Pesquisa | Biblioteca Virtual em Saúde

1.

Genetic variation in transmembrane 6 superfamily member 2 and the risk of nonalcoholic fatty liver disease and histological disease severity.

Sookoian, Silvia; Castaño, Gustavo O; Scian, Romina; Mallardi, Pablo; Fernández Gianotti, Tomas; Burgueño, Adriana L; San Martino, Julio; Pirola, Carlos J.

Hepatology ; 61(2): 515-25, 2015 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-25302781

2.

Circulating microRNA signature in non-alcoholic fatty liver disease: from serum non-coding RNAs to liver histology and disease pathogenesis.

Pirola, Carlos J; Fernández Gianotti, Tomas; Castaño, Gustavo O; Mallardi, Pablo; San Martino, Julio; Mora Gonzalez Lopez Ledesma, María; Flichman, Diego; Mirshahi, Faridodin; Sanyal, Arun J; Sookoian, Silvia.

Gut ; 64(5): 800-12, 2015 May.

Artigo em Inglês | MEDLINE | ID: mdl-24973316

3.

Cross talk between the liver microbiome and epigenome in patients with metabolic dysfunction-associated steatotic liver disease.

Pirola, Carlos Jose; Salatino, Adrian; Fernández Gianotti, Tomas; Castaño, Gustavo Osvaldo; Garaycoechea, Martin; Sookoian, Silvia.

EBioMedicine ; 101: 104996, 2024 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-38320344

4.

Epigenetic regulation of insulin resistance in nonalcoholic fatty liver disease: impact of liver methylation of the peroxisome proliferator-activated receptor Î³ coactivator 1α promoter.

Sookoian, Silvia; Rosselli, Maria Soledad; Gemma, Carolina; Burgueño, Adriana L; Fernández Gianotti, Tomas; Castaño, Gustavo O; Pirola, Carlos J.

Hepatology ; 52(6): 1992-2000, 2010 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-20890895

5.

A Rare Nonsense Mutation in the Glucokinase Regulator Gene Is Associated With a Rapidly Progressive Clinical Form of Nonalcoholic Steatohepatitis.

Pirola, Carlos J; Flichman, Diego; Dopazo, Hernán; Fernández Gianotti, Tomas; San Martino, Julio; Rohr, Cristian; Garaycoechea, Martin; Gazzi, Carla; Castaño, Gustavo O; Sookoian, Silvia.

Hepatol Commun ; 2(9): 1030-1036, 2018 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-30202818

6.

Genetic variation in long noncoding RNAs and the risk of nonalcoholic fatty liver disease.

Sookoian, Silvia; Rohr, Cristian; Salatino, Adrián; Dopazo, Hernán; Fernandez Gianotti, Tomas; Castaño, Gustavo O; Pirola, Carlos J.

Oncotarget ; 8(14): 22917-22926, 2017 Apr 04.

Artigo em Inglês | MEDLINE | ID: mdl-28206970

7.

Serum aminotransferases in nonalcoholic fatty liver disease are a signature of liver metabolic perturbations at the amino acid and Krebs cycle level.

Sookoian, Silvia; Castaño, Gustavo O; Scian, Romina; Fernández Gianotti, Tomas; Dopazo, Hernán; Rohr, Cristian; Gaj, Graciela; San Martino, Julio; Sevic, Ina; Flichman, Diego; Pirola, Carlos J.

Am J Clin Nutr ; 103(2): 422-34, 2016 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-26791191

8.

Promoter DNA methylation of farnesoid X receptor and pregnane X receptor modulates the intrahepatic cholestasis of pregnancy phenotype.

Cabrerizo, Romina; Castaño, Gustavo O; Burgueño, Adriana L; Fernández Gianotti, Tomas; Gonzalez Lopez Ledesma, María Mora; Flichman, Diego; Pirola, Carlos J; Sookoian, Silvia.

PLoS One ; 9(1): e87697, 2014.

Artigo em Inglês | MEDLINE | ID: mdl-24498169

9.

Fatty liver is associated with transcriptional downregulation of stearoyl-CoA desaturase and impaired protein dimerization.

Fernández Gianotti, Tomas; Burgueño, Adriana; Gonzales Mansilla, Noelia; Pirola, Carlos Jose; Sookoian, Silvia.

PLoS One ; 8(9): e76912, 2013.

Artigo em Inglês | MEDLINE | ID: mdl-24098813

10.

Epigenética y síndrome metabólico / Epigenetics and Metabolic Syndrome

Fernández Gianotti, Tomás; Pirola, Carlos José.

Rev. argent. endocrinol. metab ; 52(1): 35-44, mar. 2015. ilus, tab

Artigo em Espanhol | BINACIS | ID: bin-134070

11.

