Parayil Sankaran Bindu

8PUBLICATIONS
1CO-AUTHORS
Metabolic medicineGene expression (incl. microarray and other genome-wide approaches)Organic chemistry not elsewhere classifiedNeonatology
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Publications (8)

|Jun 10, 2024
Hematologic Manifestations in Primary Mitochondrial Diseases.

Arthavan Selvanathan, Juliana Teo, Bindu Parayil Sankaran

|Mar 18, 2020
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel.

Bindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar

|Apr 05, 2017
Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency.

Shwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa

|Jun 17, 2016
Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1.

Shwetha Chiplunkar, Parayil Sankaran Bindu, Madhu Nagappa

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