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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
2003 2
2004 1
2005 1
2009 1
2011 1
2012 1
2013 2
2014 1
2016 2
2018 1
2021 3
2022 1
2023 1
2024 0

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18 results

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Page 1
Congenital and infantile myotonic dystrophy.
Echenne B, Bassez G. Echenne B, et al. Handb Clin Neurol. 2013;113:1387-93. doi: 10.1016/B978-0-444-59565-2.00009-5. Handb Clin Neurol. 2013. PMID: 23622362 Review.
The congenital form appears as the most severe end of the phenotypic spectrum and may include marked neonatal hypotonia, respiratory failure, facial diplegia, contractures, and mental retardation. Brain involvement is the hallmark of childhood-onset DM1, distinguish …
The congenital form appears as the most severe end of the phenotypic spectrum and may include marked neonatal hypotonia, respiratory failure …
Association of Guillain-Barré syndrome following COVID-19 vaccination.
Chowdhury S, Chowdhury S. Chowdhury S, et al. Int J Immunopathol Pharmacol. 2023 Jan-Dec;37:3946320231199349. doi: 10.1177/03946320231199349. Int J Immunopathol Pharmacol. 2023. PMID: 37681361 Free PMC article. Review.
The average time between vaccination and symptom onset was 12.67 days. Prominent clinical features observed in the case reports included back pain, facial diplegia, weakness, and paresthesia. ...
The average time between vaccination and symptom onset was 12.67 days. Prominent clinical features observed in the case reports inclu …
Atypical presentations of inclusion body myositis: Clinical characteristics and long-term outcomes.
Alamr M, Pinto MV, Naddaf E. Alamr M, et al. Muscle Nerve. 2022 Dec;66(6):686-693. doi: 10.1002/mus.27716. Epub 2022 Sep 18. Muscle Nerve. 2022. PMID: 36052422
The most common presentation was dysphagia (50%), followed by asymptomatic hyperCKemia (24%; CK, creatine kinase), then foot drop (12%). 6% of patients presented with proximal arm weakness, 4% with axial weakness and 4% with facial diplegia. Median time from symptom …
The most common presentation was dysphagia (50%), followed by asymptomatic hyperCKemia (24%; CK, creatine kinase), then foot drop (12%). 6% …
Clinical features and outcome of Guillain-Barre syndrome in Saudi Arabia: a multicenter, retrospective study.
Alanazy MH, Bakry SS, Alqahtani A, AlAkeel NS, Alazwary N, Osman AM, Mustafa RA, Al-Harbi TM, Abdulmana SO, Amper AC, Aldughaythir Y, Ali AS, Makkawi S, Maglan A, Alamoudi L, Alsulaiman F, Alabdali M, AlShareef AA, Abuzinadah AR, Bamaga AK. Alanazy MH, et al. BMC Neurol. 2021 Jul 12;21(1):275. doi: 10.1186/s12883-021-02314-5. BMC Neurol. 2021. PMID: 34253174 Free PMC article.
All but two patients (98.7%) had weakness, 64.1% had sensory symptoms, 43.1% had facial diplegia, 33.8% had oropharyngeal weakness, 12.4% had ophthalmoplegia, and 26.3% needed mechanical ventilation. Cytoalbuminological dissociation was observed in 69.1% of t …
All but two patients (98.7%) had weakness, 64.1% had sensory symptoms, 43.1% had facial diplegia, 33.8% had oropharyngeal weak …
Guillain-Barré syndrome associated with SARS-CoV-2 infection: a scoping review.
Medeiros KS, Macêdo LTA, Souza WF, Sarmento AC, Costa APF, Gonçalves AK. Medeiros KS, et al. Rev Assoc Med Bras (1992). 2021 Feb;67(2):318-334. doi: 10.1590/1806-9282.67.2.20200716. Rev Assoc Med Bras (1992). 2021. PMID: 34406260 Free article.
