracciolo M, Casari G, Ardito B, Lastilla M, Gambardella A, Quattrone A.
    J Neurol; 2002 Oct; 249(10):1413-6. PubMed ID: 12382159
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  • 30. Slowly progressive autosomal dominant spastic paraplegia with late onset, variable expression and reduced penetrance: a basis for diagnosis and counseling.
    Burdick AB, Owens LA, Peterson CR.
    Clin Genet; 1981 Jan; 19(1):1-7. PubMed ID: 7460376
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  • 31. Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.
    Heinzlef O, Paternotte C, Mahieux F, Prud'homme JF, Dien J, Madigand M, Pouget J, Weissenbach J, Roullet E, Hazan J.
    J Med Genet; 1998 Feb; 35(2):89-93. PubMed ID: 9507385
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  • 32. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.
    Zatz M, Penha-Serrano C, Otto PA.
    J Med Genet; 1976 Jun; 13(3):217-22. PubMed ID: 1084423
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  • 33. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.
    Dürr A, Davoine CS, Paternotte C, von Fellenberg J, Cogilinicean S, Coutinho P, Lamy C, Bourgeois S, Prud'homme JF, Penet C, Mas JL, Burgunder JM, Hazan J, Weissenbach J, Brice A, Fontaine B.
    Brain; 1996 Oct; 119 ( Pt 5)():1487-96. PubMed ID: 8931574
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  • 36. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
    Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G.
    Am J Hum Genet; 1995 Jan; 56(1):183-7. PubMed ID: 7825576
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  • 38. Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
    Muglia M, Criscuolo C, Magariello A, De Michele G, Scarano V, D'Adamo P, Ambrosio G, Gabriele AL, Patitucci A, Mazzei R, Conforti FL, Sprovieri T, Morgante L, Epifanio A, La Spina P, Valentino P, Gasparini P, Filla A, Quattrone A.
    Neurogenetics; 2004 Feb; 5(1):49-54. PubMed ID: 14658060
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  • 39. Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.
    Martínez Murillo F, Kobayashi H, Pegoraro E, Galluzzi G, Creel G, Mariani C, Farina E, Ricci E, Alfonso G, Pauli RM, Hoffman EP.
    Neurology; 1999 Jul 13; 53(1):50-6. PubMed ID: 10408536
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  • 40. Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.
    De Jonghe P, Krols L, Michalik A, Hazan J, Smeyers G, Löfgren A, Weissenbach J, Martin JJ, Van Broeckhoven C.
    Eur J Hum Genet; 1996 Jul 13; 4(5):260-6. PubMed ID: 8946171
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