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5. [An unusual case of peroneal muscular atrophy with rigidity, polyneuropathy, mental retardation, and diabetes mellitus developed in familial Parkinson's disease]. Saito T; Hosoda M; Aoto K; Hasegawa H; Kowa H Rinsho Shinkeigaku; 1995 Aug; 35(8):878-83. PubMed ID: 8665730 [TBL] [Abstract][Full Text] [Related]
6. [Juvenile Sandhoff disease with local panatrophy--a case report]. Nakano R; Wakamatsu N; Tsuji S; Matsumura G; Miyatake T Rinsho Shinkeigaku; 1989 Aug; 29(8):1032-8. PubMed ID: 2532090 [TBL] [Abstract][Full Text] [Related]
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8. [A 54-year-old man with progressive proximal muscle atrophy and gynecomastia]. Anno M; Gotoh K; Hirasawa E; Mori H; Nakajima Y; Mizuno Y No To Shinkei; 1995 Jan; 47(1):87-96. PubMed ID: 7669408 [TBL] [Abstract][Full Text] [Related]
9. [A nosological study of a patient showing ataxia & lower motor neuron involvement]. Murakami N; Yoshida M; Hashizume Y; Muroga T; Takahashi A Rinsho Shinkeigaku; 1989 Sep; 29(9):1116-21. PubMed ID: 2598537 [TBL] [Abstract][Full Text] [Related]
11. [A 29-year-old man with diabetes insipidus and cerebellar ataxia and development of spinal cord swelling 15 years after the onset]. Ohkuma Y; Sato K; Ohtomo T; Ohishi H; Mitsuoka H; Mori H; Hirai S; Takubo H; Takeda N; Sato K; Mizuno Y No To Shinkei; 1997 May; 49(5):473-81. PubMed ID: 9163763 [TBL] [Abstract][Full Text] [Related]
12. N-acetyl-beta-hexosaminidase beta locus defect and juvenile motor neuron disease: a case study. Cashman NR; Antel JP; Hancock LW; Dawson G; Horwitz AL; Johnson WG; Huttenlocher PR; Wollmann RL Ann Neurol; 1986 Jun; 19(6):568-72. PubMed ID: 3014997 [TBL] [Abstract][Full Text] [Related]
13. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset]. Iwabuchi K; Kogure T; Oda T; Kato Y; Ohtani K; Endo K; Kosaka K; Amano N; Yagishita S No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819 [TBL] [Abstract][Full Text] [Related]
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18. Motor neuron disease and adult hexosaminidase A deficiency in two families: evidence for multisystem degeneration. Mitsumoto H; Sliman RJ; Schafer IA; Sternick CS; Kaufman B; Wilbourn A; Horwitz SJ Ann Neurol; 1985 Apr; 17(4):378-85. PubMed ID: 3159334 [TBL] [Abstract][Full Text] [Related]
19. [Adult form of GM2-gangliosidosis: a man and 2 sisters with hexosaminidase-A and -B deficiency (Sandhoff disease) and literature review]. Schnorf H; Bosshard NU; Gitzelmann R; Spycher MA; Isler P; Waespe W Schweiz Med Wochenschr; 1996 May; 126(18):757-64. PubMed ID: 8693300 [TBL] [Abstract][Full Text] [Related]
20. [A case of congenital non-progressive cerebellar ataxia with pigmentary retinal degeneration, fiber type disproportion and hypercreatine kinasemia]. Yamasaki T; Taniwaki T; Kikuchi H; Araki E; Arakawa K; Iwaki T; Yamada T; Kira J Rinsho Shinkeigaku; 1999 Sep; 39(9):925-9. PubMed ID: 10614155 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]