1. Catalase enzyme mutations and their association with diseases

   • László Góth
   • Péter Rass
   • Anikó Páy

   Review Article 01 December 2012 Pages: 141 - 149

   

2. Hereditary hyperekplexia caused by novel mutations of GLRA1 in Turkish families

   • Sandra L. Gilbert
   • Fatih Ozdag
   • Bruce T. Lahn

   Short Communication 01 December 2012 Pages: 151 - 155

   

3. Association of the human bradykinin B₂ receptor gene with chronic renal failure

   • Lucyna Jozwiak
   • Andrzej Drop
   • Monika Buraczynska

   Original Research Article 01 December 2012 Pages: 157 - 161

   

4. A novel 1297–1304delGCCTGCCA mutation in the exon 10 of the thyroid hormone receptor β gene causes resistance to thyroid hormone

   • Carina M. Rivolta
   • M. Susana Mallea Gil
   • Héctor M. Targovnik

   Original Research Article 01 December 2012 Pages: 163 - 169

   

5. 17α-hydroxylase deficiency

   • Maria S. Perez
   • Haydee Benencia
   • Norma B. Marquez

   Original Research Article 01 December 2012 Pages: 171 - 178

   

6. Quantitative detection of Escherichia coli from urine of patients with bacteriuria by real-time PCR

   • Nobuyuki Hinata
   • Toshiro Shirakawa
   • Akinobu Gotoh

   Original Research Article 01 December 2012 Pages: 179 - 184

   

7. Comparison of three PCR assays for the evaluation of interferon-β biological activity in patients with multiple sclerosis

   • Francesca Gilli
   • Fabiana Marnetto
   • Antonio Bertolotto

   Original Research Article 01 December 2012 Pages: 185 - 194