Epigenética y síndrome metabólico / Epigenetics and Metabolic Syndrome

Fernández Gianotti, Tomás; Pirola, Carlos José.

Rev. argent. endocrinol. metab ; 52(1): 35-44, mar. 2015. ilus, tab

Artigo em Espanhol | LILACS | ID: lil-750604

12.

Ectopic growth hormone-releasing hormone secretion by a metastatic bronchial carcinoid tumor: a case with a non hypophysial intracranial tumor that shrank during long acting octreotide treatment.

Fainstein Day, Patricia; Frohman, Lawrence; Garcia Rivello, Hernan; Reubi, Jean Claude; Sevlever, Gustavo; Glerean, Mariela; Fernandez Gianotti, Tomas; Pietrani, Marcelo; Rabadan, Alejandra; Racioppi, Silvina; Bidlingmaier, Martin.

Pituitary ; 10(3): 311-9, 2007.

Artigo em Inglês | MEDLINE | ID: mdl-17373589

13.

Pesquisa de hipotiroidismo congénito: resultados de dieciocho años de trabajo ininterrumpido en el Hospital Italiano de Buenos Aires / Survey of congenital hypothyroidism: results of eighteen years of uninterrupted work in the Hospital Italiano de Buenos Aires

Balzaretti, Marta; Kozak, Andrea; Fernández Gianotti, Tomás; Alonso, Guillermo; Jenik, Alejandro; Fainstein Day, Patricia.

Rev. Hosp. Ital. B. Aires (2004) ; 28(2): 57-62, dic. 2008. graf, tab

Artigo em Espanhol | LILACS | ID: lil-575085

14.

Carcinoma medular de tiroides familiar (CMTF): primera familia descripta con CMTF asociado a la mutación Cys611Trp del proto-oncogen RET / Familial medullary thyroid carcinoma (FMTC): first family described with FMTC associated to Cys611Trp mutation of RET proto-oncogene

Fernández Gianotti, Tomás; Fainstein Day, Patricia; Russo Picasso, María Fabiana; Knoblovits, Pablo; Figari, Marcelo.

Rev. Hosp. Ital. B. Aires (2004) ; 24(1)sept. 2004. ilus, tab

Artigo em Espanhol | LILACS | ID: lil-506961

15.

Fernandez Gianotti, Tomás.

In. Gagliardino, Juan José. La depleción del ADN mitocondrial en la patogenia del síndrome metabólico. Buenos Aires, Ministerio de Salud de la Nación, 2007. . (120229).

Monografia em Espanhol | BINACIS | ID: bin-120229

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Genetic variation in transmembrane 6 superfamily member 2 and the risk of nonalcoholic fatty liver disease and histological disease severity.

Circulating microRNA signature in non-alcoholic fatty liver disease: from serum non-coding RNAs to liver histology and disease pathogenesis.

Cross talk between the liver microbiome and epigenome in patients with metabolic dysfunction-associated steatotic liver disease.

Epigenetic regulation of insulin resistance in nonalcoholic fatty liver disease: impact of liver methylation of the peroxisome proliferator-activated receptor Î³ coactivator 1α promoter.

A Rare Nonsense Mutation in the Glucokinase Regulator Gene Is Associated With a Rapidly Progressive Clinical Form of Nonalcoholic Steatohepatitis.

Genetic variation in long noncoding RNAs and the risk of nonalcoholic fatty liver disease.

Serum aminotransferases in nonalcoholic fatty liver disease are a signature of liver metabolic perturbations at the amino acid and Krebs cycle level.

Promoter DNA methylation of farnesoid X receptor and pregnane X receptor modulates the intrahepatic cholestasis of pregnancy phenotype.

Fatty liver is associated with transcriptional downregulation of stearoyl-CoA desaturase and impaired protein dimerization.

Epigenética y síndrome metabólico / Epigenetics and Metabolic Syndrome

Epigenética y síndrome metabólico / Epigenetics and Metabolic Syndrome

Ectopic growth hormone-releasing hormone secretion by a metastatic bronchial carcinoid tumor: a case with a non hypophysial intracranial tumor that shrank during long acting octreotide treatment.

Pesquisa de hipotiroidismo congénito: resultados de dieciocho años de trabajo ininterrumpido en el Hospital Italiano de Buenos Aires / Survey of congenital hypothyroidism: results of eighteen years of uninterrupted work in the Hospital Italiano de Buenos Aires

Carcinoma medular de tiroides familiar (CMTF): primera familia descripta con CMTF asociado a la mutación Cys611Trp del proto-oncogen RET / Familial medullary thyroid carcinoma (FMTC): first family described with FMTC associated to Cys611Trp mutation of RET proto-oncogene