109 related articles for article (PubMed ID: 11071149)
1. Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation.
Miyama S; Arimoto K; Kimiya S; Tomi H
Neuropediatrics; 2000 Aug; 31(4):214-7. PubMed ID: 11071149
[TBL] [Abstract][Full Text] [Related]
2. [Complicated form of spastic paraplegia with congenital cataract: a case report].
Hirabayashi H; Takahashi W; Shinohara N; Hata T; Shinohara Y
Rinsho Shinkeigaku; 1998 Jan; 38(1):38-41. PubMed ID: 9597908
[TBL] [Abstract][Full Text] [Related]
3. [A case of complicated form of hereditary spastic paraplegia associated with hypoplasia of the corpus callosum and cataracta].
Tanaka M; Kobayashi Y; Sato M; Tsuji S
Rinsho Shinkeigaku; 1995 Jul; 35(7):798-802. PubMed ID: 8777806
[TBL] [Abstract][Full Text] [Related]
4. [Two siblings with spastic paraplegia, optic atrophy and peripheral neuropathy].
Joshita Y; Atsumi T; Miyatake T
Rinsho Shinkeigaku; 1982 Oct; 22(10):901-8. PubMed ID: 6303658
[No Abstract] [Full Text] [Related]
5. Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases.
Tang BS; Chen X; Zhao GH; Shen L; Yan XX; Jiang H; Luo W
Chin Med J (Engl); 2004 Jul; 117(7):1002-5. PubMed ID: 15265372
[TBL] [Abstract][Full Text] [Related]
6. [A case of spastic paraparesis with mental deterioration and markedly thin corpus callosum--callosal dysfunction demonstrated by magnetic stimulation].
Katayama T; Sakamoto N; Kuroda K; Yahara O; Ugawa Y
Rinsho Shinkeigaku; 1998 May; 38(5):418-22. PubMed ID: 9805987
[TBL] [Abstract][Full Text] [Related]
7. Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.
Gucuyener K; Hirfanoglu T; Ok I; Cansu A; Serdaroglu A
J Child Neurol; 2007 Feb; 22(2):214-7. PubMed ID: 17621486
[TBL] [Abstract][Full Text] [Related]
8. [Three patients of complicated form of autosomal recessive hereditary spastic paraplegia associated with hypoplasia of the corpus callosum].
Iwabuchi K; Kubota Y; Hanihara T; Nagatomo H
No To Shinkei; 1994 Oct; 46(10):941-7. PubMed ID: 7826709
[TBL] [Abstract][Full Text] [Related]
9. [A case of autosomal dominant, pure form spastic paraplegia with thinning of the corpus callosum].
Tomiyasu H; Hayashi R; Watanabe R; Honda M; Yoshii F
Rinsho Shinkeigaku; 1998 May; 38(5):435-9. PubMed ID: 9805990
[TBL] [Abstract][Full Text] [Related]
10. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11).
Winner B; Uyanik G; Gross C; Lange M; Schulte-Mattler W; Schuierer G; Marienhagen J; Hehr U; Winkler J
Arch Neurol; 2004 Jan; 61(1):117-21. PubMed ID: 14732628
[TBL] [Abstract][Full Text] [Related]
11. Thin corpus callosum and amyotrophy in spastic paraplegia--case report and review of literature.
Winner B; Gross C; Uyanik G; Schulte-Mattler W; Lürding R; Marienhagen J; Bogdahn U; Windpassinger C; Hehr U; Winkler J
Clin Neurol Neurosurg; 2006 Oct; 108(7):692-8. PubMed ID: 16102895
[TBL] [Abstract][Full Text] [Related]
12. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.
França MC; D'Abreu A; Maurer-Morelli CV; Seccolin R; Appenzeller S; Alessio A; Damasceno BP; Nucci A; Cendes F; Lopes-Cendes I
Mov Disord; 2007 Aug; 22(11):1556-62. PubMed ID: 17516453
[TBL] [Abstract][Full Text] [Related]
13. Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.
Brockmann K; Simpson MA; Faber A; Bönnemann C; Crosby AH; Gärtner J
Neuropediatrics; 2005 Aug; 36(4):274-8. PubMed ID: 16138254
[TBL] [Abstract][Full Text] [Related]
14. [A family of hereditary spastic paraplegia with dementia, ataxia, and dystonia].
Maruta K; Kondo I
Rinsho Shinkeigaku; 2001 Oct; 41(10):683-90. PubMed ID: 11993189
[TBL] [Abstract][Full Text] [Related]
15. [An autopsy case of complicated form of spastic paraplegia with amyotrophy, mental deficiency, sensory impairment, and parkinsonism].
Iwabuchi K; Yagishita S; Amano N; Yokoi S; Honda H; Tanabe T; Kinoshita J; Kosaka K
No To Shinkei; 1990 Nov; 42(11):1075-83. PubMed ID: 2076353
[TBL] [Abstract][Full Text] [Related]
16. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].
Adachi T; Imaoka K; Shirasawa A; Yamaguchi S; Kobayashi S
Rinsho Shinkeigaku; 1998 Dec; 38(12):1037-41. PubMed ID: 10349345
[TBL] [Abstract][Full Text] [Related]
17. Leber's disease with spastic paraplegia and peripheral neuropathy. Case report with nerve biopsy study.
Pagès M; Pagès AM
Eur Neurol; 1983; 22(3):181-5. PubMed ID: 6305662
[TBL] [Abstract][Full Text] [Related]
18. [A new type of complicated form of hereditary spastic paraplegia showing mental deterioration, quadriplegia with muscular atrophy, sensory disturbance, extrapyramidal disorders, and epilepsy].
Iwabuchi K; Yagishita S; Amano N; Kosaka K
Rinsho Shinkeigaku; 1991 Sep; 31(9):945-52. PubMed ID: 1769157
[TBL] [Abstract][Full Text] [Related]
19. [Optic neuropathy in Strumpell-Lorrain disease: presentation of a clinical case and literature review].
Makhoul J; Cordonnier M; Van Nechel C
Bull Soc Belge Ophtalmol; 2002; (286):9-14. PubMed ID: 12564312
[TBL] [Abstract][Full Text] [Related]
20. Spastic paraplegia 15: linkage and clinical description of three Tunisian families.
Boukhris A; Feki I; Denis E; Miladi MI; Brice A; Mhiri C; Stevanin G
Mov Disord; 2008 Feb; 23(3):429-33. PubMed ID: 18098276
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
