Cargando…

HIV-related neuromuscular diseases: nemaline myopathy, amyotrophic lateral sclerosis and bibrachial amyotrophic diplegia

The human immunodeficiency virus (HIV) causes diverse disorders of the brain, spinal cord and peripheral nerves. Rarely, polymyositis and myoglobinuria are seen. Two other neuromuscular syndromes in people with HIV antibodies are nemaline myopathy and bibrachial amyotrophic diplegia, a form of motor...

Descripción completa

Detalles Bibliográficos
Autor principal:	ROWLAND, L.P.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Pacini Editore SpA 2011
Materias:	Articles in Tribute of V. Askanas and K. Engel
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185829/ https://www.ncbi.nlm.nih.gov/pubmed/21842590

Ejemplares similares

Familial amyotrophic lateral sclerosis, a historical perspective
por: Siddique, T., et al.
Publicado: (2011)

Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle
por: Broccolini, A., et al.
Publicado: (2011)

Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy
por: Vattemi, G., et al.
Publicado: (2011)

The Microglial-Motoneuron dialogue in ALS
por: APPEL, S.H., et al.
Publicado: (2011)

Sporadic-inclusion body myositis (s-IBM) is not so prevalent in Istanbul/Turkey: a muscle biopsy based survey
por: SERDAROGLU OFLAZER, P., et al.
Publicado: (2011)

Continuous muscle activity, Morvan's syndrome and limbic encephalitis: ionic or non ionic disorders?
por: SERRATRICE, G., et al.
Publicado: (2011)

Activation of NF-kB pathway in Duchenne muscular dystrophy: relation to age
por: MESSINA, S., et al.
Publicado: (2011)

Mesoangioblasts of inclusion-body myositis: a twofold tool to study pathogenic mechanisms and enhance defective muscle regeneration
por: MOROSETTI, R., et al.
Publicado: (2011)

Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis
por: Dubourg, O., et al.
Publicado: (2011)

Strategy for genetic testing in Charcot-Marie-Disease
por: Miller, L.J., et al.
Publicado: (2011)

Progress and problems in muscle glycogenoses
por: DiMauro, S., et al.
Publicado: (2011)

Molecular biomarkers associated with respiratory insufficiency in amyotrophic lateral sclerosis
por: Pronto-Laborinho, Ana Catarina, et al.
Publicado: (2021)

Neuromuscular Junction Dismantling in Amyotrophic Lateral Sclerosis
por: Cappello, Valentina, et al.
Publicado: (2017)

Pathologic expansion in the C9orf72 gene is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis
por: Miltenberger-Miltenyi, Gabriel, et al.
Publicado: (2021)

Neuromuscular Junction Protection for the Potential Treatment of Amyotrophic Lateral Sclerosis
por: Krakora, Dan, et al.
Publicado: (2012)

Systemic inflammatory response and neuromuscular involvement in amyotrophic lateral sclerosis
por: Lu, Ching-Hua, et al.
Publicado: (2016)

Clinical and research applications of neuromuscular ultrasound in amyotrophic lateral sclerosis
por: Barnes, Stephanie L, et al.
Publicado: (2019)

Aberrant enteric neuromuscular system and dysbiosis in amyotrophic lateral sclerosis
por: Zhang, Yongguo, et al.
Publicado: (2021)

Amyotrophic lateral sclerosis
por: Wijesekera, Lokesh C, et al.
Publicado: (2009)

The role of oxidative stress in degeneration of the neuromuscular junction in amyotrophic lateral sclerosis
por: Pollari, Eveliina, et al.
Publicado: (2014)

Adducin at the Neuromuscular Junction in Amyotrophic Lateral Sclerosis: Hanging on for Dear Life
por: Krieger, Charles, et al.
Publicado: (2016)

Neuromuscular Junction Impairment in Amyotrophic Lateral Sclerosis: Reassessing the Role of Acetylcholinesterase
por: Campanari, Maria-Letizia, et al.
Publicado: (2016)

TDP-43 dysregulation and neuromuscular junction disruption in amyotrophic lateral sclerosis
por: Lépine, Sarah, et al.
Publicado: (2022)

SIRT1 deacetylase in aging‐induced neuromuscular degeneration and amyotrophic lateral sclerosis
por: Herskovits, Adrianna Z., et al.
Publicado: (2018)

Bisperoxovanadium promotes motor neuron survival and neuromuscular innervation in amyotrophic lateral sclerosis
por: Wang, Junmei, et al.
Publicado: (2021)

Amyotrophic lateral sclerosis and neuroregeneration
Publicado: (2012)

Mimickers of Amyotrophic Lateral Sclerosis
por: Dubey, Ayush, et al.
Publicado: (2019)

Destination Amyotrophic Lateral Sclerosis
por: Keon, Matt, et al.
Publicado: (2021)

Prionoids in amyotrophic lateral sclerosis
por: Gosset, Philippe, et al.
Publicado: (2022)

Amyotrophic lateral sclerosis and cerebellum
por: Kabiljo, Renata, et al.
Publicado: (2022)

Dysautonomia in Amyotrophic Lateral Sclerosis
por: Oprisan, Alexandra L., et al.
Publicado: (2023)

Novel small molecule TRVA242 targets neuromuscular junction in amyotrophic lateral sclerosis
por: Bose, Poulomee
Publicado: (2019)

A rare structural myopathy: Nemaline myopathy
por: Yeşilbaş, Osman, et al.
Publicado: (2019)

Zebrafish model for nemaline myopathy
Publicado: (2012)

Sarcomere Dysfunction in Nemaline Myopathy
por: de Winter, Josine M., et al.
Publicado: (2017)

Classification of Myopathy and Amyotrophic Lateral Sclerosis Electromyograms Using Bat Algorithm and Deep Neural Networks
por: Bakiya, A., et al.
Publicado: (2022)

Sporadic Spinal-Onset Amyotrophic Lateral Sclerosis Associated with Myopathy in Three Unrelated Portuguese Patients
por: Oliveira Santos, Miguel, et al.
Publicado: (2023)

Clinical Psychology and Amyotrophic Lateral Sclerosis
por: Pagnini, Francesco, et al.
Publicado: (2010)

Glial Cells in Amyotrophic Lateral Sclerosis
por: Lasiene, Jurate, et al.
Publicado: (2011)

The Cortical Signature of Amyotrophic Lateral Sclerosis
por: Agosta, Federica, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_1hpgq39us4q43l0ni7o6pemavq