Di Cosmo, Caterina: search on Z-Library

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1

Mct8-Deficient Mice Have Increased Energy Expenditure and Reduced Fat Mass That Is Abrogated by Normalization of Serum T 3 Levels

Di Cosmo, Caterina, Liao, Xiao-Hui, Ye, Honggang, Ferrara, Alfonso Massimiliano, Weiss, Roy E., Refetoff, Samuel, Dumitrescu, Alexandra M.

Journal:

Year:

2013

Language:

english

File:

PDF, 872 KB

english, 2013

2

Lyophilized red wine administration prolongs survival in an animal model of amyotrophic lateral sclerosis

Ennio Esposito, Cosmo Rossi, Rosalba Amodio, Augusto Di Castelnuovo, Caterina Bendotti, Tiziana Rotondo, Sergio Algeri, Domenico Rotilio

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 121 KB

english, 2000

3

Infezioni cutanee e mucose multiple in donna con agranulocitosi indotta da metimazolo

Caterina di Cosmo,Teresa Rago,Michele Marinò,Edda Vignali

Journal:

L'Endocrinologo

Year:

2003

Language:

italian

File:

PDF, 226 KB

italian, 2003

4

A Combined Therapy with Myo-Inositol and D-Chiro-Inositol Improves Endocrine Parameters and Insulin Resistance in PCOS Young Overweight Women

Benelli, Elena, Del Ghianda, Scilla, Di Cosmo, Caterina, Tonacchera, Massimo

Journal:

International Journal of Endocrinology

Year:

2016

Language:

english

File:

PDF, 1.20 MB

english, 2016

5

Identification and Functional Analysis of Novel Dual Oxidase 2 (DUOX2) Mutations in Children with Congenital or Subclinical Hypothyroidism

De Marco, Giuseppina, Agretti, Patrizia, Montanelli, Lucia, Di Cosmo, Caterina, Bagattini, Brunella, De Servi, Melissa, Ferrarini, Eleonora, Dimida, Antonio, Freitas Ferreira, Andrea Claudia, Molinaro

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2011

Language:

english

File:

PDF, 534 KB

english, 2011

6

Identification and Functional Studies of Two New Dual-Oxidase 2 (DUOX2) Mutations in a Child with Congenital Hypothyroidism and a Eutopic Normal-Size Thyroid Gland

Tonacchera, Massimo, De Marco, Giuseppina, Agretti, Patrizia, Montanelli, Lucia, Di Cosmo, Caterina, Freitas Ferreira, Andrea Claudia, Dimida, Antonio, Ferrarini, Eleonora, Ramos, Helton Estrela, Cecc

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 320 KB

english, 2009

7

Thyroid Hormone-Regulated Mouse Cerebral Cortex Genes Are Differentially Dependent on the Source of the Hormone: A Study in Monocarboxylate Transporter-8- and Deiodinase-2-Deficient Mice

Morte, Beatriz, Ceballos, Ainhoa, Diez, Diego, Grijota-Martínez, Carmen, Dumitrescu, Alexandra M., Di Cosmo, Caterina, Galton, Valerie Anne, Refetoff, Samuel, Bernal, Juan

Journal:

Year:

2010

Language:

english

File:

PDF, 285 KB

english, 2010

8

Thyroid Hormone Receptor α and Regulation of Type 3 Deiodinase

Barca-Mayo, Olga, Liao, Xiao-Hui, Alonso, Manuela, Di Cosmo, Caterina, Hernandez, Arturo, Refetoff, Samuel, Weiss, Roy E.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2011

Language:

english

File:

PDF, 61 KB

english, 2011

9

Obesity and monitoring iodine nutritional status in schoolchildren: is body mass index a factor to consider?

