Relevant bibliographies by topics / Paralysis, history

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Paralysis, history'

Author: Grafiati
Published: 4 June 2021
Last updated: 29 July 2025

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Journal articles on the topic "Paralysis, history"

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Chalissery, Albi Jose, Tudor Munteanu, Yvonne Langan, Francesca Brett, and Janice Redmond. "Diverse phenotype of hypokalaemic periodic paralysis within a family." Practical Neurology 18, no. 1 (2017): 60–65. http://dx.doi.org/10.1136/practneurol-2017-001677.

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Hypokalaemic periodic paralysis typically presents with intermittent mild-to-moderate weakness lasting hours to days. We report a case with an uncommon phenotype of late-onset myopathy without episodic paralytic attacks. Initial work-up including muscle biopsy was inconclusive. A subsequent review of the right deltoid biopsy, long exercise testing and repeated family history was helpful, followed by appropriate genetic testing. We identified a heterozygous pathogenic mutation in calcium ion channel (CACNA1S:c.1583G>A p.Arg528His) causing hypokalaemic periodic paralysis. Myopathy can present
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Kim, Youn Kyoung, and Sa-Yoon Kang. "Hyperkalemic Periodic Paralysis Caused by a Mutation in the Sodium Channel SCN4A Gene." Journal of Medicine and Life Science 11, no. 1 (2014): 5–7. http://dx.doi.org/10.22730/jmls.2014.11.1.5.

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Hyperkalemic periodic paralysis (HyperPP) is an autosomal dominant muscle sodium channelopathy characterized by recurrentepisode of reversible paralysis with concomitant hyperkalemia. The diagnosis of HyperPP is suggested by a history of attacks ofparalysis, positive family history, and the presence of myotonia. A 19-year-old man presented with recurrent generalized limbweakness since childhood. The paralysis often followed by fatigue, exercise, and fasting. His parents were clinically unaffectedand had never experienced paralytic symptoms. Electromyographic evaluation demonstrated myotonic di
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Rabinovich, Itamar. "Paralysis in Lebanon." Current History 89, no. 544 (1990): 73–76. http://dx.doi.org/10.1525/curh.1990.89.544.73.

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Vale, José, Nuno Canas, Alberto Leal, and Helena Vilar. "Paralisia periódica tireotóxica." Acta Médica Portuguesa 18, no. 5 (2012): 399–402. http://dx.doi.org/10.20344/amp.1056.

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Thyrotoxic periodic paralysis (TPP) is characterized by recurrent episodes of muscle weakness and hypokalemia associated with thyroid hyperactivity. Reported predominantly among individuals of Asian descent, TPP is a rare manifestation of hyperthyroidism in western populations. We describe a typical case of TPP in a 33-year-old portuguese male, who presented with acute tetraparesis associated with hypokalemia (K+ 2.6 mEq/L). The patient had a 8-week history of several episodes of paraparesis of variable intensity; these attacks were usually nocturnal, preceded by strenuous exercise and resolve
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Shreya, Kumar Nabin, Ahmad Ansari Fayaz, and Kumar Jha Anand. "Abstract Aim: To determine the impact of Botulinum Toxin on Cervical Dystonia and its influence on Quality of Life. Materials and Methods: This study was conducted in the Department of physical medicine and rehabilitation, ESIC Medical College, Bihta, Patna, Bihar, India. Male and female patients aged between 18 and 80 years who fulfilled the diagnostic criteria for primary CD, had good consciousness and comprehension of the HRQoL questionnaires, and could communicate in and understand Thai language were included in the study. All the patients were included and completed the study. To assess the disease-specific HRQoL, this study used the CDIP58 and CDQ-24. This study employed the SF-36 and the EQ-5D to assess patients' general HRQoL. Results: Mean duration of symptoms in enrolled patients was 5.0 years (range from 0 to 12 years). There were 16 cases of torticollis, two of laterocollis, one of anterocollis, and one of latrocollis included in the study. The previous mean number of botulinum toxin A injections received per patient was 8.85±5.32 injections, ranging from 1 to 22. After 24 weeks of treatment, the mean (SD) score of all eight domains of CDIP-58 including head and neck symptoms, pain and discomfort, upper limb activities, walking, sleep, annoyance, mood, and psychosocial functioning were significantly improved (P<0.001) (Table 2). The mean (SD) of each of the five categories of CDQ-24 was also significantly improved with P-values of 0.004, 0.001, 0.003, 0.001, and 0.0005 for stigma, emotional well-being, pain, activities of daily living, and social and family life, respectively (Table 2). After 24 weeks of treatment, the mean values of results of all eight domains of SF-36 did not significantly improved. The P-values for PF, RP, RE, VT, mental health, SF, BP, and GH are 0.726, 1.000, 0.505, 0.349, 0.115, 0.171, 0.427, and 0.380 respectively. The mean score of each category of EQ-5D including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression revealed a nonsignificant change (P>0.05). Conclusion: In conclusion, the quality of life of CD patients improved after multiple botulinum toxin A injections. Each injection of botulinum toxin A seems to have cumulative effects in multiple-injection patients. The direct mechanism behind an improvement in physical health is well understood; however, that behind mental health is less obvious. A relief of dystonia could make a positive difference to patients' relaxation state and stress level, which would account for mental improvement." International Journal of Current Pharmaceutical Review and Research 15, no. 11 (2023): 790–94. https://doi.org/10.5281/zenodo.13234062.

