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Rare genetic diseases--new opportunities and challenges through biotechnological progress and scientific knowledge.
- Source :
-
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society [Eur J Paediatr Neurol] 2002; Vol. 6 Suppl A, pp. A71-5; discussion A55-8, A65-6. - Publication Year :
- 2002
- Subjects :
- Adolescent
Basal Ganglia Diseases diagnosis
Calcinosis diagnosis
Cerebrospinal Fluid cytology
Child
Child, Preschool
Forecasting
Genetic Research
Genetic Therapy trends
Hereditary Central Nervous System Demyelinating Diseases diagnosis
Humans
Infant
Infant, Newborn
Lymphocytosis diagnosis
Syndrome
Basal Ganglia Diseases genetics
Calcinosis genetics
Hereditary Central Nervous System Demyelinating Diseases genetics
Interferon-alpha cerebrospinal fluid
Lymphocytosis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1090-3798
- Volume :
- 6 Suppl A
- Database :
- MEDLINE
- Journal :
- European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
- Publication Type :
- Academic Journal
- Accession number :
- 12365364
- Full Text :
- https://doi.org/10.1053/ejpn.2002.0579