126 related articles for article (PubMed ID: 471193)
1. Adult metachromatic leucodystrophy: clinicopathological report of two familial cases with slow course.
Tagliavini F; Pietrini V; Pilleri G; Trabattoni G; Lechi A
Neuropathol Appl Neurobiol; 1979; 5(3):233-43. PubMed ID: 471193
[TBL] [Abstract][Full Text] [Related]
2. Four cases of late onset metachromatic leucodystrophy in a family: clinical, biochemical and neuropathological studies.
Alves D; Pires MM; Guimarães A; Miranda MC
J Neurol Neurosurg Psychiatry; 1986 Dec; 49(12):1417-22. PubMed ID: 3806119
[TBL] [Abstract][Full Text] [Related]
3. Two clinicopathological cases of a dominantly inherited, adult onset orthochromatic leucodystrophy.
Letournel F; Etcharry-Bouyx F; Verny C; Barthelaix A; Dubas F
J Neurol Neurosurg Psychiatry; 2003 May; 74(5):671-3. PubMed ID: 12700318
[TBL] [Abstract][Full Text] [Related]
4. Adult metachromatic leucodystrophy.
Cole G; Proctor NS
S Afr Med J; 1974 Jul; 48(32):1371-4. PubMed ID: 4450165
[No Abstract] [Full Text] [Related]
5. Metachromatic leukodystrophy. Report of siblings with the juvenile type of metachromatic leukodystrophy.
Satoh T; Suzuki H; Monma N; Satodate R; Tanaka H; Yajima H
Acta Pathol Jpn; 1988 Aug; 38(8):1041-51. PubMed ID: 3188912
[TBL] [Abstract][Full Text] [Related]
6. Late infantile metachromatic leucodystrophy (MLD). Clinical and diagnostic evaluation in a typical case.
Rossi LN; Vassella F; Bischoff A; Wiesmann UN; Herschkowitz N
J Neurol; 1975 Oct; 210(4):291-8. PubMed ID: 52698
[TBL] [Abstract][Full Text] [Related]
7. An unusual homozygous arylsulfatase: a pseudodeficiency in a metachromatic leukodystrophy Tunisian patient.
Tinsa F; Caillaud C; Vanier MT; Bousnina D; Boussetta K; Bousnina S
J Child Neurol; 2010 Jan; 25(1):82-6. PubMed ID: 19574581
[TBL] [Abstract][Full Text] [Related]
8. [Familial metachromatic leukodystrophy as a cause of psychotic manifestations in young adults].
Wender M; Pruchnik-Wolińska D; Paprzycki W; Czartoryska B
Psychiatr Pol; 1998; 32(1):113-9. PubMed ID: 9594589
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Sporadic adult-onset leucodystrophy with axonal spheroids and pigmented glia with no mutations in the known targeted genes.
Fernández-Vega I; Pérez de Heredia-Goñi K; Santos-Juanes J; Goñi Imizcoz M; Zaldumbide L; Zarranz JJ; Ferrer I
Histopathology; 2016 Jan; 68(2):308-12. PubMed ID: 26018837
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Clinical and ultrastructural ocular histopathologic studies of adult-onset metachromatic leukodystrophy.
Quigley HA; Green WR
Am J Ophthalmol; 1976 Sep; 82(3):472-9. PubMed ID: 961798
[TBL] [Abstract][Full Text] [Related]
13. [Metachromatic leukodystrophy. Report of a case].
Nascimento OJ; Freitas MR; Alencar AA; Couto BH
Arq Neuropsiquiatr; 1980 Sep; 38(3):287-92. PubMed ID: 7469818
[TBL] [Abstract][Full Text] [Related]
14. Peripheral neuropathy detected on electrophysiological study as first manifestation of metachromatic leucodystrophy in infancy.
Martinez AC; Ferrer MT; Fueyo E; Galdos L
J Neurol Neurosurg Psychiatry; 1975 Feb; 38(2):169-74. PubMed ID: 1151398
[TBL] [Abstract][Full Text] [Related]
15. Clinicopathological differences between juvenile and late infantile metachromatic leukodystrophy.
Takashima S; Matsui A; Fujii Y; Nakamura H
Brain Dev; 1981; 3(4):365-74. PubMed ID: 6119040
[TBL] [Abstract][Full Text] [Related]
16. Late infantile metachromatic leucodystrophy in two siblings.
Koul RL; Gururaj A; Chacko AP; Elbualy MS; Bhusnurmath SR; Chand P
Indian Pediatr; 1994 Jun; 31(6):694-8. PubMed ID: 7896397
[No Abstract] [Full Text] [Related]
17. Juvenile metachromatic leucodystrophy. Case report with clinical, histopathological, ultrastructural and biochemical observations.
Haberland C; Brunngraber E; Witting L; Daniels A
Acta Neuropathol; 1973 Oct; 26(2):93-106. PubMed ID: 4763204
[No Abstract] [Full Text] [Related]
18. Metachromatic leucodystrophy: a newly identified mutation in arylsulphatase A, D281Y, found as a compound heterozygote with I179L in an adult onset case.
Halsall DJ; Halligan EP; Elsey TS; Cox TM
Hum Mutat; 1999 Nov; 14(5):447. PubMed ID: 10533072
[TBL] [Abstract][Full Text] [Related]
19. First-trimester diagnosis of metachromatic leucodystrophy.
Fensom AH; Marsh J; Jackson M; McGuire VM; Vimal C; Nicolaides K; Sheridan R
Clin Genet; 1988 Aug; 34(2):122-5. PubMed ID: 2903806
[TBL] [Abstract][Full Text] [Related]
20. [2 familial cases of metachromatic leukodystrophy of late onset].
Brault JL; Gielselmann V; Carpentier A; Lefèvre M; Turpin JC; Baumann N
Rev Neurol (Paris); 1997 Apr; 153(3):193-6. PubMed ID: 9296133
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
