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 *

120 related articles for article (PubMed ID: 228523)

  • 1. Morphological observations in the nervous system of prenatal mucopolysaccharidosis II (M. Hunter).
    Meier C; Wismann U; Herschkowitz N; Bischoff A
    Acta Neuropathol; 1979 Nov; 48(2):139-43. PubMed ID: 228523
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ultrastructural demonstration of neuronal storage in fetal Tay-Sachs disease.
    Cutz E; Lowden JA; Conen PE
    J Neurol Sci; 1974 Feb; 21(2):197-202. PubMed ID: 4374514
    [No Abstract]   [Full Text] [Related]  

  • 3. Prenatal mucopolysaccharidosis II (Hunter): a pathogenetic study.
    Wiesmann UN; Spycher MA; Meier C; Liebaers I; Herschkowitz N
    Pediatr Res; 1980 May; 14(5):749-56. PubMed ID: 6770331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ultrastructural study on nervous system of fetus with GM1-gangliosidosis type 1.
    Yamano T; Shimada M; Okada S; Yutaka T; Kato T; Inui K; Yabuuchi H; Kanzaki S; Kanda S
    Acta Neuropathol; 1983; 61(1):15-20. PubMed ID: 6414233
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Peripheral nerve involvement in Hunter syndrome (mucopolysaccharidosis II).
    Swift TR; McDonald TF
    Arch Neurol; 1976 Dec; 33(12):845-6. PubMed ID: 187158
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome).
    Chen CP; Lin SP; Tzen CY; Hwu WL; Chern SR; Chuang CK; Chiang SS; Wang W
    Genet Couns; 2007; 18(1):49-56. PubMed ID: 17515300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of adult neuronal ceroid-lipofuscinosis with the appearance of membranous cytoplasmic bodies localized in the spinal anterior horn.
    Iseki E; Amano N; Yokoi S; Yamada Y; Suzuki K; Yazaki M
    Acta Neuropathol; 1987; 72(4):362-8. PubMed ID: 3033977
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Light, fluorescence, and electron microscopic features of neuronal intranuclear hyaline inclusions associated with multisystem atrophy.
    Sung JH
    Acta Neuropathol; 1980; 50(2):115-20. PubMed ID: 6249061
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hunter's syndrome. An ultrastructural study of an autopsy case.
    Oda H; Sasaki Y; Nakatani Y; Maesaka H; Suwa S
    Acta Pathol Jpn; 1988 Sep; 38(9):1175-90. PubMed ID: 2853931
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two cases of mucopolysaccharidosis type III (Sanfilippo). An anatomopathological study.
    Martin JJ; Ceuterick C; Van Dessel G; Lagrou A; Dierick W
    Acta Neuropathol; 1979 May; 46(3):185-90. PubMed ID: 223363
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sialidosis type I carrying V217M/G243R mutations in lysosomal sialidase: an autopsy study demonstrating terminal sialic acid in lysosomal lamellar inclusions and cerebellar dysplasia.
    Uchihara T; Ohashi K; Kitagawa M; Kurata M; Nakamura A; Hirokawa K; Kasuga T; Kobayashi T
    Acta Neuropathol; 2010 Jan; 119(1):135-45. PubMed ID: 19415310
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hunter' syndrome. Ultrastructural features in young children.
    Murphy JV; Hodach AE; Gilbert EF; Deanching M; Matalon R
    Arch Pathol Lab Med; 1983 Sep; 107(9):495-9. PubMed ID: 6309115
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mucopolysaccharidosis type V. (Scheie syndrome). A postmortem study by multidisciplinary techniques with emphasis on the brain.
    Dekaban AS; Constantopoulos G; Herman MM; Steusing JK
    Arch Pathol Lab Med; 1976 May; 100(5):237-45. PubMed ID: 817693
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The gangliosidoses.
    Volk BW; Adachi M; Schneck L
    Hum Pathol; 1975 Sep; 6(5):555-69. PubMed ID: 170187
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Morphological and biochemical studies of a case of mucopolysaccharidosis II (Hunter's syndrome).
    Nagashima K; Endo H; Sakakibara K; Konishi Y; Miyachi K; Wey JJ; Suzuki Y; Onisawa J
    Acta Pathol Jpn; 1976 Jan; 26(1):115-32. PubMed ID: 132078
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pathological study on a severe sialidosis (alpha-neuraminidase deficiency).
    Yamano T; Shimada M; Matsuzaki K; Matsumoto Y; Yoshihara W; Okada S; Inui K; Yutaka T; Yabuuchi H
    Acta Neuropathol; 1986; 71(3-4):278-84. PubMed ID: 3799140
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The diagnosis of mucopolysaccharidoses by electron microscopy of skin biopsies.
    Bioulac P; Mercier M; Beylot C; Fontan D
    J Cutan Pathol; 1975; 2(4):179-90. PubMed ID: 172535
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effects of chronic vitamin E deficiency on the nervous system of the rat.
    Towfighi J
    Acta Neuropathol; 1981; 54(4):261-7. PubMed ID: 7270082
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.