Massimo Tonacchera


Ontology type: schema:Person     


Person Info

NAME

Massimo

SURNAME

Tonacchera

Publications in SciGraph latest 50 shown

  • 2018 Congenital Hypothyroidism in THYROID DISEASES
  • 2018 Toxic Adenoma and Multinodular Toxic Goiter in THYROID DISEASES
  • 2018 Congenital Hypothyroidism in THYROID DISEASES
  • 2017-06 Iodoprofilassi 11 anni dopo: progressi e prospettive in L'ENDOCRINOLOGO
  • 2017 Toxic Adenoma and Multinodular Toxic Goiter in THYROID DISEASES
  • 2016-10 Papillary thyroid cancer in a patient with congenital goitrous hypothyroidism due to a novel deletion in NIS gene in ENDOCRINE
  • 2015-09 Pregnancy outcome in women treated with methimazole or propylthiouracil during pregnancy in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2015-02 Rare diseases in clinical endocrinology: a taxonomic classification system in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2015 Iodine Deficiency from Pregnancy to Childhood in THYROID DISEASES IN CHILDHOOD
  • 2014-12 Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism in BMC ENDOCRINE DISORDERS
  • 2014-10 BRAF mutation analysis in thyroid nodules with indeterminate cytology: our experience on surgical management of patients with thyroid nodules from an area of borderline iodine deficiency in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2014-02 Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2013-12 Non-autoimmune subclinical hypothyroidism due to a mutation in TSH receptor: report on two brothers in ITALIAN JOURNAL OF PEDIATRICS
  • 2013-12 Radioiodide induces apoptosis in human thyroid tissue in culture in ENDOCRINE
  • 2013-10 Diagnostic utility of BRAFV600E mutation testing in thyroid nodules in elderly patients in BMC SURGERY
  • 2013-10 Genetic mutations in the treatment of anaplastic thyroid cancer: a systematic review in BMC SURGERY
  • 2013-10 In vivo assessment about the effects of a diet containing iodine-enriched foodstuffs. A pilot study in 30 volunteers in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2013-10 The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2013-07 Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene in EUROPEAN JOURNAL OF PEDIATRICS
  • 2013-03 The Italian screening program for primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2012-12 Metabolic engineering of the iodine content in Arabidopsis in SCIENTIFIC REPORTS
  • 2012-07 Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene in EUROPEAN JOURNAL OF PEDIATRICS
  • 2012-02 Thyroid autoimmunity may represent a predisposition for the development of fibromyalgia? in RHEUMATOLOGY INTERNATIONAL
  • 2011-11 Thyroid-stimulating hormone levels in the first days of life and perinatal factors associated with sub-optimal neuromotor outcome in pre-term infants in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2011-03 Hyperthyroidism and pregnancy. An Italian Thyroid Association (AIT) and Italian Association of Clinical Endocrinologists (AME) joint statement for clinical practice in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2011-03 Electric and magnetic fields do not modify the biochemical properties of FRTL-5 cells in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2011-03 Study of potential inhibitors of thyroid iodide uptake by using CHO cells stably expressing the human sodium/iodide symporter (hNIS) protein in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2010-12 Patients affected by vitiligo and autoimmune diseases do not show antibodies interfering with the activity of the melanocortin 1 receptor in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2007-04 Ras homolog enriched in striatum inhibits the functional activity of wild type thyrotropin, follicle-stimulating hormone, luteinizing hormone receptors and activating thyrotropin receptor mutations by altering their expression in COS-7 cells in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2006-12 Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2006-01 Uptake of amiodarone by thyroidal and non-thyroidal cell lines in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2004-10 Absence of interference of serum IgGs from patients with breast cancer and thyroid autoimmunity on the function of human iodide symporter gene stably transfected in CHO cells in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2003-10 TSH receptor and Gsα genetic analysis in children with Down’s syndrome and subclinical hypothyroidism in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2003-10 In vitro assay of thyroid disruptors affecting TSH-stimulated adenylate cyclase activity in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 1999-04 Genetic analysis of the TSH receptor gene in differentiated human thyroid carcinomas in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 1994-11 Detection of antibodies blocking thyrotropin effect using Chinese hamster ovary cells transfected with the cloned human TSH receptor in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 1993-07 Measurement of cAMP accumulation in Chinese hamster ovary cells transfected with the recombinant human TSH receptor (CHO-R): a new bioassay for human thyrotropin in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 1993-05 Thyroid autoimmunity and female gender in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 1991-12 Evaluation of L-thyroxine replacement therapy in children with congenital hypothyroidism in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 1989 TSH-Blocking Antibodies and Congenital Hypothyroidism in RESEARCH IN CONGENITAL HYPOTHYROIDISM
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