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AbstractAim: To determine the etiological spectrum of hypokalaemia periodic paralysis.Material and methods: This study was conducted in the department of Medicine, JNKTMCH, Madhepura, Bihar,India for one year. All patients admitted in the neurology ward with acute flaccid paralysis with hypokalaemia(serum potassium &lt;3.5) involving two or more limbs without sphincter and sensory disturbances were includedin the study. Medical history, previous episodes of similar weakness, hyperthyroidism, diarrhoea, vomiting, renaldisease, and drug intake were noted. Any history of similar illness in the fa
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Binder, Devin K. "A History of Todd and His Paralysis." Neurosurgery 54, no. 2 (2004): 480–87. http://dx.doi.org/10.1227/01.neu.0000103490.49537.37.

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Cabrera-Gómez, J. A., N. Echazabal-Santana, Y. Real-González, et al. "Hereditary Melkersson-Rosenthal syndrome and multiple sclerosis." Multiple Sclerosis Journal 11, no. 3 (2005): 364–66. http://dx.doi.org/10.1191/1352458505ms1164cr.

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The revision of MEDLINE from 1966 to 2003 did not report any association between multiple sclerosis (MS) and Melkersson—Rosenthal syndrome (MRS). This is a case report of a 51-year-old woman, with history of four recurrent Bell’s palsies. In 1999 she developed a right facial paralysis due to a supranuclear pyramidal lesion with right monoparesis. The family history showed five relatives with recurrent Bell’s paralysis and plicata tongue. Physical examination: right Bell’s paralysis, left supranuclear facial paralysis, furrowed tongue, right hemiparesis with pallor of the optic disks. Brain mag
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Kesavan T M, Ananda, Sreejith Kumar K C, and Sreya Raghunath. "Hypokalemic Peroidic Paralysis: The Unusual Ones in Pediatrics." Indian Journal of Trauma and Emergency Pediatrics 14, no. 1 (2022): 25–27. http://dx.doi.org/10.21088/ijtep.2348.9987.14122.3.

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Hypokalaemic periodic paralysis is an uncommon but potentially life threatening clinical syndrome. It should consider in any child with recurrent motor paralysis. A positive family history with a low potassium level during attacks, will confirm the diagnosis If recognized and treated appropriately, patients recover without any clinical squeal. No extensive investigations are needed. KCL, acetazolamide, spiranolactone and lifestyle modificationswill help them to bring to normal activity.
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Metri, Shrikanth, and Srinivas B. "PERIODIC PARALYSIS IN THYROTOXICOSIS." International Journal of Advanced Research 10, no. 04 (2022): 589–91. http://dx.doi.org/10.21474/ijar01/14587.

