Lista de obras -

Ankle-Foot Orthosis in Duchenne Muscular Dystrophy: A 4 year Experience in a Multidisciplinary Neuromuscular Disorders Clinic.

artículo científico publicado en 2016

Brain and Spinal Cord Lesions in Leprosy: A Magnetic Resonance Imaging-Based Study

artículo científico publicado en 2019

CARASIL families from India with 3 novel null mutations in the HTRA1 gene

artículo científico publicado en 2017

Caregiver burden and quality of life of patients with amyotrophic lateral sclerosis in India

scientific article published on 24 July 2018

Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant

scientific article published on 16 September 2019

Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort

artículo científico publicado en 2017

Family Caregivers' Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in India

artículo científico publicado en 2019

Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndrome

artículo científico publicado en 2017

Hirayama disease/cervical flexion-induced myelopathy progressing to spastic paraparesis: A report on three cases with literature review

scientific article published on 01 July 2018

Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle

scientific article published on 23 October 2019

In Vivo Evaluation of White Matter Abnormalities in Children with Duchenne Muscular Dystrophy Using DTI

artículo científico publicado en 2020

Intrafamilial phenotypic variations in familial cases of cervical flexion induced myelopathy/Hirayama disease.

artículo científico publicado en 2017

Leptospirosis and dengue fever: a predictive model for early differentiation based on clinical and biochemical parameters.

artículo científico publicado en 2013

MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.

artículo científico publicado en 2017

Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive pattern.

artículo científico publicado en 2016

Mutation pattern in 606 Duchenne muscular dystrophy children with a comparison between familial and non-familial forms: a study in an Indian large single-center cohort

artículo científico publicado en 2019

Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunit.

artículo científico publicado en 2018

Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South India.

artículo científico publicado en 2018

Proximal and proximo-distal bimelic amyotrophy: Evidence of cervical flexion induced myelopathy

artículo científico publicado en 2016

Reverse split hand syndrome: Dissociated intrinsic hand muscle atrophy pattern in Hirayama disease/brachial monomelic amyotrophy.

artículo científico publicado en 2016

University of Pennsylvania Smell Identification Test Abnormalities in Parkinson's Disease

artículo científico publicado en 2016

Ventral longitudinal intraspinal fluid collection: Rare presentation as brachial amyotrophy and intracranial hypotension.

artículo científico publicado en 2017

Lista de obras de

Ankle-Foot Orthosis in Duchenne Muscular Dystrophy: A 4 year Experience in a Multidisciplinary Neuromuscular Disorders Clinic.

Brain and Spinal Cord Lesions in Leprosy: A Magnetic Resonance Imaging-Based Study

CARASIL families from India with 3 novel null mutations in the HTRA1 gene

Caregiver burden and quality of life of patients with amyotrophic lateral sclerosis in India

Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant

Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort

Family Caregivers' Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in India

Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndrome

Hirayama disease/cervical flexion-induced myelopathy progressing to spastic paraparesis: A report on three cases with literature review

Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle

In Vivo Evaluation of White Matter Abnormalities in Children with Duchenne Muscular Dystrophy Using DTI

Intrafamilial phenotypic variations in familial cases of cervical flexion induced myelopathy/Hirayama disease.

Leptospirosis and dengue fever: a predictive model for early differentiation based on clinical and biochemical parameters.

MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.

Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive pattern.

Mutation pattern in 606 Duchenne muscular dystrophy children with a comparison between familial and non-familial forms: a study in an Indian large single-center cohort

Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunit.

Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South India.

Proximal and proximo-distal bimelic amyotrophy: Evidence of cervical flexion induced myelopathy

Reverse split hand syndrome: Dissociated intrinsic hand muscle atrophy pattern in Hirayama disease/brachial monomelic amyotrophy.

University of Pennsylvania Smell Identification Test Abnormalities in Parkinson's Disease

Ventral longitudinal intraspinal fluid collection: Rare presentation as brachial amyotrophy and intracranial hypotension.