Publications by authors named "Usha Dave"

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Hemoglobin Variant Analysis and Its Comparison between Conventional High-performance Liquid Chromatography Using Whole Blood versus Dried Blood Spot: High-performance Liquid Chromatography.
Rabindra Kumar Jena, Sudha Sethy, Pradyumna Kumar Dash, Mitanjali Behera, Bhushan Palande, Usha Dave

Indian J Public Health· July 2025

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Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort.
Usha Dave, Srilatha Kadali, Tajamul Hussain, Ananthaneni Radhika, Sagar Patel

Indian J Clin Biochem· April 2025

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Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Maninder Kaur, Justin Blair, Batsal Devkota, Sierra Fortunato, Dinah Clark, Usha Dave

Am J Med Genet A· August 2023

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Cornelia de Lange syndrome in diverse populations.
Leah Dowsett, Antonio R Porras, Paul Kruszka, Brandon Davis, Tommy Hu, Usha Dave

Am J Med Genet A· February 2019

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Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency.
Elsayed Abdelkreem, Radha Rama Devi Akella, Usha Dave, Sudhir Sane, Hiroki Otsuka

JIMD Rep· December 2016

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Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease.
Chitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, Mamta Muranjan, Usha Dave

J Hum Genet· May 2015

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An open-label study to elucidate the effects of standardized Bacopa monnieri extract in the management of symptoms of attention-deficit hyperactivity disorder in children.
Usha Pinakin Dave, Sunila Rajeev Dingankar, Vinod Swaroop Saxena, Joshua Allan Joseph, Bharathi Bethapudi

Adv Mind Body Med· November 2014

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Brain-Derived Neurotrophic Factor in children with Autism Spectrum Disorder.
Nikhil J Kasarpalkar, Sweta T Kothari, Usha P Dave

Ann Neurosci· October 2014

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Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease.
Chitra Ankleshwaria, Mehul Mistri, Ashish Bavdekar, Mamta Muranjan, Usha Dave

J Hum Genet· April 2014

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Mutational Screening and Prenatal Diagnosis in Cornelia de Lange syndrome.
Usha Dave, Dhanlaxmi Shetty

J Obstet Gynaecol India· February 2014

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Plasma chitotriosidase activity in children with lysosomal storage disorders.
Jayesh J Sheth, Frenny J Sheth, Nrupesh J Oza, Prakash S Gambhir, Usha P Dave

Indian J Pediatr· February 2010

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