Fugazzola Laura

Top coauthors of Fugazzola Laura

Beck-Peccoz Paolo (31 papers)

Cirello Valentina (25 papers)

Persani Luca (22 papers)

Vannucchi Guia (18 papers)

Perrino Michela (15 papers)

List of Fugazzola Laura publications

2016

Muzza Marina, Colombo Carla, Cirello Valentina, Perrino Michela, Vicentini Leonardo, Fugazzola Laura 2016. "Oxidative stress and the subcellular localization of the telomerase reverse transcriptase (TERT) in papillary thyroid cancer." Molecular and cellular endocrinology doi:10.1016/j.mce.2016.05.005
Busnelli Andrea, Somigliana Edgardo, Ferrari Stefania, Filippi Francesca, Vannucchi Guia, et al. 2016. "THE LONG-TERM IMPACT OF CONTROLLED OVARIAN HYPERSTIMULATION ON THYROID FUNCTION." Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 22 (4) doi:10.4158/EP15933.OR
de Filippis Tiziana, Marelli Federica, Nebbia Gabriella, Porazzi Patrizia, Corbetta Sabrina, et al. 2016. "JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects." The Journal of clinical endocrinology and metabolism 101 (3) doi:10.1210/jc.2015-3403
Cirello Valentina, Fugazzola Laura 2016. "Novel insights into the link between fetal cell microchimerism and maternal cancers." Journal of cancer research and clinical oncology doi:10.1007/s00432-015-2110-3
Shi Xiaoguang, Liu Rengyun, Basolo Fulvio, Giannini Riccardo, Shen Xiaopei, et al. 2016. "Differential Clinicopathological Risk and Prognosis of Major Papillary Thyroid Cancer Variants." The Journal of clinical endocrinology and metabolism 101 (1) doi:10.1210/jc.2015-2917
Lunati Maria Elena, Grancini Valeria, Colombo Carla, Palmieri Eva, Resi Veronica, et al. 2016. "Basal and stimulated calcitonin levels in patients with type 2 diabetes did not change during 1 year of Liraglutide treatment." Metabolism: clinical and experimental 65 (1) doi:10.1016/j.metabol.2015.09.010

2015

Cirello Valentina, Colombo Carla, Perrino Michela, De Leo Simone, Muzza Marina, et al. 2015. "Fetal cell microchimerism in papillary thyroid cancer: A role in the outcome of the disease." International journal of cancer 137 (12) doi:10.1002/ijc.29653
Worden Francis, Fassnacht Martin, Shi Yuankai, Hadjieva Tatiana, Bonichon Françoise, et al. 2015. "Safety and tolerability of sorafenib in patients with radioiodine-refractory thyroid cancer." Endocrine-related cancer 22 (6) doi:10.1530/ERC-15-0252
Grassi Elisa Stellaria, Vezzoli Valeria, Negri Irene, Lábadi Árpád, Fugazzola Laura, et al. 2015. "SP600125 has a remarkable anticancer potential against undifferentiated thyroid cancer through selective action on ROCK and p53 pathways." Oncotarget 6 (34) doi:10.18632/oncotarget.5799
Busnelli Andrea, Vannucchi Guia, Paffoni Alessio, Faulisi Sonia, Fugazzola Laura, et al. 2015. "Levothyroxine dose adjustment in hypothyroid women achieving pregnancy through IVF." European journal of endocrinology / European Federation of Endocrine Societies 173 (4) doi:10.1530/EJE-15-0151
Vannucchi Guia, De Leo Simone, Perrino Michela, Rossi Stefania, Tosi Delfina, et al. 2015. "Impact of estrogen and progesterone receptor expression on the clinical and molecular features of papillary thyroid cancer." European journal of endocrinology / European Federation of Endocrine Societies 173 (1) doi:10.1530/EJE-15-0054
Cirello Valentina, Rizzo Roberta, Crippa Milena, Campi Irene, Bortolotti Daria, et al. 2015. "Fetal cell microchimerism: a protective role in autoimmune thyroid diseases." European journal of endocrinology / European Federation of Endocrine Societies 173 (1) doi:10.1530/EJE-15-0028
Castagna Maria G, Fugazzola Laura, Maino Fabio, Covelli Danila, Memmo Silvia, et al. 2015. "Reference range of serum calcitonin in pediatric population." The Journal of clinical endocrinology and metabolism 100 (5) doi:10.1210/jc.2014-4508
Muzza Marina, Colombo Carla, Rossi Stefania, Tosi Delfina, Cirello Valentina, et al. 2015. "Telomerase in differentiated thyroid cancer: promoter mutations, expression and localization." Molecular and cellular endocrinology 399 doi:10.1016/j.mce.2014.10.019
Colombo Carla, Minna Emanuela, Rizzetti Maria Grazia, Romeo Paola, Lecis Daniele, et al. 2015. "The modifier role of RET-G691S polymorphism in hereditary medullary thyroid carcinoma: functional characterization and expression/penetrance studies." Orphanet journal of rare diseases 10 doi:10.1186/s13023-015-0231-z
Xing Mingzhao, Alzahrani Ali S, Carson Kathryn A, Shong Young Kee, Kim Tae Yong, et al. 2015. "Association between BRAF V600E mutation and recurrence of papillary thyroid cancer." Journal of clinical oncology : official journal of the American Society of Clinical Oncology 33 (1) doi:10.1200/JCO.2014.56.8253

