ACNP - Italian Periodicals Catalogue

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Results: 1-25 | 26-35

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LIMITS TO THE USE OF THE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE 6-PHOSPHOGLUCONATE DEHYDROGENASE INDEX FOR THE DETECTION OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY

Authors: MOSCA A PALEARI R SOLLAINO C BARELLA S GALANELLO R

Citation: A. Mosca et al., LIMITS TO THE USE OF THE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE 6-PHOSPHOGLUCONATE DEHYDROGENASE INDEX FOR THE DETECTION OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY, CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 36(9), 1998, pp. 737-738

HB-SASSARI[ALPHA-126(H9)ASP-]HIS] RESULTS FROM A (G)UNDER-BAR-AC-](C)UNDER-BAR-AC MUTATION IN THE ALPHA-1-GLOBIN GENE

Authors: PAGLIETTI E BARELLA S SATTA S PERRA C CAO A GALANELLO R

Citation: E. Paglietti et al., HB-SASSARI[ALPHA-126(H9)ASP-]HIS] RESULTS FROM A (G)UNDER-BAR-AC-](C)UNDER-BAR-AC MUTATION IN THE ALPHA-1-GLOBIN GENE, Hemoglobin, 22(1), 1998, pp. 65-67

ALPHA-THALASSEMIA CARRIER IDENTIFICATION BY DNA ANALYSIS IN THE SCREENING FOR THALASSEMIA

Authors: GALANELLO R SOLLAINO C PAGLIETTI E BARELLA S PERRA C DONEDDU I PIRRONI MG MACCIONI L CAO A

Citation: R. Galanello et al., ALPHA-THALASSEMIA CARRIER IDENTIFICATION BY DNA ANALYSIS IN THE SCREENING FOR THALASSEMIA, American journal of hematology, 59(4), 1998, pp. 273-278

EVALUATION OF THE BETHA GENE-1 KIT FOR THE QUALITATIVE DETECTION OF THE 8 MOST COMMON MEDITERRANEAN BETA-THALASSEMIA MUTATIONS

Authors: UGOZZOLI LA LOWERY JD REYES AA LIN CIP RE A LOCATI F GALANELLO R MACIONI L MAGGIO A GIAMBONA A LOUTRADI A BOUSSIOU M WALLACE RB

Citation: La. Ugozzoli et al., EVALUATION OF THE BETHA GENE-1 KIT FOR THE QUALITATIVE DETECTION OF THE 8 MOST COMMON MEDITERRANEAN BETA-THALASSEMIA MUTATIONS, American journal of hematology, 59(3), 1998, pp. 214-222

HETEROZYGOUS BETA-THALASSEMIA WITH THALASSEMIA-INTERMEDIA PHENOTYPE

Authors: GASPERINI D PERSEU L MELIS MA MACCIONI L SOLLAINO MC PAGLIETTI E CAO A GALANELLO R

Citation: D. Gasperini et al., HETEROZYGOUS BETA-THALASSEMIA WITH THALASSEMIA-INTERMEDIA PHENOTYPE, American journal of hematology, 57(1), 1998, pp. 43-47

HOMOZYGOUS BETA(0)39 NONSENSE MUTATION ASSOCIATED WITH C-]T AT 158G(Y)HPFH AND 4BP DELETION (-225-222) IN THE PROMOTER OF THE (A)Y GENE

Authors: GONZALEZ FA ROPERO P MARTI E SANCHEZ J ARMADA B ANGUITA E ROSATELLI C GALANELLO R VILLEGAS A

Citation: Fa. Gonzalez et al., HOMOZYGOUS BETA(0)39 NONSENSE MUTATION ASSOCIATED WITH C-]T AT 158G(Y)HPFH AND 4BP DELETION (-225-222) IN THE PROMOTER OF THE (A)Y GENE, British Journal of Haematology, 102(1), 1998, pp. 47-47

HB PUTTELANGE [BETA-140(H19)ALA-]VAL] IN AN ITALIAN MAN WITH POLYCYTHEMIA

Authors: GALANELLO R PALEARI R PERSEU L BARELLA S MACCIONI L CAO A MULAS G COCCO E MOSCA A

Citation: R. Galanello et al., HB PUTTELANGE [BETA-140(H19)ALA-]VAL] IN AN ITALIAN MAN WITH POLYCYTHEMIA, Hemoglobin, 21(1), 1997, pp. 17-26

MOLECULAR DIAGNOSIS AND CARRIER SCREENING FOR BETA-THALASSEMIA

Authors: CAO A SABA L GALANELLO R ROSATELLI C

Citation: A. Cao et al., MOLECULAR DIAGNOSIS AND CARRIER SCREENING FOR BETA-THALASSEMIA, JAMA, the journal of the American Medical Association, 278(15), 1997, pp. 1273-1277

