165 related articles for article (PubMed ID: 33363)
1. [Juvenile form of metachromatic leukodystrophy. Clinical variant of sulfatidosis].
Turpin JC; Elchardus JF; Morice J; Georges MC; Dubois G
Pediatrie; 1978; 3(7):629-36. PubMed ID: 33363
[No Abstract] [Full Text] [Related]
2. [Arylsulfatase A deficiency-metachromatic leukodystrophy].
Eto Y
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):749-52. PubMed ID: 2908400
[No Abstract] [Full Text] [Related]
3. [Diagnostic problems in children with metachromatic leukodystrophy].
Michałowicz R; Ignatowicz R; Potakiewicz W; Kmieć T; Onyszkiewicz J; Radelicka H
Wiad Lek; 1986 Nov; 39(21):1494-8. PubMed ID: 2883775
[No Abstract] [Full Text] [Related]
4. Enzymic detection of metachromatic leukodystrophy patients and heterozygotes.
Jordan TW; Casey B; Weston HJ
N Z Med J; 1977 May; 85(587):369-72. PubMed ID: 23508
[TBL] [Abstract][Full Text] [Related]
5. Treatment of late infantile metachromatic leukodystrophy by bone marrow transplantation.
Krivit W; Shapiro E; Kennedy W; Lipton M; Lockman L; Smith S; Summers CG; Wenger DA; Tsai MY; Ramsay NK
N Engl J Med; 1990 Jan; 322(1):28-32. PubMed ID: 1967188
[No Abstract] [Full Text] [Related]
6. Arylsulfatases A and B in leukocytes: a comparative statistical study of late infantile and juvenile forms of metachromatic leukodystrophy and controls.
Dubois G; Turpin JC; Georges MC; Baumann N
Biomedicine; 1980 Feb; 33(1):2-4. PubMed ID: 6102873
[TBL] [Abstract][Full Text] [Related]
7. Metachromatic leukodystrophy: clinical and enzymatic parameters.
McKhann GM
Neuropediatrics; 1984 Sep; 15 Suppl():4-10. PubMed ID: 6152812
[TBL] [Abstract][Full Text] [Related]
8. [Metachromatic leukodystrophy in childhood. Description of a case].
Parenti D; Ricci R; Scoppetta C; Segni G
Minerva Pediatr; 1978 Aug; 30(15):1243-50. PubMed ID: 30037
[No Abstract] [Full Text] [Related]
9. Marked clinical difference between two sibs affected with juvenile metachromatic leukodystrophy.
Clarke JT; Skomorowski MA; Chang PL
Am J Med Genet; 1989 May; 33(1):10-3. PubMed ID: 2568751
[TBL] [Abstract][Full Text] [Related]
10. [Lysosomal diseases [metachromatic leukodystrophy (adult), Krabbe's disease (adult)]].
Kuriyama M
Nihon Rinsho; 2004 Jan; 62 Suppl():393-8. PubMed ID: 15011393
[No Abstract] [Full Text] [Related]
11. Metachromatic leukodystrophy and pseudoarylsulfatase A deficiency in a Danish family.
Tønnesen T; Bro PV; Brøndum Nielsen K; Lykkelund C
Acta Paediatr Scand; 1983 Mar; 72(2):175-8. PubMed ID: 6132516
[TBL] [Abstract][Full Text] [Related]
12. [Enzymologic detection of metachromatic leukodystrophy: limitations in prenatal diagnosis].
Turpin JC
Sem Hop; 1977 Dec; 53(42):2445-6. PubMed ID: 23583
[No Abstract] [Full Text] [Related]
13. Genetic heterogeneity in metachromatic leukodystrophy.
Kihara H
Am J Hum Genet; 1982 Mar; 34(2):171-81. PubMed ID: 6122378
[No Abstract] [Full Text] [Related]
14. Detection of arylsulfatase A in leukocytes and urines of late infantile metachromatic leukodystrophy. Report of 3 cases.
Wang DF; Zhao KW; Zeng JS; Li LQ; Sun YX; Gao QZ
Chin Med J (Engl); 1988 Nov; 101(11):793-7. PubMed ID: 2907984
[No Abstract] [Full Text] [Related]
15. A variant form of metachromatic leukodystrophy without arylsulfatase deficiency.
Hahn AF; Gordon BA; Hinton GG; Gilbert JJ
Ann Neurol; 1982 Jul; 12(1):33-6. PubMed ID: 6126151
[TBL] [Abstract][Full Text] [Related]
16. [Metachromatic leukodystrophy].
Eto Y; Hasegawa Y; Kurosawa K
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):379-84. PubMed ID: 9645087
[No Abstract] [Full Text] [Related]
17. Bone marrow transplantation in metachromatic leukodystrophy.
Lipton M; Lockman LA; Ramsay NK; Kersey JH; Jacobson RI; Krivit W
Birth Defects Orig Artic Ser; 1986; 22(1):57-67. PubMed ID: 2870748
[No Abstract] [Full Text] [Related]
18. Clinical and biochemical study of 29 Brazilian patients with metachromatic leukodystrophy.
Artigalás O; Lagranha VL; Saraiva-Pereira ML; Burin MG; Lourenço CM; van der Linden H; Santos ML; Rosemberg S; Steiner CE; Kok F; de Souza CF; Jardim LB; Giugliani R; Schwartz IV
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S257-62. PubMed ID: 20596894
[TBL] [Abstract][Full Text] [Related]
19. Atypical metachromatic leukodystrophy? Problems with the biochemical diagnosis.
Tønnesen T; Vrang C; Wiesmann UN; Christomanou H; Lou HO
Hum Genet; 1984; 67(2):170-3. PubMed ID: 6146562
[TBL] [Abstract][Full Text] [Related]
20. Presymptomatic diagnosis: metachromatic leukodystrophy or pseudo arylsulphatase A deficiency?
Kihara H; Fluharty AL; Ng WG; Leider W
J Inherit Metab Dis; 1982; 5(4):215-7. PubMed ID: 6133034
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
