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Results: 1-17 |
Results: 17
CARBOHYDRATE-DEFICIENT TRANSFERRIN ASSAY IN PEDIATRICS AND PREGNANCY - EXPRESSION OF RESULTS
Authors: TAMARO G SIMEONE R MANGIAROTTI M CAROZZI M CIANA G MARTINI C BEMBI B
Citation: G. Tamaro et al., CARBOHYDRATE-DEFICIENT TRANSFERRIN ASSAY IN PEDIATRICS AND PREGNANCY - EXPRESSION OF RESULTS, International journal of clinical & laboratory research, 28(2), 1998, pp. 140-140
LOW-DOSE ENZYME REPLACEMENT THERAPY IN PE DIATRIC TYPE-1 GAUCHERS-DISEASE
Authors: BEMBI B DONDA MG MARTINI C ZANATTA M BOSCOLO R KATOUZIAN F CIANA G
Citation: B. Bembi et al., LOW-DOSE ENZYME REPLACEMENT THERAPY IN PE DIATRIC TYPE-1 GAUCHERS-DISEASE, Rivista italiana di pediatria, 24(1), 1998, pp. 93-98
TOTAL GLYCOLIPID AND GLUCOSYLCERAMIDE CONTENT IN SERUM AND URINE OF PATIENTS WITH GAUCHERS-DISEASE TYPE-3 BEFORE AND AFTER ENZYME REPLACEMENT THERAPY
Authors: GORNATI R BEMBI B TONG XW BOSCOLO R BERRA B
Citation: R. Gornati et al., TOTAL GLYCOLIPID AND GLUCOSYLCERAMIDE CONTENT IN SERUM AND URINE OF PATIENTS WITH GAUCHERS-DISEASE TYPE-3 BEFORE AND AFTER ENZYME REPLACEMENT THERAPY, Clinica chimica acta, 271(2), 1998, pp. 151-161
NEURONOPATHIC FORMS OF GAUCHERS-DISEASE
Authors: ERIKSON A BEMBI B SCHIFFMANN R
Citation: A. Erikson et al., NEURONOPATHIC FORMS OF GAUCHERS-DISEASE, Bailliere's clinical haematology, 10(4), 1997, pp. 711-723
SHORT-TERM EFFECTS OF PAMIDRONATE IN PATIENTS WITH GAUCHERS-DISEASE AND SEVERE SKELETAL INVOLVEMENT
Authors: CIANA G CUTTINI M BEMBI B
Citation: G. Ciana et al., SHORT-TERM EFFECTS OF PAMIDRONATE IN PATIENTS WITH GAUCHERS-DISEASE AND SEVERE SKELETAL INVOLVEMENT, The New England journal of medicine, 337(10), 1997, pp. 712-712
INTRAVENOUS PAMIDRONATE TREATMENT IN OSTEOGENESIS IMPERFECTA
Authors: BEMBI B PARMA A BOTTEGA M CESCHEL S ZANATTA M MARTINI C CIANA G
Citation: B. Bembi et al., INTRAVENOUS PAMIDRONATE TREATMENT IN OSTEOGENESIS IMPERFECTA, The Journal of pediatrics, 131(4), 1997, pp. 622-625
TREATMENT OF PATIENTS WITH NIEMANN-PICK TYPE IS USING REPEATED AMNIOTIC EPITHELIAL-CELLS IMPLANTATION - CORRECTION OF AGGREGATION AND COAGULATION ABNORMALITIES
Authors: CERNECA F ANDOLINA M SIMEONE R BOSCOLO R CIANA G BEMBI B
Citation: F. Cerneca et al., TREATMENT OF PATIENTS WITH NIEMANN-PICK TYPE IS USING REPEATED AMNIOTIC EPITHELIAL-CELLS IMPLANTATION - CORRECTION OF AGGREGATION AND COAGULATION ABNORMALITIES, Clinical pediatrics, 36(3), 1997, pp. 141-146
OCCURRENCE OF PARKINSONS-SYNDROME IN TYPE-I GAUCHER DISEASE
Authors: NEUDORFER O GILADI N ELSTEIN D ABRAHAMOV A TUREZKITE T AGHAI E RECHES A BEMBI B ZIMRAN A
Citation: O. Neudorfer et al., OCCURRENCE OF PARKINSONS-SYNDROME IN TYPE-I GAUCHER DISEASE, Quarterly Journal of Medicine, 89(9), 1996, pp. 691-694
A DESCRIPTION OF 2 CASES OF FACTOR-V DEFICIENCY
Authors: CERNECA F PARCO S SIMEONE R BEMBI B GIORGI R