HYPERBILIRUBINEMIA IN HETEROZYGOUS BETA-THALASSEMIA IS RELATED TO CO-INHERITED GILBERTS-SYNDROME

Authors: GALANELLO R PERSEU L MELIS MA CIPOLLINA L BARELLA S GIAGU N TURCO MP MACCIONI O CAO A

Citation: R. Galanello et al., HYPERBILIRUBINEMIA IN HETEROZYGOUS BETA-THALASSEMIA IS RELATED TO CO-INHERITED GILBERTS-SYNDROME, British Journal of Haematology, 99(2), 1997, pp. 433-436

HYPERBILIRUBINEMIA AND GILBERTS-SYNDROME IN THALASSEMIA MAJOR AND INTERMEDIA

Authors: GALANELLO R CIPOLLINA L BARELLA LS GIAGU L LAI E CAO A

Citation: R. Galanello et al., HYPERBILIRUBINEMIA AND GILBERTS-SYNDROME IN THALASSEMIA MAJOR AND INTERMEDIA, Blood, 90(10), 1997, pp. 572-572

SIMULTANEOUS AUTOMATED-DETERMINATION OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE AND 6-PHOSPHOGLUCONATE DEHYDROGENASE-ACTIVITIES IN WHOLE-BLOOD

Authors: MOSCA A PALEARI R ROSTI E LUZZANA M BARELLA S SOLLAINO C GALANELLO R

Citation: A. Mosca et al., SIMULTANEOUS AUTOMATED-DETERMINATION OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE AND 6-PHOSPHOGLUCONATE DEHYDROGENASE-ACTIVITIES IN WHOLE-BLOOD, European journal of clinical chemistry and clinical biochemistry, 34(5), 1996, pp. 431-438

CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF A VARIANT TRANSLOCATIONASSOCIATED WITH ACUTE PROMYELOCYTIC LEUKEMIA AND INVOLVING CHROMOSOME-11, CHROMOSOME-15 AND CHROMOSOME-17

Authors: CASULA L ARCHIDIACONO N PAU MG ADDIS M MURA R GALANELLO R BIDDAU P CAO A NUCARO A

Citation: L. Casula et al., CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF A VARIANT TRANSLOCATIONASSOCIATED WITH ACUTE PROMYELOCYTIC LEUKEMIA AND INVOLVING CHROMOSOME-11, CHROMOSOME-15 AND CHROMOSOME-17, Leukemia, 10(10), 1996, pp. 1655-1657

BLOOD-GLUCOSE NORMALIZATION-INDUCED HEMOLYSIS IN 3 ADOLESCENTS WITH TYPE-1 DIABETES-MELLITUS AT ONSET AND UNKNOWN G-6-PD DEFICIENCY

Authors: VANELLI M LUCENTINI L PICCO P GALANELLO R CHIARI G ADINOLFI B STREET ME

Citation: M. Vanelli et al., BLOOD-GLUCOSE NORMALIZATION-INDUCED HEMOLYSIS IN 3 ADOLESCENTS WITH TYPE-1 DIABETES-MELLITUS AT ONSET AND UNKNOWN G-6-PD DEFICIENCY, Journal of pediatric endocrinology & metabolism, 9(2), 1996, pp. 193-196

CLINICAL-EXPERIENCE OF MANAGEMENT OF THALASSEMIA - THE SARDINIAN EXPERIENCE

Authors: CAO A GALANELLO R ROSATELLI MC ARGIOLU F DEVIRGILIIS S

Citation: A. Cao et al., CLINICAL-EXPERIENCE OF MANAGEMENT OF THALASSEMIA - THE SARDINIAN EXPERIENCE, Seminars in hematology, 33(1), 1996, pp. 66-75

GENETIC-BASIS OF HYPERBILIRUBINEMIA IN HETEROZYGOUS BETA-THALASSEMIA

Authors: GALANELLO R PERSEU L MELIS MA BARELLA S GIAGU N TURCO MP MACCIONI O CAO A

Citation: R. Galanello et al., GENETIC-BASIS OF HYPERBILIRUBINEMIA IN HETEROZYGOUS BETA-THALASSEMIA, Blood, 88(10), 1996, pp. 2825-2825

MOLECULAR-BASIS OF THALASSEMIA MAJOR

Authors: GALANELLO R

Citation: R. Galanello, MOLECULAR-BASIS OF THALASSEMIA MAJOR, International journal of pediatric hematology/oncology, 2(5), 1995, pp. 383-396

