Search Results - "Mainali, Gayatra"

A Case of Autosomal Recessive Intellectual Developmental Disorder Type 5 Presenting with Epilepsy by Hasan, Mahpara, Mainali, Gayatra, Aliu, Ermal, Paudel, Sita

“…Autosomal recessive intellectual developmental disorder type 5 (MRT5, OMIM # 611091) is caused by biallelic pathogenic variants, leading to loss of function of…”
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Role of Neurovascular Compression of Oculomotor Nerve in Ophthalmoplegic Migraine by Bui, Linda T, Mainali, Gayatra, Naik, Sunil, Cockroft, Kevin, Thamburaj, Krishnamoorthy

“…Ophthalmoplegic migraine is considered to occur more commonly in children than in adults. It commonly affects the oculomotor nerve among the cranial nerves…”
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Importance of Genetic Testing in Children With Generalized Epilepsy by Heebner, Madison, Mainali, Gayatra, Wei, Sharon, Kumar, Ashutosh, Naik, Sunil, Pradhan, Sandeep, Kandel, Prakash, Tencer, Jaclyn, Carney, Paul, Paudel, Sita

“…Epilepsy is a neurological disorder characterized by the predisposition for recurrent unprovoked seizures. It can broadly be classified as focal, generalized,…”
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A Review of the Multi-Systemic Complications of a Ketogenic Diet in Children and Infants with Epilepsy by Newmaster, Kyra, Zhu, Zahra, Bolt, Elizabeth, Chang, Ryan J, Day, Christopher, Mhanna, Asmaa, Paudel, Sita, Farooq, Osman, Swaminathan, Arun, Acharya, Prakrati, Cheungpasitporn, Wisit, Gupta, Siddharth, Samanta, Debopam, Mahfooz, Naeem, Mainali, Gayatra, Carney, Paul R, Naik, Sunil

“…Ketogenic diets (KDs) are highly effective in the treatment of epilepsy. However, numerous complications have been reported. During the initiation phase of the…”
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Use of Integrative, Complementary, and Alternative Medicine in Children with Epilepsy: A Global Scoping Review by Zhu, Zahra, Dluzynski, Daniela, Hammad, Nouran, Pugalenthi, Deepika, Walser, Sarah A, Mittal, Rea, Samanta, Debopam, Brown, Melanie L, Asadi-Pooya, Ali A, Kakooza-Mwesige, Angelina, Spalice, Alberto, Capponi, Martina, Lekoubou, Alain, Kumar, Ashutosh, Paudel, Sita, Carney, Paul R, Mainali, Gayatra, Naik, Sunil

“…(1) Background: Epilepsy is one of the most common chronic neurological disorders in childhood. Complementary and alternative medicine (CAM) use is highly…”
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5.4 MANAGEMENT OF DRUG-INDUCED MOVEMENT DISORDERS (DIMDS): A CHILD NEUROLOGIST’S PERSPECTIVE by Mainali, Gayatra

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Pitt Hopkins-Like Syndrome 1 with novel CNTNAP2 mutation in siblings (2828) by Mittal, Rea, Alieue, Erma, Mainali, Gayatra, Ladda, Roger, Kumar, Ashutosh

“…Abstract only…”
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Author response: Teaching NeuroImages: A rare case of Jacobsen syndrome with global diffuse hypomyelination of brain by Patel, Himadri, Kumar, Ashutosh, Raymond, Gerald, Mainali, Gayatra

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Teaching NeuroImages: A rare case of Jacobsen syndrome with global diffuse hypomyelination of brain by Patel, Himadri, Kumar, Ashutosh, Raymond, Gerald, Mainali, Gayatra

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A Comprehensive Review of Neurologic Manifestations of COVID-19 and Management of Pre-existing Neurologic Disorders in Children by Kim, Yunsung, Walser, Sarah A., Asghar, Sheila J., Jain, Rohit, Mainali, Gayatra, Kumar, Ashutosh

