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Relevant bibliographies by topics / Anterior horn cell disease

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Academic literature on the topic 'Anterior horn cell disease'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Anterior horn cell disease"

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Ryan, Monique M., Claire M. Cooke-Yarborough, Peter G. Procopis, and Robert A. Ouvrier. "Anterior horn cell disease and olivopontocerebellar hypoplasia." Pediatric Neurology 23, no. 2 (2000): 180–84. http://dx.doi.org/10.1016/s0887-8994(00)00166-1.

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Vuopala, Katri, Jaakko Ignatius, and Riitta Herva. "Lethal arthrogryposis with anterior horn cell disease." Human Pathology 26, no. 1 (1995): 12–19. http://dx.doi.org/10.1016/0046-8177(95)90109-4.

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Gaitanis, John N., Hugh J. McMillan, Allan Wu, and Basil T. Darras. "Electrophysiologic Evidence for Anterior Horn Cell Disease in Amyoplasia." Pediatric Neurology 43, no. 2 (2010): 142–47. http://dx.doi.org/10.1016/j.pediatrneurol.2010.03.018.

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Desai, J. A., and M. Melanson. "Teaching NeuroImages: Anterior horn cell hyperintensity in Hirayama disease." Neurology 77, no. 12 (2011): e73-e73. http://dx.doi.org/10.1212/wnl.0b013e31822f02d0.

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Görgen-Pauly, Ute, Jürgen Sperner, Irwin Reiss, Hans-Björn Gehl, and Erich Reusche. "Familial pontocerebellar hypoplasia type I with anterior horn cell disease." European Journal of Paediatric Neurology 3, no. 1 (1999): 33–38. http://dx.doi.org/10.1053/ejpn.1999.0177.

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Torne, Krupa, and Neeta Sutay. "A rare presentation of anterior horn cell disease in children." European Journal of Paediatric Neurology 21 (June 2017): e109. http://dx.doi.org/10.1016/j.ejpn.2017.04.941.

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Corbett, Joel, Stephen Walsh, Sandeep Bhuta, and Arman Sabet. "105 Snake eyes in the thoracic spine." Journal of Neurology, Neurosurgery & Psychiatry 89, no. 6 (2018): A41.3—A42. http://dx.doi.org/10.1136/jnnp-2018-anzan.104.

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IntroductionBilateral anterior horn cell hyperintensity on spinal imaging (‘snake eyes’ sign) is seen in pathologies including cervical spondylosis, spinal cord infarction and Hirayama’s disease. Below is the first report of lower limb monomelic amyotrophy (MMA) with thoracic spine snake eyes sign. We present a case report of lower limb MMA with bilateral anterior horn hyperintensity, and literature review of cases with this clinico-radiologic presentation.CaseA 47 year old man presented with an 11 year history of asymmetric, progressive, proximal right lower limb weakness and wasting followin

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de Carvalho, M., and M. Swash. "Fasciculation-cramp syndrome preceding anterior horn cell disease: an intermediate syndrome?" Journal of Neurology, Neurosurgery & Psychiatry 82, no. 4 (2010): 459–61. http://dx.doi.org/10.1136/jnnp.2009.194019.

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Wongworawat, Yan Chen, Yin Allison Liu, Ravi Raghavan, et al. "Aggressive FUS-Mutant Motor Neuron Disease Without Profound Spinal Cord Pathology." Journal of Neuropathology & Experimental Neurology 79, no. 4 (2020): 365–69. http://dx.doi.org/10.1093/jnen/nlaa011.

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Abstract A 29-year-old man presented with rapidly progressive severe neck weakness, asymmetrical bilateral upper extremity weakness, bulbar dysfunction, profound muscle wasting, and weight loss. Within 1 year, his speech became unintelligible, he became gastrostomy- and tracheostomy/ventilator-dependent, and wheelchair bound. Electrophysiology suggested motor neuron disease. Whole exome sequencing revealed a heterozygous pathogenic variant in the fused in sarcoma gene (FUS), c.1574C&gt;T,p. R525L, consistent with autosomal dominant amyotrophic lateral sclerosis. Autopsy revealed extensive

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Pisharam, N. Thekkootu, T. Solomon, and R. Sharma. "Anterior horn cell and encephalopathic variant of Fabry's disease — The neuro-Fabry." Journal of the Neurological Sciences 333 (October 2013): e455-e456. http://dx.doi.org/10.1016/j.jns.2013.07.1626.

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Dissertations / Theses on the topic "Anterior horn cell disease"

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Chroni, Elisabeth. "F chronodispersion and F tacheodispersion : a study of conduction properties of motor nerve fibres in normal and pathological conditions." Thesis, King's College London (University of London), 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320463.

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Kezic, Jelena Marie. "A study of the monocyte-derived cell populations of the uveal tract and retina in homeostatic conditions and during the early stages of ocular autoimmune disease." University of Western Australia. School of Anatomy and Human Biology, 2008. http://theses.library.uwa.edu.au/adt-WU2009.0084.

