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Articles de revues sur le sujet "Painful Nerve Disease"

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Guerrero-Moreno, Adrian, Hong Liang, Nathan Moreau, et al. "Corneal Nerve Abnormalities in Painful Dry Eye Disease Patients." Biomedicines 9, no. 10 (2021): 1424. http://dx.doi.org/10.3390/biomedicines9101424.

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Background: This study aimed to compare the corneal nerve structural abnormalities detected using in vivo confocal microscopy (IVCM) in patients with neuropathic corneal pain (NCP) secondary to primary meibomian gland dysfunction (MGD) or autoimmune dry eye (AIDE). Methods: A two-stage retrospective nested case–control study was conducted. First, data from patients with either MGD or AIDE were assessed, selecting only cases with no corneal pain (VAS = 0) or severe pain (VAS ≥ 8). Ocular signs and symptoms of the 238 selected patients were compared between painful and painless cases. Next, pain
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Santosh, Kamble *. Bhagwat Poul Prachi Udapurkar Kailash Biyani. "Peripheral Neuropathy: Diagnosis, Management and Pharmacotherapy." Journal of Pharma Research 5, no. 2 (2016): 25–29. https://doi.org/10.5281/zenodo.1116570.

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<strong>ABSTRACT</strong> <strong>N</strong>europathy a disease of nerve is the common cause of pain in modern world. Chronic neuropathic pain is the most disturbing symptom of lesions in the peripheral nervous system that can be of many forms. Peripheral neuropathy is often distressing may produce disabilities or even found to be fatal. There are several things that cause neuropathies, understanding of the different types of neuropathies as well as their causes, symptoms, treatment options and prognoses is important for management of the painful disease. Symptoms of different painful neuropat
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Santosh, Kamble *. Bhagwat Poul Prachi Udapurkar Kailash Biyani. "Peripheral Neuropathy: Diagnosis, Management and Pharmacotherapy." Journal of Pharma Research 5, no. 2 (2017): 25–29. https://doi.org/10.5281/zenodo.1116578.

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<strong>ABSTRACT</strong> <strong>N</strong>europathy a disease of nerve is the common cause of pain in modern world. Chronic neuropathic pain is the most disturbing symptom of lesions in the peripheral nervous system that can be of many forms. Peripheral neuropathy is often distressing may produce disabilities or even found to be fatal. There are several things that cause neuropathies, understanding of the different types of neuropathies as well as their causes, symptoms, treatment options and prognoses is important for management of the painful disease. Symptoms of different painful neuropat
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Godel, Tim, Philipp Bäumer, Mirko Pham, et al. "Human dorsal root ganglion in vivo morphometry and perfusion in Fabry painful neuropathy." Neurology 89, no. 12 (2017): 1274–82. http://dx.doi.org/10.1212/wnl.0000000000004396.

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Objective:To evaluate functional and morphometric magnetic resonance neurography of the dorsal root ganglion and peripheral nerve segments in patients with Fabry painful neuropathy.Methods:In this prospective study, the lumbosacral dorsal root ganglia and proximal peripheral nerve segments of the lower extremity were examined in 11 male patients with Fabry disease by a standardized 3T magnetic resonance neurography protocol. Volumes of L3 to S2 dorsal root ganglia, perfusion parameters of L5-S1 dorsal root ganglia and the spinal nerve L5, and the cross-sectional area of the proximal sciatic ne
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Gaydhanker, Anuradha Prasanna, and Prasanna Shravan Gaydhanker. "A study on trigeminal nerve: Does superior cerebellar artery causes trigeminal neuralgia." Indian Journal of Clinical Anatomy and Physiology 9, no. 3 (2022): 174–78. http://dx.doi.org/10.18231/j.ijcap.2022.037.

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Our brain is the most complex organ in our body which conducts various complex functions and this level of complexity is operated by different structures of the brain. The complexity of relaying information between brain and different parts of the body is conducted by 12 pairs of cranial nerves. Out of 12 pairs of cranial nerves, the most complex and largest nerve is know as trigeminal nerve which is responsible for sensation of face and motor functions such as biting and chewing. Sometimes due to offendation of this nerve typically by Superior Cerebellar Artery leads to most excruciating pain
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Bourque, Christopher N., Brian A. Anderson, C. Martin del Campo, and Anders A. F. Sima. "Sensorimotor Perineuritis – An Autoimmune Disease?" Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 12, no. 2 (1985): 129–33. http://dx.doi.org/10.1017/s0317167100046837.

