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Results:
1-8
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Results: 8
Authors:
AMARAL O
MARCAO A
PINTO E
MIRANDA MCS
Citation: O. Amaral et al., MUTATION ANALYSIS OF THE 3 MOST COMMON LYSOSOMAL STORAGE DISORDERS INPORTUGAL, European journal of human genetics, 6, 1998, pp. 1027-1027
Authors:
LACERDA L
FORTUNA A
SILVA E
AMARAL O
MIRANDA CS
Citation: L. Lacerda et al., STUDY OF CHARACTERISTIC SECONDARY BIOCHEMICAL-ABNORMALITIES OF GAUCHER-DISEASE IN PATIENTS SUBMITTED TO ENZYME SUPPLEMENTATION THERAPY, European journal of human genetics, 6, 1998, pp. 1090-1090
Authors:
AMARAL O
MARCAO A
PINTO E
ZIMRAN A
MIRANDA MCS
Citation: O. Amaral et al., DISTINCT HAPLOTYPE IN NON-ASHKENAZI GAUCHER PATIENTS WITH N370S MUTATION, Blood cells, molecules, & diseases, 23(22), 1997, pp. 415-416
Authors:
AMARAL O
PINTO E
FORTUNA M
LACERDA L
MIRANDA MCS
Citation: O. Amaral et al., TYPE-1 GAUCHER DISEASE - IDENTIFICATION OF N396T AND PREVALENCE OF GLUCOCEREBROSIDASE MUTATIONS IN THE PORTUGUESE, Human mutation, 8(3), 1996, pp. 280-281
Authors:
LACERDA L
AMARAL O
PINTO R
AERTS J
MIRANDA MCS
Citation: L. Lacerda et al., THE N370S MUTATION IN THE GLUCOCEREBROSIDASE GENE OF PORTUGUESE TYPE-1 GAUCHER PATIENTS - LINKAGE TO THE PVUII POLYMORPHISM, Journal of inherited metabolic disease, 17(1), 1994, pp. 85-88
Authors:
AMARAL O
FORTUNA AM
LACERDA L
PINTO R
MIRANDA MCS
Citation: O. Amaral et al., MOLECULAR CHARACTERIZATION OF TYPE-1 GAUCHER DISEASE FAMILIES AND PATIENTS - INTRAFAMILIAL HETEROGENEITY AT THE CLINICAL-LEVEL, Journal of Medical Genetics, 31(5), 1994, pp. 401-404
Authors:
LACERDA L
AMARAL O
PINTO R
OLIVEIRA P
AERTS J
MIRANDA MCS
Citation: L. Lacerda et al., GAUCHER DISEASE - N370S GLUCOCEREBROSIDASE GENE-FREQUENCY IN THE PORTUGUESE POPULATION, Clinical genetics, 45(6), 1994, pp. 298-300
Authors:
LACERDA L
AMARAL O
PINTO R
AERTS J
MIRANDA MCS
Citation: L. Lacerda et al., IDENTIFICATION OF GAUCHER DISEASE CARRIERS - GLUCOCEREBROSIDASE ANTIGEN AND DNA ANALYSIS, Biochemical medicine and metabolic biology, 50(2), 1993, pp. 190-196
Risultati:
1-8
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