Microchimerism and Endocrine DisordersFUGAZZOLA, Laura; CIRELLO, Valentina; BECK-PECCOZ, Paolo et al.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 5, pp 1452-1461, issn 0021-972X, 10 p.Article

Life-threatening metabolic alkalosis in Pendred syndromeKANDASAMY, Narayanan; FUGAZZOLA, Laura; EVANS, Mark et al.European journal of endocrinology. 2011, Vol 165, Num 1, pp 167-170, issn 0804-4643, 4 p.Article

Comparison of Calcium and Pentagastrin Tests for the Diagnosis and Follow-Up of Medullary Thyroid CancerCOLOMBO, Carla; VERGA, Uberta; FUGAZZOLA, Laura et al.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 3, pp 905-913, issn 0021-972X, 9 p.Article

The tight relationship between papillary thyroid cancer, autoimmunity and inflammation: clinical and molecular studiesMUZZA, Marina; DEGL'INNOCENTI, Debora; COLOMBO, Carla et al.Clinical endocrinology (Oxford. Print). 2010, Vol 72, Num 5, pp 702-708, issn 0300-0664, 7 p.Article

The expression of wild-type pendrin (SLC26A4) in human embryonic kidney (HEK 293 Phoenix) cells leads to the activation of cationic currentsDOSSENA, Silvia; MACCAGNI, Antonella; ZOROWKA, Patrick et al.European journal of endocrinology. 2005, Vol 153, Num 5, pp 693-699, issn 0804-4643, 7 p.Article

A novel tyrosine-kinase selective inhibitor, sunitinib, induces transient hypothyroidism by blocking iodine uptakeMANNAVOLA, Deborah; COCO, Paola; VANNUCCHI, Guia et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 9, pp 3531-3534, issn 0021-972X, 4 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

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

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

Different responses to chronic somatostatin analogues in patients with central hyperthyroidismMANNAVOLA, Deborah; PERSANI, Luca; VANNUCCHI, Guia et al.Clinical endocrinology (Oxford. Print). 2005, Vol 62, Num 2, pp 176-181, issn 0300-0664, 6 p.Article

Differential diagnosis between Pendred and pseudo-Pendred syndromes: Clinical, radiologic, and molecular studiesFUGAZZOLA, Laura; CERUTTI, Nadia; MANNAVOLA, Deborah et al.Pediatric research. 2002, Vol 51, Num 4, pp 479-484, issn 0031-3998Article

Association Between BRAFV600E Mutation and Mortality in Patients With Papillary Thyroid CancerMINGZHAO XING; ALZAHRANI, Ali S; ROBENSHTOK, Eyal et al.JAMA, the journal of the American Medical Association. 2013, Vol 309, Num 14, pp 1493-1501, issn 0098-7484, 9 p.Article

A High Percentage of BRAF^V600E Alleles in Papillary Thyroid Carcinoma Predicts a Poorer OutcomeGUERRA, Anna; FUGAZZOLA, Laura; MAROTTA, Vincenzo et al.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 7, pp 2333-2340, issn 0021-972X, 8 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

Frequent association between MEN 2A and cutaneous lichen amyloidosisVERGA, Uberta; FUGAZZOLA, Laura; CAMBIAGHI, Stefano et al.Clinical endocrinology (Oxford. Print). 2003, Vol 59, Num 2, pp 156-161, issn 0300-0664, 6 p.Article

Congenital Hypothyroidism With Eutopic Thyroid Gland: Analysis of Clinical and Biochemical Features at Diagnosis and After Re-EvaluationRABBIOSI, Sarah; VIGONE, Maria Cristina; CORTINOVIS, Francesca et al.The Journal of clinical endocrinology and metabolism. 2013, Vol 98, Num 4, pp 1395-1402, issn 0021-972X, 8 p.Article

The Primary Occurrence of BRAF^V600E Is a Rare Clonal Event in Papillary Thyroid CarcinomaGUERRA, Anna; ROSARIA SAPIO, Maria; VITALE, Mario et al.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 2, pp 517-524, issn 0021-972X, 8 p.Article

Clinical and molecular features of differentiated thyroid cancer diagnosed during pregnancyVANNUCCHI, Guia; PERRINO, Michela; ROSSI, Stefania et al.European journal of endocrinology. 2010, Vol 162, Num 1, pp 145-151, issn 0804-4643, 7 p.Article

Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitroMUZZA, Marina; CORDELLA, Daniela; BOMBLED, Johny et al.European journal of endocrinology. 2010, Vol 162, Num 4, pp 771-777, issn 0804-4643, 7 p.Article

High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene : clinical characterization and functional studies of the mutated SLC26A4 proteinFUGAZZOLA, Laura; CIRELLO, Valentina; PAULMICHL, Markus et al.European journal of endocrinology. 2007, Vol 157, Num 3, pp 331-338, issn 0804-4643, 8 p.Article

BRAF mutations in an Italian cohort of thyroid cancersFUGAZZOLA, Laura; MANNAVOLA, Deborah; CIRELLO, Valentina et al.Clinical endocrinology (Oxford. Print). 2004, Vol 61, Num 2, pp 239-243, issn 0300-0664, 5 p.Article

Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacementFUGAZZOLA, Laura; PERSANI, Luca; MANNAVOLA, Deborah et al.Clinical endocrinology (Oxford. Print). 2003, Vol 59, Num 2, pp 230-236, issn 0300-0664, 7 p.Article