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ABSTRACT:The literature contains a single description of sensory perineuritis (Asbury et al 1972). These patients demonstrated a painful, distal, sensory neuropathy, and examination of peripheral nerve biopsies revealed focal thickening and inflammatory infiltrates of the perineurium. We report a patient with sensorimotor peripheral nerve dysfunction, accompanied by progressive slowing of nerve conduction velocity. Examination of a sural nerve biopsy demonstrated focal thickening of the perineurium, inflammatory infiltrates, and necrosis of perineurial cells. Immunohistology revealed a patchy
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Bashlachev, M. G., G. Yu Evzikov, and V. A. Parfenov. "Clinical manifestations, diagnosis, and surgical treatment of compressive common peroneal neuropathy at the level of the fibular head." Neurology, Neuropsychiatry, Psychosomatics 13, no. 1 (2021): 18–23. http://dx.doi.org/10.14412/2074-2711-2021-1-18-23.

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Common peroneal neuropathy (CPN) is the most common tunnel neuropathy in the lower extremities, many issues of diagnosis and treatment of which require further study.Objective: to analyze the clinical manifestations of CPN, methods of its diagnosis and treatment results.Patients and methods. Eighty patients (31 women and 49 men) aged 18 to 82 years (mean age, 51 years) with compressive CPN were followed up during 2012–2018. Unilateral CPN and bilateral CPN were found in 76 and 4 patients, respectively. Eighty-four common peroneal nerve decompression operations were performed.Results and discus
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Paovic, Jelena, Predrag Paovic, Ivica Bojkovic, Mirjana Nagulic, and Vojislav Sredovic. "Tolosa-Hunt syndrome - diagnostic problem of painful ophthalmoplegia." Vojnosanitetski pregled 69, no. 7 (2012): 627–30. http://dx.doi.org/10.2298/vsp1207627p.

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Background. Tolosa-Hunt syndrome (THS) is an uncommon disease caused by non-specific inflammation of the cavernous sinus, superior orbital fissure and the apex of the orbit. The disease is characterized by periorbital pain, paresis of the bulbomotor and quick response to steroid treatment. The orbital process may lead to optic nerve atrophy. According to the International Headache Society Classification of 2004, the diagnostic protocol includes magnetic resonance imaging (MRI) and biopsy. Case reports. We presented 46-year old male patient, with THS. The patient had unilateral periorbital pain
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Sabovchyk, Andriy Ya. "EFFECT OF NON-ALCOHOLIC FATTY LIVER DISEASE ON THE COURSE OF DIABETIC POLYNEUROPATHY IN PATIENTS WITH TYPE 2 DIABETES MELLITUS." Wiadomości Lekarskie 76, no. 11 (2023): 2395–400. http://dx.doi.org/10.36740/wlek202311109.

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The aim: To study the peculiarities of diabetic polyneuropathy in patients with type 2 diabetes mellitus and concomitant NAFLD. Materials and methods: We examined 75 patients with type 2 diabetes mellitus, including 31 (41.3%) women and 44 (58.7%) men. The main group included 35 patients with NAFLD (46.7%), and the control group included 40 patients without NAFLD (53.3%). The severity of polyneuropathy was assessed using the Toronto clinical neuropathy score. The presence of neuropathic pain syndrome in patients allowed us to divide patients into groups with painful or painless forms of diabet
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Podgorac, Ana, Jasna Zidverc-Trajkovic, Zagorka Jovanovic, et al. "Tolosa-Hunt syndrome: is it really necessary to show granuloma? - The report of eight cases." Vojnosanitetski pregled 74, no. 3 (2017): 287–93. http://dx.doi.org/10.2298/vsp150703180p.

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Introduction. Tolosa?Hunt syndrome (THS) is a rare entity, characterized by unilateral orbital pain associated with paresis of one or more of the oculomotor cranial nerves and caused by a granulomatous inflammation in the cavernous sinus, superior orbital fissure or orbit. The low prevalence of THS with a broad spectrum of other disorders that could cause painful ophtalmoplegia resulted in a stricter diagnostic criteria of THS in the latest edition of the International Classification of Headache Disorders. Current criteria require demonstration of granuloma by magnetic resonance imaging or bio
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Thèses sur le sujet "Painful Nerve Disease"

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Guzman, Ruben J. (Ruben Jacobo). "Effect of whole-body vibration on painful diabetic peripheral neuropathy." Thesis, 2012. http://hdl.handle.net/1957/30035.

