SUBPOPULATIONS OF T LYMPHOCYTES IN PRIMARY BILIARY CIRRHOSISCANCELLIERI V; SCARONI C; VERNACE SJ et al.1981; CLIN. IMMUNOL. IMMUNOPATHOL.; ISSN 0090-1229; USA; DA. 1981; VOL. 20; NO 2; PP. 255-260; BIBL. 38 REF.Article

INFEZIONE DA VIRUS B NEI PAZIENTI CON ACRODERMATIE PAPULOSA. = INFECTION A VIRUS B CHEZ LES PATIENTS ATTEINTS D'ACRODERMITE PAPULEUSESCARONI C; CANCELLIERI V; BORZIO F et al.1978; FOLIA ALLERGOL. IMMUNOL. CLIN.; ITA; DA. 1978; VOL. 25; NO 2; PP. 165-168; ABS. ENG; BIBL. 15 REF.Article

CRYPTIC 21-HYDROXYLASE DEFICIENCY IN FAMILIES OF PATIENTS WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIALEVINE LS; DUPONT B; LORENZEN F et al.1980; J. CLIN. ENDOCRINOL. METAB.; ISSN 0021-972X; USA; DA. 1980; VOL. 51; NO 6; PP. 1316-1324; BIBL. 36 REF.Article

GENETIC AND HORMONAL CHARACTERIZATION OF CRYPTIC 21-HYDROXYLASE DEFICIENCYLEVINE LS; DUPONT B; LORENZEN F et al.1981; J. CLIN. ENDOCRINOL. METAB.; ISSN 0021-972X; USA; DA. 1981; VOL. 53; NO 6; PP. 1193-1198; BIBL. 12 REF.Article

PERIPHERAL AND RENAL VEIN PLASMA RENIN ACTIVITY IN HYPERTENSIVE UROLOGICAL PATIENTSARMANINI D; FALLO F; OPOCHER G et al.1982; BR. J. UROL.; ISSN 0007-1331; GBR; DA. 1982; VOL. 54; NO 4; PP. 348-353; BIBL. 19 REF.Article

HLA GENOTYPES AND HLA-LINKED GENETIC MARKERS IN ITALIAN PATIENTS WITH CLASSICAL 21-HYDROXYLASE DEFICIENCYPOLLACK MS; NEW MI; O'NEILL GJ et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 3; PP. 331-337; BIBL. 27 REF.Article

DELTA INFECTION AND LIVER DISEASE IN HEMOPHILIC CARRIERS OF HEPATITIS B SURFACE ANTIGENRIZZETTO M; MORELLO C; MANNUCCI PM et al.1982; J. INFECT. DIS.; ISSN 0022-1899; USA; DA. 1982; VOL. 145; NO 1; PP. 18-22; BIBL. 15 REF.Article

Incidentally discovered adrenal tumors : Endocrine and scintigraphic correlatesBARZON, L; SCARONI, C; SONINO, N et al.The Journal of clinical endocrinology and metabolism. 1998, Vol 83, Num 1, pp 55-62, issn 0021-972XArticle

Pharmacokinetics of oral and rectal flurbiprofen in childrenSCARONI, C; MAZZONI, P. L; DAMICO, E et al.European journal of clinical pharmacology. 1984, Vol 27, Num 3, pp 367-369, issn 0031-6970Article

HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21 OHDS)SCARONI, C; ORLANDINI, E; VENTURI PASINI, C et al.Journal of endocrinological investigation (Testo stampato). 1986, Vol 9, Num 1, pp 65-70, issn 0391-4097Article

Effect of metoprolol+chlorthalidone on the cardio-circulatory response to isometric exercise in essential hypertensionFALLO, F; BUI, F; SCARONI, C et al.Current therapeutic research. 1983, Vol 34, Num 4, pp 581-586, issn 0011-393XArticle

Unilateral adrenal tumor, erectile dysfunction and infertility in a patient with 21-hydroxylase deficiency: Effects of glucocorticoid treatment and surgerySCARONI, C; FAVIA, G; LUMACHI, F et al.Experimental and clinical endocrinology & diabetes. 2003, Vol 111, Num 1, pp 41-43, issn 0947-7349, 3 p.Article

Deletion within the CYP17 gene together with insertion of foreign DNA is the cause of combined complete 17α-hydroxylase/17,20-lyase deficiency in an Italian patientBIASON, A; MANTERO, F; SCARONI, C et al.Molecular endocrinology (Baltimore, Md.). 1991, Vol 5, Num 12, pp 2037-2045, issn 0888-8809Article

Single-dose pharmacokinetics of flurbiprofen granules and tablets in healthy volunteersBENVENUTI, C; GAMBARO, V; LODI, F et al.International journal of clinical pharmacology, therapy and toxicology (1980). 1989, Vol 27, Num 7, pp 334-337, issn 0174-4879Article

Pharmacokinetics of two new oral formulations of ibuprofenBENVENUTI, C; CANCELLIERI, V; GAMBARO, V et al.International journal of clinical pharmacology, therapy and toxicology (1980). 1986, Vol 24, Num 6, pp 308-312, issn 0174-4879Article

Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau diseasePIERMAROCCHI, S; LO GIUDICE, G; PILOTTO, E et al.Graefe's archive for clinical and experimental ophthalmology. 2000, Vol 238, Num 7, pp 615-620, issn 0721-832XArticle

Peroxisome proliferator-activated receptor γ in the human pituitary gland: Expression and splicing pattern in adenomas versus normal pituitaryOCCHI, G; ALBIGER, N; BERLUCCHI, S et al.Journal of neuroendocrinology. 2007, Vol 19, Num 7, pp 552-559, issn 0953-8194, 8 p.Article

Volumetric MRI analysis of hippocampal subregions in Cushing's disease: A model for glucocorticoid neural modulationTOFFANIN, T; NIFOSI, F; MANTERO, F et al.European psychiatry. 2011, Vol 26, Num 1, pp 64-67, issn 0924-9338, 4 p.Article

Steroids and hypertensionMANTERO, F; ARMANINI, D; BOSCARO, M et al.Journal of steroid biochemistry and molecular biology. 1991, Vol 40, Num 1-3, pp 35-44, issn 0960-0760Conference Paper

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Predictors of morbidity and mortality in acromegaly: an Italian surveyAROSIO, M; REIMONDO, G; MINUTO, F et al.European journal of endocrinology. 2012, Vol 167, Num 2, pp 189-198, issn 0804-4643, 10 p.Article