Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family

por Dongerdiye, Rashmi, Sampagar, Abhilasha, Devendra, Rati, Warang, Prashant, Kedar, Prabhakar
Publicado 2021

Successful management of Methemoglobinemia and G6PD deficiency in a patient posted for surgical excision of branchial cyst

por Arun, V J, Deorukhkar, Anuradha, Rafi, Aboobacker Mohamed, Charles, Deepak, Devendra, Rati, Innah, Susheela J, Kedar, Prabhakar
Publicado 2022