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Introduction. Painful diabetic peripheral neuropathy (DPN) is a common complication of diabetes that interferes with daily living and causes severe pain. Pharmacotherapy is the accepted treatment strategy, however, this strategy is associated with high cost, minimal reductions in pain, and adverse side effects. Thus, a critical need exists to develop alternative treatment strategies. Purpose. To determine if a 12-week whole-body vibration (WBV) intervention reduces pain in adults with DPN. Methods. Twenty-one adults with physician confirmed painful DPN volunteered to take part in a 26-week tim
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Livres sur le sujet "Painful Nerve Disease"

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Shaibani, Aziz. Muscle Stiffness and Cramps. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199898152.003.0020.

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Muscle stiffness is a nonspecific term meaning limited muscle mobility that is not due to weakness. It is opposite to flexibility. Muscle and joint pain may be described as stiffness. Painful sustained muscle cramps are usually associated with muscle stiffness. A careful history is paramount. Exercise-induced muscle cramps are usually myopathic (metabolic or mitochondrial myopathy), while resting and nocturnal cramps are neurogenic (neuropathy, motor neuron disease, etc). Metabolic cramps are electrically silent. Focal or generalized stiffness is typically seen in stiff person syndrome. Upper
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Shaibani, Aziz. Muscle Stiffness and Cramps. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0020.

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Muscle stiffness as a nonspecific term means limited muscle mobility. Muscle and joint pain may be described as stiffness. Painful, sustained muscle cramps are usually associated with muscle stiffness. A careful history is paramount. Exercise-induced muscle cramps are usually myopathic (metabolic or mitochondrial myopathy) while resting, and nocturnal cramps are neurogenic [neuropathy, motor neuron disease (MND), etc.]. Metabolic cramps are electrically silent. Focal or generalized stiffness is typically seen in stiff person syndrome (SPS). Upper motor neuron (UMN) lesions are associated with
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Leung, Doris G. Neuropathies Associated with Infection or Toxic Exposure. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0113.

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Among the many causes of peripheral neuropathy are those mediated by environmental exposure to infectious and toxic agents. The most common neuropathy associated with HIV is HIV-associated distal sensory polyneuropathy (HIV-DSP). The clinical presentation of HIV-DSP is one of a distal, symmetric, often painful, small-fiber sensory axonal polyneuropathy. Other infectious causes of neuropathy include hepatitis C, leprosy, Lyme disease, rabies, and diphtheria, and antibiotic drugs such as isoniazid can also cause neuropathy. Heavy metals and a variety of other toxins including chemotherapeutic ag
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Scadding, John. Neuropathic pain. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0386.

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Pain signalled by a normal sensory system, nociceptive pain, serves a vital protective function. The peripheral and central nervous somatosensory systems permit rapid localization and identification of the nature of painful stimuli, prior to appropriate action to minimize or avoid potentially tissue damaging events. A reduction or absence of pain resulting from neurological disease emphasizes the importance of this normal protective function of pain. For example, tissue destruction occurs frequently in peripheral nerve diseases which cause severe sensory loss such as leprosy, and in central di
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Wallace, William 1791-1838. Physiological Enquiry Respecting the Action of Moxa: And Its Utility in Inveterate Cases of Sciatica, Lumbago, Paraplegia, Epilepsy, and Some Other Painful, Paralytic, and Spasmodic Diseases of the Nerves and Muscles. Creative Media Partners, LLC, 2021.

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Chapitres de livres sur le sujet "Painful Nerve Disease"

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Paudel, Byapak, Nitin Maruti Adsul, Hyeun Sung Kim, and Bentham Science Publisher Il-Tae Jang. "Transforaminal Epiduroscopic Basivertebral Nerve Laser Ablation for Chronic Low Back Pain Associated with Modic Changes." In Contemporary Endoscopic Spine Surgery. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815051544122030013.

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Among different causes of chronic low back pain, Modic changes of the endplates have been identified as an MRI-image representation of end stage degenerative disc disease. Painful innervation of these degenerative endplates from within the vertebral body by arborization of the basivertebral nerve towards these endplates has been demonstrated. Ablation of the basivertebral nerve has been identified as one possible way to treat chronic low back pain. This chapter describes the transforaminal epiduroscopic laser ablation of the basivertebral nerve and its associated clinical outcomes.
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Dowling, Álvaro, Juan Carlos Vera, Jorge Felipe Ramírez León, William Omar Contreras López, Morgan P. Lorio, and Kai-Uwe Lewandrowski. "Allogeneic Stem Cell Therapy for Painful Intermediate Lumbar Degenerative Discs." In Regenerative Medicine & Peripheral Nerve Endoscopy. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815274462124010012.

