Screening for GALC to make neonatal diagnosis and initial neonatal stem cell treatment with umbilical cord blood
Author:
Publisher
Wiley
Subject
Transplantation,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-3046.2003.00032.x/fullpdf
Reference21 articles.
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2. Residual galactosylsphingosine (psychosine) beta-galactosidase activities and associated GALC mutations in late and very late onset Krabbe disease;Harzer;Clin Chim Acta,2002
3. Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications;Wenger;Hum Mutat,1997
4. Lysosomal storage diseases;Gieselmann;Biochim Biophys Acta,1995
5. Microglia the effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage disease;Krivit;Cell Transplant,1995
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