SEARCH STRATEGY: The search was conducted through Medline, Web of Science, Embase, CINAHAL, Latin-American and Caribbean Literature in Health Sciences (LILACS), clinicaltrials.gov, SCOPUS, and the Cochrane Central Register of Controlled Trials. SELECTION CRITERIA: Observationa
SEARCH STRATEGY: The search was conducted through Medline, Web of Science, Embase, CINAHAL, Latin-American and Caribbean Literature in Healt …
Concomitant Guillain-Barre syndrome with COVID-19: a case report.
Mackenzie N, Lopez-Coronel E, Dau A, Maloof D, Mattar S, Garcia JT, Fontecha B, Lanata CM, Guillen-Burgos HF. Mackenzie N, et al. BMC Neurol. 2021 Mar 23;21(1):135. doi: 10.1186/s12883-021-02162-3. BMC Neurol. 2021. PMID: 33757457 Free PMC article.
BACKGROUND: During the Coronavirus disease 2019 (COVID-19) pandemic, different neurological manifestations have been observed. However, only a few cases of Guillain-Barre syndrome (GBS) and COVID-19 have been reported. ...Previous symptoms such as ageusia, anosmia and inte …
BACKGROUND: During the Coronavirus disease 2019 (COVID-19) pandemic, different neurological manifestations have been observed. Howeve …
Long-term outcome of Guillain-Barré syndrome in children.
Roodbol J, de Wit MC, Aarsen FK, Catsman-Berrevoets CE, Jacobs BC. Roodbol J, et al. J Peripher Nerv Syst. 2014 Jun;19(2):121-6. doi: 10.1111/jns5.12068. J Peripher Nerv Syst. 2014. PMID: 24863162
The objective of this study is to determine the long-term outcome and consequences of Guillain-Barre syndrome (GBS) in children. This is an observational cross-sectional cohort study of children diagnosed with GBS (0-18 years old) at the Sophia Children's Hospital in Rotte …
The objective of this study is to determine the long-term outcome and consequences of Guillain-Barre syndrome (GBS) in children. This is an …
Brainstem calcification in Möbius syndrome.
Dooley JM, Stewart WA, Hayden JD, Therrien A. Dooley JM, et al. Pediatr Neurol. 2004 Jan;30(1):39-41. doi: 10.1016/s0887-8994(03)00408-9. Pediatr Neurol. 2004. PMID: 14738949
Mobius syndrome is characterized by congenital facial diplegia, and may be associated with limb or orofacial malformations. ...The calcification was detected as early as 7 days of age and did not change with time, suggesting a static condition of prenatal onset. The …
Mobius syndrome is characterized by congenital facial diplegia, and may be associated with limb or orofacial malformations. .. …
Caries Experience in Individuals with Moebius Syndrome.
Castro T, Ortega AO, Mussi MC, Braga MM, Gallottini M. Castro T, et al. Pediatr Dent. 2016 Jan-Feb;38(1):68-71. Pediatr Dent. 2016. PMID: 26892218
PURPOSE: Moebius syndrome (MS) is a rare congenital facial diplegia characterized by partial or complete sixth and seventh cranial nerve palsy. ...All individuals were evaluated for the presence of caries using the ICDAS. For statistical analysis, different ICDAS …
PURPOSE: Moebius syndrome (MS) is a rare congenital facial diplegia characterized by partial or complete sixth and seventh cra …
Anti-MuSK myasthenia gravis with prolonged remission.
Bouwyn JP, Magnier P, Bédat-Millet AL, Ahtoy P, Maltête D, Lefaucheur R. Bouwyn JP, et al. Neuromuscul Disord. 2016 Jul;26(7):453-4. doi: 10.1016/j.nmd.2016.04.008. Epub 2016 Apr 8. Neuromuscul Disord. 2016. PMID: 27161384
We report the case of a 22-year-old man who presented with diplopia on lateral gaze to both sides, facial diplegia, nasal dysarthria and dysphagia. Repetitive nerve stimulation of the trapezius and orbicularis oculi muscles showed amplitude decrements of 19% and 41% …
We report the case of a 22-year-old man who presented with diplopia on lateral gaze to both sides, facial diplegia, nasal dysa …
18 results