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Results 1 to 25 of 299

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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

MOLECULAR MECHANISM ACCOUNTING FOR MILDER TYPES OF THALASSEMIA MAJORFURBETTA M; TUVERI T; ROSATELLI C et al.1983; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1983; VOL. 103; NO 1; PP. 35-39; BIBL. 20 REF.Article

ANEMIES HEREDITAIRES: BASES GENETIQUES, CARACTERISTIQUES CLINIQUES, DIAGNOSTIC ET TRAITEMENTBOYO A; CAO A; DER KALOUSTIAN V et al.1983; BULLETIN OF THE WORLD HEALTH ORGANIZATION; ISSN 0366-4996; CHE; DA. 1983; VOL. 61; NO 2; PP. 179-198; 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

CHRONIC LIVER DISEASE IN TRANSFUSION-DEPENDENT THALASSAEMIA: HEPATITIS B VIRUS MARKER STUDIESDE VIRGILIIS S; FIORELLI G; FARGION S et al.1980; J. CLIN. PATHOL.; ISSN 0021-9746; GBR; DA. 1980; VOL. 33; NO 10; PP. 949-953; BIBL. 22 REF.Article

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

SCHWARTZ-JAMPEL SYNDROME. CLINICAL, ELECTROPHYSIOLOGICAL AND HISTOPATHOLOGICAL STUDY OF A SEVERE VARIANT.CAO A; CIANCHETTI C; CALISTI L et al.1978; J. NEUROL. SCI.; NETHERL.; DA. 1978; VOL. 35; NO 2-3; PP. 175-187; BIBL. 1 P.Article

A CASE OF EXTRA SMALL ACROCENTRIC BISATELLITED CHROMOSOME IN A NON MONGOLOID CHILDFURBETTA M; ROSI G; BIAGIONI M et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 3; PP. 259-263; BIBL. 11 REF.Article

A CASE OF TRISOMY OF THE SHORT ARMS OF CHROMOSOME NO 4 WITH TRANSLOCATION T (4 P 21 P; 4 Q 21 Q) IN THE MOTHER = UN CAS DE TRISOMIE DES BRAS COURTS DU CHROMOSOME NO 4 AVEC TRANSLOCATION T (4 P 21 P; 4 Q 21 Q) CHEZ LA MERE)FURBETTA M; ROSI G; COSSU P et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 2; PP. 87-91; BIBL. 13 REF.Article

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

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