“…Since the first reports of SARS-CoV-2 infection from China, multiple studies have been published regarding the epidemiologic aspects of COVID-19 including…”
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Periodic Paralysis in the Phenotypic Spectrum of CLCN1 Gene Mutation (P1.6-048) by Patel, Himadri, Tiwana, Harmanpreet, Mainali, Gayatra, Wicklund, Matthew, Kumar, Ashutosh

“…Abstract only…”
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Complementary and Alternative Medicine (CAM) use in Children with Epilepsy by Zhu, Zahra, Mittal, Rea, Walser, Sarah A., Lehman, Erik, Kumar, Ashutosh, Paudel, Sita, Mainali, Gayatra

“…Complementary and alternative medicine (CAM) use by the pediatric population with epilepsy in rural Pennsylvania was studied to characterize the prevalence,…”
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Use of Complementary and Alternative Medicine in Children with Neuromuscular Disorders Followed at Penn State Health Pediatric Muscular Dystrophy Association Care Center Clinic by Mittal, Rea, Maltese, Caroline, Bolt, Elizabeth, Paul, Dustin, Mainali, Gayatra, Naik, Sunil, Paudel, Sita, Lehman, Erik, Kumar, Ashutosh

“…The exact prevalence of complementary and alternative medicine (CAM) use is not known in pediatric patients with neuromuscular diseases followed by any of the…”
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Encephalitis with Extensive Cortical Brain Magnetic Resonance Imaging Changes Secondary to Myelin Oligodendrocyte Glycoprotein Antibody Disease by Satyasi, Vivek, Mainali, Gayatra, Chatterjee, Jahnavi, Paudel, Sita

“…Patient: Male, 17-month-old Final Diagnosis: Fluid attenuated inversion recovery (FLAIR) imaging showing cortical hyperintense lesions in…”
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Complications of intrathecal baclofen pumps in children: experience from a tertiary care center by Ghosh, Debabrata, Mainali, Gayatra, Khera, Jena, Luciano, Mark

“…Intrathecal baclofen (ITB) therapy is useful in treating spasticity and dystonia but it has many complications, more so in children. The main aim of the study…”
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Use of Complementary and Alternative Medicine in Children With Tourette Syndrome by Patel, Himadri, Nguyen, KieuHanh, Lehman, Erik, Mainali, Gayatra, Duda, Laura, Byler, Debra, Kumar, Ashutosh

“…Introduction: Tourette syndrome is a neuropsychiatric condition defined by motor and phonic tics with onset in childhood. Many families have concerns regarding…”
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Neurobehavioral Issues in the Phenotypic Spectrum of Variations in OTX2 (P1.6-043) by Patel, Himadri, Tiwana, Harmanpreet, Chalia, Mayur, Yelton, Melissa, Mainali, Gayatra, Raymond, Gerald, Kumar, Ashutosh

“…Abstract only…”
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Pharmaceutical Interventions for Tourette’s Syndrome by Duda, Laura, Mainali, Gayatra

“…Tourette’s syndrome is a childhood-onset neuropsychiatric disorder characterized by motor and vocal tics that are chronic (duration of >1 year) (Kurlan N Engl…”
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Response to Correspondence “Complementary and Alternative…but Please Not Secret” by Patel, Himadri, Nguyen, KieuHanh, Lehman, Erik, Mainali, Gayatra, Duda, Laura, Byler, Debra, Kumar, Ashutosh

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Pitt Hopkins-Like Syndrome 1 with Novel CNTNAP2 Mutation in Siblings by Mittal, Rea, Kumar, Ashutosh, Ladda, Roger, Mainali, Gayatra, Aliu, Ermal

“…Pitt Hopkins-like syndrome 1 (PTHLS1, OMIM # 610042) is an ultra-rare autosomal recessive condition with a prevalence of <1/1,000,000. Intragenic deletions of…”
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