BP
Bindu Parayil Sankaran
Research areas: Biochemistry, Genetics and Molecular Biology · Clinical Biochemistry · Metabolism and Genetic Disorders · Mitochondrial Function and Pathology · Neurological diseases and metabolism
0000-0002-1914-9505
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Publications (15)
- Hematologic Manifestations in Primary Mitochondrial Diseases Save
- Paroxysmal Dystonia in a Child with Enoyl-CoA Hydratase Short-Chain 1 (ECHS1) Mutations Save
- Teaching NeuroImage: Bilateral Nucleus Tractus Solitarius Lesions in Neurogenic Respiratory Failure Save
- Functional Network Connectivity Imprint In Febrile Seizures Save
- Child Neurology: Hereditary Folate Malabsorption Save
- Infantile Onset Encephalomyopathy, Heart Block, and Sensorineural Hearing Loss: RMND1-Associated Mitochondrial Disease Save
- Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel Save
- Child Neurology: Ethylmalonic encephalopathy Save
- <p>Sjogren-Larsson Syndrome: Mechanisms and Management</p> Save
- Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency Save
- Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency Save
- Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1 Save
- Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome Save
- Audiological findings in Infantile Refsum disease Save
- Oculomotor Apraxia in Gaucher Disease Save