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Teaching NeuroImage: Neuroimaging Features of Wilson Disease

Neurology, 2024-02, Vol.102 (3), p.e208078

2024

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Use of Ketogenic Diet in Two Indian Children with a Rare Early-Onset Epileptic Encephalopathy

Indian journal of pediatrics, 2023-04, Vol.90 (4), p.414-414

2023

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Cogan's Lid Twitch Sign in a Child with Congenital Myasthenia

Neuropediatrics, 2024-04, Vol.55 (2), p.148

2024

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Paroxysmal Neuropathic Pruritus in Patients With Chiari Malformation Type I: A Rare Phenotype

Pediatric neurology, 2023-03, Vol.140, p.65-67

2023

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Kikuchi-Fujimoto Disease Secondary to Disseminated Brucellosis in an Adolescent Boy

The Pediatric infectious disease journal, 2023-02, Vol.42 (2), p.e55

2023

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Primary Diffuse Leptomeningeal Melanomatosis in an Indian Child With Review of Literature

Pediatric neurology, 2024-03, Vol.152, p.23-29

2024

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Acute Flaccid Paralysis due to Pyruvate Dehydrogenase E1-Alpha Deficiency

Indian journal of pediatrics, 2024-05, Vol.91 (5), p.518-518

2024

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Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF Gene

Indian journal of pediatrics, 2023-08, Vol.90 (8), p.835-835

2023

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Knobloch Syndrome - Triad of Occipital Encephalocele, Retino-Choroidal Detachment and Epilepsy

Indian journal of pediatrics, 2024-03, Vol.91 (3), p.306-306

2024

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Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene

Indian journal of pediatrics, 2024-03, Vol.91 (3), p.317-317

2024

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Clinical Profile, Follow-up, and Role of Neuroimaging in Pediatric Guillain-Barré Syndrome in the COVID Era: An Ambispective Study

Journal of child neurology, 2023-05, Vol.38 (6-7), p.407-413

2023

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Associated movement disorder as a clue for the diagnosis of paroxysmal kinesigenic dyskinesia in a child with focal epilepsy

Journal of neurosciences in rural practice, 2023-07, Vol.14 (3), p.558-559, Article 558

2023

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Add-on Thiamin as an Adjunct in the Treatment of Children with Neuro-Wilson Disease

Indian journal of pediatrics, 2023, Vol.90 (1), p.95-95

2023

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SARS-COV-2 Infection in a Term Neonate Presenting with Respiratory Failure on Day 3 of Life

Indian journal of pediatrics, 2021-01, Vol.88 (1), p.99-100

2021

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A rare case of intermediate phenotype Niemann-Pick disease with a rare pathogenic variant of 1624C>T in SMPD1 gene

Journal of neurosciences in rural practice, 2023-01, Vol.14 (1), p.189-190, Article 189

2023

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A child with global developmental delay and excessive startles: Never overlook the family history

Journal of neurosciences in rural practice, 2022-10, Vol.13 (4), p.808-809, Article 808

2022

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Chromosome Xp22.3 deletion syndrome with X-linked ichthyosis, Kallmann syndrome, short stature, generalized epilepsy, hearing loss, attention deficit hyperactivity disorder, and intellectual disability – A rare report with review of literature

Journal of neurosciences in rural practice, 2024-07, Vol.15, p.425-430, Article 425

2024

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Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene

Indian journal of pediatrics, 2024, Vol.91 (3), p.317-317

2024

Volltextzugriff (PDF)

Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF Gene

Indian journal of pediatrics, 2023, Vol.90 (8), p.835-835

2023

Volltextzugriff (PDF)

SARS-COV-2 Infection in a Term Neonate Presenting with Respiratory Failure on Day 3 of Life

Indian journal of pediatrics, 2021, Vol.88 (1), p.99-100

2021

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White-rot fungus mediated green synthesis of zinc oxide nanoparticles and their impregnation on cellulose to develop environmental friendly antimicrobial fibers

3 Biotech, 2021-06, Vol.11 (6), p.269-269, Article 269

2021

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Zinc oxide derived from zinc(II)/acetoxime system: formation pathway and solar-driven photocatalytic and antimicrobial applications

Journal of sol-gel science and technology, 2019-09, Vol.91 (3), p.644-653

2019

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Chemically modified germanium(IV) alkoxides: molecular precursors for nano-sized germania

Materials research innovations, 2020-02, Vol.24 (2), p.123-128

2020

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Antibacterial effect of glycerol assisted ZnO nanoparticles synthesized by white rot fungus Phanerochaete chrysosporium

Materials today : proceedings, 2021, Vol.43, p.2855-2860

2021

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Clonidine versus dexmedetomidine as premedication to intrathecal 0.5% bupivacaine: A randomized, double-blind, prospective study

Bali journal of anesthesiology, 2021-10, Vol.5 (4), p.252-259

2021

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Teaching NeuroImage: Neuroimaging Features of Wilson Disease

Use of Ketogenic Diet in Two Indian Children with a Rare Early-Onset Epileptic Encephalopathy

Cogan's Lid Twitch Sign in a Child with Congenital Myasthenia

Paroxysmal Neuropathic Pruritus in Patients With Chiari Malformation Type I: A Rare Phenotype

Kikuchi-Fujimoto Disease Secondary to Disseminated Brucellosis in an Adolescent Boy

Primary Diffuse Leptomeningeal Melanomatosis in an Indian Child With Review of Literature

Acute Flaccid Paralysis due to Pyruvate Dehydrogenase E1-Alpha Deficiency

Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF Gene

Knobloch Syndrome - Triad of Occipital Encephalocele, Retino-Choroidal Detachment and Epilepsy

Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene

Clinical Profile, Follow-up, and Role of Neuroimaging in Pediatric Guillain-Barré Syndrome in the COVID Era: An Ambispective Study

Associated movement disorder as a clue for the diagnosis of paroxysmal kinesigenic dyskinesia in a child with focal epilepsy

Add-on Thiamin as an Adjunct in the Treatment of Children with Neuro-Wilson Disease

SARS-COV-2 Infection in a Term Neonate Presenting with Respiratory Failure on Day 3 of Life

A rare case of intermediate phenotype Niemann-Pick disease with a rare pathogenic variant of 1624C>T in SMPD1 gene

A child with global developmental delay and excessive startles: Never overlook the family history

Chromosome Xp22.3 deletion syndrome with X-linked ichthyosis, Kallmann syndrome, short stature, generalized epilepsy, hearing loss, attention deficit hyperactivity disorder, and intellectual disability – A rare report with review of literature

Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene

Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF Gene

SARS-COV-2 Infection in a Term Neonate Presenting with Respiratory Failure on Day 3 of Life

White-rot fungus mediated green synthesis of zinc oxide nanoparticles and their impregnation on cellulose to develop environmental friendly antimicrobial fibers

Zinc oxide derived from zinc(II)/acetoxime system: formation pathway and solar-driven photocatalytic and antimicrobial applications

Chemically modified germanium(IV) alkoxides: molecular precursors for nano-sized germania

Antibacterial effect of glycerol assisted ZnO nanoparticles synthesized by white rot fungus Phanerochaete chrysosporium

Clonidine versus dexmedetomidine as premedication to intrathecal 0.5% bupivacaine: A randomized, double-blind, prospective study

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