2014

Vannucchi Guia, Covelli Danila, Perrino Michela, De Leo Simone, Fugazzola Laura 2014. "Ultrasound-guided percutaneous ethanol injection in papillary thyroid cancer metastatic lymph-nodes." Endocrine 47 (2) doi:10.1007/s12020-014-0215-0
Cirello Valentina, Fugazzola Laura 2014. "Positive effect of fetal cell microchimerism on tumor presentation and outcome in papillary thyroid cancer." Chimerism 5 (3-4) doi:10.1080/19381956.2015.1107254
Longo Marcella, Cassoli Ing Paolo, Fugazzola Laura, Vannucchi Guia, Lanzoni Monica, Castaldi Silvana 2014. "Feasibility study for the introduction of a new treatment method for benign thyroid nodules in a teaching and research hospital." Journal of evaluation in clinical practice 20 (5) doi:10.1111/jep.12177
Tresoldi Alberto S, Sburlati Laura F, Rodari Marcello, Schinkelshoek Mink, Perrino Michela, et al. 2014. "Radioiodine ablation with 1,850 MBq in association with rhTSH in patients with differentiated thyroid cancer." Journal of endocrinological investigation 37 (8) doi:10.1007/s40618-014-0088-3
Simbolo Michele, Mian Caterina, Barollo Susi, Fassan Matteo, Mafficini Andrea, et al. 2014. "High-throughput mutation profiling improves diagnostic stratification of sporadic medullary thyroid carcinomas." Virchows Archiv : an international journal of pathology 465 (1) doi:10.1007/s00428-014-1589-3
Mian Caterina, Perrino Michela, Colombo Carla, Cavedon Elisabetta, Pennelli Gianmaria, et al. 2014. "Refining calcium test for the diagnosis of medullary thyroid cancer: cutoffs, procedures, and safety." The Journal of clinical endocrinology and metabolism 99 (5) doi:10.1210/jc.2013-4088
Benaglia Laura, Busnelli Andrea, Somigliana Edgardo, Leonardi Marta, Vannucchi Guia, et al. 2014. "Incidence of elevation of serum thyroid-stimulating hormone during controlled ovarian hyperstimulation for in vitro fertilization." European journal of obstetrics, gynecology, and reproductive biology 173 doi:10.1016/j.ejogrb.2013.11.003

