Hasil Pencarian - Rati Devendra

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  1. 1
    Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family

    Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family oleh Rashmi Dongerdiye, Abhilasha Sampagar, Rati Devendra, Prashant Warang, Prabhakar Kedar

    Diterbitkan 2021-07-01
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  2. 2
    Successful management of Methemoglobinemia and G6PD deficiency in a patient posted for surgical excision of branchial cyst

    Successful management of Methemoglobinemia and G6PD deficiency in a patient posted for surgical excision of branchial cyst oleh V J Arun, Anuradha Deorukhkar, Aboobacker Mohamed Rafi, Deepak Charles, Rati Devendra, Susheela J Innah, Prabhakar Kedar

    Diterbitkan 2022-01-01
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  3. 3
    G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India

    G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India oleh Rati Devendra, Vinod Gupta, Somashekhar S. Biradar, Pradeep Bhat, Shantharam Hegde, S. L. Hoti, Malay B. Mukherjee, Harsha V. Hegde

    Diterbitkan 2020-01-01
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