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Journal articles on the topic 'Guillain-Barré'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Cibulčík, František. "Guillain-Barré polyradiculoneuritis." Neurologie pro praxi 17, no. 1 (2016): 11–15. http://dx.doi.org/10.36290/neu.2016.003.

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2

Manfroi, Bárbara, and Letícia Aranega Dalari. "Síndrome de Guillain-Barré / Guillain-Barré Syndrome." Brazilian Journal of Health Review 5, no. 1 (2022): 2565–72. http://dx.doi.org/10.34119/bjhrv5n1-229.

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3

Sharma, Kamal, Supatida Tengsupakul, Omar Sanchez, Rozaleen Phaltas, and Paul Maertens. "Guillain–Barré syndrome with unilateral peripheral facial and bulbar palsy in a child: A case report." SAGE Open Medical Case Reports 7 (January 2019): 2050313X1983875. http://dx.doi.org/10.1177/2050313x19838750.

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Guillain–Barré syndrome is characterized by progressive motor weakness, sensory changes, dysautonomia, and areflexia. Cranial nerve palsies are frequent in Guillain–Barré syndrome. Among cranial nerve palsies in Guillain–Barré syndrome, facial nerve palsy is the most common affecting around half of the cases. Facial palsy in Guillain–Barré syndrome is usually bilateral. We describe a pediatric Guillain–Barré syndrome variant presenting with unilateral peripheral facial palsy and dysphagia. A 5-year-old boy had progressive lower extremity weakness and pain 3 days prior to onset of unilateral pe

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4

Bondi, Steven, Elizabeth Carroll, and Jaydeep Bhatt. "Taking a Strohl Through History: Putting Strohl Back in Guillain-Barré-Strohl Syndrome." Journal of Neuromuscular Diseases 7, no. 4 (2020): 521–22. http://dx.doi.org/10.3233/jnd-200545.

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Guillain-Barré Syndrome is a popular eponym that comes from a 1916 paper by Drs. Guillain, Barré, and Strohl. These physicians described two soldiers in the French Sixth Army during World War I who developed acute progressive motor weakness. Although Drs. Guillain and Barré have continued to be included in the syndrome’s eponym, Dr. Strohl has been forgotten despite having strongly contributed to the original paper. The reasons previously mentioned for Dr. Strohl’s absence appear trivial in contemporary practice and thus, his name deserves to be reintroduced to Guillain-Barré-Strohl Syndrome.

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5

Shahrizaila, Nortina, and Nobuhiro Yuki. "Guillain-Barré Syndrome Animal Model: The First Proof of Molecular Mimicry in Human Autoimmune Disorder." Journal of Biomedicine and Biotechnology 2011 (2011): 1–5. http://dx.doi.org/10.1155/2011/829129.

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Molecular mimicry between self and microbial components has been proposed as the pathogenic mechanism of autoimmune diseases, and this hypothesis is proven in Guillain-Barré syndrome. Guillain-Barré syndrome, the most frequent cause of acute neuromuscular paralysis, sometimes occurs afterCampylobacter jejunienteritis. Gangliosides are predominantly cell-surface glycolipids highly expressed in nervous tissue, whilst lipo-oligosaccharides are major components of the Gram-negative bacteriumC. jejuniouter membrane. IgG autoantibodies to GM1 ganglioside were found in the sera from patients with Gui

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6

Morshed, Md Mahabub, AKM Ferdous Rahman, Syed Tariq Reza, Muhammad Asaduzzaman, Mohammad Selim, and Mohammad Asrafuzzaman. "A case of a recurrent GBS." Bangladesh Critical Care Journal 5, no. 2 (2017): 135–38. http://dx.doi.org/10.3329/bccj.v5i2.34397.

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Background: Guillain-Barré syndrome is an acquired polyradiculo-neuropathy, often preceded by an antecedent event. It is a monophasic disease but a recurrence rate of 16 % is documented in a subset group of patients.Case presentation: Thirty-five-years-old female with past history of near complete recovery following Guillain-Barré syndrome 17 years back presented with acute, ascending symmetrical flaccid quadriparasis extending to bulbar muscles and respiratory compromise needing mechanical ventilation. Nerve conduction study revealed AMAN variant of Guillain-Barré syndrome. Cerebrospinal flu

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7

Surbakti, Stefanie Meitha Putri Sejahtera, and Aida Fitri. "Mortality of Guillain Barre Syndrome and Myasthenic Crisis in Haji Adam Malik Central General Hospital Medan January 2021- December 2022." Asian Australasian Neuro and Health Science Journal (AANHS-J) 6, no. 2 (2024): 35–41. http://dx.doi.org/10.32734/aanhsj.v6i2.17730.