2013

Xing Mingzhao, Alzahrani Ali S, Carson Kathryn A, Viola David, Elisei Rossella, et al. 2013. "Association between BRAF V600E mutation and mortality in patients with papillary thyroid cancer." JAMA : the journal of the American Medical Association 309 (14) doi:10.1001/jama.2013.3190
Rabbiosi Sarah, Vigone Maria Cristina, Cortinovis Francesca, Zamproni Ilaria, Fugazzola Laura, et al. 2013. "Congenital hypothyroidism with eutopic thyroid gland: analysis of clinical and biochemical features at diagnosis and after re-evaluation." The Journal of clinical endocrinology and metabolism 98 (4) doi:10.1210/jc.2012-3174
Fugazzola Laura, De Leo Simone, Perrino Michela 2013. "The optimal range of RET mutations to be tested: European comments to the guidelines of the American Thyroid Association." Thyroid research 6 Suppl 1 doi:10.1186/1756-6614-6-S1-S8
Fugazzola Laura 2013. "Stimulated calcitonin cut-offs by different tests." European thyroid journal 2 (1) doi:10.1159/000346020
Porcu Eleonora, Medici Marco, Pistis Giorgio, Volpato Claudia B, Wilson Scott G, et al. 2013. "A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function." PLoS genetics 9 (2) doi:10.1371/journal.pgen.1003266
Marino Marco, Cirello Valentina, Gnarini Valentina, Colombo Carla, Pignatti Elisa, et al. 2013. "Are pre-miR-146a and PTTG1 associated with papillary thyroid cancer?" Endocrine connections 2 (4) doi:10.1530/EC-13-0066
Ciampi Raffaele, Mian Caterina, Fugazzola Laura, Cosci Barbara, Romei Cristina, et al. 2013. "Evidence of a low prevalence of RAS mutations in a large medullary thyroid cancer series." Thyroid : official journal of the American Thyroid Association 23 (1) doi:10.1089/thy.2012.0207

2012

Romei Cristina, Fugazzola Laura, Puxeddu Efisio, Frasca Francesco, Viola David, et al. 2012. "Modifications in the papillary thyroid cancer gene profile over the last 15 years." The Journal of clinical endocrinology and metabolism 97 (9) doi:10.1210/jc.2012-1269
Ciampi Raffaele, Mian Caterina, Fugazzola Laura, Cosci Barbara, Romei Cristina, et al. 2012. "EVIDENCE OF A LOW PREVALENCE OF RAS MUTATIONS IN A LARGE MEDULLARY THYROID CANCER SERIES." Thyroid : official journal of the American Thyroid Association doi:10.1089/thy.2012-0207
Guerra Anna, Fugazzola Laura, Marotta Vincenzo, Cirillo Massimo, Rossi Stefania, et al. 2012. "A high percentage of BRAFV600E alleles in papillary thyroid carcinoma predicts a poorer outcome." The Journal of clinical endocrinology and metabolism 97 (7) doi:10.1210/jc.2011-3106
Fugazzola Laura, Cirello Valentina, Beck-Peccoz Paolo 2012. "Microchimerism and endocrine disorders." The Journal of clinical endocrinology and metabolism 97 (5) doi:10.1210/jc.2011-3160
Cirello Valentina, Bazzini Claudia, Vezzoli Valeria, Muzza Marina, Rodighiero Simona, et al. 2012. "Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss." Molecular and cellular endocrinology 351 (2) doi:10.1016/j.mce.2012.01.013
Colombo Carla, Verga Uberta, Mian Caterina, Ferrero Stefano, Perrino Michela, et al. 2012. "Comparison of calcium and pentagastrin tests for the diagnosis and follow-up of medullary thyroid cancer." The Journal of clinical endocrinology and metabolism 97 (3) doi:10.1210/jc.2011-2033
Guerra Anna, Sapio Maria Rosaria, Marotta Vincenzo, Campanile Elisabetta, Rossi Stefania, et al. 2012. "The primary occurrence of BRAF(V600E) is a rare clonal event in papillary thyroid carcinoma." The Journal of clinical endocrinology and metabolism 97 (2) doi:10.1210/jc.2011-0618

2011

Kandasamy Narayanan, Fugazzola Laura, Evans Mark, Chatterjee Krishna, Karet Fiona 2011. "Life-threatening metabolic alkalosis in Pendred syndrome." European journal of endocrinology / European Federation of Endocrine Societies 165 (1) doi:10.1530/EJE-11-0101
Fugazzola Laura, Cirello Valentina, Beck-Peccoz Paolo 2011. "Fetal microchimerism as an explanation of disease." Nature reviews. Endocrinology 7 (2) doi:10.1038/nrendo.2010.216