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Thyrotoxic periodic paralysis (TPP) is one of the rare manifestation thyrotoxicosis. In this case report, we present a 36-year-old man, who had lower limb weakness for one day on waking up.He has no family history of thyroid or neurological problems.Any cause of thyrotoxicosis maybe sufficient to trigger attacks in susceptible patients. In order to permanently repair the problem, the underlying hyperthyroid status must be rectified.
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Borg, Tiffanie-Marie, Amy Sarah Warwick, and Mas Ahmed. "The child with facial nerve palsy." InnovAiT: Education and inspiration for general practice 14, no. 12 (2021): 742–48. http://dx.doi.org/10.1177/17557380211046283.

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In this article we summarise the educational aspects regarding the clinical presentation, diagnosis and management of children presenting with facial nerve paralysis, highlighting the importance of family history. We report two cases of hereditary facial nerve paralysis managed by the authors: one a child with familial facial nerve palsy, and the other a child with Melkersson–Rosenthal syndrome. The history in both cases revealed multiple family members with the same disorder.
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Dissertations / Theses on the topic "Paralysis, history"

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Hurn, Juliet D. "The history of general paralysis of the insane in Britain, 1830 to 1950." Thesis, University College London (University of London), 1998. http://discovery.ucl.ac.uk/1349281/.

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This thesis explores the history of ideas about, and responses to, general paralysis of the insane (GPI) - specifically in the context of the developing profession of psychiatry in Britain. It considers GPI as an objective disease entity whose subjective definition was nevertheless open to negotiation; for example, in deciding how central was overt insanity, or how GPI should be differentiated from the allied disease of tabes dorsalis. It explores how psychiatrists' interest in organicism and the science of medicine - and their attempts to raise the status of their specialty - both informed th
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Bryant, Jacob Owen. "The Invisible Enemy: The Effects of Polio on the American War Effort during World War II, 1941-1945." Digital Commons @ East Tennessee State University, 2012. https://dc.etsu.edu/etd/1404.

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This thesis looks at the social, political, and military effects of epidemic polio on America's war effort during World War II. The primary sources consulted include newspapers, military medical reports, photographs, memoirs, speeches, and archival collections. It looks at the effects of polio on the home front, more specifically how epidemics and the rising rates of polio were a detriment to the civilian war effort. It also focuses on the American military's preparation for and response to polio outbreaks among troops both at home and abroad. Finally, it discusses the experiences of the servi
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Matos, José Antônio Souza. "A escola e o percurso educativo de pessoas com paralisia cerebral: estudo de caso." Faculdade de Educação, 2011. http://repositorio.ufba.br/ri/handle/ri/18858.

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Submitted by José Antônio Matos (jasmatos@bol.com.br) on 2016-04-14T20:18:18Z No. of bitstreams: 1 DISSERTAÇÃO MESTRADO JOSE ANTONIO S MATOS.pdf: 503684 bytes, checksum: 84fbe8c234c1dcd1c9202b3862d9290a (MD5)<br>Approved for entry into archive by Maria Auxiliadora da Silva Lopes (silopes@ufba.br) on 2016-04-15T17:45:33Z (GMT) No. of bitstreams: 1 DISSERTAÇÃO MESTRADO JOSE ANTONIO S MATOS.pdf: 503684 bytes, checksum: 84fbe8c234c1dcd1c9202b3862d9290a (MD5)<br>Made available in DSpace on 2016-04-15T17:45:33Z (GMT). No. of bitstreams: 1 DISSERTAÇÃO MESTRADO JOSE ANTONIO S MATOS.pdf: 503684 byt
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Macia, Frédéric. "Paralysie supranucléaire progressive : histoire naturelle, marqueurs cliniques et neuroradiologiques." Bordeaux 2, 2000. http://www.theses.fr/2000BOR23006.

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MAY, REGINE. "De la syphilis au sida, de la paralysie cerebrale a la demence du sida." Lille 2, 1994. http://www.theses.fr/1994LIL2M085.

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NEGRELLO, LAURENT. "La maladie de guy de maupassant : revue de la litterature." Lyon 1, 1993. http://www.theses.fr/1993LYO1M322.

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Mawdsley, Stephen Edward. "Fighting polio : selling the gamma globulin field trials, 1950-1953." Thesis, University of Cambridge, 2012. https://www.repository.cam.ac.uk/handle/1810/252270.

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Mai, Nadin. "The aesthetics of absence and duration in the post-trauma cinema of Lav Diaz." Thesis, University of Stirling, 2015. http://hdl.handle.net/1893/22990.

