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Journal Abstract Search
159 related items for PubMed ID: 6582228
1. 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 [Abstract] [Full Text] [Related]
2. [Hereditary spastic paraplegia associated with peripheral neuropathy. Contribution of a family]. García-Albea E, Peña P, Cabello A, Calandre L. Rev Clin Esp; 1979 Jan 31; 152(2):155-9. PubMed ID: 220681 [No Abstract] [Full Text] [Related]
3. Familial spastic paraplegia-clinical and pathologic studies in a large kindred. Sack GH, Huether CA, Garg N. Johns Hopkins Med J; 1978 Oct 31; 143(4):117-21. PubMed ID: 703033 [Abstract] [Full Text] [Related]
4. X-linked hereditary spastic paraplegia. Raggio JF, Thurmon TF, Anderson EE. J La State Med Soc; 1973 Jan 31; 125(1):4-5. PubMed ID: 4684346 [No Abstract] [Full Text] [Related]
5. [Familial spastic paraplegia in 3 families]. Fujiwara H, Akabori O, Akashi K, Moriya S. Seikei Geka; 1971 Jan 31; 22(6):471-6. PubMed ID: 5104423 [No Abstract] [Full Text] [Related]
6. Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia. Speer MC, Kingston HM, Boustany RM, Gaskell PC, Robinson LC, Lennon F, Wolpert CM, Yamaoka LH, Kahler SG, Hogan EL. Am J Med Genet; 1995 Aug 14; 60(4):307-11. PubMed ID: 7485266 [Abstract] [Full Text] [Related]
7. Hereditary neurologic disorders, characterized by ataxia. Immunological in vitro parameters and HLA. Pedersen L, Platz P, Raun NE. Acta Pathol Microbiol Scand C; 1980 Dec 14; 88(6):281-6. PubMed ID: 7246142 [Abstract] [Full Text] [Related]
8. [The clinical characteristics of a pedigree with incompletely penetrated autosomal dominant hereditary spastic paraplegia and its exclusion analysis of genetic loci]. Zhao GH, Ren ZJ, Liu XM, Li SJ, Guo P, Shen L, Xia K, Tang BS. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Jun 14; 25(3):304-7. PubMed ID: 18543222 [Abstract] [Full Text] [Related]
9. Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34. Valente EM, Brancati F, Caputo V, Bertini E, Patrono C, Costanti D, Dallapiccola B. Ann Neurol; 2002 Jun 14; 51(6):681-5. PubMed ID: 12112072 [Abstract] [Full Text] [Related]
10. [Clinical manifestations and mode of inheritance of hereditary spastic paraplegia in 20 families]. Gao HW. Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1985 Feb 14; 18(1):24-6. PubMed ID: 3987454 [No Abstract] [Full Text] [Related]
11. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J. Nat Genet; 1993 Oct 14; 5(2):163-7. PubMed ID: 8252041 [Abstract] [Full Text] [Related]
12. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24. Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L. Neurology; 2009 Jun 02; 72(22):1893-8. PubMed ID: 19357379 [Abstract] [Full Text] [Related]
13. [Complicated spastic paraplegia with sex-linked inheritance (report of a family)]. Galassi G, Penne A, Colombo A, Forabosco A. Acta Neurol (Napoli); 1977 Jun 02; 32(6):746-56. PubMed ID: 605830 [No Abstract] [Full Text] [Related]
14. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study. Erichsen AK, Koht J, Stray-Pedersen A, Abdelnoor M, Tallaksen CM. Brain; 2009 Jun 02; 132(Pt 6):1577-88. PubMed ID: 19339254 [Abstract] [Full Text] [Related]
15. Hereditary spastic paraplegia (a review of two families with eight case reports). Rath RN, Das RK, Panda RK, Santhalia RR. J Assoc Physicians India; 1978 Jun 02; 26(6):535-40. PubMed ID: 721758 [No Abstract] [Full Text] [Related]
16. [Hereditary spastic paraplegia. Case report and review with special reference to current neurophysiologic examination methods]. Urnes O. Tidsskr Nor Laegeforen; 1983 May 30; 103(15):1249-51. PubMed ID: 6879555 [No Abstract] [Full Text] [Related]
17. Familial spastic paraplegia: a clinical and electrodiagnostic evaluation. Owens LA, Peterson CR, Burdick AB. Arch Phys Med Rehabil; 1982 Aug 30; 63(8):357-61. PubMed ID: 7115028 [Abstract] [Full Text] [Related]
18. [Involvement of the peripheral motor neuron in hereditary spastic paraplegia (author's transl)]. Malin JP. EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1976 Sep 30; 7(3):140-5. PubMed ID: 829059 [Abstract] [Full Text] [Related]
19. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34. Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B. Brain; 2006 Sep 30; 129(Pt 9):2332-40. PubMed ID: 16672289 [Abstract] [Full Text] [Related]
20. [Strümpell Lorrain's familial spasmodic paraplegia. An anatomical and clinical review and report on a new case (author's transl)]. Buge A, Escourolle R, Rancurel G, Gray F, Pertuiset BF. Rev Neurol (Paris); 1979 Sep 30; 135(4):329-37. PubMed ID: 504864 [Abstract] [Full Text] [Related] Page: [Next] [New Search]