2010

Schulte Klaus-Martin, Machens Andreas, Fugazzola Laura, McGregor Alan, Diaz-Cano Salvador, et al. 2010. "The clinical spectrum of multiple endocrine neoplasia type 2a caused by the rare intracellular RET mutation S891A." The Journal of clinical endocrinology and metabolism 95 (9) doi:10.1210/jc.2010-0375
Romei Cristina, Mariotti Stefano, Fugazzola Laura, Taccaliti Augusto, Pacini Furio, et al. 2010. "Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes." European journal of endocrinology / European Federation of Endocrine Societies 163 (2) doi:10.1530/EJE-10-0333
Cirello Valentina, Perrino Michela, Colombo Carla, Muzza Marina, Filopanti Marcello, et al. 2010. "Fetal cell microchimerism in papillary thyroid cancer: studies in peripheral blood and tissues." International journal of cancer. Journal international du cancer 126 (12) doi:10.1002/ijc.24993
Muzza Marina, Degl'Innocenti Debora, Colombo Carla, Perrino Michela, Ravasi Elena, et al. 2010. "The tight relationship between papillary thyroid cancer, autoimmunity and inflammation: clinical and molecular studies." Clinical endocrinology 72 (5) doi:10.1111/j.1365-2265.2009.03699.x
Muzza Marina, Cordella Daniela, Bombled Johny, Bressac-de Paillerets Brigitte, Guizzardi Fabiana, et al. 2010. "Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro." European journal of endocrinology / European Federation of Endocrine Societies 162 (4) doi:10.1530/EJE-09-0929
Fugazzola Laura, Cirello Valentina, Beck-Peccoz Paolo 2010. "Fetal cell microchimerism in human cancers." Cancer letters 287 (2) doi:10.1016/j.canlet.2009.05.017
Vannucchi Guia, Perrino Michela, Rossi Stefania, Colombo Carla, Vicentini Leonardo, et al. 2010. "Clinical and molecular features of differentiated thyroid cancer diagnosed during pregnancy." European journal of endocrinology / European Federation of Endocrine Societies 162 (1) doi:10.1530/EJE-09-0761

2009

Dossena Silvia, Rodighiero Simona, Vezzoli Valeria, Nofziger Charity, Salvioni Elisabetta, et al. 2009. "Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome." Journal of molecular endocrinology 43 (3) doi:10.1677/JME-08-0175
Perrino Michela, Vannucchi Guia, Vicentini Leonardo, Cantoni Gianmaria, Dazzi Davide, et al. 2009. "Outcome predictors and impact of central node dissection and radiometabolic treatments in papillary thyroid cancers < or =2 cm." Endocrine-related cancer 16 (1) doi:10.1677/ERC-08-0119

2008

Cirello Valentina, Recalcati Maria Paola, Muzza Marina, Rossi Stefania, Perrino Michela, et al. 2008. "Fetal cell microchimerism in papillary thyroid cancer: a possible role in tumor damage and tissue repair." Cancer research 68 (20) doi:10.1158/0008-5472.CAN-08-0672
Fugazzola Laura, Muzza Marina, Mian Caterina, Cordella Daniela, Barollo Susi, et al. 2008. "RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series." Clinical endocrinology 69 (3) doi:10.1111/j.1365-2265.2008.03218.x
Zamproni Ilaria, Grasberger Helmut, Cortinovis Francesca, Vigone Maria Cristina, Chiumello Giuseppe, et al. 2008. "Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism." The Journal of clinical endocrinology and metabolism 93 (2) doi:10.1210/jc.2007-2020

2007

Fugazzola Laura, Persani Luca, Vannucchi Guia, Carletto Marco, Mannavola Deborah, et al. 2007. "Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy." European journal of nuclear medicine and molecular imaging 34 (9) doi:10.1007/s00259-007-0377-6
Mannavola Deborah, Coco Paola, Vannucchi Guia, Bertuelli Rossella, Carletto Marco, et al. 2007. "A novel tyrosine-kinase selective inhibitor, sunitinib, induces transient hypothyroidism by blocking iodine uptake." The Journal of clinical endocrinology and metabolism 92 (9) doi:10.1210/jc.2007-0586
Fugazzola Laura, Cirello Valentina, Dossena Silvia, Rodighiero Simona, Muzza Marina, et al. 2007. "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 protein." European journal of endocrinology / European Federation of Endocrine Societies 157 (3) doi:10.1530/EJE-07-0263
Verga Uberta, Ferrero Stefano, Vicentini Leonardo, Brambilla Tatiana, Cirello Valentina, et al. 2007. "Histopathological and molecular studies in patients with goiter and hypercalcitoninemia: reactive or neoplastic C-cell hyperplasia?" Endocrine-related cancer 14 (2) doi:10.1677/ERC-06-0053

