Publications by authors named "Emilia Vieira"

18Publications

New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy.

J Hum Genet 2014 Aug 10;59(8):454-64. Epub 2014 Jul 10.

1] Departamento de Ciências Biológicas, Laboratório de Bioquímica, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal [2] Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.

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August 2014

Bilirubin levels and redox status in a young healthy population.

Acta Haematol 2013 6;130(1):57-60. Epub 2013 Mar 6.

Laboratório de Bioquímica, Departamento de Ciências Biológicas, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal.

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September 2013

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.

Blood Cells Mol Dis 2012 Mar 9;48(3):166-72. Epub 2012 Feb 9.

Departamento de Ciências Biológicas, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Portugal.

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March 2012

Bilirubin dependence on UGT1A1 polymorphisms, hemoglobin, fasting time and body mass index.

Am J Med Sci 2012 Feb;343(2):114-118

Department of Biological Sciences, Biochemistry Laboratory, Faculty of Pharmacy of Oporto University, Porto; Institute for Cellular and Molecular Biology, Oporto University, Porto, Portugal. Electronic address:

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February 2012

Gene symbol: UGT1A1. Disease: Crigler-Najjar syndrome 1.

Hum Genet 2008 Oct;124(3):301

Instituto Politécnico de Bragança, Escola Superior de Saúde, Dr. António Bernardino de Almeida, NA, 4200-072 Porto, Bragança, Portugal.

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October 2008

Molecular characterization of a Portuguese patient with Shwachman-Diamond syndrome.

J Pediatr Gastroenterol Nutr 2005 Jul;41(1):115-6

Serviço de Pediatria, Hospital Central Especializado de Crianças Maria Pia, Porto, Portugal.

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July 2005

A new case of (TA)8 allele in the UGT1A1 gene promoter in a Caucasian girl with Gilbert syndrome.

Pediatr Hematol Oncol 2004 Jul-Aug;21(5):371-4

Serviço de Hematologia, Hospital de Crianças Maria Pia, Porto, Portugal.

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January 2005

[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome].

Acta Med Port 2002 Nov-Dec;15(6):409-12

Serviço de Hematologia, Hospital Maria Pia, Serviços de Hematologia Clínica e Pediátrica, Hospital Geral de Santo António, Unidade de Genética Molecular, Instituto de Genética Doutor Jacinto de Magalhães, Porto.

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May 2003