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The eye contains closely related but widely different tissues, offering a unique opportunity to investigate the phenotype and function of monocyte-derived cell populations within functionally unique microenvironments in a single complex organ. The uveal tract and retina contain rich networks of immune cells that reside and traffic through the eye, these cells having been implicated in various ocular inflammatory processes and immune-mediated diseases. One such inflammatory condition is human posterior uveitis, an autoimmune disease mainly affecting the retina. As current treatments for posteri

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Books on the topic "Anterior horn cell disease"

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Pitt, Matthew. Needle EMG findings in different pathologies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.003.0007.

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In this chapter, the inability of electromyography (EMG) to be able to further progress the diagnosis of myopathy on its own—requiring muscle biopsy and other modalities such as genetics to complete this process—is emphasized. The role of EMG particularly in the era of genetics is discussed. Findings in neurogenic abnormality are next described and the important hereditary conditions such as spinal muscular atrophy (SMA), distal SMA, Brown–Vialetto–Van Laere syndrome, segmental anterior horn cell disease, conditions with progressive bulbar palsy, SMARD1, and pontocerebellar hypoplasia with spi

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Thakore, Nimish, and Erik P. Pioro. Types of Motor Neuron Diseases. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0022.

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Disorders of lower motor neurons (LMNs, or anterior horn cells) and upper motor neurons (UMNs), jointly termed motor neuron disorders (MNDs), are diverse and numerous. The prototypical MND, namely amyotrophic lateral sclerosis (ALS), a relentlessly progressive lethal disorder of adults, is the subject of another section and will not be discussed further here. Other MNDs include spinal muscular atrophy (SMA), of which there are four types: Kennedy’s disease, Brown-Violetto-Van Laere, and Fazio-Londe syndromes, lower motor neuron disorders as part of neurodegenerations and secondary motor neuron

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Constantinescu, Cris S., and Su-Yin Lim. Weakness. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0044.

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Muscle weakness may reflect systemic disease (such as sepsis or severe hypokalaemia) or a neuromuscular disorder. The origin of neuromuscular weakness may be localized to upper motor neurons, lower motor neurons (including nerve roots, plexus, and peripheral nerves), anterior horn cells, neuromuscular junctions, or muscles. The mode of onset of weakness, its time course, and the findings on general and neurological examination will usually differentiate between the possible diagnoses. The approach to the patient with suspected neuromuscular weakness is described in this chapter.

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Forsyth, Rob, and Richard Newton. Specific conditions. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198784449.003.0004.

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This chapter adopts a systematic approach to common diagnoses in paediatric neurology, aetiologies, management to include investigation and treatment, and outcome. For each condition current knowledge on cause and underlying biology is summarized. A rational approach to investigation and treatment is summarized for each topic. These include: acquired brain injury; autoimmune and autoinflammatory disease of the CNS; cerebral palsy and neurodisability which covers feeding, communication, special senses, and respiratory disease; demyelinating disease; epilepsy including its impact on daily life;

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Donaghy, Michael. The clinical approach. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0030.

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This chapter describes the appropriate clinical approach to take when presented with a patient reporting a neurological symptom. Just under 10 per cent of the population consult their general practitioner about a neurological symptom each year in the United Kingdom. About 10 per cent of these are referred for a specialist opinion, usually to a neurologist. Nine conditions account for roughly 75 per cent of general neurological referrals and are diagnosed initially on purely clinical grounds, with the other 25 per cent representing the full range of other, potentially very rare, neurological di

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Katirji, Bashar. Electrodiagnostic Findings in Neuromuscular Disorders. Edited by Bashar Katirji. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190603434.003.0004.

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Neuromuscular disorders are often classified into four major categories: anterior horn cell disorders, peripheral neuropathies, neuromuscular junction disorders and myopathies. This chapter discusses the electrodiagnostic and clinical EMG findings in these various neuromuscular disorders. Peripheral neuropathies are subdivided into focal mononeuropathies, radiculopathies, plexopathies and generalized peripheral polyneuropathies. Focal peripheral nerve lesions and generalized peripheral polyneuropathies may be axonal or demyelinating, and manifest quite distinctly on nerve conduction studies. N

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Fuglsang-Frederiksen, Anders, Kirsten Pugdahl, and Hatice Tankisi. Quantitative electromyography. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0008.

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Several quantitative electromyography (QEMG) methods are used for diagnosing and monitoring in patients with neuromuscular disorders. At weak effort of the muscle, motor unit potential (MUP) analyses as individual MUP, multi-MUP, and macro-EMG are diagnostically sensitive and well tested. At higher effort of the muscle, interference pattern analyses such as the turns amplitude analysis are also diagnostically sensitive. Other potential diagnostic methods are power spectrum analysis, muscle fibre conduction velocity analysis, and some surface EMG methods. In patients with myopathy, QEMG has an

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Crum, Brian A., Eduardo E. Benarroch, and Robert D. Brown. Neurologic Disorders Categorized by Anatomical Involvement. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199755691.003.0523.