De Angelis, Simona, Bagnasco, Marcello, Moleti, Mariacarla, Regalbuto, Concetto, Tonacchera, Massimo, Vermiglio, Francesco, Medda, Emanuela, Rotondi, Daniela, Di Cosmo, Caterina, dimida, antonio, Rago

Journal:

Year:

2020

File:

PDF, 1.13 MB

2020

10

Genetic analysis of the PAX8 gene in children with congenital hypothyroidism and dysgenetic or eutopic thyroid glands: identification of a novel sequence variant

Massimo Tonacchera, Maria Elena Banco, Lucia Montanelli, Caterina Di Cosmo, Patrizia Agretti, Giuseppina De Marco, Eleonora Ferrarini, Arash Ordookhani, Anna Perri, Luca Chiovato, Ferruccio Santini, P

Journal:

Clinical Endocrinology

Year:

2007

Language:

english

File:

PDF, 254 KB

english, 2007

11

Genetic Analysis of TTF-2 Gene in Children with Congenital Hypothyroidism and Cleft Palate, Congenital Hypothyroidism, or Isolated Cleft Palate

Tonacchera, Massimo, Banco, Mariaelena, Lapi, Paola, Di Cosmo, Caterina, Perri, Anna, Montanelli, Lucia, Moschini, Lidia, Gatti, Gianluca, Gandini, Daniele, Massei, Alessandro, Agretti, Patrizia, De M

Journal:

Year:

2004

Language:

english

File:

PDF, 176 KB

english, 2004

12

A Thyroid Hormone Analog with Reduced Dependence on the Monocarboxylate Transporter 8 for Tissue Transport

Di Cosmo, Caterina, Liao, Xiao-Hui, Dumitrescu, Alexandra M., Weiss, Roy E., Refetoff, Samuel

Journal:

Year:

2009

Language:

english

File:

PDF, 190 KB

english, 2009

13

Manifestazioni cliniche delle mutazioni del trasportatore degli ormoni tiroidei MCT8

Caterina Di Cosmo

Journal:

L'Endocrinologo

Year:

2013

Language:

italian

File:

PDF, 541 KB

italian, 2013

14

Benign Nonfunctioning Thyroid Adenomas Are Characterized by a Defective Targeting to Cell Membrane or a Reduced Expression of the Sodium Iodide Symporter Protein

Tonacchera, Massimo, Viacava, Paolo, Agretti, Patrizia, de Marco, Giuseppina, Perri, Anna, di Cosmo, Caterina, de Servi, Melissa, Miccoli, Paolo, Lippi, Francesco, Naccarato, Antonio Giuseppe, Pincher

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2002

Language:

english

File:

PDF, 295 KB

english, 2002

15

Weight Loss Associated with Bariatric Surgery Does Not Restore Short Telomere Length of Severe Obese Patients After 1 Year

Formichi, Caterina, Cantara, Silvia, Ciuoli, Cristina, Neri, Ornella, Chiofalo, Francesco, Selmi, Federico, Tirone, Andrea, Colasanto, Giuseppina, Di Cosmo, Leonardo, Vuolo, Giuseppe, Pacini, Furio

Journal:

Obesity Surgery

Year:

2014

Language:

english

File:

PDF, 327 KB

english, 2014

16

Clinical features, risk of mass enlargement, and development of endocrine hyperfunction in patients with adrenal incidentalomas: a long-term follow-up study

Falcetta, Pierpaolo, Orsolini, Francesca, Benelli, Elena, Agretti, Patrizia, Vitti, Paolo, Di Cosmo, Caterina, Tonacchera, Massimo

Journal:

Endocrine (Springer)

Year:

2020

File:

PDF, 699 KB

2020

17

Clinical and Molecular Characterization of a Novel Selenocysteine Insertion Sequence-Binding Protein 2 ( SBP2 ) Gene Mutation (R128X)

Di Cosmo, Caterina, McLellan, Neil, Liao, Xiao-Hui, Khanna, Kum Kum, Weiss, Roy E., Papp, Laura, Refetoff, Samuel

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 183 KB

english, 2009

18

An essential physiological role for MCT8 in bone in male mice

Leitch, Victoria D., Di Cosmo, Caterina, Liao, Xiao-Hui, O'Boy, Sam, Galliford, Thomas M., Evans, Holly, Croucher, Peter I., Boyde, Alan, Dumitrescu, Alexandra, Weiss, Roy E., Refetoff, Samuel, Willia