2006

Mannavola Deborah, Vannucchi Guia, Fugazzola Laura, Cirello Valentina, Campi Irene, et al. 2006. "TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature." Journal of molecular medicine (Berlin, Germany) 84 (10) doi:10.1007/s00109-006-0078-9
Cordella Daniela, Muzza Marina, Alberti Luisella, Colombo Paolo, Travaglini Pietro, et al. 2006. "An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma." Endocrine-related cancer 13 (3) doi:10.1677/erc.1.01144
Dossena Silvia, Rodighiero Simona, Vezzoli Valeria, Bazzini Claudia, Sironi Chiara, et al. 2006. "Fast fluorometric method for measuring pendrin (SLC26A4) Cl-/I- transport activity." Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 18 (1-3) doi:10.1159/000095164
Dossena Silvia, Vezzoli Valeria, Cerutti Nadia, Bazzini Claudia, Tosco Marisa, et al. 2006. "Functional characterization of wild-type and a mutated form of SLC26A4 identified in a patient with Pendred syndrome." Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 17 (5-6) doi:10.1159/000094137

2005

Dossena Silvia, Maccagni Antonella, Vezzoli Valeria, Bazzini Claudia, Garavaglia Maria Lisa, et al. 2005. "The expression of wild-type pendrin (SLC26A4) in human embryonic kidney (HEK 293 Phoenix) cells leads to the activation of cationic currents." European journal of endocrinology / European Federation of Endocrine Societies 153 (5) doi:10.1530/eje.1.02018
Borrello Maria Grazia, Alberti Luisella, Fischer Andrew, Degl'innocenti Debora, Ferrario Cristina, et al. 2005. "Induction of a proinflammatory program in normal human thyrocytes by the RET/PTC1 oncogene." Proceedings of the National Academy of Sciences of the United States of America 102 (41) doi:10.1073/pnas.0503039102
Vigone Maria Cristina, Fugazzola Laura, Zamproni Ilaria, Passoni Arianna, Di Candia Stefania, et al. 2005. "Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings." Human mutation 26 (4) doi:10.1002/humu.9372
Vannucchi Guia, Chiti Arturo, Mannavola Deborah, Dazzi Davide, Rodari Marcello, et al. 2005. "Radioiodine treatment of non-toxic multinodular goitre: effects of combination with lithium." European journal of nuclear medicine and molecular imaging 32 (9) doi:10.1007/s00259-005-1818-8
Fugazzola Laura, Mannavola Deborah, Vigone Maria Cristina, Cirello Valentina, Weber Giovanna, et al. 2005. "Total iodide organification defect: clinical and molecular characterization of an Italian family." Thyroid : official journal of the American Thyroid Association 15 (9) doi:10.1089/thy.2005.15.1085
Mannavola Deborah, Persani Luca, Vannucchi Guia, Zanardelli Maddalena, Fugazzola Laura, et al. 2005. "Different responses to chronic somatostatin analogues in patients with central hyperthyroidism." Clinical endocrinology 62 (2) doi:10.1111/j.1365-2265.2004.02192.x

2004

Fugazzola Laura, Mannavola Deborah, Cirello Valentina, Vannucchi Guia, Muzza Marina, et al. 2004. "BRAF mutations in an Italian cohort of thyroid cancers." Clinical endocrinology 61 (2) doi:10.1111/j.1365-2265.2004.02089.x

2003

Verga Uberta, Fugazzola Laura, Cambiaghi Stefano, Pritelli Chiara, Alessi Elvio, et al. 2003. "Frequent association between MEN 2A and cutaneous lichen amyloidosis." Clinical endocrinology 59 (2) doi:
Fugazzola Laura, Persani Luca, Mannavola Deborah, Reschini Eugenio, Vannucchi Guia, et al. 2003. "Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacement." Clinical endocrinology 59 (2) doi:

2002

Fugazzola Laura, Mihalich Alessandra, Persani Luca, Cerutti Nadia, Reina Michela, et al. 2002. "Highly sensitive serum thyroglobulin and circulating thyroglobulin mRNA evaluations in the management of patients with differentiated thyroid cancer in apparent remission." The Journal of clinical endocrinology and metabolism 87 (7) doi:
Fugazzola Laura, Cerutti Nadia, Mannavola Deborah, Crino Antonino, Cassio Alessandra, et al. 2002. "Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies." Pediatric research 51 (4) doi:10.1203/00006450-200204000-00013