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Results 1 to 25 of 197

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HAEMATOLOGICAL AND OBSTETRIC ASPECTS OF ANTENATAL DIAGNOSIS OF BETA -THALASSAEMIA: EXPERIENCE WITH 200 CASESCAO A; FURBETTA M; ANGIUS A et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 2; PP. 81-87; BIBL. 36 REF.Article

DIAGNOSIS OF THE BETA O THALASSEMIA TRAIT AT BIRTHFURBETTA M; ANGIUS A; TUVERI T et al.1981; HEMOGLOBIN; USA; DA. 1981; VOL. 5; NO 3; PP. 217-229; BIBL. 18 REF.Article

GENETIC AND MOLECULAR DIVERSITY IN NONDELETION HB H DISEASEHIGGS DR; PRESSLEY L; ALDRIDGE B et al.1981; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1981; VOL. 78; NO 9; PP. 5833-5837; BIBL. 22 REF.Article

BETA 0 THALASSEMIA IN SARDINIA IS CAUSED BY A NONSENSE MUTATIONTRECARTIN RF; LIEBHABER SA; CHANG JC et al.1981; J. CLIN. INVEST.; ISSN 0021-9738; USA; DA. 1981; VOL. 68; NO 4; PP. 1012-1017; BIBL. 38 REF.Article

A CASE OF D13 RING CHROMOSOMECOSSU P; DIANA G; MAMELI M et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 111-114; BIBL. 10 REF.Article

A FAMILY OF JUVENILE PROXIMAL SPINAL MUSCULAR ATROPHY WITH DOMINANT INHERITANCE.CAO A; CIANCHETTI C; CALISTI L et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 2; PP. 131-135; BIBL. 22 REF.Article

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

AN ANALYTICAL APPROACH TO SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY WITH THE ATTENUATION EFFECTSOUSSALINE FP; CAO A; LECOQ G et al.1982; EUROPEAN JOURNAL OF NUCLEAR MEDICINE; ISSN 0340-6997; DEU; DA. 1982; VOL. 7; NO 11; PP. 487-493; BIBL. 12 REF.Article

GLUCOSE-6-PHOSPHATE DEHYDROGENASE RED BLOOD CELL PHENOTYPE IN GD MEDITERRANEAN HETEROZYGOUS FEMALES AND HEMIZYGOUS MALES AT BIRTHSANNA G; FRAU F; DE VIRGILIIS S et al.1981; PEDIATR. RES.; ISSN 0031-3998; USA; DA. 1981; VOL. 15; NO 11; PP. 1443-1446; BIBL. 16 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

POLYMORPHISM OF DNA SEQUENCE IN THE BETA -GLOBIN GENE REGION. APPLICATION TO PRENATAL DIAGNOSIS OF BETA O THALASSEMIA IN SARDINIAYUET WAI KAN; LEE KY; FURBETTA M et al.1980; NEW ENGL. J. MED.; USA; DA. 1980; VOL. 302; NO 4; PP. 185-188; BIBL. 23 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

ATROFIA MUSCOLARE SPINALE PROSSIMALE TIPO II. STUDIO CLINICO, ELETTROFISIOLOGICO, ISTOPATOLOGICO ED ISTOCHIMICO = L'ATROPHIE MUSCULAIRE SPINALE PROXIMALE TYPE II. ETUDE CLINIQUE, ELECTROPHYSIOLOGIQUE, HISTOPATHOLOGIQUE ET HISTOCHIMIQUETANGHERONI W; CAO A; CIANCHETTI C et al.1974; MINERVA PEDIATR.; ITAL.; DA. 1974; VOL. 26; NO 22; PP. 1125-1145; BIBL. 1P.1/2Article

CHARACTERIZATION OF SERUM ALKALINE PHOSPHATASE IN INFANCY AND CHILDHOOD = LA CARACTERISATION DE LA PHOSPHATASE SERIQUE ALCALINE CHEZ LE NOURRISSON ET L'ENFANTCAO A; COPPA G; TRABALZA N et al.1972; Z. KINDERHEILKDE; DTSCH.; DA. 1972; VOL. 113; NO 4; PP. 289-296; ABS. ALLEM.; BIBL. 1P.1/2Serial Issue

IRON CHELATION IN TRANSFUSION-DEPENDENT THALASSEMIA WITH CHRONIC HEPATITISDE VIRGILIIS S; COSSU P; SANNA G et al.1982; ACTA HAEMATOL.; ISSN 0001-5792; CHE; DA. 1982; VOL. 67; NO 1; PP. 49-56; BIBL. 22 REF.Article

ALPHA-THALASSEMIA IN TWO MEDITERRANEAN POPULATIONSPIRASTU M; LEE KY; DOZY AM et al.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 60; NO 2; PP. 509-512; BIBL. 18 REF.Article

DIFFICULTIES IN ANTENATAL DIAGNOSIS OF INHERITED HAEMOGLOBINOPATHIES: GAMMA -CHAIN VARIANTSFURBETTA M; ANGIUS A; XIMENES A et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 47; NO 2; PP. 319-321; BIBL. 6 REF.Article

IRON OVERLOAD AND DESFORRIOXAMINE CHELATION THERAPY IN BETA -THALASSEMIA INTERMEDIACOSSU P; TOCCAFONDI C; VARDEU F et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 137; NO 3; PP. 267-271; BIBL. 14 REF.Article

PRENATAL DIAGNOSIS OF THALASSAEMIA MAJOR RESULTING FROM LEPORE/BETA -THALASSAEMIA GENOTYPEFURBETTA M; ANGIUS A; FALCHI AM et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 6; PP. 476-478; BIBL. 8 REF.Article

PREVENTION OF HOMOZYGOUS BETA -THALASSEMIA BY CARRIER SCREENING AND PRENATAL DIAGNOSIS IN SARDINIACAO A; GALANELLO R; MELIS MA et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 4; PP. 592-605; BIBL. 39 REF.Article

BETA -THALASSAEMIA TYPES IN SOUTHERN SARDINIACAO A; FURBETTA M; XIMENES A et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 3; PP. 196-199; BIBL. 19 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

PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA ASSOCIATED WITH RETINAL PIGMENT EPITHELIOPATHY = OPHTALMOPLEGIE PROGRESSIVE EXTERNE ASSOCIEE A UNE EPITHELIOPATHIE DE L'EPITHELIUM PIGMENTAIRE RETINIENDANIELE S; CIANCHETTI C; CAO A et al.1975; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1975; VOL. 80; NO 4; PP. 585-590; BIBL. 1 P. 1/2Article

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

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