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

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

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

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

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

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

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