Report of the Spanish Gaucher's disease registry: Clinical and genetic characteristics

Haematologica

Volumn 85, Issue 8, 2000, Pages 792-799

  Giraldo, P ^a   Pocovi, M ^a   Perez Calvo, J I ^a   Rubio Felix, D ^a   Giralt, M ^a  

^a HOSPITAL UNIVERSITARIO MIGUEL SERVET   (Spain)

Author keywords

ERT; Genotype; Incidence; Phenotypic diversity; Quality of life; Type I Gaucher's disease

Indexed keywords

ACID PHOSPHATASE; GLYCOSIDASE; HEMOGLOBIN;

ADOLESCENT; ADULT; AGE DISTRIBUTION; ALLELISM; ARTICLE; CHILD; CLINICAL FEATURE; ENZYME REPLACEMENT; FEMALE; GAUCHER DISEASE; GENE MUTATION; HEMOGLOBIN DETERMINATION; HUMAN; JEW; LEUKOCYTE COUNT; LIVER DYSFUNCTION; MAJOR CLINICAL STUDY; MALE; QUALITY OF LIFE; RACE DIFFERENCE; SPAIN; THROMBOCYTE COUNT;

ADOLESCENT; ADULT; AGE DISTRIBUTION; ALLELES; AMINO ACID SUBSTITUTION; ANTHROPOMETRY; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; COMBINED MODALITY THERAPY; FEMALE; GAUCHER DISEASE; GENE FREQUENCY; GENOTYPE; GLUCOSYLCERAMIDASE; HUMAN; INFANT; MALE; MIDDLE AGE; POINT MUTATION; QUALITY OF LIFE; QUESTIONNAIRES; REGISTRIES; SEVERITY OF ILLNESS INDEX; SPAIN; SPLENECTOMY; SUPPORT, NON-U.S. GOV'T; TREATMENT OUTCOME;

EID: 0033826442     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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