Search Results - Ajit, Valaparambil Karthika

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  1. 1
    A genotype–phenotype description in two Indian patients: Broadening the spectrum in VRK1‐related complex motor disorders

    A genotype–phenotype description in two Indian patients: Broadening the spectrum in VRK1‐related complex motor disorders by Ajit, Valaparambil Karthika, Nair, Sruthi Sivaraman, Anjali, Sethu Madhavan, Vidyadharan, Pravi, Urulangodi, Madhusoodanan, Menon, Ramshekhar N., Sundaram, Soumya

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  2. 2
    Movement Disorders in GRIA2‐Related Disorder – Expanding the Genetic Spectrum of Developmental Dyskinetic Encephalopathy

    Movement Disorders in GRIA2‐Related Disorder – Expanding the Genetic Spectrum of Developmental Dyskinetic Encephalopathy by Vijayaraghavan, Asish, Urulangodi, Madhusoodanan, Ajit Valaparambil, Karthika, Sundaram, Soumya, Krishnan, Syam

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  3. 3
    Steroid Responsive Encephalopathy Associated with Autoimmune Thyroiditis (SREAT): Authors' Reply

    Steroid Responsive Encephalopathy Associated with Autoimmune Thyroiditis (SREAT): Authors' Reply by Karthika, Ajit Valaparambil, Madhavan, Sheeja, Kunju, P A Mohammed, Kalpana, D

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  4. 4
    Clinical Utility of Proband Only Clinical Exome Sequencing in Neurodevelopmental Disorders

    Clinical Utility of Proband Only Clinical Exome Sequencing in Neurodevelopmental Disorders by Valaparambil, Karthika Ajit, Fasaludeen, Alfiya, Priya, Lakshmi, Menon, Ramshekhar N., Menon, Ramesh, Sundaram, Soumya

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  5. 5
    Status Epilepticus in Coenzyme A Synthase Protein-Associated Neurodegeneration - Expanding the Clinical Phenotype

    Status Epilepticus in Coenzyme A Synthase Protein-Associated Neurodegeneration - Expanding the Clinical Phenotype by Ajit, Valaparambil Karthika, Selvaraj, Prabhu, Divya, KP, Thomas, Bejoy, Menon, Ramshekhar N., Sundaram, Soumya

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