94 related articles for article (PubMed ID: 18494795)
1. Late onset hexosaminidase A deficiency in a young adult.
Peters AS; Markovic K; Schramm A; Schwab S; Heuss D
Eur J Neurol; 2008 Jul; 15(7):e70-1; author reply e72-3. PubMed ID: 18494795
[No Abstract] [Full Text] [Related]
2. [Late onset Tay-Sachs disease may mimic adult SMA].
Praline J; Guennoc AM; Vourc'h P; Sedel F; Andres CR; Corcia P
Rev Neurol (Paris); 2011; 167(6-7):549-50. PubMed ID: 21481906
[No Abstract] [Full Text] [Related]
3. Late-onset Tay-Sachs disease.
Barritt AW; Anderson SJ; Leigh PN; Ridha BH
Pract Neurol; 2017 Oct; 17(5):396-399. PubMed ID: 28739864
[TBL] [Abstract][Full Text] [Related]
4. Late-onset Tay-Sachs disease: the spectrum of peripheral neuropathy in 30 affected patients.
Shapiro BE; Logigian EL; Kolodny EH; Pastores GM
Muscle Nerve; 2008 Aug; 38(2):1012-5. PubMed ID: 18642377
[TBL] [Abstract][Full Text] [Related]
5. Paranoid delusion as lead symptom in two siblings with late-onset Tay-Sachs disease and a novel mutation in the HEXA gene.
Stendel C; Gallenmüller C; Peters K; Bürger F; Gramer G; Biskup S; Klopstock T
J Neurol; 2015; 262(4):1072-3. PubMed ID: 25860343
[No Abstract] [Full Text] [Related]
6. Cerebellar atrophy and muscle weakness: late-onset Tay-Sachs disease outside Jewish populations.
Steiner KM; Brenck J; Goericke S; Timmann D
BMJ Case Rep; 2016 Mar; 2016():. PubMed ID: 27033294
[No Abstract] [Full Text] [Related]
7. Late-onset hexosaminidase A deficiency mimicking primary lateral sclerosis.
Godeiro-Junior C; Felicio AC; Benites V; Chieia MA; Oliveira AS
Arq Neuropsiquiatr; 2009 Mar; 67(1):105-6. PubMed ID: 19330222
[No Abstract] [Full Text] [Related]
8. Tay-Sachs disease: a case report.
Arisoy AE; Ozden S; Ciliv G; Ozalp I
Turk J Pediatr; 1995; 37(1):51-6. PubMed ID: 7732608
[TBL] [Abstract][Full Text] [Related]
9. Late-onset Tay-Sachs disease presenting as a childhood stutter.
Shapiro BE; Natowicz MR
J Neurol Neurosurg Psychiatry; 2009 Jan; 80(1):94-5. PubMed ID: 19091716
[No Abstract] [Full Text] [Related]
10. Late onset Tay-Sachs disease in mice with targeted disruption of the Hexa gene: behavioral changes and pathology of the central nervous system.
Miklyaeva EI; Dong W; Bureau A; Fattahie R; Xu Y; Su M; Fick GH; Huang JQ; Igdoura S; Hanai N; Gravel RA
Brain Res; 2004 Mar; 1001(1-2):37-50. PubMed ID: 14972652
[TBL] [Abstract][Full Text] [Related]
11. Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis.
Vielhaber S; Winkler K; Kirches E; Kunz D; Büchner M; Feistner H; Elger CE; Ludolph AC; Riepe MW; Kunz WS
J Neurol Sci; 1999 Oct; 169(1-2):133-9. PubMed ID: 10540022
[TBL] [Abstract][Full Text] [Related]
12. Polyglucosan body disease myopathy: an unusual presentation.
Vucic S; Pamphlett R; Wills EJ; Yiannikas C
Muscle Nerve; 2007 Apr; 35(4):536-9. PubMed ID: 17221878
[TBL] [Abstract][Full Text] [Related]
13. [Tay-Sachs disease: a case report. Interest of ultrastructural studies of cultured skin fibroblasts (author's transl)].
Charbonne F; Rousseau P; Malpuech G; Geneix A
Arch Fr Pediatr; 1980 Jan; 37(1):51-3. PubMed ID: 7469686
[TBL] [Abstract][Full Text] [Related]
14. Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosis.
Drory VE; Birnbaum M; Peleg L; Goldman B; Korczyn AD
Muscle Nerve; 2003 Jul; 28(1):109-12. PubMed ID: 12811781
[TBL] [Abstract][Full Text] [Related]
15. Late-onset Tay-Sachs disease presenting as catatonic schizophrenia: diagnostic and treatment issues.
Rosebush PI; MacQueen GM; Clarke JT; Callahan JW; Strasberg PM; Mazurek MF
J Clin Psychiatry; 1995 Aug; 56(8):347-53. PubMed ID: 7635850
[TBL] [Abstract][Full Text] [Related]
16. Hemiplegic ALS: Mills syndrome.
Rajabally YA; Hbahbih M; Abbott RJ
Neurology; 2005 Jun; 64(11):1984-5. PubMed ID: 15955966
[No Abstract] [Full Text] [Related]
17. A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: a clinical, pathological and genetic report.
Yamamoto-Watanabe Y; Watanabe M; Okamoto K; Fujita Y; Jackson M; Ikeda M; Nakazato Y; Ikeda Y; Matsubara E; Kawarabayashi T; Shoji M
J Neurol Sci; 2010 Sep; 296(1-2):59-63. PubMed ID: 20621307
[TBL] [Abstract][Full Text] [Related]
18. Mechanism of interrupted saccades in patients with late-onset Tay-Sachs disease.
Optican LM; Rucker JC; Keller EL; Leigh RJ
Prog Brain Res; 2008; 171():567-70. PubMed ID: 18718355
[TBL] [Abstract][Full Text] [Related]
19. [An unusual combination of myasthenia with late-disease-onset and lateral amyotrophic sclerosis].
Sanadze AG; Kasatkina LF
Zh Nevrol Psikhiatr Im S S Korsakova; 2010; 110(11 Pt 1):52-5. PubMed ID: 21329015
[No Abstract] [Full Text] [Related]
20. The "cherry red" spot.
Leavitt JA; Kotagal S
Pediatr Neurol; 2007 Jul; 37(1):74-5. PubMed ID: 17628229
[No Abstract] [Full Text] [Related]
[Next] [New Search]
