130 related articles for article (PubMed ID: 4804153)
1. [Quantitative metachromasia with pseudoisocyanin: a new method for the determination of sulphatides, and for use in the diagnosis of metachromatic leucodystrophy (sulphatide lipidosis) (author's transl)].
Harzer K; Benz HU
Z Klin Chem Klin Biochem; 1973 Nov; 11(11):471-5. PubMed ID: 4804153
[No Abstract] [Full Text] [Related]
2. [Clinical and histological diagnosis of a case of familial adult metachromatic leucodystrophy (author's transl)].
Czmok E; Regli F; Bischoff A; Harzer K; Benz HU
J Neurol; 1974; 207(3):189-204. PubMed ID: 4137382
[No Abstract] [Full Text] [Related]
3. Deficiency of lactosyl sulfatide sulfatase in metachromatic leucodystrophy (sulfatidosis).
Harzer K; Benz HU
Hoppe Seylers Z Physiol Chem; 1974 Jun; 355(6):744-8. PubMed ID: 4140140
[No Abstract] [Full Text] [Related]
4. Biochemical abnormalities of metachromatic leukodystrophy in an adult psychiatric population.
Mahon-Haft H; Stone RK; Johnson R; Shah S
Am J Psychiatry; 1981 Oct; 138(10):1372-4. PubMed ID: 6117201
[No Abstract] [Full Text] [Related]
5. Deficiency of seminolipid sulphatase activity in brain tissue of metachromatic leucodystrophy.
Yamaguchi S; Aoki K; Handa S; Yamakawa T
J Neurochem; 1975 May; 24(5):1087-9. PubMed ID: 237979
[No Abstract] [Full Text] [Related]
6. Human urinary sulfatides in patients with sulfatidosis (metachromatic leukodystrophy).
Philippart M; Sarlieve L; Meurant C; Mechler L
J Lipid Res; 1971 Jul; 12(4):434-41. PubMed ID: 5164093
[TBL] [Abstract][Full Text] [Related]
7. Auditory evoked brainstem response and high-performance liquid chromatography sulfatide assay as early indices of metachromatic leukodystrophy.
Brown FR; Shimizu H; McDonald JM; Moser AB; Marquis P; Chen WW; Moser HW
Neurology; 1981 Aug; 31(8):980-5. PubMed ID: 6115337
[No Abstract] [Full Text] [Related]
8. Determination of urinary sulfatides and other lipids by combination of reversed-phase and thin-layer chromatographies.
Berná L; Asfaw B; Conzelmann E; Cerný B; Ledvinová J
Anal Biochem; 1999 May; 269(2):304-11. PubMed ID: 10222002
[TBL] [Abstract][Full Text] [Related]
9. Apparent biochemical homozygosity in two obligatory heterozygotes for metachromatic leukodystrophy.
Lott IT; Dulaney JT; Milunsky A; Hoefnagel D; Moser HW
J Pediatr; 1976 Sep; 89(3):438-40. PubMed ID: 8599
[No Abstract] [Full Text] [Related]
10. Metachromatic leucodystrophy-a generalized lipidosis. Determination of sulfatides in urine, blood plasma and cerebrospinal fluid.
HAGBERG B; SVENNERHOLM L
Acta Paediatr (Stockh); 1960 Nov; 49():690-4. PubMed ID: 13710472
[No Abstract] [Full Text] [Related]
11. Characterization of urinary sulfatides in metachromatic leukodystrophy using electrospray ionization-tandem mass spectrometry.
Whitfield PD; Sharp PC; Johnson DW; Nelson P; Meikle PJ
Mol Genet Metab; 2001 May; 73(1):30-7. PubMed ID: 11350180
[TBL] [Abstract][Full Text] [Related]
12. Sulfatide excreting heterozygous carrier of juvenile metachromatic leukodystrophy or asymptomatic patient of adult metachromatic leukodystrophy.
Harzer K; Recke AS
Humangenetik; 1975 Oct; 29(4):299-307. PubMed ID: 1176145
[TBL] [Abstract][Full Text] [Related]
13. [Prenatal diagnosis of a case of metachromatic leucodystrophy (author's transl)].
Harzer K; Zahn V; Stengel-Rutkowski S; Gley EO
Dtsch Med Wochenschr; 1975 Apr; 100(17):951-3. PubMed ID: 1122864
[TBL] [Abstract][Full Text] [Related]
14. Staining of sulphatides in metachromatic leukodystrophy with Alcian blue at high salt concentrations.
Lampert IA; Lewis PD
Histochemistry; 1975 Jun; 43(3):269-73. PubMed ID: 50307
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. [Metachromatic leukodystrophy--a neurolipidosis].
Nyberg-Hansen R
Tidsskr Nor Laegeforen; 1973 Apr; 93(12):835-7. PubMed ID: 4201739
[No Abstract] [Full Text] [Related]
17. Comparison of properties of the enzymes involved in metachromatic leukodystrophy and in Tay-Sachs disease.
Jatzkewitz H
Biochem Soc Symp; 1972; (35):141-50. PubMed ID: 4614800
[No Abstract] [Full Text] [Related]
18. Studies on the function of the activator of sulphatase A.
Fischer G; Jatzkewitz H
Adv Exp Med Biol; 1978; 101():573-82. PubMed ID: 27072
[TBL] [Abstract][Full Text] [Related]
19. Sulfogalactosylsphingosine sulfatase. Characteristics of the enzyme and its deficiency in metachromatic leukodystrophy in human cultured skin fibroblasts.
Eto Y; Wiesmann U; Herschkowitz NN
J Biol Chem; 1974 Aug; 249(15):4955-60. PubMed ID: 4846753
[No Abstract] [Full Text] [Related]
20. Sulfatide excretion in metachromatic leukodystrophy.
Lott IT; Dulaney JT
Am J Hum Genet; 1978 Mar; 30(2):228-9. PubMed ID: 655169
[No Abstract] [Full Text] [Related]
[Next] [New Search]
