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Results: 1-16 |
Results: 16
COMPARISON OF CLINICAL-RADIOLOGICAL AND MOLECULAR FINDINGS IN HYPOCHONDROPLASIA
Authors: PRINSTER C CARRERA P DELMASCHIO M WEBER G MAGHNIE M VIGONE MC MORA S TONINI G RIGON F BELUFFI G SEVERI F CHIUMELLO G FERRARI M
Citation: C. Prinster et al., COMPARISON OF CLINICAL-RADIOLOGICAL AND MOLECULAR FINDINGS IN HYPOCHONDROPLASIA, American journal of medical genetics, 75(1), 1998, pp. 109-112
HYPERTENSIVE CARDIOMEGALY CAUSED BY AN ALDOSTERONE-SECRETING ADENOMA IN A NEWBORN
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
FINAL HEIGHT IN NONGROWTH HORMONE-DEFICIENT CHILDREN TREATED WITH GROWTH-HORMONE
Authors: BERNASCONI S STREET ME VOLTA C MAZZARDO G BARTOLOTTA E BENSO L BONA G BORRELLI P BUZI F CAPPA M CHIABOTTO P DELUCA F DESANCTIS V KLAIN U LOCHE S MORABITO F PIETTA R PULLANO V RADETTI G RIGON F SARTORIO A TONINI G
Citation: S. Bernasconi et al., FINAL HEIGHT IN NONGROWTH HORMONE-DEFICIENT CHILDREN TREATED WITH GROWTH-HORMONE, Clinical endocrinology, 47(3), 1997, pp. 261-266
BIOCHEMICAL SELECTION OF PREPUBERTAL PATIENTS WITH ANDROGEN INSENSITIVITY SYNDROME BY SEX HORMONE-BINDING GLOBULIN RESPONSE TO THE HUMAN CHORIONIC-GONADOTROPIN TEST
Authors: BERTELLONI S FEDERICO G BARONCELLI GI CAVALLO L CORSELLO G LIOTTA A RIGON F SAGGESE G
Citation: S. Bertelloni et al., BIOCHEMICAL SELECTION OF PREPUBERTAL PATIENTS WITH ANDROGEN INSENSITIVITY SYNDROME BY SEX HORMONE-BINDING GLOBULIN RESPONSE TO THE HUMAN CHORIONIC-GONADOTROPIN TEST, Pediatric research, 41(2), 1997, pp. 266-271
INTRAPERITONEAL AND SUBCUTANEOUS ADMINISTRATION OF RECOMBINANT HUMAN GROWTH-HORMONE IN CCPD CHILDREN - A PHARMACOKINETIC STUDY
Authors: MONTINI G TODERINI L BOCCAZZI A RIGON F ANDREETTA B MURER L DALLAMICO R ZACCHELLO G
Citation: G. Montini et al., INTRAPERITONEAL AND SUBCUTANEOUS ADMINISTRATION OF RECOMBINANT HUMAN GROWTH-HORMONE IN CCPD CHILDREN - A PHARMACOKINETIC STUDY, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1047-1047
OUTPATIENT MANAGEMENT OF THE ADOLESCENT P ATIENT WITH ANOREXIA
Authors: POZZAN GB RIGON F GREGGIO NA CONDINI A
Citation: Gb. Pozzan et al., OUTPATIENT MANAGEMENT OF THE ADOLESCENT P ATIENT WITH ANOREXIA, Rivista italiana di pediatria, 22(4), 1996, pp. 697-699
FREQUENCY, CLINICAL AND LABORATORY FEATURES OF THYROIDITIS IN GIRLS WITH TURNERS-SYNDROME
Authors: RADETTI G MAZZANTI L PAGANINI C BERNASCONI S RUSSO G RIGON F CACCIARI E
Citation: G. Radetti et al., FREQUENCY, CLINICAL AND LABORATORY FEATURES OF THYROIDITIS IN GIRLS WITH TURNERS-SYNDROME, Acta paediatrica, 84(8), 1995, pp. 909-912
BLOOD ZINC LEVELS IN PATIENTS WITH DOWNS- SYNDROME - RESULTS OF A MULTICENTER STUDY
