檢索結果 - Udani, Vrajesh

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  1. 1
    Posterior Reversible Encephalopathy Syndrome: An Expanding Phenotype

    Posterior Reversible Encephalopathy Syndrome: An Expanding Phenotype 由 Udani, Vrajesh

    出版 2020
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  2. 2
    Pediatric epilepsy: The Indian experience

    Pediatric epilepsy: The Indian experience 由 Gadgil, Pradnya, Udani, Vrajesh

    出版 2011
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  3. 3
    A Retrospective Analysis of the Long-Term Outcome of Drug-Resistant Epilepsy in Children Treated in Urban India

    A Retrospective Analysis of the Long-Term Outcome of Drug-Resistant Epilepsy in Children Treated in Urban India 由 Raimalwalla, Toranj, Udani, Vrajesh, Mhatre, Dimpi

    出版 2018
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  4. 4
    Panthotenate Kinase‐Associated Neurodegeneration Has a Founder Mutation (c.215_216insa) in Indian Agrawal Patients

    Panthotenate Kinase‐Associated Neurodegeneration Has a Founder Mutation (c.215_216insa) in Indian Agrawal Patients 由 Udani, Vrajesh, Das, Soma, Chhabria, Rahul

    出版 2016
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  5. 5
    Partial Manifestation of Anti‐NMDA‐R Encephalitis with Predominant Movement Disorder

    Partial Manifestation of Anti‐NMDA‐R Encephalitis with Predominant Movement Disorder 由 Udani, Vrajesh, Desai, Neelu, Botre, Abhijeet

    出版 2015
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  6. 6
    Mutational Analysis of Methyl‐CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome

    Mutational Analysis of Methyl‐CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome 由 Das, Dhanjit Kumar, Udani, Vrajesh, Sanghavi, Daksha, Adhia, Rashmi, Maitra, Anurupa

    出版 2013
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  7. 7
    Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic

    Paroxysmal Nonepileptic Events in a Pediatric Epilepsy Clinic 由 Mandli, Ashfak H., Desai, Neelu A., Badheka, Rahul S., Udani, Vrajesh P.

    出版 2021
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  8. 8
    Leukocyte Phosphomannomutase and Phosphomannose Isomerase Activity in an Indian Cohort

    Leukocyte Phosphomannomutase and Phosphomannose Isomerase Activity in an Indian Cohort 由 Dave, Mihika B., Dherai, Alpa J., Udani, Vrajesh P., Ashavaid, Tester F.

    出版 2020
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  9. 9
    Comparison of transferrin isoform analysis by capillary electrophoresis and HPLC for screening congenital disorders of glycosylation

    Comparison of transferrin isoform analysis by capillary electrophoresis and HPLC for screening congenital disorders of glycosylation 由 Dave, Mihika B., Dherai, Alpa J., Udani, Vrajesh P., Hegde, Anaita U., Desai, Neelu A., Ashavaid, Tester F.

    出版 2017
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  10. 10
    Paroxysmal Asymmetric Dystonic Arm Posturing—A Less Recognized but Characteristic Manifestation of ATP1A3‐related disease

    Paroxysmal Asymmetric Dystonic Arm Posturing—A Less Recognized but Characteristic Manifestation of ATP1A3‐related disease 由 Balint, Bettina, Stephen, Christopher D., Udani, Vrajesh, Sankhla, Charulata Savant, Barad, Narendrakumar H., Lang, Anthony E., Bhatia, Kailash P.

    出版 2019
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  11. 11
    Analytical Method Validation for Estimation of Neurotransmitters (Biogenic Monoamines) from Cerebrospinal Fluid Using High Performance Liquid Chromatography

    Analytical Method Validation for Estimation of Neurotransmitters (Biogenic Monoamines) from Cerebrospinal Fluid Using High Performance Liquid Chromatography 由 Lokhande, Rohan V., Bhagure, Ganesh R., Dherai, Alpa J., Naik, Prasad R., Udani, Vrajesh P., Desai, Neelu A., Ashavaid, Tester F.

    出版 2021
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