Resultados de búsqueda - Yoganathan, Sangeetha

Stroke in a Child with Dengue Encephalopathy por Yoganathan, Sangeetha, Sudhakar, Sniya Valsa, Priyambada, Leena, Thomas, Maya

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A Tale of Treatable Infantile Neuroregression and Diagnostic Dilemma with Glutaric Aciduria Type I por Yoganathan, Sangeetha, Varman, Mugil, Oommen, Samuel Philip, Thomas, Maya

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Clinical Profile, Prognostic Indicators, and Therapeutic Outcomes of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: A Single-Center Experience from South India por Muthusamy, Karthik, Thomas, Maya, Yoganathan, Sangeetha, Sudhakar, Sniya Valsa

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A tropical menace of co-infection of Japanese encephalitis and neurocysticercosis in two children por Yoganathan, Sangeetha, Sudhakar, Sniya Valsa, Thomas, Maya Mary, Yadav, Vikas Kapildeo

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Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy por Muthusamy, Karthik, Yoganathan, Sangeetha, Thomas, Maya Mary, Alexander, Mathew, Verghese, Valsan Philip

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Predictors of Outcome in Children with Status Epilepticus during Resuscitation in Pediatric Emergency Department: A Retrospective Observational Study por Santhanam, Indumathy, Yoganathan, Sangeetha, Sivakumar, V. Akila, Ramakrishnamurugan, Rubini, Sathish, Sharada, Thandavarayan, Murali

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Imaging findings in TRPM6-Related hypomagnesemia with secondary hypocalcemia por Malik, Prateek, Bidkar, Sayli Umakant, Yoganathan, Sangeetha, Mathai, Sarah, Danda, Sumita, Koshy, Beena

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Candida tropicalis brain abscess in a neonate: An emerging nosocomial menace por Yoganathan, Sangeetha, Chakrabarty, Biswaroop, Gulati, Sheffali, Kumar, Ajay, Kumar, Atin, Singh, Manmohan, Xess, Immaculata

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Novel Imaging Finding and Novel Mutation in an Infant with Molybdenum Cofactor Deficiency, a Mimicker of Hypoxic-Ischaemic Encephalopathy por YOGANATHAN, Sangeetha, SUDHAKAR, SniyaVALSA, THOMAS, Maya, KUMAR DUTTA, Atanu, DANDA, Sumita, CHANDRAN, Mahalakshmi

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Menkes disease and response to copper histidine: An Indian case series por Yoganathan, Sangeetha, Sudhakar, Sniya Valsa, Arunachal, Gautham, Thomas, Maya, Subramanian, Annadurai, George, Renu, Danda, Sumita

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Child with D-2-Hydroxyglutaric Aciduria Type II: A Rare Neurometabolic Disorder por Srinivasaraghavan, Rangan, Sharma, Suvasini, Kratz, Lisa, Malik, Prateek, Yoganathan, Sangeetha, Danda, Sumita, Oommen, Samuel Philip

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Oculodigital Sign: A Clinical Clue for Diagnosis por Yoganathan, Sangeetha, Kumar, Madhan, John, Deepa, Danda, Sumita, Oommen, Samuel P., Umakant, Sayli B., Thomas, Maya

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Revisiting magnetic resonance imaging pattern of Krabbe disease – Lessons from an Indian cohort por Muthusamy, Karthik, Sudhakar, Sniya Valsa, Thomas, Maya, Yoganathan, Sangeetha, Christudass, Christhunesa S., Chandran, Mahalakshmi, Panwala, Hirenkumar, Gibikote, Sridhar

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Study of Refractory Status Epilepticus from a Tertiary Care Center por Kohli, Sahil, Pasangulapati, Suresh Babu, Yoganathan, Sangeetha, Rynjah, Gideon Lyngsyun, Prabhakar, A. T., Aaron, Sanjith, Alexander, Mathew, Mathew, Vivek

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Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase Deficiency por Yoganathan, Sangeetha, Arunachal, Gautham, Kratz, Lisa, Varman, Mugil, Thomas, Maya, Sudhakar, Sniya Valsa, Oommen, Samuel Philip, Danda, Sumita

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Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1 por Yoganathan, Sangeetha, Arunachal, Gautham, Kratz, Lisa, Varman, Mugil, Thomas, Maya, Sudhakar, Sniya V., Oommen, Samuel P., Danda, Sumita

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Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder por Yoganathan, Sangeetha, Srinivasaraghavan, Rangan, Chandran, Mahalakshmi, Kratz, Lisa, Koshy, Beena, Sudhakar, Sniya Valsa, Arunachal, Gautham, Thomas, Maya, Danda, Sumita

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Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder por Yoganathan, Sangeetha, Arunachal, Gautham, Kratz, Lisa, Varman, Mugil, Sudhakar, Sniya Valsa, Oommen, Samuel Philip, Jain, Shikha, Thomas, Maya, Babuji, Manimegalai

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The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study por Varala, Sirisha, George, Renu, Mathew, Lydia, Russell, Paul, Koshy, Beena, Oommen, Samuel P., Thomas, Maya, Muthusamy, Karthik, Yoganathan, Sangeetha, Jeyaseelan, L, Muliyil, Jayaprakash

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Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia por Tuschl, Karin, Meyer, Esther, Valdivia, Leonardo E., Zhao, Ningning, Dadswell, Chris, Abdul-Sada, Alaa, Hung, Christina Y., Simpson, Michael A., Chong, W. K., Jacques, Thomas S., Woltjer, Randy L., Eaton, Simon, Gregory, Allison, Sanford, Lynn, Kara, Eleanna, Houlden, Henry, Cuno, Stephan M., Prokisch, Holger, Valletta, Lorella, Tiranti, Valeria, Younis, Rasha, Maher, Eamonn R., Spencer, John, Straatman-Iwanowska, Ania, Gissen, Paul, Selim, Laila A. M., Pintos-Morell, Guillem, Coroleu-Lletget, Wifredo, Mohammad, Shekeeb S., Yoganathan, Sangeetha, Dale, Russell C., Thomas, Maya, Rihel, Jason, Bodamer, Olaf A., Enns, Caroline A., Hayflick, Susan J., Clayton, Peter T., Mills, Philippa B., Kurian, Manju A., Wilson, Stephen W.

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