Screening for GALC to make neonatal diagnosis and initial neonatal stem cell treatment with umbilical cord blood
- 21 March 2003
- journal article
- research article
- Published by Wiley in Pediatric Transplantation
- Vol. 7 (2) , 83-85
- https://doi.org/10.1034/j.1399-3046.2003.00032.x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Hematopoietic Stem-Cell Transplantation in Globoid-Cell LeukodystrophyNew England Journal of Medicine, 1998
- Molecular genetics of Krabbe disease (globoid cell leukodystrophy): Diagnostic and clinical implicationsHuman Mutation, 1997
- Diagnosis of Inborn Errors of Metabolism from Blood Spots by Acylcarnitines and Amino Acids Profiling Using Automated Electrospray Tandem Mass SpectrometryPediatric Research, 1995
- Microglia: The Effector Cell for Reconstitution of the Central Nervous System following Bone Marrow Transplantation for Lysosomal and Peroxisomal Storage DiseasesCell Transplantation, 1995
- The future for treatment by bone marrow transplantation for adrenoleukodystrophy, metachromatic leukodystrophy, globoid cell leukodystrophy and Hurler syndromeJournal of Inherited Metabolic Disease, 1995
- Allogeneic bone marrow transplantation for lysosomal storage diseasesThe Lancet, 1995
- Lysosomal storage diseasesBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1995
- Gene theraphy of lysosomal storage disordersBritish Medical Bulletin, 1995
- Neonatal screening for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis: four years' experienceBMJ, 1994
- Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolismJournal of Inherited Metabolic Disease, 1990