Julaine Florence

Rajarajeswari Medical College and Hospital — India

Biochemistry, Genetics and Molecular Biology · Life Sciences

51h-index10.9kcitations115works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(64), Neurogenetic and Muscular Disorders Research(27), Muscle activation and electromyography studies(17), Cerebral Palsy and Movement Disorders(15), Amyotrophic Lateral Sclerosis Research(12)

Publications114 total

Evaluation of Drug Utilization in Coronary Artery Disease in Tertiary Care Centre: A Cross Sectional Study
Journal of Pharmaceutical Research International·2025Open Access
Experimental Model of Chest Trauma: A Clinically Relevant Model of Retained Hemothorax Amenable to Testing Intrapleural Fibrinolytic Therapy
2024
Investigating Late-Onset Pompe Prevalence in Neuromuscular Medicine Academic Practices
Neurology Genetics·2021· 7 citedOpen Access
Consensus Guidelines for Improving Quality of Assessment and Training for Neuromuscular Diseases
Frontiers in Genetics·2021· 11 citedOpen Access
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy
Journal of Comparative Effectiveness Research·2021· 15 citedOpen Access
Prevalence of neuropathy in patients with minimally symptomatic hyperCKemia (2484)
Neurology·2021
The <scp>CINRG</scp> Becker Natural History Study: Baseline characteristics
Muscle & Nerve·2020· 22 citedOpen Access
Systemic mutational rescue in <i>Escherichia coli</i> elicited by a valency dependent, high affinity protein DNA interaction
2020Open Access
Electrical impedance myography for reducing sample size in Duchenne muscular dystrophy trials
Annals of Clinical and Translational Neurology·2019· 32 citedOpen Access
The IPANEMA Study: Top Line Results from an Investigator-Initiated Multi-site Late-onset Pompe Disease Prevalence Study (P5.4-005)
Neurology·2019
Twice‐weekly glucocorticosteroids in infants and young boys with Duchenne muscular dystrophy
Muscle & Nerve·2019· 45 cited
Assessment of disease progression in dysferlinopathy
Neurology·2019· 26 citedOpen Access
A natural history study of Becker muscular dystrophy by the CINRG investigators
Neuromuscular Disorders·2017
Characterization of Strength and Function in Ambulatory Adults With GNE Myopathy
Journal of Clinical Neuromuscular Disease·2017· 16 citedOpen Access
A dedicated electrical impedance myography device in the assessment of Duchenne muscular dystrophy. (P5.102)
Neurology·2017
Comparison of Loudness Growth Function in Normal Hearing Individuals and Impaired Aided Hearing
Advanced Science Letters·2017· 1 cited
Fixed dynamometry is more sensitive than vital capacity or ALS rating scale
Muscle & Nerve·2017· 20 cited
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy
The American Journal of Human Genetics·2016· 72 citedOpen Access
Table of Contents
Muscle & Nerve·2016Open Access
Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophy
Neurology·2016· 167 citedOpen Access
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Frequent Co-authors

Alan Pestronk(19), Anne M. Connolly(17), Jerry R. Mendell(14), Craig M. McDonald(14), Wendy King(11), Erik Henricson(11), Diana M. Escolar(10), Kevin M. Flanigan(9), John Day(9), Paula R. Clemens(8), Jeanine Schierbecker(8), Michelle Eagle(8), J. Philip Miller(7), Shree Pandya(7), Richard S. Finkel(7), Richard T. Abresch(7), Eduard Gappmaier(7), Allan M. Glanzman(7), Katherine D. Mathews(7), Robert T. Leshner(6)