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Aiming to make an intervention in both emerging Slow Cinema and classical Trauma Cinema scholarship, this thesis demonstrates the ways in which the post-trauma cinema of Filipino filmmaker Lav Diaz merges aesthetics of cinematic slowness with narratives of post-trauma in his films Melancholia (2008), Death in the Land of Encantos (2007) and Florentina Hubaldo, CTE (2012). Diaz has been repeatedly considered as representative of what Jonathan Romney termed in 2004 “Slow Cinema”. The director uses cinematic slowness for an alternative approach to an on-screen representation of post-trauma. Contr
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Books on the topic "Paralysis, history"

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Killalea, Anne. The great scourge: The Tasmanian infantile paralysis epidemic, 1937-1938. Tasmanian Historical Research Association, 1995.

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Smelser, Neil J. Social paralysis and social change: British working-class education in the nineteenth century. University of California Press, 1991.

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Koontz, Dean R. Le temps paralysé. J'ai Lu, 1990.

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universitet), European Conference on South Asian Studies (18th 2004 Lunds. Paralysed tongue: An anthology of Dalit studies. Pagemaker, 2005.

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McMahon, John M. Paralysin cave: Impotence, perception, and text in the Satyrica of Petronius. Brill, 1998.

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1869-1964, Aguinaldo Emilio, Aguinaldo Emilio 1869-1964, Calairo, Emmanuel Franco, editor, translator, and National Historical Commission (Philippines), eds. Saloobin: Mga sagot ni Hen. Emilio Aguinaldo sa mga paratang ng dakilang lumpo = Sentiments : Gen. Emilio Aguinaldo's response to the accusations of the sublime paralytic. National Historical Commission of the Philippines, 2002.

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Gaurier, Bruno. André Trannoy: Handicap et mobilisation. Desclée de Brouwer, 1998.

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Elsom, John. State of Paralysis: A Cultural History of Brexit. Lutterworth Press, The, 2019.

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Elsom, John. State of Paralysis: A Cultural History of Brexit. Lutterworth Press, The, 2019.

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Elsom, John. State of Paralysis: A Cultural History of Brexit. Lutterworth Press, The, 2019.

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Book chapters on the topic "Paralysis, history"

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Loza-Rubio, Elizabeth, and Juan Antonio Montaño-Hirose. "A History of Paralytic Bovine Rabies Transmitted by Vampire Bats in Mexico." In History of Rabies in the Americas: From the Pre-Columbian to the Present, Volume II. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-25405-5_4.

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Lekka, Vasia. "Unrolling the Archives’ Thread: Epilepsy and Epileptics at the National Hospital for the Paralysed and Epileptic." In Boston Studies in the Philosophy and History of Science. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-06293-8_3.

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Sharpless, Brian A., and Karl Doghramji. "The History of Sleep Paralysis in Folklore and Myth." In Sleep Paralysis. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199313808.003.0003.

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Winnicott, Donald W. "Facial Nerve Paralysis." In The Collected Works of D. W. Winnicott. Oxford University Press, 2016. http://dx.doi.org/10.1093/med:psych/9780190271336.003.0023.

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Wray, Shirley H. "Vertical Gaze and Syndromes of the Midbrain." In Eye Movement Disorders in Clinical Practice. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199921805.003.0007.

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reviews the architecture of the midbrain and extensively discusses the linkage of specific diagnostic signs to areas of the midbrain. Paralysis of up- and downgaze, pretectal pupils, eyelid and vergence disorders are among the signs discussed. Here again, case studies and video displays allow detailed presentations of patient history, analysis, diagnosis, and treatment of a range of disorders characterized by supranuclear vertical gaze paralysis: the pretectal syndrome, the Sylvian aqueduct syndrome, syndromes of the top of the basilar artery, and a rare case of supranuclear paralysis of downg
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Winnicott, Donald W. "Facial Nerve Paralysis, Associated with Fits." In The Collected Works of D. W. Winnicott. Oxford University Press, 2016. http://dx.doi.org/10.1093/med:psych/9780190271336.003.0024.

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"The Agrarian State and the Company: Parasitism and Paralysis." In An Economic History of India. Routledge, 2002. http://dx.doi.org/10.4324/9780203420584-4.

