Authors:
ARMANINI D
SPINELLA P
SIMONCINI M
BASSO A
ZOVATO S
POZZAN GB
DEPALO CB
BUCCIANTE G
KARBOWIAK I
Citation: D. Armanini et al., REGULATION OF CORTICOSTEROID RECEPTORS IN PATIENTS WITH ANOREXIA-NERVOSA AND CUSHINGS-SYNDROME, Journal of Endocrinology, 158(3), 1998, pp. 435-439
Authors:
POZZAN GB
ARMANINI D
CECCHETTO G
OPOCHER G
RIGON F
FASSINA A
ZACCHELLO F
Citation: Gb. Pozzan et al., HYPERTENSIVE CARDIOMEGALY CAUSED BY AN ALDOSTERONE-SECRETING ADENOMA IN A NEWBORN, Journal of endocrinological investigation, 20(2), 1997, pp. 86-89
Authors:
GRISOLIA G
GUARISO G
POZZAN GB
PERINI C
ZERBINATI L
CASELLA S
CATTELAN C
ZANCAN L
Citation: G. Grisolia et al., CHILDREN WITH NONORGANIC FAILURE-TO-THRIV E, THEIR PARENTS, THE PEDIATRICIAN AND THE CHILD-PSYCHIATRIST, Rivista italiana di pediatria, 22(5), 1996, pp. 752-759
Authors:
RUBELLO D
POZZAN GB
CASARA D
GIRELLI ME
BOCCATO S
RIGON F
BACCICHETTI C
PICCOLO M
BETTERLE C
BUSNARDO B
Citation: D. Rubello et al., NATURAL COURSE OF SUBCLINICAL HYPOTHYROIDISM IN DOWNS-SYNDROME - PROSPECTIVE-STUDY RESULTS AND THERAPEUTIC CONSIDERATIONS, Journal of endocrinological investigation, 18(1), 1995, pp. 35-40
Authors:
POZZAN GB
BOCCATO S
RIGON F
GIROTTO S
RUBELLO D
BACCICHETTI C
ZACCHELLO F
Citation: Gb. Pozzan et al., UNUSUAL PREVALENCE OF HYPERTHYROIDISM IN PATIENTS WITH DOWN-SYNDROME IN THE VENETO REGION, Rivista italiana di pediatria, 20(6), 1994, pp. 701-703
Authors:
POZZAN GB
RIGON F
MONCIOTTI C
DARIO C
CAROLLO C
CHIANDETTI L
Citation: Gb. Pozzan et al., HAMARTOMA OF TUBER-CINEREUM AND PRECOCIOU S PUBERTY IN A 10-MONTH MALE, Rivista italiana di pediatria, 20(3), 1994, pp. 269-271
Authors:
ARAGONA F
RAGAZZI R
POZZAN GB
DECARO R
MUNARI PF
MILANI C
GLAZEL GP
Citation: F. Aragona et al., CORRELATION OF TESTICULAR VOLUME, HISTOLOGY AND LHRH TEST IN ADOLESCENTS WITH IDIOPATHIC VARICOCELE, European urology, 26(1), 1994, pp. 61-66
Authors:
GREGGIO NA
CAMERAN M
RIGON F
RADETTI G
TIOZZO MP
POZZAN GB
ZACCHELLO F
Citation: Na. Greggio et al., THE SAME MOLECULAR GENOTYPE MAY EXPRESS DIFFERENT DISEASE PHENOTYPES IN 21-HYDROXYLASE DEFICIENCY, American journal of human genetics, 53(3), 1993, pp. 905-905