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au.\*:("GALANELLO, R")

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ALPHA GLOBIN GENE ANALYSIS IN A SARDINIAN FAMILY WITH INTERACTING ALPHA AND BETA THALASSAEMA GENESMELIS MA; GALANELLO R; CAO A et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 53; NO 4; PP. 667-671; BIBL. 12 REF.Article

QUANTITATION OF HBA2 WITH DE-52 MICROCHROMATOGRAPHY IN WHOLE BLOOD AS SCREENING TEST FOR BETA -THALASSEMIA HETEROZYGOTES.GALANELLO R; MELIS MA; MURONI P et al.1977; ACTA HAEMATOL.; SUISSE; DA. 1977; VOL. 57; NO 1; PP. 32-36; BIBL. 8 REF.Article

HEMOGLOBIN A2 IN IRON DEFICIENT BETA -THALASSEMIA HETEROZYGOTESGALANELLO R; RUGGERI R; ADDIS M et al.1981; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1981; VOL. 5; NO 6; PP. 613-618; BIBL. 7 REF.Article

PROSPECTIVE STUDY OF RED BLOOD CELL INDICES, HEMOGLOBIN A2, AND HEMOGLOBIN F IN INFANTS HETEROZYGOUS FOR BETA -THALASSEMIAGALANELLO R; MELIS MA; RUGGERI R et al.1981; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1981; VOL. 99; NO 1; PP. 105-108; BIBL. 14 REF.Article

Genotype-phenotype correlations in β-thalassemiasCAO, A; GALANELLO, R; ROSATELLI, M. C et al.Blood reviews. 1994, Vol 8, Num 1, pp 1-12, issn 0268-960XArticle

SERUM FERRITIN LEVELS IN HEMOGLOBIN H DISEASEGALANELLO R; NELIS MA; PAGLIETTI E et al.1983; ACTA HAEMATOLOGICA; ISSN 0001-5792; CHE; DA. 1983; VOL. 69; NO 1; PP. 56-58; BIBL. 7 REF.Article

INTERACTION OF ALPHA - AND DELTA BETA O-THALASSAEMIA: HAEMATOLOGICAL FEATURES AND GLOBIN CHAIN SYNTHESIS ANALYSISGALANELLO R; FU BETTA M; MELIS MA et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 1; PP. 40-42; BIBL. 18 REF.Article

INTERACTION BETWEEN THE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND THALASSAEMIA GENES AT PHENOTYPE LEVELSANNA G; FRAU F; MELIS MA et al.1980; BRIT. J. HAEMATOL.; GBR; DA. 1980; VOL. 44; NO 4; PP. 555-561; BIBL. 16 REF.Article

HAEMATOLOGICAL CHARACTERISTICS OF THE BETA 0 THALASSAEMIA TRAIT IN SARDINIAN CHILDRENGALANELLO R; DE VIRGILIIS S; ADDIS M et al.1980; J. CLIN. PATHOL.; ISSN 0021-9746; GBR; DA. 1980; VOL. 33; NO 10; PP. 946-948; BIBL. 12 REF.Article

Percentile curves for red cell indices of β°-thalassaemia heterozygotes in infancy and childhoodGALANELLO, R; LILLIU, F; BERTOLINO, F et al.European journal of pediatrics. 1991, Vol 150, Num 6, pp 413-415, issn 0340-6199Article

HEMATOLOGICAL CHARACTERISTICS OF SARDINIAN ALPHA -THALASSEMIA CARRIERS DETECTED IN A POPULATION STUDYMELIS MA; ROSATELLI C; FALCHI AM et al.1980; ACTA HAEMATOL.; CHE; DA. 1980; VOL. 63; NO 1; PP. 32-36; BIBL. 10 REF.Article

ALPHA -THALASSAEMIA IN SARDINIAN INFANTSGALANELLO R; DIANA G; FURBETTA M et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 5; PP. 357-362; BIBL. 25 REF.Article

Thallassemias in sardinia : molecular pathology, phenotype-genotype correlation, and preventionCAO, A; ROSATELLI, C; PIRASTU, M et al.The American journal of pediatric hematology/oncology. 1991, Vol 13, Num 2, pp 179-188, issn 0192-8562Article

Mechanism of Hb F stimulation by S-stage compounds: in vitro studies with bone marrow cells exposed to 5-azacytidine, Ara-C, or hydroxyureaGALANELLO, R; STAMATOYANNOPOULOS, G; PAPAYANNOPOULOU, T et al.The Journal of clinical investigation. 1988, Vol 81, Num 4, pp 1209-1216, issn 0021-9738Article

Stimulation of F-cell production in patients with sicklecell anemia treated with cytarabine or hydroxyureaVEITH, R; GALANELLO, R; PAPAYANNOPOULOU, T et al.The New England journal of medicine. 1985, Vol 313, Num 25, pp 1571-1575, issn 0028-4793Article

DELTA BETA (F)-THALASSAEMIA IN SARDINIACAO A; MELIS MA; GALANELLO R et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 3; PP. 184-192; BIBL. 36 REF.Article

INTERACTION OF ALPHA AND BETA THALASSAEMIA GENES IN TWO SARDINIAN FAMILIESFURBETTA M; GALANELLO R; XIMENES A et al.1979; BRIT. J. HAEMATOL.; GBR; DA. 1979; VOL. 41; NO 2; PP. 203-210; BIBL. 22 REF.Article

α-Thalassemia carrier identification by DNA analysis in the screening for thalassemiaGALANELLO, R; SOLLAINO, C; PAGLIETTI, E et al.American journal of hematology. 1998, Vol 59, Num 4, pp 273-278, issn 0361-8609Article

Variability of the immunoglobulin heavy chain constant region locus : a population studyBRUSCO, A; CARIOTA, U; BOTTARO, A et al.Human genetics. 1995, Vol 95, Num 3, pp 319-326, issn 0340-6717Article

Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin β-thalassemia intermedia patientsGALANELLO, R; BARELLA, S; TURCO, M. P et al.Blood. 1994, Vol 83, Num 2, pp 561-565, issn 0006-4971Article

Prenatal diagnosis of inherited hemoglobinopathiesCAO, A; ROSATELLI, C; GALANELLO, R et al.Indian journal of pediatrics. 1989, Vol 56, Num 6, pp 707-717, issn 0019-5456, 11 p.Article

A genetic combination of silent β-thalassaemia, high Hb A2 β-thalassaemia, and single α globin gene deletion causing mild thalassaemia intermadiaGALANELLO, R; MACCIONI, L; ROSATELLI, M. C et al.Journal of medical genetics. 1984, Vol 21, Num 2, pp 153-156, issn 0022-2593Article

Cholelithiasis and Gilbert's syndrome in homozygous β-thalassaemiaGALANELLO, R; PIRAS, S; BARELLA, S et al.British journal of haematology. 2001, Vol 115, Num 4, pp 926-928, issn 0007-1048Article

Cytogenetic and molecular characterization of a variant translocation associated with acute promyelocytic leukemia and involving chromosomes 11, 15 and 17CASULA, L; ARCHIDIACONO, N; GRAZIA PAU, M et al.Leukemia. 1996, Vol 10, Num 10, pp 1655-1657, issn 0887-6924Article

Healing of broken human chromosomes by the addition of telomeric repeatsFLINT, J; CRADDOCK, C. F; VILLEGAS, A et al.American journal of human genetics. 1994, Vol 55, Num 3, pp 505-512, issn 0002-9297Article

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