Results 31 to 40 of about 25,100 (235)

Basilar invagination: A mimicker of bulbar-onset amyotrophic lateral sclerosis

eNeurologicalSci, 2021
Amyotrophic lateral sclerosis (ALS) is characterized by progressive onset motor deficits with heterogenous presentations ranging from dysarthria to foot drop.
Jason Seng Hong Tan, Shirley Lee, Fu Liong Hiew   +2 more
doaj   +1 more source

Combined Acupuncture and Shirodhara as an Effective Treatment Approach in the Management of Progressive Bulbar Palsy: A Case Report

Annapurna Journal of Health Sciences, 2023
N ...
Jaya Satyal, Pradeep Kc, R. Kc, Aabha Sharma, A. Chandra   +4 more
semanticscholar   +1 more source

Utility of the new Movement Disorder Society clinical diagnostic criteria for Parkinson's disease applied retrospectively in a large cohort study of recent onset cases [PDF]

, 2017
Objective: To examine the utility of the new Movement Disorder Society (MDS) diagnostic criteria in a large cohort of Parkinson's disease (PD) patients.
,, Bajaj, Nin, Barker, Roger A., Ben-Shlomo, Yoav, Burn, David J., Foltynie, Tom, Grosset, Donald G., Grosset, Katherine A., Hardy, John, Lawton, Michael A., Malek, Naveed, Morris, Huw R., Williams, Nigel M., Wood, Nicholas   +13 more
core   +5 more sources

A Rare case of Miller Fisher Syndrome with Ophthalmoplegia with Bulbar Palsy with Bifacial Weakness with Progressive Quadriparesi

Indian Journal of Emergency Medicine, 2022
A 20 years old female came to ED with c/o giddiness since 4 days, headache since 3 days with diplopia with slurring of speech, lower limb weakness, difficulty in swallowing, and dropping of left eyelid since 1 day.
Ritul Srivastava, P. Govil, Kishalay Datta   +2 more
semanticscholar   +1 more source

Progressive Bulbar Palsy

Developmental Medicine & Child Neurology, 1969
SUMMARYProgressive bulbar palsy is very rare in childhood. A probable case diagnosed in Greece is presented. After a short review of the literature the clinical and laboratory findings are described. The main clinical features were progressive affection of the bulbar nuclei over one year without involvement of the long tracts.
Gregoriou, M., Matsaniotis, N., Papadakis, G.   +2 more
openaire   +3 more sources

Adrenomyeloneuropathy with bulbar palsy: A rare association

Annals of Indian Academy of Neurology, 2014
Adrenomyeloneuropathy (AMN) is a variant of adrenoleukodystrophy (ALD), an X-linked recessive peroxisomal disorder associated with accumulation of very long chain fatty acids (VLCFA). Mutations of this gene lead to abnormal peroxisomal β-oxidation, which
Vishal Annaji Chafale, Satish Arunkumar Lahoti, Atanu Biswas, Arijit Roy, Asit Kumar Senapati   +4 more
doaj   +1 more source

Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis [PDF]

, 2010
The finding of TDP-43 as a major component of ubiquitinated protein inclusions in amyotrophic lateral sclerosis (ALS) has led to the identification of 30 mutations in the transactive response-DNA binding protein (TARDBP) gene, encoding TDP-43.
A Yokoseki, BA Hosler, C Lomen-Hoerth, C Vance, Christopher J. McDermott, D Neary, DR Rosen, E Buratti, E Buratti, E Kabashi, Emily F. Goodall, F Gros-Louis, GM Ringholz, H Daoud, Hannah C. Hollinger, I Gijselinck, IF Wang, IR Mackenzie, J Kirby, J Sreedharan, J. Robin Highley, Janine Kirby, JJ Kew, Judith A. Hartley, Karen E. Morrison, L Benajiba, L Corrado, M Morita, M Neumann, MJ Strong, MJ Winton, NJ Rutherford, P Kuhnlein, PA Mercado, Pamela J. Shaw, Paul G. Ince, PM Andersen, R Bo Del, R Lemmens, Rachel Hibberd, RJ Guerreiro, Rudo Masanzu, SH Ou, Stephen B. Wharton, VM Deerlin Van, William Smith, YM Ayala   +46 more
core   +1 more source

UNUSUAL PRESENTATION OF BRAINSTEM GLIOMA AS PROGRESSIVE BULBAR PALSY

Journal of Evolution of Medical and Dental Sciences, 2015
R. Šumak, R. Muddurangappa, S. Srinath
semanticscholar   +2 more sources

Acute Thyrotoxic Bulbar Myopathy with Encephalopathic Behaviour: An Uncommon Complication of Hyperthyroidism

Case Reports in Endocrinology, 2013
Objective. Acute thyrotoxic bulbar palsy is rare, severe, and rapidly progressive. We describe a case of thyrotoxicosis with bulbar palsy, encephalopathy, and pyramidal tract dysfunction. Case Report. 64-year-old white male with toxic multinodular goiter
Neeraja J. Boddu, Sridhar Badireddi, Karl David Straub, John Schwankhaus, Rajani Jagana   +4 more
doaj   +1 more source

Brown-Vialetto-Van Laere syndrome [PDF]

, 2008
The Brown-Vialetto-Van Laere syndrome (BVVL) is a rare neurological disorder characterized by progressive pontobulbar palsy associated with sensorineural deafness. Fifty-eight cases have been reported in just over 100 years.
Sivakumar Sathasivam
core   +1 more source