Volumen 5, Asunto 2 (2016)

Reporte de un caso

Two Novel Mutations in the AGK Gene: Two Case Reports with Sengers Syndrome

  • Deniz Kor, Berna Seker Yılmaz, Ozden Ozgur Horoz, Gulay Ceylaner, Selcuk Sızmaz, Fadli Demir and Neslihan Onenli Mungan

Reporte de un caso

Hereditary Xanthinuria with Recurrent Urolithiasis Occurring in Infancy

  • Afef Bahlous, Mehdi M’rad, Eya Kalaie, Mouna Bouksila, Manef Gasmi, Amira Mohsni, Kahena Bouzid and Jaouida Abdelmoula

Artículo de revisión

A Rapid Real-Time PCR Assay for CYP2C19 Gene Variants to Optimize the Use of Clopidogrel and Other Anti-Platelet Drugs for PCI Stent Patients

  • Khandrika L, Parsam V, Mahalingam M, Musmoori SG, Nandan U,Dange S, Sahoo PK, Rath PC and Jain J