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The management of mid-stage degenerative disc disease presenting with pain remains contentious, attributed in part to the scarcity of conclusive clinical trials. Allogeneic mesenchymal stem cells (MSCs), procured from donors, emerge as a viable alternative to autologous stem cell therapy. These MSCs are characterized by their accessibility and the streamlined administration process suitable for procedure-room settings, particularly for addressing discogenic lumbar pain. Within this manuscript, the authors delineate their proprietary protocol involving allogeneic MSC application, detailing the
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Mendell, Jerry R. "α-Galactosidase A Deficiency: Fabry Disease." In Diagnosis and Management of Peripheral Nerve Disorders. Oxford University PressNew York, NY, 2001. http://dx.doi.org/10.1093/oso/9780195133011.003.0025.

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Abstract Fabry disease is a rare, inborn error of glycosphingolipid catabolism, inherited as an Xlinked recessive disorder with an incidence of only 1 in 40,000. Deficient activity of the lysosomal hydrolase, cx-galactosidase A, causes a symptom complex of acroparesthesias, angiokeratoma, corneal and lenticular opacities, and anhidrosis. In 1897, two dermatologists independently described the condition: Fabry in Germany and Anderson in Great Britain. Fabry disease is the preferred eponymic designation used in most places in the world, except in England where is it called Anderson-Fabry disease
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Scrivani, Steven J., Shehryar N. Khawaja, and Zahid H. Bajwa. "The Cranial Neuralgias and Other Neuropathic Head Pain." In Comprehensive Review of Headache Medicine, 2nd ed., edited by Morris Levin. Oxford University PressNew York, 2025. https://doi.org/10.1093/med/9780190888770.003.0016.

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Abstract Neuropathic pain disorder is a painful condition that is caused by a lesion or disease of the somatosensory nervous system. Cranial neuralgia is a type of neuropathic pain disorder in which lancinating pain is experienced along the distribution of a cranial nerve or nerves. There are a number of established neuralgias that present in the head and neck region. These disorders are unique and have a specific cluster of signs and symptoms, and they necessitate specific treatment and care. This chapter reviews the definition, classification, clinical features, pathophysiology, differential
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Novak, Vera, and Jerry R. Mendell. "Evaluation of the Peripheral Neuropathy Patient Using Autonomic Reflex Tests." In Diagnosis and Management of Peripheral Nerve Disorders. Oxford University PressNew York, NY, 2001. http://dx.doi.org/10.1093/oso/9780195133011.003.0005.

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Abstract Autonomic nervous system involvement is an important feature of many acute and chronic peripheral neuropathies (Table 5-1). Neuropathies may affect both somatic and autonomic nerves, or less often, autonomic nervous system failure may be the major or sole manifestation of the condition. In either case, autonomic reflex testing has emerged as an important diagnostic tool. Examples where autonomic reflex tests are valuable include acute panautonomia (Chapter 9), pure autonomic failure, and paraneoplastic intestinal pseudoobstruction. In patients with small cell carcinoma of the lung, au
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Moore, Andrew, Jayne Edwards, Jodie Barden, and Henry McQuay. "Topical capsaicin for pain relief." In Bandolier’s Little Book of Pain. Oxford University PressNew York, NY, 1992. http://dx.doi.org/10.1093/oso/9780192632470.003.0049.

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Abstract Capsaicin is an alkaloid derived from chillies. It first entered European knowledge after Columbus’ second voyage to the New World in 1494. There is evidence that capsaicin can deplete substance P in local nerve sensory terminals. Substance P is thought to be associated with initiation and transmission of painful stimuli, as well as a number of diseases including arthritis, psoriasis and inflammatory bowel disease. Inclusion criteria were randomised, double-blind, placebo-controlled trials of topical capsaicin for pain relief; data extractable to show proportion of patients showing im
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Cornblath, David R., Jerry R. Mendell, and John T. Kissel. "Evaluation of the Patient with Peripheral Neuropathy: The Challenges." In Diagnosis and Management of Peripheral Nerve Disorders. Oxford University PressNew York, NY, 2001. http://dx.doi.org/10.1093/oso/9780195133011.003.0001.

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Abstract The physician encountering a patient with suspected peripheral neuropathy is faced with three basic challenges. The first and most obvious challenge is to determine if the patient’s complaints and the physical findings are the result of a peripheral neuropathy, as similar symptoms can occasionally arise from disorders of the brain, spinal cord, anterior horn cell, neuromuscular junction, or muscle. The second challenge involves formulation of a complete differential diagnosis that will lead to proper identification of the type and cause of neuropathy. The third and perhaps most import
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Jitprapaikulsan, Jiraporn, M. Tariq Bhatti, Eric R. Eggenberger, Marie D. Acierno, and John J. Chen. "A Woman With Subacute Painful Vision Loss." In Mayo Clinic Cases in Neuroimmunology, edited by Andrew McKeon, B. Mark Keegan, and W. Oliver Tobin. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780197583425.003.0001.

