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 *

115 related articles for article (PubMed ID: 5465441)

  • 61. EEG findings in late infantile metachromatic and globoid cell leucodystrophy.
    Blom S; Hagberg B
    Electroencephalogr Clin Neurophysiol; 1967 Mar; 22(3):253-9. PubMed ID: 4163824
    [No Abstract]   [Full Text] [Related]  

  • 62. Galactocerebrosidase deficiency in globoid cell leucodystrophy of late onset.
    Young E; Wilson J; Patrick AD; Crome L
    Arch Dis Child; 1972 Jun; 47(253):449-50. PubMed ID: 5034675
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Mental retardation in children. II. Leucodystrophies.
    Joshua GE; Jadhav M; Bhaktaviziam A; Mokashi S
    Indian Pediatr; 1974 Jan; 11(1):53-9. PubMed ID: 4839581
    [No Abstract]   [Full Text] [Related]  

  • 64. Metachromatic leucodystrophy (sulphatide lipidoses). Juvenile type: case report.
    Taori GM; Mathew NT; Bhaktaviziam A; Bachhawat BK
    Indian J Med Res; 1969 May; 57(5):914-20. PubMed ID: 5820439
    [No Abstract]   [Full Text] [Related]  

  • 65. The patterns of arylsulphatases A and B in human normal and metachromatic leucodystrophy tissues and their relationship to the cerebroside sulphatase activity.
    Harzer K; Stinshoff K; Mraz W; Jatzkewitz H
    J Neurochem; 1973 Feb; 20(2):279-87. PubMed ID: 4698279
    [No Abstract]   [Full Text] [Related]  

  • 66. Electron microscopic studies of metachromatic leucodystrophy. IV. Liver and kidney alterations.
    Résibois A
    Pathol Eur; 1971; 6(3):278-98. PubMed ID: 4107144
    [No Abstract]   [Full Text] [Related]  

  • 67. The diagnostic value of sural nerve biopsy in metachromatic leucodystrophy and other conditions with low leucocyte arylsulphatase A activities.
    Vos AJ; Joosten EM; Gabreëls-Festen AA; Gabreëls FJ; Notermans SL; Lamers KJ
    Neuropediatrics; 1982 Feb; 13(1):42-6. PubMed ID: 6123090
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Krabbe's globoid cell leukodystrophy: deficiency of glactocerebrosidase in serum, leukocytes, and fibroblasts.
    Suzuki Y; Suzuki K
    Science; 1971 Jan; 171(3966):73-5. PubMed ID: 5538703
    [TBL] [Abstract][Full Text] [Related]  

  • 69. [Infantile metachromatic leukodystrophy (4 cases)].
    Maraví E; Bueno M; Martínez-Lage JM; Villanueva JA
    Arch Neurobiol (Madr); 1970; 33(2):207-32. PubMed ID: 4194760
    [No Abstract]   [Full Text] [Related]  

  • 70. Defective sulfatide synthesis in Krabbe's disease (globoid leukodystrophy).
    Austin J; Bachhawat B; Armstrong D; Stumpf D; Kretschmer L; Mitchell C; Van Zee B
    J Neuropathol Exp Neurol; 1968 Jan; 27(1):141-2. PubMed ID: 5656559
    [No Abstract]   [Full Text] [Related]  

  • 71. Urinary screening of globoid-cell leukodystrophy.
    Suzuki K; Suzuki Y; Desnick RJ; Desnick SJ; Dawson G
    N Engl J Med; 1971 Jul; 285(4):238-9. PubMed ID: 5087736
    [No Abstract]   [Full Text] [Related]  

  • 72. E.E.G. studies in 22 children with sulphatide lipidosis (metachromatic leucodystrophy).
    Mastropaolo C; Pampiglione G; Stephens R
    Dev Med Child Neurol; 1971 Feb; 13(1):20-31. PubMed ID: 5554949
    [No Abstract]   [Full Text] [Related]  

  • 73. An activator of cerebroside sulphatase in human normal liver and in cases of congenital metachromatic leukodystrophy.
    Jatzkewitz H; Stinshoff K
    FEBS Lett; 1973 May; 32(1):129-31. PubMed ID: 4715673
    [No Abstract]   [Full Text] [Related]  

  • 74. [Combination of metachromatic leucodystrophy and mucopolysaccharidosis: a disease entity (mucosulfatidosis)].
    Rampini S; Isler W; Baerlocher K; Bischoff A; Ulrich J; Plüss HJ
    Helv Paediatr Acta; 1970 Nov; 25(5):436-61. PubMed ID: 4250178
    [No Abstract]   [Full Text] [Related]  

  • 75. Metachromatic form of diffuse cerebral sclerosis. VI. A rapid test for the sulfatase A deficiency in metachromatic leukodystrophy (MLD) urine.
    Austin J; Armstrong D; Shearer L; McAfee D
    Arch Neurol; 1966 Mar; 14(3):259-69. PubMed ID: 5905074
    [No Abstract]   [Full Text] [Related]  

  • 76. Variable course of Canavan disease in two boys with early infantile aspartoacylase deficiency.
    von Moers A; Sperner J; Michael T; Scheffner D; Schutgens RH
    Dev Med Child Neurol; 1991 Sep; 33(9):824-8. PubMed ID: 1936635
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Sudanophilic leucodystrophy with meningeal angiomatosis in two brothers: infantile form of diffuse sclerosis with meningeal angiomatosis.
    Hooft C; Deloore G; Van Bogaert L; Guazzi GC
    J Neurol Sci; 1965; 2(1):30-51. PubMed ID: 4167605
    [No Abstract]   [Full Text] [Related]  

  • 78. [Metachromatic leucodystrophy. A genetic study of a familial adult form of metachromatic leucodystrophy (author's transl)].
    Czmok E; Regli F; Harzer K; Benz HU
    Arch Psychiatr Nervenkr (1970); 1974; 219(4):369-75. PubMed ID: 4447458
    [No Abstract]   [Full Text] [Related]  

  • 79. Globoid cell leucodystrophy.
    Kelly TE
    Arch Dis Child; 1973 Feb; 48(2):165. PubMed ID: 4690524
    [No Abstract]   [Full Text] [Related]  

  • 80. Treatment of metachromatic leukodystrophy in fibroblasts by enzyme replacement.
    Wiesmann UN; Rossi EE; Herschkowitz NN
    N Engl J Med; 1971 Mar; 284(12):672-3. PubMed ID: 5545612
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.