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Introduction: Neuromuscular disorders are disorders of the neuro system that impact the muscular system. Among them are Guillain-Barré Syndrome and Myasthenic Crisis. Guillain-Barré syndrome is an autoimmune disorder of the nervous system that is polyradiculoneuropathic, characterized by weakness that radiates from the legs to the arms, torso, and face. Myasthenic crisis is a state of acute respiratory failure due to the exacerbation of Myasthenia Gravis. These two diseases are the most common types of neurodiseases found in hospital ICU patients. Objective: Determining the mortality rate of G

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8

Shahrizaila, Nortina, Helmar C. Lehmann, and Satoshi Kuwabara. "Guillain-Barré syndrome." Lancet 397, no. 10280 (2021): 1214–28. http://dx.doi.org/10.1016/s0140-6736(21)00517-1.

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9

Mirian, Ario, Michael W. Nicolle, and Adrian Budhram. "Guillain–Barré syndrome." Canadian Medical Association Journal 193, no. 11 (2021): E378. http://dx.doi.org/10.1503/cmaj.202710.

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10

Chung, Aimee, and Melissa Deimling. "Guillain-Barré Syndrome." Pediatrics in Review 39, no. 1 (2018): 53–54. http://dx.doi.org/10.1542/pir.2017-0189.

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11

Kankam, Cygethia Gayle, and Robert Sallis. "Guillain-Barré syndrome." Postgraduate Medicine 101, no. 3 (1997): 279–90. http://dx.doi.org/10.3810/pgm.1997.03.189.

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12

Payus, Alvin O., Tan HUI Jan, and Azman A. Raymond. "Guillain–Barré syndrome." Clinical Medicine 20, no. 6 (2020): e281.1-e281. http://dx.doi.org/10.7861/clinmed.let.20.6.6.

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13

Pritchard, Jane. "Guillain-Barré syndrome." Clinical Medicine 10, no. 4 (2010): 399–401. http://dx.doi.org/10.7861/clinmedicine.10-4-399.

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14

Crawford, Doreen, and Annette Dearmun. "Guillain-Barré syndrome." Nursing Children and Young People 29, no. 2 (2017): 17. http://dx.doi.org/10.7748/ncyp.29.2.17.s20.

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15

Zia, Muhammad Ahmed, Yasser Masood, and Muhammad Kashif Salman. "GUILLAIN-BARRÉ SYNDROME;." Professional Medical Journal 25, no. 04 (2018): 538–44. http://dx.doi.org/10.29309/tpmj/18.4320.

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16

Rosen, Beth A. "Guillain-Barré Syndrome." Pediatrics In Review 33, no. 4 (2012): 164–71. http://dx.doi.org/10.1542/pir.33.4.164.

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17

Zia, Muhammad Ahmed, Yasser Masood, and Muhammad Kashif Salman. "GUILLAIN-BARRÉ SYNDROME." Professional Medical Journal 25, no. 04 (2018): 538–44. http://dx.doi.org/10.29309/tpmj/2018.25.04.342.

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Objectives: To determine the outcome of autonomic disturbances in childrenwith Guillain Barre Syndrome. Study Design: Case series study. Setting: Pediatric ICU andNeurology ward of Nishtar Medical University/hospital Multan. Period: 9th June 2014 to 8th June2015. Methods: 48 children having age less than 18 years. Clinical examination of centralnervous system was conducted by single examiner to see presence of acute flaccid paralysisand to detect autonomic dysfunction. Cerebrospinal fluid analysis for albumino-cytologicdissociation, electromyography and nerve conduction studies was done in eve

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18

Sutherland, John M. "Guillain–Barré syndrome." Medical Journal of Australia 146, no. 3 (1987): 122–23. http://dx.doi.org/10.5694/j.1326-5377.1987.tb120149.x.

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19

Davidson, G. P., and K. Abbott. "Guillain‐Barré syndrome." Medical Journal of Australia 146, no. 7 (1987): 401. http://dx.doi.org/10.5694/j.1326-5377.1987.tb120326.x.

