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1

Adult metachromatic leukodystrophy: disorganized schizophrenia-like symptoms and postpartum depression in 2 sisters.

Kumperscak HG, Paschke E, Gradisnik P, Vidmar J, Bradac SU. Kumperscak HG, et al. J Psychiatry Neurosci. 2005 Jan;30(1):33-6. J Psychiatry Neurosci. 2005. PMID: 15644995 Free PMC article.

2

Adult metachromatic leukodystrophy: a new mutation in the schizophrenia-like phenotype with early neurological signs.

Kumperscak HG, Plesnicar BK, Zalar B, Gradisnik P, Seruga T, Paschke E. Kumperscak HG, et al. Psychiatr Genet. 2007 Apr;17(2):85-91. doi: 10.1097/YPG.0b013e3280298280. Psychiatr Genet. 2007. PMID: 17413447

3

[Homicide and hebephrenia-like syndrome in metachromatic leukodystrophy].

Rentrop M, Hakk K, Freisleder FJ, Kissling W, Kockott G. Rentrop M, et al. Nervenarzt. 1999 Mar;70(3):276-80. doi: 10.1007/s001150050434. Nervenarzt. 1999. PMID: 10231817 German.

4

Characterization of urinary sulfatides in metachromatic leukodystrophy using electrospray ionization-tandem mass spectrometry.

Whitfield PD, Sharp PC, Johnson DW, Nelson P, Meikle PJ. Whitfield PD, et al. Mol Genet Metab. 2001 May;73(1):30-7. doi: 10.1006/mgme.2001.3165. Mol Genet Metab. 2001. PMID: 11350180

5

Metachromatic leukodystrophy without arylsulfatase A deficiency: a new case of saposin-B deficiency.

Deconinck N, Messaaoui A, Ziereisen F, Kadhim H, Sznajer Y, Pelc K, Nassogne MC, Vanier MT, Dan B. Deconinck N, et al. Eur J Paediatr Neurol. 2008 Jan;12(1):46-50. doi: 10.1016/j.ejpn.2007.05.004. Epub 2007 Jul 5. Eur J Paediatr Neurol. 2008. PMID: 17616409

6

Elevated sulfatide excretion in heterozygotes of metachromatic leukodystrophy: dependence on reduction of arylsulfatase A activity.

Molzer B, Sundt-Heller R, Kainz-Korschinsky M, Zobel M. Molzer B, et al. Am J Med Genet. 1992 Nov 1;44(4):523-6. doi: 10.1002/ajmg.1320440429. Am J Med Genet. 1992. PMID: 1359786

7

Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.

Kihara H, Ho CK, Fluharty AL, Tsay KK, Hartlage PL. Kihara H, et al. Pediatr Res. 1980 Mar;14(3):224-7. doi: 10.1203/00006450-198003000-00009. Pediatr Res. 1980. PMID: 6104322

8

Investigations of micro-organic brain damage (MOBD) in heterozygotes of metachromatic leukodystrophy.

Tylki-Szymańska A, Ługowska A, Chmielik J, Kotowicz J, Jakubowska-Winecka A, Zobel M, Berger J, Molzer B. Tylki-Szymańska A, et al. Am J Med Genet. 2002 Jul 15;110(4):315-9. doi: 10.1002/ajmg.10369. Am J Med Genet. 2002. PMID: 12116203

9

[Frontotemporal dementia in metachromatic leukodystrophy].

Kozian R, Sieber N, Thiergart S. Kozian R, et al. Fortschr Neurol Psychiatr. 2007 Sep;75(9):549-51. doi: 10.1055/s-2007-980065. Epub 2007 Jun 13. Fortschr Neurol Psychiatr. 2007. PMID: 17566965 German.

10

Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy.

Berger J, Löschl B, Bernheimer H, Lugowska A, Tylki-Szymanska A, Gieselmann V, Molzer B. Berger J, et al. Am J Med Genet. 1997 Mar 31;69(3):335-40. Am J Med Genet. 1997. PMID: 9096767

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