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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 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

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

SERUM FERRITIN, LIVER IRON STORES, AND LIVER HISTOLOGY IN CHILDREN WITH THALASSAEMIADE VIRGILIIS S; SANNA G; CORNACCHIA G et al.1980; ARCH. DIS. CHILDH.; GBR; DA. 1980; VOL. 55; NO 1; PP. 43-45; BIBL. 13 REF.Article

FAVISM IN GDMEDITERRANEAN HETEROZYGOUS FEMALESSANNA G; DE VIRGILIIS S; PALMAS C et al.1979; PEDIATR. RES.; USA; DA. 1979; VOL. 13; NO 7; PP. 812-816; BIBL. 14 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

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

STUDIO CLINICO ED IMMUNOLOGICO DI QUATRO PAZIENTI IN ETA PEDIATRICA CON MUCOCANDIDOSI IRONICA ASSOCIATA AD IPOPARATIROIDISMO = ETUDE CLINIQUE ET IMMUNOLOGIQUE DE QUATRE PATIENTS DE PEDIATRIE ATTEINTS DE CANDIDOSE CUTANEOMUQUEUSE CHRONIQUE ASSOCIEE A UNE HYPOPARATHYROIDIEMANTOVANI G; DE VIRGILIIS S; PUDDU A et al.1982; BOLLETTINO DELL'ISTITUTO SIEROTERAPICO MILANESE; ISSN 0021-2547; ITA; DA. 1982; VOL. 61; NO 3; PP. 239-244; ABS. ENG; BIBL. 23 REF.Article

AGENESIS OF THE CORPUS CALLOSUM, INFANTILE SPASMS, SPASTIC QUADRIPLEGIA, MICROCEPHALY AND SEVERE MENTAL RETARDATION IN THREE SIBLINGS.CAO A; CIANCHETTI C; SIGNORINI E et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 5; PP. 290-296; BIBL. 1 P.Article

Subacute sclerosing panencephalitis and hypoparathyroidismCIANCHETTI, C; DE VIRGILIIS, S; MARROSU, M. G et al.European neurology. 1985, Vol 24, Num 3, pp 149-152, issn 0014-3022Article

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

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

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

Clinical experience of management of thalassemia : The Sardinian experienceCAO, A; GALANELLO, R; ROSATELLI, M. C et al.Seminars in hematology. 1996, Vol 33, Num 1, pp 66-75, issn 0037-1963Article

Acute lymphoblastic leukemia in a child with constitutional ring chromosome 21FALCHI, A. M; OROFINO, M. G; NUCARO, A. L et al.Cancer genetics and cytogenetics. 1987, Vol 27, Num 2, pp 219-224, issn 0165-4608Article

Early and severe neurological features in a Wilson disease patient compound heterozygous for two frameshift mutationsANGIUS, A; DESSI, V; LOVICU, M et al.European journal of pediatrics. 1998, Vol 157, Num 2, pp 128-129, issn 0340-6199Article

Cerebellar vermis defect, oligophrenia, congenital ataxia, and hepatic fibrocirrhosis without coloboma and renal abnormalities: Report of three casesCOPPOLA, G; VAJRO, P; DE VIRGILIIS, S et al.Neuropediatrics. 2002, Vol 33, Num 4, pp 180-185, issn 0174-304XArticle

Saturation of the 5q31-q33 candidate region for coeliac diseasePERCOPO, S; BABRON, M.-C; WHALEN, M et al.Annals of human genetics. 2003, Vol 67, Num 3, pp 265-268, issn 0003-4800, 4 p.Article

In siblings of celiac children, rectal gluten challenge reveals gluten sensitization not restricted to celiac HLATRONCONE, R; GRECO, L; MAYER, M et al.Gastroenterology (New York, NY. 1943). 1996, Vol 111, Num 2, pp 318-324, issn 0016-5085Article

HLA-DQB1*O305 and -DQB1*0304 alleles among sardinians : evolutionary and practical implications for oligotypingCUCCA, F; FRAU, F; LAMPIS, R et al.Human immunology. 1994, Vol 40, Num 2, pp 143-149, issn 0198-8859Article

Depletion of trace elements and acute ocular toxicity induced by desferrioxamine in patients with thalassaemiaDE VIRGILIIS, S; CONGIA, M; TURCO, M. P et al.Archives of disease in childhood. 1988, Vol 63, Num 3, pp 250-255, issn 0003-9888Article

Immune reaction against the cytoskeleton in coeliac diseaseCLEMENTE, M. G; MUSU, M. P; FRAU, F et al.Gut. 2000, Vol 47, Num 4, pp 520-526, issn 0017-5749Article

A novel cystic fibrosis mutation : deletion of seventeen nucleotides at the exon 10-intron 10 boundary of the CFTR gene, in a Sardinian patientLEONI, G. B; ROSATELLI, M. C; COSSU, G et al.Human molecular genetics (Print). 1993, Vol 2, Num 1, pp 83-84, issn 0964-6906Article

Two cytochromes P450 are major hepatocellular autoantigens in autoimmune polyglandular syndrome type 1CLEMENTE, M. G; MELONI, A; OBERMAYER-STRAUB, P et al.Gastroenterology (New York, NY. 1943). 1998, Vol 114, Num 2, pp 324-328, issn 0016-5085Article

A gene dosage effect of the DQA1*0501/DQB1*0201 allelic combination influences the clinical heterogeneity of celiac diseaseCONGIA, M; CUCCA, F; FRAU, F et al.Human immunology. 1994, Vol 40, Num 2, pp 138-142, issn 0198-8859Article

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