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20

Sutherland, John M. "Guillain‐Barré syndrome." Medical Journal of Australia 147, no. 2 (1987): 106. http://dx.doi.org/10.5694/j.1326-5377.1987.tb133293.x.

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21

Wakerley, Benjamin R., and Nobuhiro Yuki. "Guillain–Barré syndrome." Expert Review of Neurotherapeutics 15, no. 8 (2015): 847–49. http://dx.doi.org/10.1586/14737175.2015.1065732.

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22

Yuki, Nobuhiro, and Hans-Peter Hartung. "Guillain–Barré Syndrome." New England Journal of Medicine 366, no. 24 (2012): 2294–304. http://dx.doi.org/10.1056/nejmra1114525.

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23

Ginn, David R. "Guillain-Barré syndrome." Postgraduate Medicine 90, no. 5 (1991): 145–56. http://dx.doi.org/10.1080/00325481.1991.11701079.

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24

Sheikh, Kazim A. "Guillain-Barré Syndrome." CONTINUUM: Lifelong Learning in Neurology 26, no. 5 (2020): 1184–204. http://dx.doi.org/10.1212/con.0000000000000929.

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25

England, John D. "Guillain-Barré Syndrome." Annual Review of Medicine 41, no. 1 (1990): 1–6. http://dx.doi.org/10.1146/annurev.me.41.020190.000245.

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26

Ho, Tony, and John Griffin. "Guillain - Barré syndrome." Current Opinion in Neurology 12, no. 4 (1999): 389–94. http://dx.doi.org/10.1097/00019052-199908000-00004.

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27

Donofrio, Peter D. "Guillain-Barré Syndrome." CONTINUUM: Lifelong Learning in Neurology 23, no. 5 (2017): 1295–309. http://dx.doi.org/10.1212/con.0000000000000513.

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28

Pascuzzi, Robert. "Guillain-Barré Syndrome." Critical Care Medicine 20, no. 5 (1992): 718. http://dx.doi.org/10.1097/00003246-199205000-00035.

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29

Piquero Fernández, Carlos, Carolina Saenz Lafourcada, and Ana Pinel González. "Recurrent Guillain Barré." Medicina Clínica (English Edition) 163, no. 10 (2024): 530–31. http://dx.doi.org/10.1016/j.medcle.2024.06.008.

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30

Putri, Gyang Hanandita Gusti, Nectarine Natasya Regitta Yasmin, and Shahdevi Nandar Kurniawan. "GUILLAIN-BARRÉ SYNDROME." JPHV (Journal of Pain, Vertigo and Headache) 4, no. 2 (2023): 46–50. http://dx.doi.org/10.21776/ub.jphv.2023.004.02.4.

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Guillain-Barré Syndrome (GBS) is an infection-preceded autoimmune disease attacking myelin sheath of neurons through molecular mimicry, causing neuron demyelination and conduction disruption. GBS is classified into four subtypes: Acute Inflammatory Demyelinating (AIDP), Acute Motor Axonal Neuropathy (AMAN), Acute Motor Sensory Axonal Neuropathy (AMSAN), and Miller Fisher Syndrome. It affects spinal radix which resulted in polyneuropathy, showing mainly symptoms of ascending paresis of the extremity and areflexia. Cerebrospinal fluid evaluation is essential to distinguish GBS from its vast diff

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31

Kumar, Sanjeev, Priyanka Rani, Janardan Sharma, and Anand Kumar Rai. "Guillain–Barré Syndrome." International Journal of Nutrition, Pharmacology, Neurological Diseases 12, no. 3 (2022): 163–69. http://dx.doi.org/10.4103/ijnpnd.ijnpnd_17_22.

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Background: Guillain–Barré syndrome (GBS) is an immune-mediated acute polyradiculoneuropathy with different subtypes, clinical features, and demographics. Nerve conduction study is important in differentiating axonal and demyelinating form of GBS. Diagnosis of various subtypes is essential as they have different pathophysiology and prognosis. Objective: The study was aimed to evaluate the different subtype spectrum of GBS in our patient population cohort and to look for the clinical features, demographics, and electrophysiological profile variations among the patients with GBS. Materials and M

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32

Lewis, Richard, and Ximena Arcila-Londono. "Guillain-Barré Syndrome." Seminars in Neurology 32, no. 03 (2012): 179–86. http://dx.doi.org/10.1055/s-0032-1329196.

