Menabò S; Balsamo A; Nicoletti A; Gennari M; Pirazzoli P; Cicognani A; Baldazzi L., Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage., «HORMONE RESEARCH», 2008, 70(2), pp. 124 - 128 [articolo]
Nicoletti A.; Baldazzi L.; Menabò S.; Balsamo A.; Gennari M.; Buzi F.; Pasini A.; Cicognani A., A molecular analysis of candidate genes for hypospadias in Italian subjects, in: , «HORMONE RESEARCH», 2007, 68 (S1) P03-669, pp. 207 - 207 (atti di: 46th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Helsinki, Finland, June 27-30, 2007) [atti di convegno-abstract]
Pirazzoli P.; Nicoletti A.; Gennari M.; Baldazzi L.; Balsamo A.; Mencarelli F.; Cicognani A., A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father, in: , «HORMONE RESEARCH», 2007, 68 (S1) P03-658, pp. 204 - 204 (atti di: 46th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Helsinki, Finland, June 27-30, 2007) [atti di convegno-abstract]
Balsamo A.; Cicognani A.; Gennari M.; Sippel W.G.; Menabò S.; Baronio F.; Riepe F., Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three gene SNPs, in: , «HORMONE RESEARCH», 2007, 68 (S1) PO2-340, pp. 105 - 105 (atti di: 46th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Helsinki, Finland, 27-30, 2007) [atti di convegno-abstract]
A.Balsamo; A.Cicognani; M.Gennari; W.G.Sippell; S.Menabò; F.Baronio; F.G.Riepe, Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1, «EUROPEAN JOURNAL OF ENDOCRINOLOGY», 2007, 156, pp. 249 - 256 [articolo]
Santoro N.; Cirillo G.; Romano T.; ..; Balsamo A.; Gennari M.; ..; Miraglia del Giudice E., Melanocortin-4-receptor molecular screening in a group of phenotypically selected obese children: report of two new mutations and lack of association to the early onset of the disease, in: , «HORMONE RESEARCH», 2007, 68 suppl1 FC8-113, pp. 34 - 34 (atti di: 46th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Helsinki, Finland, June 27-30, 2007) [atti di convegno-abstract]
S.Cazzato; F.Bernardi; A.Balsamo; I.Corsini; M.Gennari; S.Colonna; L.Bertelli; A.Cicognani., Studio della funzionalità polmonare nel bambino obeso., in: SIEDP, Abstract book, FIDENZA, Mattioli 1885 spa, 2007, pp. 210 - 211 (atti di: XVI Congresso Nazionale SIEDP, Parma, 11-13 ottobre 2007) [atti di convegno-abstract]
Antelli A; Baldazzi L; Balsamo A; Pirazzoli P; Nicoletti A; Gennari M;
Cicognani A., Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism.
Eur J Endocrinol, «EUROPEAN JOURNAL OF ENDOCRINOLOGY», 2006, 155, pp. 201 - 205 [articolo]
Pirazzoli P; Lanari M; Zucchini S; Gennari M; Pagotto U; De Iasio R; Pasquali R; Cassio A; Cicognani A; Cacciari E., Active and total ghrelin concentrations in the newborn, «JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM», 2005, 18, pp. 379 - 384 [articolo]
A. Balsamo;S. Forti;M. Bal;M. Gennari;R. Di Iasio;S. Gualandi;D. Elleri;A. Cicognani, Relationships between ghrelin, hypothalamic-pituitary-adrenal- and GH/IGF1 axes in patients treated for congenital adrenal
hyperplasia, in: , «HORMONE RESEARCH», 2005, 64, pp. 340 - 340 (atti di: European Society for Paediatric Endocrinology (ESPE) / Lawson Wilkins Pediatric Endocrine Society (LWPES)
7th Joint Meeting in collaboration with APEG, APPES, JSPE and SLEP, Lyon, September 2005) [atti di convegno-abstract]
Nicoletti A; Baldazzi L; Balsamo A; Barp L; Pirazzoli P; Gennari M; Radetti G; Cacciari E; Cicognani A., SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects., «CLINICAL ENDOCRINOLOGY», 2005, 63, pp. 375 - 380 [articolo]
F. Baronio;P. Pirazzoli;M. Gennari;G. Frank;V. Rosetti;A. Cicognani, Statural growth and final height after transsphenoidal surgery for Cushing's disease in 7 children, in: , «HORMONE RESEARCH», 2005, 64, pp. 221 - 222 (atti di: European Society for Paediatric Endocrinology (ESPE) / Lawson Wilkins Pediatric Endocrine Society (LWPES)
7th Joint Meeting in collaboration with APEG, APPES, JSPE and SLEP, Lyon, September 2005) [atti di convegno-abstract]
A.Balsamo; S.Piazzi; M.Bal; C.Retetangos; M.Gennari; F.Baronio; A.Cassio; A.Cicognani., Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003)., in: Atti del VIII Congresso Nazionale SISN, CATANZARO, n.s., 2004(atti di: VIII Congresso Nazionale SISN (associato con SISMME e GENCLI), Catanzaro, 7-10, Luglio, 2004) [atti di convegno-abstract]
A.Balsamo; M.Gennari; MC.Pittalis; P.Biso; L.Baldazzi; L.Mazzanti; R.De Castro; A.Cicognani., Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p)., in: Intersex – from gene to gender, LUBECCA, O.Hiort, 2004(atti di: I Congrtesso Internazionale “Intersex – from gene to gender”, Lubecca, Germania, April 1-3, 2004) [atti di convegno-abstract]
A.Balsamo; L.Baldazzi; L.Barp; F.Baronio; M.Gennari; C.Retetangos; A.Cassio; A.Cicognani; E.Cacciari., Height outcome and pubertal development in CYP21 genotyped CAH male patients, in: Human Growth in Sickness and in Health, FIRENZE, s.n, 2004(atti di: X International Congress of Auxology “Human Growth in Sickness and in Health”, Florence, July 4-7, 2004) [atti di convegno-abstract]
