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au.\*:("CAMASCHELLA C")

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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

Juvenile haemochromatosisCAMASCHELLA, C.Baillière's clinical gastroenterology. 1998, Vol 12, Num 2, pp 227-235, issn 0950-3528Article

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

Molecular genetics and control of iron metabolism in hemochromatosisPIETRANGELO, A; CAMASCHELLA, C.Haematologica - Journal of hematology. 1998, Vol 83, Num 5, pp 456-461Article

L'HBF NELLE SINDROMI TALASSEMICHE = L'HEMOGLOBINE F DANS LES SYNDROMES THALASSEMIQUESMAZZA U; CAMASCHELLA C; GUERRASIO A et al.1978; G. ACCAD. MED. TORINO; ITA; DA. 1978 PUBL. 1979; VOL. 141; NO 1-12; PP. 81-82; BIBL. 2 REF.Article

Thalassemia intermediaCAMASCHELLA, C; CAPPELLINI, M. D.Haematologica (Roma). 1995, Vol 80, Num 1, pp 58-68, issn 0390-6078Article

LA LAPAROTOMIA DIAGNOSTICA NELLA MALATTIA DI HODGKIN. = LA LAPAROTOMIE DIAGNOSTIQUE DANS LA MALADIE DE HODGKINROLFO F; ARDIZZONE G; CAMASCHELLA C et al.1977; MINERVA CHIR.; ITAL.; DA. 1977; VOL. 32; NO 20; PP. 1265-1274; ABS. ANGL.; BIBL. 32 REF.Article

GAMMA CHAIN COMPOSITION IN FIVE ITALIAN NEWBORNS HETEROZYGOUS FOR HB F MALTA GGAMMA 117 HIS->ARGMAZZA U; MELONI T; DAVID O et al.1980; BRIT. J. HAEMATOL.; GBR; DA. 1980; VOL. 44; NO 1; PP. 93-99; BIBL. 2 P.Article

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

MOLECULAR COMPARISON OF DELTA BETA -THALASSEMIA AND HEREDITARY PERSISTANCE OF FETAL HEMOGLOBIN DNAS: EVIDENCE OF A REGULATORY AREA.OTTOLENGHI S; GIGLIONI B; TARAMELLI R et al.1982; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 7; PP. 2347-2351; BIBL. 32 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

Hereditary hemochromatosis : Recent advances in molecular genetics and clinical managementCAMASCHELLA, C; PIPERNO, A.Haematologica (Roma). 1997, Vol 82, Num 1, pp 77-84, issn 0390-6078Conference Paper

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

Feasibility of molecular diagnosis of α-Thalassemia in the evaluation of microcytosisSIVERA, P; ROETTO, A; MAZZA, U et al.Haematologica (Roma). 1997, Vol 82, Num 5, pp 592-593, issn 0390-6078Article

POLYMORPHISM OF HUMAN FETAL HAEMOGLOBIN STUDIED BY ISOELECTRIC FOCUSINGCHEN MAROTEL J; BEUZARD Y; KAC TRUNG B et al.1980; F.E.B.S. LETTERS; NLD; DA. 1980; VOL. 115; NO 1; PP. 68-70; BIBL. 16 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

GY AND AY GLOBIN CHAINS SEPARATION AND QUANTITATION BY ISOELECTRIC FOCUSINGCOMI P; GIGLIONI B; OTTOLENGHI S et al.1979; BIOCHEM. BIOPHYS. RES. COMMUNIC.; USA; DA. 1979; VOL. 87; NO 1; PP. 1-8; BIBL. 17 REF.Article

A spontaneous mutation causing unstable Hb Hammersmith : detection of the β42 TTT→TCT change by CCM and direct sequencingDIANZANI, I; RAMUS, S; COTTON, R. G. H et al.British journal of haematology. 1991, Vol 79, Num 1, pp 127-129, issn 0007-1048Article

Clinical and haematological improvement induced by etidronate in a patient with idiopathic myelofibrosis and oesteosclerosisSIVERA, P; CESANO, L; GUERRASIO, A et al.British journal of haematology. 1994, Vol 86, Num 2, pp 397-398, issn 0007-1048Article

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