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Liveson, Jay Allan. "Congenital Bilateral Sixth and Seventh Palsies." In Peripheral Neurology. Oxford University PressNew York, NY, 2000. http://dx.doi.org/10.1093/oso/9780195135633.003.0088.

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Abstract A I0-year-old girl was referred for preoperative evaluation of her cranial nerve function. Since birth she had bilateral facial and lateral rectus paralysis. There was a maternal history of miscarriage and a prolonged labor. Patient had a normal development and above-average intelligence.
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Gilleard, Onur, and Kalliroi Tzafetta. "Anatomy and physiology of the facial nerve and aetiology of facial nerve palsy." In Oxford Textbook of Plastic and Reconstructive Surgery, edited by Maniram Ragbir. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780199682874.003.0216.

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Facial paralysis can have significant functional and social consequences and presents a challenging reconstructive problem for plastic surgeons. Detailed knowledge of facial nerve anatomy and an understanding of the natural history of the different conditions which result in facial palsy is a prerequisite for clinicians who are involved in the management of this devastating affliction.
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Caldwell, Peter C. "Modernization and Its Discontents." In Democracy, Capitalism, and the Welfare State. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198833819.003.0005.

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The period from the mid-1960s to the early 1970s has been characterized by historians as one of “planning euphoria.” This enthusiasm was especially evident in the Social Democrats’ ambitious plans for steering the economy and reshaping society through social policy. At the same time, however, social theorists on both right and left criticized these efforts for their tendency toward alienation and bureaucratization. On the right, Hans Freyer and Arnold Gehlen predicted that secondary institutions would end human creativity, ushering in a period of post-history; Ernst Forsthoff feared state para
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Conference papers on the topic "Paralysis, history"

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Zabel, Marianne, Johannes Woitzik, Andreas Radeloff, and Katrin Radeloff. "New-onset left vocal fold palsy with a 10-years history of left tongue paralysis." In 94th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1767199.

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Gardiner, A., and R. Bilancia. "P110 The untold tale of diaphragmatic paralysis: epidemiology, natural history and decision-making for surgical repair." In British Thoracic Society Winter Meeting 2022, QEII Centre, Broad Sanctuary, Westminster, London SW1P 3EE, 23 to 25 November 2022, Programme and Abstracts. BMJ Publishing Group Ltd and British Thoracic Society, 2022. http://dx.doi.org/10.1136/thorax-2022-btsabstracts.246.

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Santos, João Nicoli Ferreira dos, Izadora Fonseca Zaiden Soares, and Lis Gomes Silva. "Unilateral opercular lesion mimicking opercular syndrome." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.601.

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Introduction: Foix-Chavany-Marie syndrome, also known as opercular syndrome, consists of voluntary orofacial muscle paralysis due to bilateral lesions in the anterior frontotemporal operculum. Classically, there is an automatic-voluntary dissociation, with impairment of speech and chewing. We present a case of a patient who had a similar presentation to opercular syndrome, secondary to unilateral ischemic lesion in the right frontal operculum. Case report: A 55-year-old, right-handed, black woman with history of arterial hypertension was admitted to the emergency department presenting left-sid
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Engan, Mette, Merete Engeseth, Ingvild Engesæter, et al. "Prevalence and consequences of left vocal cord paralysis in young adults born extremely premature with a history of neonatal patent ductus arteriosus surgery." In ERS International Congress 2020 abstracts. European Respiratory Society, 2020. http://dx.doi.org/10.1183/13993003.congress-2020.4793.

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Madruga, Kauan Alves Sousa, Luiz Fernando Melo Lima, Pedro Victor Oliveira Araújo, Vitória Bittencourt de Carvalho, and Bruna Da Cruz Beyruth Borges. "Septic Cavernous Sinus Thrombosis due to Pneumococcal Meningitis in A 6 Months Infant." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.479.

