Search Results - Manickam, Agaath

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  1. 1
    Analysis of Genome Wide Associated Variants rs2651899 (PRDM16), rs11172113 (LRP1), and rs10166942 (TRPM8) of Migraine in the Indian Episodic Migraineurs

    Analysis of Genome Wide Associated Variants rs2651899 (PRDM16), rs11172113 (LRP1), and rs10166942 (TRPM8) of Migraine in the Indian Episodic Migraineurs by Manickam, Agaath Hedina, Ramasamy, Sivasamy

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  2. 2
    Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy

    Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy by Manickam, Agaath Hedina, Michael, Minu Jenifer, Ramasamy, Sivasamy

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  3. 3
    Mutations in the Voltage Dependent Calcium Channel CACNA1A (P/Q type alpha 1A subunit) Causing Neurological Disorders - An Overview

    Mutations in the Voltage Dependent Calcium Channel CACNA1A (P/Q type alpha 1A subunit) Causing Neurological Disorders - An Overview by Manickam, Agaath, Ramasamy, Sivasamy

    Published in Neurology India
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  4. 4
    Chemotherapeutic Resistance Genes of Breast Cancer Patients – An Overview

    Chemotherapeutic Resistance Genes of Breast Cancer Patients – An Overview by Ajith, Anagha Kollamparambil, Subramani, Sasikala, Manickam, Agaath Hedina, Ramasamy, Sivasamy

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  5. 5
    Raynaud's phenomenon secondary to erenumab in a patient with chronic migraine

    Raynaud's phenomenon secondary to erenumab in a patient with chronic migraine by Manickam, Agaath Hedina, Buture, Alina, Tomkins, Esther, Ruttledge, Martin

    Published in Clinical case reports
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  6. 6
    Raynaud's phenomenon secondary to erenumab in a patient with chronic migraine

    Raynaud's phenomenon secondary to erenumab in a patient with chronic migraine by Manickam, Agaath Hedina, Buture, Alina, Tomkins, Esther, Ruttledge, Martin

    Published in Clinical case reports
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