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List of works by Paolo Emidio Macchia

A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation.

scientific article published in July 2007

A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea

scientific article

A preservation method that allows recovery of intact RNA from tissues dissected by laser capture microdissection.

scientific article

Adherence to the Mediterranean Diet and Circulating Levels of Sirtuin 4 in Obese Patients: A Novel Association

scientific article

Amiodarone Induced Thyrotoxicosis

scientific article published on 24 April 2015

Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate loci.

scientific article

Benign hereditary chorea: clinical and neuroimaging features in an Italian family.

scientific article published on July 2010

Bioelectrical phase angle and psoriasis: a novel association with psoriasis severity, quality of life and metabolic syndrome

scientific article published on 10 May 2016

Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism

scientific article published on December 2010

Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2).

scientific article

Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skipping

scientific article published on 01 March 2002

Dietary polyphenols and chromatin remodeling

scientific article published on 10 September 2015

EFFICACY AND SAFETY OF RADIOFREQUENCY THERMAL ABLATION IN THE TREATMENT OF THYROID NODULES WITH PRESSURE SYMPTOMS IN ELDERLY PATIENTS

scientific article published on 01 September 2007

Effects of treatment modalities for Graves' hyperthyroidism on Graves' orbitopathy: a 2015 Italian Society of Endocrinology Consensus Statement.

scientific article published on 27 February 2015

FOXE1 polymorphisms: a new piece in the puzzle of thyroid dysgenesis

scientific article published on 01 January 2007

Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene

scientific article (publication date: November 1999)

Flavor identification inversely correlates with body mass index (BMI)

scientific article published on 20 April 2020

Flavor perception test: evaluation in patients with Kallmann syndrome

scientific article published on 25 July 2015

Genetic Defects in Thyroid Hormone Supply

scientific article published on 24 April 2015

Germline Polymorphisms of the VEGF Pathway Predict Recurrence in Nonadvanced Differentiated Thyroid Cancer.

scientific article published on 16 November 2016

Glucose-induced expression of the homeotic transcription factor Prep1 is associated with histone post-translational modifications in skeletal muscle

scientific article published on 9 October 2015

High-dose intravenous corticosteroid therapy for Graves' ophthalmopathy

scientific article published in March 2001

Identification and functional characterization of a novel mutation in the NKX2-1 gene: comparison with the data in the literature

scientific article

Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alpha

scholarly article

Influence of nutrition on somatotropic axis: Milk consumption in adult individuals with moderate-severe obesity

scientific article published on 18 December 2015

Influences of Age, Sex and Smoking Habit on Flavor Recognition in Healthy Population

scientific article published on 04 February 2020

Iodine deficiency among Italian children and adolescents assessed through 24-hour urinary iodine excretion

scientific article published on 01 April 2019

Long period fiber grating nano-optrode for cancer biomarker detection

scientific article published on 13 February 2016

Mediterranean Diet and Phase Angle in a Sample of Adult Population: Results of a Pilot Study

scientific article published on 17 February 2017

Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis

scientific article

Molecular genetics of congenital hypothyroidism

scientific article

Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis

scientific article published on 01 March 2009

Mutations in the Gene EncodingThyroid Transcription Factor-1 (TTF-1) Are Not a Frequent Cause of Congenital Hypothyroidism (CH) with Thyroid Dysgenesis ⬇️

scientific article published on June 1, 1997

Nutrition and psoriasis: is there any association between the severity of the disease and adherence to the Mediterranean diet?

scientific article

Nutrition: a key environmental dietary factor in clinical severity and cardio-metabolic risk in psoriatic male patients evaluated by 7-day food-frequency questionnaire

scientific article

Orbital scintigraphy with [111In-diethylenetriamine pentaacetic acid-D-phe1]-octreotide predicts the clinical response to corticosteroid therapy in patients with Graves' ophthalmopathy

scientific article published in November 1998

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

scientific article

Pregnancy outcome in women treated with methimazole or propylthiouracil during pregnancy.

scientific article published on 4 April 2015

Preliminary results demonstrating the impact of Mediterranean diet on bone health

scientific article

Quercetin and its derivative Q2 modulate chromatin dynamics in adipogenesis and Q2 prevents obesity and metabolic disorders in rats

scientific article published on 08 April 2019

RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor

scientific article

Reply to A Olivieri et al

scientific article published on 01 November 2019

Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis

scientific article published on 08 November 2010

Search for abnormalities of nuclear corepressors, coactivators, and a coregulator in families with resistance to thyroid hormone without mutations in thyroid hormone receptor beta or alpha genes

scientific article published on 01 October 2000

Similarities and differences in the reproductive phenotypes of women with congenital hypogonadotrophic hypogonadism caused by GNRHR mutations and women with polycystic ovary syndrome

scientific article published on 01 January 2019

Structural defects of a Pax8 mutant that give rise to congenital hypothyroidism

scientific article published in 1999

The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease

scientific article published on 20 March 2019

The molecular causes of thyroid dysgenesis: a systematic review

scientific article published on 22 May 2013

Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes

scientific article published in January 2002

Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I

scientific article published on 01 December 1995

Thyroid nodules and related symptoms are stably controlled two years after radiofrequency thermal ablation

scientific article published in March 2009

Thyroid nodules treated with percutaneous radiofrequency thermal ablation: a comparative study

scientific article published on 27 September 2012

[Endemic goiter: clinical picture and evolution]

scientific article published on 01 January 1998

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