Bilaketaren emaitzak - 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 nork Rashmi Dongerdiye, Abhilasha Sampagar, Rati Devendra, Prashant Warang, Prabhakar Kedar

    Argitaratua 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 nork V J Arun, Anuradha Deorukhkar, Aboobacker Mohamed Rafi, Deepak Charles, Rati Devendra, Susheela J Innah, Prabhakar Kedar

    Argitaratua 2022-01-01
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  3. 3

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

    Argitaratua 2020-01-01
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