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33

Kountouras, Jannis, Georgia Deretzi, Nikolaos Grigoriadis, et al. "Guillain-Barré syndrome." Lancet Neurology 7, no. 12 (2008): 1080–81. http://dx.doi.org/10.1016/s1474-4422(08)70247-3.

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34

Li, Hai-Feng, and Yan-Chen Xie. "Guillain-Barré syndrome." Lancet Neurology 7, no. 12 (2008): 1081–82. http://dx.doi.org/10.1016/s1474-4422(08)70248-5.

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35

Lo, YL. "Guillain-Barré syndrome." Lancet Neurology 7, no. 12 (2008): 1082–83. http://dx.doi.org/10.1016/s1474-4422(08)70249-7.

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36

Kashyap, Ajit Singh, Kuldip Parkash Anand, and Surekha Kashyap. "Guillain-Barré syndrome." Lancet 367, no. 9509 (2006): 472. http://dx.doi.org/10.1016/s0140-6736(06)68173-7.

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37

Saxena, Akshay Kumar. "Guillain-Barré syndrome." Lancet 367, no. 9509 (2006): 472. http://dx.doi.org/10.1016/s0140-6736(06)68174-9.

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38

Chaudhuri, Abhijit. "Guillain-Barré syndrome." Lancet 367, no. 9509 (2006): 472–73. http://dx.doi.org/10.1016/s0140-6736(06)68175-0.

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39

Simmons, Susan. "Guillain-Barré syndrome." Nursing Critical Care 5, no. 2 (2010): 40–45. http://dx.doi.org/10.1097/01.ccn.0000369218.38874.ee.

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40

Miller, Robert G. "Guillain-Barré syndrome." Postgraduate Medicine 77, no. 7 (1985): 57–64. http://dx.doi.org/10.1080/00325481.1985.11699008.

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41

Ansar, Vibhuti, and Nojan Valadi. "Guillain-Barré Syndrome." Primary Care: Clinics in Office Practice 42, no. 2 (2015): 189–93. http://dx.doi.org/10.1016/j.pop.2015.01.001.

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42

Hahn, Angelika F. "Guillain-Barré syndrome." Lancet 352, no. 9128 (1998): 635–41. http://dx.doi.org/10.1016/s0140-6736(97)12308-x.

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43

Bosch, E. Peter. "GUILLAIN-BARRÉ SYNDROME." Neurologist 4, no. 4 (1998): 211–26. http://dx.doi.org/10.1097/00127893-199807000-00005.

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44

Willison, Hugh J., Bart C. Jacobs, and Pieter A. van Doorn. "Guillain-Barré syndrome." Lancet 388, no. 10045 (2016): 717–27. http://dx.doi.org/10.1016/s0140-6736(16)00339-1.

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45

Fulgham, J. R., and Eelco F. M. Wijdicks. "GUILLAIN-BARRÉ SYNDROME." Critical Care Clinics 13, no. 1 (1997): 1–15. http://dx.doi.org/10.1016/s0749-0704(05)70293-1.

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46

Hughes, Richard AC, and David R. Cornblath. "Guillain-Barré syndrome." Lancet 366, no. 9497 (2005): 1653–66. http://dx.doi.org/10.1016/s0140-6736(05)67665-9.

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47

Pritchard, Jane, and Richard AC Hughes. "Guillain-Barré syndrome." Lancet 363, no. 9427 (2004): 2186–88. http://dx.doi.org/10.1016/s0140-6736(04)16512-4.

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48

Wijdicks, Eelco F. M., and Christopher J. Klein. "Guillain-Barré Syndrome." Mayo Clinic Proceedings 92, no. 3 (2017): 467–79. http://dx.doi.org/10.1016/j.mayocp.2016.12.002.

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49

Pasanen, Mark E. "Guillain-Barré Syndrome." Hospital Medicine Clinics 4, no. 2 (2015): 177–90. http://dx.doi.org/10.1016/j.ehmc.2014.12.005.

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50

Doorn, Pieter A., and Frans G. A. Meché. "Guillain-Barré Syndrome." Clinical Immunotherapeutics 2, no. 2 (1994): 89–99. http://dx.doi.org/10.1007/bf03259259.

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