Allogeneic BMT followed by substrate reduction therapy in a child with subacute Tay-Sachs disease [5]

Bone Marrow Transplantation

Volumn 36, Issue 10, 2005, Pages 925-926

  Jacobs, J F M ^a   Willemsen, M A A P ^a   Groot Loonen, J J ^a   Wevers, R A ^a   Hoogerbrugge, P M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BETA N ACETYLHEXOSAMINIDASE A; BUSULFAN; CYCLOPHOSPHAMIDE; CYCLOSPORIN A; MIGLUSTAT; THYMOCYTE ANTIBODY; VALPROIC ACID;

ALLOGENIC BONE MARROW TRANSPLANTATION; BRAIN ATROPHY; BRAIN VENTRICLE; CASE REPORT; CHILDHOOD DISEASE; DETERIORATION; ELECTROENCEPHALOGRAPHY; ENZYME ACTIVITY; EPILEPTIC DISCHARGE; FEMALE; GRAFT VERSUS HOST REACTION; HUMAN; HUMAN CELL; LETTER; MOTOR PERFORMANCE; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE; SIDE EFFECT; SPEECH DISORDER; SUBARACHNOID SPACE; TAY SACHS DISEASE; VISUAL DISORDER;

1-DEOXYNOJIRIMYCIN; BONE MARROW TRANSPLANTATION; CHILD; FEMALE; HUMANS; NERVOUS SYSTEM DISEASES; TAY-SACHS DISEASE; TRANSPLANTATION, HOMOLOGOUS;

EID: 27844543404     PISSN: 02683369     EISSN: 14765365     Source Type: Journal    
DOI: 10.1038/sj.bmt.1705155     Document Type: Letter

References (6)

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5. Jeyakumar M, Butters TD, Dwek RA, Platt FM. Glycosphingolipid lysosomal storage diseases: Therapy and pathogenesis. Neuropathol Appl Neurobiol 2002; 28: 343-357.
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