Authors: BOCCATO S BACCICHETTI C RIGON F BALESTRAZZI P COCCHI G MEMO L GEMMA G RASOREQUARTINO A
Citation: S. Boccato et al., BLOOD ZINC LEVELS IN PATIENTS WITH DOWNS- SYNDROME - RESULTS OF A MULTICENTER STUDY, Rivista italiana di pediatria, 21(6), 1995, pp. 900-901
A CASE OF ADRENOCORTICAL CARCINOMA OF NEO NATAL ONSET
Authors: VISENTIN A MARZARO M FABRIS F FURLANETTO A ARRIGONI GA CABERLOTTO L RABASSINI S CARLI M RIGON F DELIA R
Citation: A. Visentin et al., A CASE OF ADRENOCORTICAL CARCINOMA OF NEO NATAL ONSET, Rivista italiana di pediatria, 21(1), 1995, pp. 124-127
NATURAL COURSE OF SUBCLINICAL HYPOTHYROIDISM IN DOWNS-SYNDROME - PROSPECTIVE-STUDY RESULTS AND THERAPEUTIC CONSIDERATIONS
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
MOLECULAR APPRAISAL IN TURNER SYNDROME PATIENTS
Authors: GREGGIO NA LICURSI A ARTIFONI L CAENAZZO L PONZANO E RIGON F ZACCHELLO F
Citation: Na. Greggio et al., MOLECULAR APPRAISAL IN TURNER SYNDROME PATIENTS, American journal of human genetics, 57(4), 1995, pp. 638-638
TURNERS-SYNDROME IN ITALY - FAMILIAL CHARACTERISTICS, NEONATAL DATA, STANDARDS FOR BIRTH-WEIGHT AND FOR HEIGHT AND WEIGHT FROM INFANCY TO ADULTHOOD
Authors: BERNASCONI S LARIZZA D BENSO L VOLTA C VANNELLI S MILANI S AICARDI G BERARDI R BORRELLI P BOSCHERINI B PASQUINO AM BUZI F CACCIARI E MAZZANTI L CAVALLO L CHIUMELLO G NIZZOLI G DAMMACCO F DELUCA F DEMATTEIS F DESANCTIS C MATARAZZO P DESANCTIS V DIMAIO S GABRIELLI O GIOVANNELLI G BALESTRAZZI P KLAIN U MORABITO F MAZZILLI G PINTOR C RADETTI G RIGON F LICURSI A SAGGESE G SEVERI F LAMANNA S SPADA A STOPPOLONI GP TATO L TONINI G
Citation: S. Bernasconi et al., TURNERS-SYNDROME IN ITALY - FAMILIAL CHARACTERISTICS, NEONATAL DATA, STANDARDS FOR BIRTH-WEIGHT AND FOR HEIGHT AND WEIGHT FROM INFANCY TO ADULTHOOD, Acta paediatrica, 83(3), 1994, pp. 292-298
FINAL HEIGHT IN GIRLS WITH CENTRAL PRECOCIOUS PUBERTY - COMPARISON OF2 DIFFERENT LUTEINIZING-HORMONE-RELEASING HORMONE AGONIST TREATMENTS
Authors: ANTONIAZZI F CISTERNINO M NIZZOLI G BOZZOLA M CORRIAS A DELUCA F DESANCTIS C RIGON F ZAMBONI G BERNASCONI S CHIUMELLO G SEVERI F TATO L
Citation: F. Antoniazzi et al., FINAL HEIGHT IN GIRLS WITH CENTRAL PRECOCIOUS PUBERTY - COMPARISON OF2 DIFFERENT LUTEINIZING-HORMONE-RELEASING HORMONE AGONIST TREATMENTS, Acta paediatrica, 83(10), 1994, pp. 1052-1056
UNUSUAL PREVALENCE OF HYPERTHYROIDISM IN PATIENTS WITH DOWN-SYNDROME IN THE VENETO REGION
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
HAMARTOMA OF TUBER-CINEREUM AND PRECOCIOU S PUBERTY IN A 10-MONTH MALE
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
THE SAME MOLECULAR GENOTYPE MAY EXPRESS DIFFERENT DISEASE PHENOTYPES IN 21-HYDROXYLASE DEFICIENCY
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
Risultati: 1-16 |