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LA MAPPA AMINOACIDICA DEL PEPTIDE ABNORME NELL' IDENTIFICAZIONE DELL' HB J OXFORD = LA CARTE AMINOACIDIQUE DES PEPTIDES ANORMAUX DANS L'IDENTIFICATION DE L'HB J OXFORDPICH PG; MAZZA U; SAGLIO G et al.1975; HAEMATOLOGICA; ITAL.; DA. 1975; VOL. 60; NO 1; PP. 38-45; ABS. ANGL.; BIBL. 2 P.Article

Single or multistep origin of hemopoietic tumors : the condition of clonality studiesLO COCO, F; SAGLIO, G.Leukemia. 1995, Vol 9, Num 9, pp 1586-1589, issn 0887-6924Article

Recent advances in diagnosis of hemoglobinopathiesCAMASCHELLA, C; SAGLIO, G.Critical reviews in oncology/hematology. 1993, Vol 14, Num 2, pp 89-105, issn 1040-8428Article

MODELITA' DI ESSPRESSIONE DEI GENI GAMMA NEL PASSAGIO DALL'ERITROPOIESI FETALE A QUELLA ADULTA = MODALITES D'EXPRESSION DES GENES GAMMA DANS LE PASSAGE DE L'ERYTHROPOIESE FOETALE A L'ERYTHROPOIESE ADULTESAGLIO G; DAVID O; FABRIS C et al.1978; G. ACCAD. MED. TORINO; ITA; DA. 1978 PUBL. 1979; VOL. 141; NO 1-12; PP. 78-80; BIBL. 6 REF.Article

Cytogenetic remission induced by interferon-α in a myeloproliferative disorder with trisomy 8PETRINI, M; SIMI, P; SAGLIO, G et al.British journal of haematology. 1996, Vol 92, Num 4, pp 941-943, issn 0007-1048Article

ANALYSIS OF THE Y CHAINS IN A HOMOZYGOTE FOR HPFH NEGRO TYPE AND IN THREE RELATED HETEROZYGOTESGUERRASIO A; ACQUAYE CTA; OLDHAM JH et al.1980; ACTA HAEMATOL.; CHE; DA. 1980; VOL. 63; NO 3; PP. 146-150; BIBL. 20 REF.Article

CLINICAL AND HAEMATOLOGICAL DATA IN 254 CASES OF BETA-THALASSAEMIA TRAIT IN ITALYMAZZA U; SAGLIO G; CALIGARIS CAPPIO F et al.1976; BRIT. J. HAEMATOL.; G.B.; DA. 1976; VOL. 33; NO 1; PP. 91-99; BIBL. 21 REF.Article

OMOZIGOSI DREPANOCITICA DI ECCEZIONALE SOPRAVOIVENZA: CASO CLINICO = HOMOZYGOTIE DREPANOCYTAIRE AVEC SURVIE EXCEPTIONNELLE: CAS CLINIQUECIOCCA VASINO MA; FURLANI C; BERTELLO PD et al.1979; MINERVA MED.; ITA; DA. 1979; VOL. 70; NO 5; PP. 413-417; ABS. ENG; BIBL. 14 REF.Article

INTERACTION BETWEEN HB HASHARON AND ALPHA -THALASSEMIA: AN APPROACH TO THE PROBLEM OF THE NUMBER OF HUMAN ALPHA LOCI.PICH P; SAGLIO G; CAMASCHELLA C et al.1978; BLOOD; U.S.A.; DA. 1978; VOL. 51; NO 2; PP. 339-346; BIBL. 1 P.Article

THE RELATIONSHIP BETWEEN ANEMIA, FECAL, STECOBILINOGEN, ERYTHROCYTE SURVIVAL, AND GLOBIN SYNTHESIS IN HETEROZYGOTES FOR BETA -THALASSEMIA. = LES RELATIONS ENTRE L'ANEMIE, LE STERCOBILINOGENE FECAL, LA DUREE DE VIE DES ERYTHROCYTES ET LA SYNTHESE DE LA GLOBINE CHEZ LES SUJETS PRESENTANT UNE BETA -THALASSEMIE A L'ETAT HETEROZYGOTEGALLO E; PICH P; RICCO G et al.1975; BLOOD; U.S.A.; DA. 1975; VOL. 46; NO 5; PP. 693-698; BIBL. 20 REF.Article