Journal:

Year:

2017

Language:

english

File:

PDF, 24.85 MB

english, 2017

19

Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene

Patrizia Agretti, Giuseppina De Marco, Caterina Di Cosmo…

Journal:

European Journal of Pediatrics

Year:

2013

Language:

english

File:

PDF, 218 KB

english, 2013

20

Distinct Roles of Deiodinases on the Phenotype of Mct8 Defect: A Comparison of Eight Different Mouse Genotypes

Liao, Xiao-Hui, Di Cosmo, Caterina, Dumitrescu, Alexandra M., Hernandez, Arturo, Van Sande, Jacqueline, St. Germain, Donald L., Weiss, Roy E., Galton, Valerie Anne, Refetoff, Samuel

Journal:

Year:

2011

Language:

english

File:

PDF, 1.98 MB

english, 2011

21

Low Prevalence of Thyrotropin Receptor Mutations in a Large Series of Subjects with Sporadic and Familial Nonautoimmune Subclinical Hypothyroidism

Tonacchera, Massimo, Perri, Anna, De Marco, Giuseppina, Agretti, Patrizia, Banco, Maria Elena, Di Cosmo, Caterina, Grasso, Lucia, Vitti, Paolo, Chiovato, Luca, Pinchera, Aldo

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2004

Language:

english

File:

PDF, 231 KB

english, 2004

22

Diiodothyropropionic Acid (DITPA) in the Treatment of MCT8 Deficiency

Verge, Charles F., Konrad, Daniel, Cohen, Michal, Di Cosmo, Caterina, Dumitrescu, Alexandra M., Marcinkowski, Teresa, Hameed, Shihab, Hamilton, Jill, Weiss, Roy E., Refetoff, Samuel

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2012

Language:

english

File:

PDF, 1.79 MB

english, 2012

23

Papillary thyroid cancer in a patient with congenital goitrous hypothyroidism due to a novel deletion in NIS gene

Agretti, Patrizia, Bagattini, Brunella, De Marco, Giuseppina, Di Cosmo, Caterina, Dionigi, Gianlorenzo, Vitti, Paolo, Tonacchera, Massimo

Journal:

Endocrine (Springer)

Year:

2016

Language:

english

File:

PDF, 515 KB

english, 2016

24

Thyroglobulin in Orbital Tissues from Patients with Thyroid-Associated Ophthalmopathy: Predominant Localization in Fibroadipose Tissue

Lisi, Simonetta, Marinò, Michele, Pinchera, Aldo, Mazzi, Barbara, di Cosmo, Caterina, Sellari-Franceschini, Stefano, Chiovato, Luca

Journal:

Year:

2002

Language:

english

File:

PDF, 219 KB

english, 2002

25

The Syndrome of Inherited Partial SBP2 Deficiency in Humans

Dumitrescu, Alexandra M., Cosmo, Caterina Di, Liao, Xiao-Hui, Weiss, Roy E., Refetoff, Samuel

Journal:

Antioxidants & Redox Signaling

Year:

2010

Language:

english

File:

PDF, 4.70 MB

english, 2010

26

Disruption of the Melanin-Concentrating Hormone Receptor 1 (MCH1R) Affects Thyroid Function

Chung, Shinjae, Liao, Xiao-Hui, Di Cosmo, Caterina, Van Sande, Jacqueline, Wang, Zhiwei, Refetoff, Samuel, Civelli, Olivier

Journal:

Year:

2012

Language:

english

File:

PDF, 1.35 MB

english, 2012

27

Identification of TSH receptor mutations in three families with resistance to TSH

Massimo Tonacchera, Caterina Di Cosmo, Giuseppina De Marco, Patrizia Agretti, Mariaelena Banco, Anna Perri, Elena Gianetti, Lucia Montanelli, Paolo Vitti, Aldo Pinchera

Journal:

Clinical Endocrinology

Year:

2007

Language:

english

File:

PDF, 242 KB

english, 2007

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