Central Hypothyroidism: Pathogenic, Diagnostic, and Therapeutic ChallengesPERSANI, Luca.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 9, pp 3068-3078, issn 0021-972X, 11 p.Article

Syndromes de résistance aux hormones thyroïdiennes par mutations du récepteur T3R β: avancées dans la compréhension des mécanismes : Résistance aux hormones thyroïdiennesBECK-PECCOZ, Paolo; MANNAVOLA, Deborah; PERSANI, Luca et al.MTE. Médecine thérapeutique endocrinologie. 2002, Vol 4, Num 1, pp 27-33, issn 1295-9359Article

Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) geneDI PASQUALE, Elisa; BECK-PECCOZ, Paolo; PERSANI, Luca et al.American journal of human genetics. 2004, Vol 75, Num 1, pp 106-111, issn 0002-9297, 6 p.Article

Primary ovarian insufficiency: X chromosome defects and autoimmunityPERSANI, Luca; ROSSETTI, Raffaella; CACCIATORE, Chiara et al.Journal of autoimmunity (Print). 2009, Vol 33, Num 1, pp 35-41, issn 0896-8411, 7 p.Article

ThyrotropinomasBECK-PECCOZ, Paolo; PERSANI, Luca.Endocrinology and metabolism clinics of North America. 2008, Vol 37, Num 1, issn 0889-8529, viii-ix, 123-134 [14 p.]Article

Isolated follicle-stimulating hormone (FSH) deficiency in a young man with normal virilization who did not have mutations in the FSHβ geneMANTOVANI, Giovanna; BORGATO, Stefano; BECK-PECCOZ, Paolo et al.Fertility and sterility. 2003, Vol 79, Num 2, pp 434-436, issn 0015-0282, 3 p.Article

Investigating the paradox of hypothyroidism and increased serum thyrotropin (TSH) levels in Sheehan's syndrome : Characterization of TSH carbohydrate content and bioactivityOLIVEIRA, Juliana H. A; PERSANI, Luca; BECK-PECCOZ, Paolo et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 4, pp 1694-1699, issn 0021-972XArticle

Oxytocin-induced cell growth proliferation in human myometrial cells and leiomyomasBUSNELLI, Marta; RIMOLDI, Valeria; VIGANO, Paola et al.Fertility and sterility. 2010, Vol 94, Num 5, pp 1869-1874, issn 0015-0282, 6 p.Article

Diagnostic and therapeutic challenges of acquired thyrotropic deficiencyPERSANI, Luca; BONOMI, Marco; RADIN, Raffaella et al.Annales d'endocrinologie. 2012, Vol 73, Num 2, pp 138-140, issn 0003-4266, 3 p.Conference Paper

Hyperplastic pituitary gland, high serum glycoprotein hormone α-subunit, and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSHβ geneBONOMI, Marco; PROVERBIO, Maria Carla; WEBER, Giovanna et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 4, pp 1600-1604, issn 0021-972XArticle

Relevant cAMP-specific phosphodiesterase isoforms in human pituitary : Effect of Gsα mutationsPERSANI, Luca; BORGATO, Stefano; LANIA, Andrea et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 8, pp 3795-3800, issn 0021-972XArticle

Circulating thyrotropin bioactivity in sporadic central hypothyroidismPERSANI, Luca; FERRETTI, Elisabetta; BORGATO, Stefano et al.The Journal of clinical endocrinology and metabolism. 2000, Vol 85, Num 10, pp 3631-3635, issn 0021-972XArticle

A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failureCORRE, Tanguy; SCHUETTLER, Julia; BIONE, Silvia et al.Human reproduction (Oxford. Print). 2009, Vol 24, Num 8, pp 2023-2028, issn 0268-1161, 6 p.Article

Highly sensitive serum thyroglobulin and circulating thyroglobulin mRNA evaluations in the management of patients with differentiated thyroid cancer in apparent remissionFUGAZZOLA, Laura; MIHALICH, Alessandra; DI BLASIO, Anna Maria et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 7, pp 3201-3208, issn 0021-972XArticle

Activator Protein-1 and Smad Proteins Synergistically Regulate Human Follicle-Stimulating Hormone β-Promoter ActivityYING WANG; FORTIN, Jérome; LAMBA, Pankaj et al.Endocrinology (Philadelphia). 2008, Vol 149, Num 11, pp 5577-5591, issn 0013-7227, 15 p.Article

A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in lacaune sheepBODIN, Loys; DI PASQUALE, Elisa; FABRE, Stéphane et al.Endocrinology (Philadelphia). 2007, Vol 148, Num 1, pp 393-400, issn 0013-7227, 8 p.Article

A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidismALBERTI, Luisella; PROVERBIO, Maria Carla; COSTAGLIOLA, Sabine et al.European journal of endocrinology. 2001, Vol 145, Num 3, pp 249-254, issn 0804-4643Article

Serum thyrotropin concentrations and bioactivity during sleep deprivation in depressionORTH, David N; SHELTON, Richard C; NICHOLSON, Wendell E et al.Archives of general psychiatry. 2001, Vol 58, Num 1, pp 77-83, issn 0003-990XArticle

Disruptions of Global and Jagged1-Mediated Notch Signaling Affect Thyroid Morphogenesis in the ZebrafishPORAZZI, Patrizia; MARELLI, Federica; BENATO, Francesca et al.Endocrinology (Philadelphia). 2012, Vol 153, Num 11, pp 5645-5658, issn 0013-7227, 14 p.Article

Sortilin Is a Putative Postendocytic Receptor of ThyroglobulinBOTTA, Roberta; LISI, Simonetta; PERSANI, Luca et al.Endocrinology (Philadelphia). 2009, Vol 150, Num 1, pp 509-518, issn 0013-7227, 10 p.Article

Biallelic Inactivation of the Dual Oxidase Maturation Factor 2 (DUOXA2) Gene as a Novel Cause of Congenital HypothyroidismZAMPRONI, Ilaria; GRASBERGER, Helmut; CORTINOVIS, Francesca et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 2, pp 605-610, issn 0021-972X, 6 p.Article

Somatic mutational analysis of DAX1 in testes from men with idiopathic azoospermiaMANTOVANI, Giovanna; MANCINI, Mario; GAZZANO, Giacomo et al.Fertility and sterility. 2005, Vol 84, Num 5, pp 1542-1544, issn 0015-0282, 3 p.Article

RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian seriesFUGAZZOLA, Laura; MUZZA, Marina; BECK-PECCOZ, Paolo et al.Clinical endocrinology (Oxford. Print). 2008, Vol 69, Num 3, pp 418-425, issn 0300-0664, 8 p.Article

DAX1 and X-linked adrenal hypoplasia congenita : clinical and molecular analysis in five patientsMANTOVANI, Giovanna; DE MENIS, Ernesto; BORRETTA, Giorgio et al.European journal of endocrinology. 2006, Vol 154, Num 5, pp 685-689, issn 0804-4643, 5 p.Article

TBG deficiency : description of two novel mutations associated with complete TBG deficiency and review of the literatureMANNAVOLA, Deborah; VANNUCCHI, Guia; FUGAZZOLA, Laura et al.Journal of molecular medicine (Berlin. Print). 2006, Vol 84, Num 10, pp 864-871, issn 0946-2716, 8 p.Article