These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 512688)

  • 1. Peripheral intraaxonal storage in Tay-Sachs' disease (GM2-gangliosidosis type 1.
    Schmitt HP; Berlet H; Volk B
    J Neurol Sci; 1979 Dec; 44(1):115-24. PubMed ID: 512688
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Changes in the voluntary muscles and the peripheral nerves in an autopsy case of MPS type II (Hunter).
    Schmitt HP
    Neuropediatrics; 1981 Feb; 12(1):83-91. PubMed ID: 6789225
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spinal ganglia and peripheral nerves from a patent with Tay-Sachs disease. Morphological and ganglioside studies.
    Abe T; Ogawa K; Fuziwara H; Urayama K; Nagashima K
    Acta Neuropathol; 1985; 66(3):239-44. PubMed ID: 2990149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A freeze-fracture study on GM2 gangliosidosis.
    Volk B
    Clin Neuropathol; 1986; 5(2):88-92. PubMed ID: 3708958
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease.
    Taniike M; Yamanaka S; Proia RL; Langaman C; Bone-Turrentine T; Suzuki K
    Acta Neuropathol; 1995; 89(4):296-304. PubMed ID: 7610760
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An autopsy case of Tay-Sachs disease--with special reference to axonal swellings of the central nervous system and freeze-fracture replication studies of the membranous cytoplasmic bodies.
    Shirabe T; Hirokawa M; Asaki H
    Folia Psychiatr Neurol Jpn; 1980; 34(4):515-23. PubMed ID: 7262729
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fine needle aspiration cytology of Tay-Sachs disease. A case report.
    Ul Haque A
    Acta Cytol; 1995; 39(4):762-5. PubMed ID: 7631552
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Murine Sialidase Neu3 facilitates GM2 degradation and bypass in mouse model of Tay-Sachs disease.
    Seyrantepe V; Demir SA; Timur ZK; Von Gerichten J; Marsching C; Erdemli E; Oztas E; Takahashi K; Yamaguchi K; Ates N; Dönmez Demir B; Dalkara T; Erich K; Hopf C; Sandhoff R; Miyagi T
    Exp Neurol; 2018 Jan; 299(Pt A):26-41. PubMed ID: 28974375
    [TBL] [Abstract][Full Text] [Related]  

  • 9. B1 variant of GM2 gangliosidosis in a 12-year-old patient.
    Goebel HH; Stolte G; Kustermann-Kuhn B; Harzer K
    Pediatr Res; 1989 Jan; 25(1):89-93. PubMed ID: 2521932
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GM2 gangliosidosis variant B1 neuroradiological findings.
    Grosso S; Farnetani MA; Berardi R; Margollicci M; Galluzzi P; Vivarelli R; Morgese G; Ballestri P
    J Neurol; 2003 Jan; 250(1):17-21. PubMed ID: 12527987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Tay-Sachs disease: a report of 2 autopsy cases].
    Cui QC; Zhou CJ; Liu TH
    Zhonghua Bing Li Xue Za Zhi; 1994 Aug; 23(4):235-6. PubMed ID: 7805156
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Retinal amacrine cell involvement in Tay-Sachs disease.
    Nagashima K; Kikuchi F; Suzuki Y; Abe T
    Acta Neuropathol; 1981; 53(4):333-6. PubMed ID: 7223376
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two siblings, including a fetus, with Tay-Sachs disease.
    Yamada E; Matsumoto M; Hazama F; Momoi T; Sudo M
    Acta Pathol Jpn; 1981 Nov; 31(6):1053-61. PubMed ID: 7315310
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytology, growth characteristics and cellular alterations following SV40-induced transformation of human foetal brain cells derived from a Gm2 gangliosidosis and control.
    Brooks SE; Amsterdam D; Hoffman LM; Adachi M; Schneck L
    J Cell Sci; 1979 Aug; 38():211-23. PubMed ID: 230195
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase B.
    Burck U; Harzer K; Goebel HH; Elze KL; Held KR; Carstens L
    Neuropadiatrie; 1980 May; 11(2):161-75. PubMed ID: 6255371
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Diagnosis of G(M2) gangliosidosis in routine practice].
    Karpenko A; Elleder M; Jirásek A; Ledvinová J
    Cesk Patol; 1991 Mar; 27(1-2):48-54. PubMed ID: 1893430
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Morphology of the gangliosidoses.
    Goebel HH
    Neuropediatrics; 1984 Sep; 15 Suppl():97-106. PubMed ID: 6100800
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sialidase-mediated depletion of GM2 ganglioside in Tay-Sachs neuroglia cells.
    Igdoura SA; Mertineit C; Trasler JM; Gravel RA
    Hum Mol Genet; 1999 Jun; 8(6):1111-6. PubMed ID: 10332044
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Adult GM2 gangliosidosis in association with Tay-Sachs disease: a new phenotype.
    Navon R; Argov Z; Brand N; Sandbank U
    Neurology; 1981 Nov; 31(11):1397-1401. PubMed ID: 6458776
    [No Abstract]   [Full Text] [Related]  

  • 20. Evidence for a chronic axonal atrophy in oculopharyngeal "muscular dystrophy".
    Probst A; Tackmann W; Stoeckli HR; Jerusalem F; Ulrich J
    Acta Neuropathol; 1982; 57(2-3):209-16. PubMed ID: 7124348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.