Citation: F. Cerneca et al., A DESCRIPTION OF 2 CASES OF FACTOR-V DEFICIENCY, Haemophilia, 1(3), 1995, pp. 200-201
INFANTILE SIALIC-ACID STORAGE DISEASE - BIOCHEMICAL-STUDIES
Authors: BERRA B GORNATI R RAPELLI S GATTI R MANCINI GMS CIANA G BEMBI B
Citation: B. Berra et al., INFANTILE SIALIC-ACID STORAGE DISEASE - BIOCHEMICAL-STUDIES, American journal of medical genetics, 58(1), 1995, pp. 24-31
CEREBROSPINAL-FLUID INFUSION OF ALGLUCERASE IN THE TREATMENT OF ACUTENEURONOPATHIC GAUCHERS-DISEASE
Authors: BEMBI B CIANA G ZANATTA M BOTTEGA M PELOS G GORNATI R BERRA B
Citation: B. Bembi et al., CEREBROSPINAL-FLUID INFUSION OF ALGLUCERASE IN THE TREATMENT OF ACUTENEURONOPATHIC GAUCHERS-DISEASE, Pediatric research, 38(3), 1995, pp. 425-425
A RARE G6490-]A SUBSTITUTION AT THE LAST NUCLEOTIDE OF EXON-10 OF THEGLUCOCEREBROSIDASE GENE IN 2 UNRELATED ITALIAN GAUCHER PATIENTS
Authors: SERI M FILOCAMO M CORSOLINI F BEMBI B BARBERA C GATTI R
Citation: M. Seri et al., A RARE G6490-]A SUBSTITUTION AT THE LAST NUCLEOTIDE OF EXON-10 OF THEGLUCOCEREBROSIDASE GENE IN 2 UNRELATED ITALIAN GAUCHER PATIENTS, Clinical genetics, 48(3), 1995, pp. 123-127
AMINOHYDROXYPROPYLIDENE-BIPHOSPHONATE IN THE TREATMENT OF BONE-LESIONS IN A CASE OF GAUCHERS-DISEASE TYPE-3
Authors: BEMBI B AGOSTI E BOEHM P NASSIMBENI G ZANATTA M VIDONI L
Citation: B. Bembi et al., AMINOHYDROXYPROPYLIDENE-BIPHOSPHONATE IN THE TREATMENT OF BONE-LESIONS IN A CASE OF GAUCHERS-DISEASE TYPE-3, Acta paediatrica, 83(1), 1994, pp. 122-124
Y418C - A NOVEL MUTATION IN EXON-9 OF THE GLUCOCEREBROSIDASE GENE OF A PATIENT WITH GAUCHER-DISEASE CREATES A NEW BGLI SITE
Authors: TUTEJA R TUTEJA N LILLIU F BEMBI B GALANELLO R CAO A BARALLE FE
Citation: R. Tuteja et al., Y418C - A NOVEL MUTATION IN EXON-9 OF THE GLUCOCEREBROSIDASE GENE OF A PATIENT WITH GAUCHER-DISEASE CREATES A NEW BGLI SITE, Human genetics, 94(3), 1994, pp. 314-315
ENZYME REPLACEMENT TREATMENT IN TYPE-1 AND TYPE-3 GAUCHERS-DISEASE
Authors: BEMBI B ZANATTA M CARROZZI M BARALLE F GORNATI R BERRA B AGOSTI E
Citation: B. Bembi et al., ENZYME REPLACEMENT TREATMENT IN TYPE-1 AND TYPE-3 GAUCHERS-DISEASE, Lancet, 344(8938), 1994, pp. 1679-1682
SEVERE FAILURE-TO-THRIVE AND LIVER DYSFUNCTION AS THE MAIN MANIFESTATIONS OF A NEW VARIANT OF NIEMANN-PICK DISEASE
Authors: REIF S SPIRER Z MESSER G BARATZ M BEMBI B BUJANOVER Y
Citation: S. Reif et al., SEVERE FAILURE-TO-THRIVE AND LIVER DYSFUNCTION AS THE MAIN MANIFESTATIONS OF A NEW VARIANT OF NIEMANN-PICK DISEASE, Clinical pediatrics, 33(10), 1994, pp. 628-630
1448C MUTATION LINKED TO THE PV1.1- GENOTYPE IN ITALIAN PATIENTS WITHGAUCHER DISEASE
Authors: TUTEJA R BEMBI B AGOSTI E BARALLE FE
Citation: R. Tuteja et al., 1448C MUTATION LINKED TO THE PV1.1- GENOTYPE IN ITALIAN PATIENTS WITHGAUCHER DISEASE, Human molecular genetics, 2(6), 1993, pp. 781-784
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