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TRATTAMENTO DEL MORBO DI HODGKIN: REVISIONE DI 90 CASI = TRAITEMENT DE LA MALADIE DE HODGKIN. REVUE DE 90 CASBUCHI G; MAZZA U; SAGLIO G et al.1979; ARCH. SCI. MED.; ITA; DA. 1979; VOL. 136; NO 2; PP. 295-302; ABS. ENG; BIBL. 59 REF.Article

FREQUENZA DEL TRATTO TALASSEMICO E DEL DEFICIT DI G-6-PD NELLA POPALAZIONE SCOLASTICA DI COMMUNI DELLA CINTURA TORINESE = FREQUENCE DE LA THALASSEMIE ET DU DEFICIT EN G-6-PD DANS LA POPULATION SCOLAIRE DES COMMUNES DE LA CEINTURE DE TURINSCAPPATICCI E; MINIERO R; TORTA F et al.1975; MINERVA PEDIATR.; ITAL.; DA. 1975; VOL. 27; NO 7; PP. 419-425; ABS. ANGL.; BIBL. 24 REF.Article

COMPOSITION OF THE GAMMA -CHAINS OF HUMAN FETAL HEMOGLOBIN AT BIRTH AND DURING INTRAUTERINE LIFESAGLIO G; MAZZA U; CAMASCHELLA C et al.1979; ACTA HAEMATOL.; CHE; DA. 1979; VOL. 62; NO 1; PP. 45-50; BIBL. 16 REF.Article

INDAGINI BIOCHIMICHE E CLINICHE SU DUE NUOVI CASI ITALIANI DI ETEROZIGOSI PER L'HB G-FERRARA = ETUDES BIOCHIMIQUES ET CLINIQUES SUR 2 NOUVEAUX CAS ITALIENS D'HETEROZYGOTIE POUR L'HEMOGLOBINE G-FERRAREGUERRASIO A; SAGLIO G; CAMASCHELLA C et al.1979; BOLL. SOC. ITAL. BIOL. SPER.; ITA; DA. 1979; VOL. 55; NO 10; PP. 967-973; ABS. ENG; BIBL. 17 REF.Article

SIGNIFICANCE OF A NEW TYPE OF HUMAN FETAL HEMOGLOBIN CARRYING A REPLACEMENT ISOLEUCINE->THREONINE AT POSITION 75 (E19) OF THE GAMMA CHAINRICCO G; MAZZA U; TURI RM et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 3; PP. 305-313; BIBL. 19 REF.Article

GGAMMA AND AGAMMA GLOBIN CHAIN SYNTHESIS IN BONE MARROW AND PERIPHERAL BLOOD OF BETA -THALASSAEMIA HOMOZYGOTESSAGLIO G; CAMASCHELLA C; GUERRASIO A et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 52; NO 2; PP. 225-231; BIBL. 2 P.Article

ELECTROPHORETIC SEPARATION OF ^AY AND ^GY HUMAN GLOBIN CHAINS IN NONIDET P-40GUERRASIO A; SAGLIO G; MAZZA U et al.1979; CLIN. CHIM. ACTA; NLD; DA. 1979; VOL. 99; NO 1; PP. 7-11; BIBL. 10 REF.Article

WT1 transcript amount discriminates secondary or reactive eosinophilia from idiopathic hypereosinophilic syndrome or chronic eosinophilic leukemiaCILLONI, D; MESSA, F; ROSSO, V et al.Leukemia. 2007, Vol 21, Num 7, pp 1442-1450, issn 0887-6924, 9 p.Article

Significant reduction of the hybrid BCR/ABL transcripts after induction and consolidation therapy is a powerful predictor of treatment response in adult philadelphia-positive acute lymphoblastic leukemiaPANE, F; CIMINO, G; MECUCCI, C et al.Leukemia. 2005, Vol 19, Num 4, pp 628-635, issn 0887-6924, 8 p.Article

Frequent mutation of bcl-6 proto-oncogene in high grade, but not low grade, MALT lymphomas of the gastrointestinal tractGAIDANO, G; CAPELLO, D; GLOGHINI, A et al.Haematologica - Journal of hematology. 1999, Vol 84, Num 7, pp 582-588Article

Rearrangements of bcl-6, bcl-2, c-myc and 6q deletion in B-diffuse large-cell lymphoma : Clinical relevance in 71 patientsVITOLO, U; GAIDANO, G; PASTORE, C et al.Annals of oncology. 1998, Vol 9, Num 1, pp 55-61, issn 0923-7534Article

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