Analysis of fatty acids and sphingosines from urinary sulfatides in a patient with metachromatic leukodystrophy by gas chromatography — Mass spectrometry

Author:

Nishio Hisahide,Kodama Soichi,Matsuo Tamotsu

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. A controlled study of enzymatic activities in three human disorders of glycolipid metabolism;Austin;J Neurochem,1963

2. Metachromatic leucodystrophy: review of 38 cases;MacFaul;Arch Dis Child,1982

3. Metachromatic form of diffuse cerebral sclerosis. 2. Diagnosis during life by isolation of metachromatic lipids from urine;Austin;Neurology (NY),1957

4. The excretion of urinary sulfatides in health and neurological disease;Hagberg;Acta Paediatr Scand,1965

5. Histochemical and biochemical studies of urinary lipids in metachromatic leukodystrophy and Fabry's disease;Pilz;J Lab Clin Med,1973

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