Progressive muscular atrophy

T Liewluck, DS Saperstein - Neurologic clinics, 2015 - neurologic.theclinics.com
PMA is a rare, sporadic, adult-onset, clinically isolated LMN syndrome due to the
degeneration of LMNs, including anterior horn cells and brainstem motor nuclei. It is …

Amyotrophic lateral sclerosis and motor neuron syndromes in Asia

N Shahrizaila, G Sobue, S Kuwabara… - Journal of Neurology …, 2016 - jnnp.bmj.com
While the past 2 decades have witnessed an increasing understanding of amyotrophic
lateral sclerosis (ALS) arising from East Asia, particularly Japan, South Korea, Taiwan and …

[HTML][HTML] An emerging role for stress granules in neurodegenerative disease and hearing loss

JL Martin, SJ Dawson, JE Gale - Hearing Research, 2022 - Elsevier
Stress granules (SGs) are membrane-less cytosolic assemblies that form in response to
stress (eg, heat, oxidative stress, hypoxia, viral infection and UV). Composed of mRNA, RNA …

Monomelic amyotrophy: clinical profile and natural history of 279 cases seen over 35 years (1976–2010)

A Nalini, M Gourie-Devi, K Thennarasu… - … Lateral Sclerosis and …, 2014 - Taylor & Francis
Our objective was to study the clinical characteristics and natural history of monomelic
amyotrophy (MMA). We used a retrospective study of 279 patients diagnosed to have either …

Complex genetic origin of Indian populations and its implications

R Tamang, L Singh, K Thangaraj - Journal of biosciences, 2012 - Springer
Indian populations are classified into various caste, tribe and religious groups, which
altogether makes them very unique compared to rest of the world. The long-term firm socio …

Genomic view on the peopling of India

R Tamang, K Thangaraj - Investigative genetics, 2012 - Springer
India is known for its vast human diversity, consisting of more than four and a half thousand
anthropologically well-defined populations. Each population differs in terms of language …

Brown-Vialetto-Van Laere syndrome: a riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

A Koy, F Pillekamp, T Hoehn, H Waterham, D Klee… - Pediatric …, 2012 - Elsevier
Brown-Vialetto-Van Laere syndrome (Online Mendelian Inheritance in Man number 211530)
is a neurodegenerative disorder characterized by pontobulbar palsy affecting cranial nerves …

SOD1 (A4V)‐mediated ALS presenting with lower motor neuron facial diplegia and unilateral vocal cord paralysis

JS Salameh, N Atassi, WS David - Muscle & Nerve: Official …, 2009 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a progressive degenerative neuromuscular disease
that presents with upper and lower motor neuron signs. Although the majority of ALS cases …

Neurological associations in auditory neuropathy spectrum disorder: Results from a tertiary hospital in South India

A Lepcha, RK Chandran, M Alexander… - Annals of Indian …, 2015 - journals.lww.com
Aims: To find out the prevalence and types of neurological abnormalities associated in
auditory neuropathy spectrum disorder in a large tertiary referral center. Settings and …

Mitochondrial DNA variations in Madras motor neuron disease

P Govindaraj, A Nalini, N Krishna, A Sharath, NA Khan… - Mitochondrion, 2013 - Elsevier
Although the Madras motor neuron disease (MMND) was found three decades ago, its
genetic basis has not been elucidated, so far. The symptom at onset was impaired hearing …