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Context: Septic Cavernous Sinus Thrombosis (CST) is a rare and potentially lethal illness that clinicians still occasionally see. We describe the evolution of a 6 months old infant patient who had a history of delayed vaccination and acquired a Pneumococcal Meningitis, leading to septic CTS. Case report: The patient was admitted with the complaint of constant crying and vomiting. The physical exam noticed: bulging of the bregmatic fontanelle, Glasgow Coma Score = 11, and bad general state. The clinical picture had begun one week before the hospitalization, but the fever had started just three
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Silva, Agnes Laura, Beatriz Iolanda de Sene Ferregutti Pinheiro, Laura de Lourdes Cardoso e. Silva, et al. "Pseudotumor demyelination lesion associated with bevacizumab in oncological treatment." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.770.

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Introduction: Bevacizumab is a monoclonal antibody directed against the human isoform of vascular endothelial growth factor A (VEGF-A) and inhibits angiogenesis. Case: Female patient, 54-year-old, with a history of intestinal adenocarcinoma associated with peritoneal carcinomatosis being treated with bevacizumab. The patient started to present a deviation of the labial rhyme to the right, which showed the presence of left facial paralysis with a central pattern on the neurological physical examination, without other alterations. Magnetic resonance imaging of the brain showed a nodular lesion c
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Moreira, João Victor Aguiar, Isabela Maria Bernardes Goulart, Diogo Fernandes dos Santos, et al. "Bilateral diaphragmatic eventration and alveolar hypoventilation in congenital myotonic dystrophy." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.533.

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Context: Congenital myotonic dystrophy (CMD) is a subtype of type 1 myotonic dystrophy presented in the neonatal period associated with a 16–40% mortality rate. CMD cause significant morbidity and mortality and often require intensive intervention at birth because of hypotonia, respiratory failure and feeding difficulties. It can cause respiratory problems including ineffective cough, recurrent pulmonary infections, orthopnea, dyspnea, poor sleep, apnea and snoring. However, there are few descriptions about diaphragmatic impairment in CMD. We present a baby who had bilateral diaphragmatic even
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Idrissa, AA, S. Atti, RK Wasaulua, et al. "Sequelae following an epidemic of meningococcal meningitis in Niger." In MSF Scientific Day International 2023. MSF-USA, 2023. http://dx.doi.org/10.57740/wg9g-dq47.

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INTRODUCTION MSF supported Niger’s Ministry of Health (MoH) in responding to a serogroup C meningococcal meningitis epidemic in Magaria and Dungass Districts in 2022. WHO’s global roadmap for defeating meningitis by 2030 emphasises appropriate care for meningitis sequelae, but this is not yet part of standard epidemic response. Meningitis sequelae in the African meningitis belt are poorly described, hampering access to rehabilitation services. To better orient future care for sequelae, we performed a follow-up survey of survivors 9 months after the 2022 epidemic. METHODS WHO case definitions w
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Pizzutti, Alice Elisa, and Luíza Fruett M. de Lima. "Clinical case of intervertebral disc disease (IVDD)." In III SEVEN INTERNATIONAL MULTIDISCIPLINARY CONGRESS. Seven Congress, 2023. http://dx.doi.org/10.56238/seveniiimulti2023-078.

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IVDD is an intervertebral disc injury characterized by extrusion of the disc into the spinal canal, compressing the spinal cord and causing limb paralysis. Diagnosis involves anamnesis, clinical history, physical and neurological examination. Treatment is clinical or surgical, depending on the degree, extent and location. The present report aims to describe the clinical therapeutic evolution of low-grade thoracolumbar IVDD. A male dachshund, 4 years old, 7 kg, with walking difficulties was seen at the UPF Veterinary Hospital. He manifested ambulatory paraparesis and decreased proprioception in
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Silva, Evelliny Gomes, Arthur Cesário de Holanda, Vitor Maia Arca, et al. "“Wake-up” onset of pharyngocervicobrachial variant of Guillain-Barré syndrome: a case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.565.

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Guillain-Barré syndrome (GBS) is the most common cause of acute flaccid paralysis in the world. There are variants. Of the cranial forms, the following stand out: the classic form, facial diplegia with distal paresthesias, pharyngo-cervico-brachial form, polyneuritis cranialis, Miller-Fisher syndrome and Bickerstaff encephalitis. This study aimed to report the case of a 73-year-old male patient, diabetic, former smoker and alcoholic, who presented at the Neurology outpatient clinic of a tertiary hospital in Pernambuco, after emergency care and 19 days of symptoms, reported as sudden cervical w
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