Rezultati - Udani, Vrajesh

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  1. 1
    Posterior Reversible Encephalopathy Syndrome: An Expanding Phenotype

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

    Izdano 2020
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  2. 2
    Pediatric epilepsy: The Indian experience

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

    Izdano 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 od Raimalwalla, Toranj, Udani, Vrajesh, Mhatre, Dimpi

    Izdano 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 od Udani, Vrajesh, Das, Soma, Chhabria, Rahul

    Izdano 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 od Udani, Vrajesh, Desai, Neelu, Botre, Abhijeet

    Izdano 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 od Das, Dhanjit Kumar, Udani, Vrajesh, Sanghavi, Daksha, Adhia, Rashmi, Maitra, Anurupa

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

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

    Izdano 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 od Dave, Mihika B., Dherai, Alpa J., Udani, Vrajesh P., Ashavaid, Tester F.

    Izdano 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 od Dave, Mihika B., Dherai, Alpa J., Udani, Vrajesh P., Hegde, Anaita U., Desai, Neelu A., Ashavaid, Tester F.

    Izdano 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 od Balint, Bettina, Stephen, Christopher D., Udani, Vrajesh, Sankhla, Charulata Savant, Barad, Narendrakumar H., Lang, Anthony E., Bhatia, Kailash P.

    Izdano 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 od Lokhande, Rohan V., Bhagure, Ganesh R., Dherai, Alpa J., Naik, Prasad R., Udani, Vrajesh P., Desai, Neelu A., Ashavaid, Tester F.

    Izdano 2021
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