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Neurological disorders of the brain, spine, and peripheral nervous system are examined. Symptoms and signs related to disorders of the cerebral cortex may lead to alterations in cognition and consciousness. Unilateral neurologic symptoms involving a single neurologic symptom commonly localize to the cerebral cortex. Abnormalities of speech and language are localized to the dominant cerebral hemisphere, whereas abnormalities of the nondominant hemisphere may lead to visuospatial deficits, confusion, or neglect of the contralateral side of the body. The hypothalamus is important in many function

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Katirji, Bashar. Electromyography in Clinical Practice. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190603434.001.0001.

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Clinical Electromyography in Clinical Practice provides case-based learning of clinical Electromyography (EMG) with a main mission of reducing the gap between theory and practice in the field of electrodiagnostic medicine. The book format includes four introductory chapters that acquaint the discipline and scope of the EMG Examination to the beginners. This include chapters on nerve conduction studies, needle EMG, and specialized testing including late responses, repetitive nerve stimulation and single fiber EMG. Discussion on the electrodiagnostic and clinical EMG findings in the numerous neu

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Book chapters on the topic "Anterior horn cell disease"

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Mitchell, J. D. "Disorders of the Anterior Horn Cell." In Spinal Cord Disease. Springer London, 1997. http://dx.doi.org/10.1007/978-1-4471-0911-2_20.

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Mitchell, J. D. "Disorders of the Anterior Horn Cell." In Spinal Cord Disease. Springer London, 1997. http://dx.doi.org/10.1007/978-1-4471-0569-5_20.

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Salih, Mustafa A. M., and Peter B. Kang. "Anterior Horn Cell Diseases." In Clinical Child Neurology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-43153-6_39.

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Mitchell, J. D. "Anterior Horn Cell Diseases." In Clinical Medicine and the Nervous System. Springer London, 1992. http://dx.doi.org/10.1007/978-1-4471-3353-7_15.

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Salih, Mustafa A. M. "Anterior Horn Cell Diseases." In Textbook of Clinical Pediatrics. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-02202-9_370.

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Perkin, G. D. "Myasthenia gravis Anterior horn cell disease." In Diagnostic Tests in Neurology. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4899-3320-1_10.

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Swash, Michael, and Martin S. Schwartz. "Diseases of Anterior Horn Cells." In Neuromuscular Diseases. Springer London, 1997. http://dx.doi.org/10.1007/978-1-4471-3834-1_6.

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Swash, Michael, and Martin Schwartz. "Diseases of Anterior Horn Cells." In Neuromuscular Diseases. Springer London, 1988. http://dx.doi.org/10.1007/978-1-4471-3526-5_6.

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Swaab, D. F., E. Fliers, and E. Goudsmit. "Differential Cell Loss in (Peptide) Neurons in the Anterior Hypothalamus with Aging and Alzheimer’s Disease: Lack of Changes in Cell Density." In Neurology. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70007-1_14.

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Uchida, Kenzo, Hideaki Nakajima, Shoei Furukawa, Tomoo Inukai, Yasuhisa Maezawa, and Hisatoshi Baba. "Morphological Changes in Anterior Horn Cells, Immunoreactivity to Neurotrophic Factors, and Neuronal Cell Death of Spinal Cord Lesions in the Spinal Hyperostotic Mouse (twy/twy) with Chronic Mechanical Cord Compression." In Neuroprotection and Regeneration of the Spinal Cord. Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54502-6_9.

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Conference papers on the topic "Anterior horn cell disease"

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Tseng, JC, HH Cheng, RJ Hu, and LY Lu. "AB0119 Primary sjogren’s syndrome associated with anterior horn cell disorder." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.302.

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Tseng, JC, HH Cheng, RJ Hu, and LY Lu. "AB0120 Primary sjogren’s syndrome associaed with anterior horn cell disorder." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.303.

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Khurana, Anil, Paramjeet Kaur, Ashok K. Chauhan, Yashpal Verma, and Nupur Bansal. "Extra ovarian adult granulosa cell tumor of omentum: A report of a rare entity." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685372.

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Aims: Extra ovarian granulosa cell tumor (GCT) is extremely rare tumor, assumed to arise from the ectopic gonadal tissue along the embryonal route of the genital ridge. A case of extra ovarian granulosa cell tumor of omentum in a 69 year old female presented here. Materials and Methods: A 69 years old postmenopausal, hypertensive female presented with complaints of pain in right lumber and iliac region of one month duration. Pain was off and on and intermittent. The patient had a history of hysterectomy 12 years ago for fibroid uterus. Results: Ultrasound examination of abdomen showed a hypoec

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