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Neuromuscular Disorders : NMD|March 24, 2009
Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) geneHeinz Jungbluth, Suzanne Lillis, Haiyan Zhou, et al.
Journal of the Neurological Sciences|January 26, 2019
Interleukin-6 and amyotrophic lateral sclerosisAna Pronto-Laborinho, Susana Pinto, Marta Gromicho, et al.
Archives of Neurology|October 10, 2007
Familial early-onset dementia with tau intron 10 + 16 mutation with clinical features similar to those of Alzheimer diseaseMark Doran, Daniel G du Plessis, Eric J Ghadiali, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 11, 2012
Primary lateral sclerosis: predicting functional outcomeVânia Almeida, Mamede de Carvalho, Manuel Scotto, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 29, 2021
Electromyographic findings in primary lateral sclerosis during disease progressionCláudia Santos Silva, Miguel Oliveira Santos, Marta Gromicho, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 27, 2022
Thyroid dysfunction in Portuguese amyotrophic lateral sclerosis patientsCláudia Santos Silva, Marta Gromicho, Miguel Oliveira Santos, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 9, 2023
Demographic changes in a large motor neuron disease cohort in Portugal: a 27 year experienceInês Alves, Marta Gromicho, Miguel Oliveira Santos, et al.
Journal of Neuromuscular Diseases|March 1, 2021
Plasma Creatinine Level Does Not Predict Respiratory Function in Amyotrophic Lateral SclerosisJoão Morgadinho, Ana Catarina Pronto-Laborinho, Vasco A Conceição, et al.
Journal of the Neurological Sciences|January 14, 2022
Respiratory function tests in amyotrophic lateral sclerosis: The role of maximal voluntary ventilationMamede de Carvalho, Sofia R Fernandes, Mariana Pereira, et al.
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