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A 51-year-old White woman sought care for vision loss 1 week after a nonspecific upper respiratory tract infection. She reported pain in both eyes exacerbated by eye movement, which lasted for several days, followed by bilateral vision loss to the level of counting fingers–only vision. Optic neuritis was diagnosed, and she was treated with 1 g intravenous methylprednisolone for 3 days. Her vision improved substantially, and the pain resolved during the corticosteroid treatment. However, 1 week later, she woke up with right eye pain and vision loss. She was again treated with 5 days of intraven
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Kandil, Abdullah, and Danielle Perret. "Classification of Neuropathic Pain." In Neuropathic Pain, edited by Jianguo Cheng. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190298357.003.0002.

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Neuropathic pain encompasses a category of chronic pain conditions that are caused by disease or lesion of the somatosensory nervous system. Depending on the location of the lesion or disease, neuropathic pain can be categorized as peripheral, central, or mixed. Peripheral neuropathic pain includes such common pain conditions as painful diabetic neuropathy, postherpetic neuralgia, radiculopathies, post-amputation stump pain, various nerve entrapment syndromes, and neuropathies due to immune, hereditary, metabolic, and toxic factors. Central neuropathic pain is pain caused by stroke, spinal cor
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Farne, Hugo, Edward Norris-Cervetto, and James Warbrick-Smith. "Limb weakness." In Oxford Cases in Medicine and Surgery. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780198716228.003.0032.

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The definition of weakness is important, because many patients who self-describe a ‘weak limb’ will actually have a clumsy limb (ataxia), a numb limb (reduced sensation), or a limb that is too painful to move. The time course of the onset of the symptoms in general reflects the time course of the underlying pathology: • Sudden onset (seconds to minutes) usually implies either trauma (e.g. displaced vertebral fractures due to major trauma) or certain vascular insults (e.g. stroke, transient ischaemic attack (TIA)). • Subacute onset (hours to days) suggests a progressive demyelination (e.g. Guil
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Actes de conférences sur le sujet "Painful Nerve Disease"

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Braga, Anna Carlinda Arantes de Almeida, Patryk Marques da Silva Rosa, Luiza Monteiro dos Santos, et al. "Optic Neuritis and its several etiologies." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.742.

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Introduction: Optic neuritis (ON) is characterized by a condition of the optic nerve´s demyelinating inflammation, unilateral or bilateral involvement, which can lead to painful visual loss, color blindness, and other neurological and systemic impairments. Because it has several etiologies, ON is underdiagnosed and the studies seek an integrative review to identify the causes and differential diagnoses for the proper management. Methods: An analysis of scientific publications in the Pubmed and ScienceDirect databases was realized using the descriptors Optic Neuritis and diagnosis. Results: The
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Marin, Carolina Maria, Gustavo Carvalho Costa, Emilia Correa Souto, et al. "Charcot arthropathy in the elbow caused by hydrosiringomyelia." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.148.

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Introduction: Syringomyelia is a chronic disease of the spinal cord that leads to damage to nerve fibers in the spinothalamic tract. The changes in these structures responsible for the thermal and painful sensitivity lead to an abnormal innervation of the joints, which can lead to neuropathic arthropathy, called Charcot arthropathy. Syringomyelia is the main cause of Charcot arthropathy in the upper limbs, and the most involving joints are the shoulder and elbow. It is a rare condition and its recognition allows for early diagnosis and proper management. Case report: A 50-year-old female patie
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Moraes, Lucas Grobério Moulim de, Caroline Colnago Demuner, Giselle Alves de Oliveira, Paula Zago Melo Dias, and Marcelo Ramos Muniz. "Pseudochoreoathetosis in a patient with idiopathic sensitive ganglionopathy: a case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.520.

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Sensitive ganglionopathy has been associated with systemic diseases. In general, this rare neurological syndrome predates the onset of systemic symptoms. It affects selectively large nerve fibers and, accordingly, is manifested with loss of protopathic touch, vibratory perception, and proprioception. We describe a case of pseudochoreoathetosis in an elderly female patient with idiopathic sensitive ganglionopathy, manisfested with unsteadiness and weight loss in the last six months. The patient had systemic arterial hypertension, and a history of tobacco and alcohol abuses. The neurological exa
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