CONTROVERSIES IN PHARMACOTHERAPY OF BETA- THALASSEMIA

Authors: GALANELLO R DIPALMA A

Citation: R. Galanello et A. Dipalma, CONTROVERSIES IN PHARMACOTHERAPY OF BETA- THALASSEMIA, Rivista italiana di pediatria, 21(4), 1995, pp. 456-458

VARIABILITY OF THE IMMUNOGLOBULIN HEAVY-CHAIN CONSTANT-REGION LOCUS -A POPULATION STUDY

Authors: BRUSCO A CARIOTA U BOTTARO A BOCCAZZI C PLEBANI A UGAZIO AG GALANELLO R GUERRA MG CARBONARA AO

Citation: A. Brusco et al., VARIABILITY OF THE IMMUNOGLOBULIN HEAVY-CHAIN CONSTANT-REGION LOCUS -A POPULATION STUDY, Human genetics, 95(3), 1995, pp. 319-326

EVALUATION OF AN AUTOMATIC HPLC ANALYZER FOR THALASSEMIA AND HEMOGLOBIN-VARIANTS SCREENING

Authors: GALANELLO R BARELLA S GASPERINI D PERSEU L PAGLIETTI E SOLLAINO C PADERI L PIRRONI MG MACCIONI L MOSCA A

Citation: R. Galanello et al., EVALUATION OF AN AUTOMATIC HPLC ANALYZER FOR THALASSEMIA AND HEMOGLOBIN-VARIANTS SCREENING, Journal of automatic chemistry, 17(2), 1995, pp. 73-76

A PROMOTER MUTATION, C-]T AT POSITION -92, LEADING TO SILENT BETA-THALASSEMIA

Authors: ROSATELLI MC FAA V MELONI A FIORENZA F GALANELLO R GASPERINI D AMENDOLA G CAO A

Citation: Mc. Rosatelli et al., A PROMOTER MUTATION, C-]T AT POSITION -92, LEADING TO SILENT BETA-THALASSEMIA, British Journal of Haematology, 90(2), 1995, pp. 483-485

RELATIONSHIP BETWEEN TRANSFUSION REGIMEN AND SUPPRESSION OF ERYTHROPOIESIS IN BETA-THALASSEMIA MAJOR

Authors: CAZZOLA M DESTEFANO P PONCHIO L LOCATELLI F BEGUIN Y DESSI C BARELLA S CAO A GALANELLO R

Citation: M. Cazzola et al., RELATIONSHIP BETWEEN TRANSFUSION REGIMEN AND SUPPRESSION OF ERYTHROPOIESIS IN BETA-THALASSEMIA MAJOR, British Journal of Haematology, 89(3), 1995, pp. 473-478

THE PROGNOSIS FOR ADULTS WITH THALASSEMIA MAJOR - SARDINIA 1995

Authors: LAI E BELLUZZO N MURACA M DANEMAN R CAO A DEVIRGILIIS S LISCI V GALANELLO R OLIVIERI NF

Citation: E. Lai et al., THE PROGNOSIS FOR ADULTS WITH THALASSEMIA MAJOR - SARDINIA 1995, Blood, 86(10), 1995, pp. 989-989

BETA-DEGREES-THALASSEMIA INTERMEDIA IN SARDINIA

Authors: GALANELLO R LAI E CAO A

Citation: R. Galanello et al., BETA-DEGREES-THALASSEMIA INTERMEDIA IN SARDINIA, Blood, 86(10), 1995, pp. 1927-1927

A NOVEL DELTA(0) THALASSEMIA MUTATION - TGG-]TAG (TRP-]STOP) AT CODON-37

Authors: GASPERINI D PERSEU L COSSU P PODDA R CAO A GALANELLO R

Citation: D. Gasperini et al., A NOVEL DELTA(0) THALASSEMIA MUTATION - TGG-]TAG (TRP-]STOP) AT CODON-37, Human mutation, 3(1), 1994, pp. 71-72

INTERFERON-ALPHA-2A THERAPY IN CML - DISAPPEARANCE OF BCR ABL TRANSCRIPT IN A CASE OF LONG-LASTING CONTINUOUS CYTOGENETIC CONVERSION/

Authors: PARDINI S ADDIS M DORE F BONFIGLI S NIEDDU RM GALANELLO R LONGINOTTI M PAU MG

Citation: S. Pardini et al., INTERFERON-ALPHA-2A THERAPY IN CML - DISAPPEARANCE OF BCR ABL TRANSCRIPT IN A CASE OF LONG-LASTING CONTINUOUS CYTOGENETIC CONVERSION/, Haematologica, 79(6), 1994, pp. 540-541

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