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

Year Number of Results
1975 1
1977 1
1985 1
1987 1
1990 2
1991 1
1992 1
1993 2
1994 4
1995 1
1996 1
1997 1
1998 2
1999 3
2000 2
2001 1
2002 1
2003 4
2004 3
2005 4
2007 1
2008 1
2009 1
2010 4
2011 4
2012 2
2013 4
2014 3
2015 5
2016 2
2017 4
2018 2
2019 3
2020 1
2021 4
2023 2
2024 0

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72 results

Results by year

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Page 1
Wound botulism.
Cherington M, Ginsburg S. Cherington M, et al. Arch Surg. 1975 Apr;110(4):436-8. doi: 10.1001/archsurg.1975.01360100078014. Arch Surg. 1975. PMID: 1147760
Results of bacteriologic and immunologic tests were not revealing, but the subsequent course of progressing, and retrogressing, bulbar signs and symptoms with eventual nearcomplete recovery confirmed the diagnosis. ...
Results of bacteriologic and immunologic tests were not revealing, but the subsequent course of progressing, and retrogressing, bulbar …
Acute muscular weakness in children.
Torricelli RPJE. Torricelli RPJE. Arq Neuropsiquiatr. 2017 Apr;75(4):248-254. doi: 10.1590/0004-282X20170026. Arq Neuropsiquiatr. 2017. PMID: 28489146 Free article. Review.
Early detection of hyperCKemia may lead to a myositis diagnosis, and hypokalemia points to the diagnosis of periodic paralysis. Ophthalmoparesis, ptosis and bulbar signs are suggestive of myasthenia gravis or botulism. Distal weakness and hyporeflexia are clinical f …
Early detection of hyperCKemia may lead to a myositis diagnosis, and hypokalemia points to the diagnosis of periodic paralysis. Ophthalmopar …
Alexander disease.
Gordon N. Gordon N. Eur J Paediatr Neurol. 2003;7(6):395-9. doi: 10.1016/j.ejpn.2003.09.004. Eur J Paediatr Neurol. 2003. PMID: 14623218
The infantile type shows enlargement of the head, retarded development and evidence of a severe neurological disorder. The juvenile sufferers are more likely to exhibit bulbar signs, and may not be significantly retarded. Among adults the condition can fluctuate, an …
The infantile type shows enlargement of the head, retarded development and evidence of a severe neurological disorder. The juvenile sufferer …
Recurrent childhood myoglobinuria.
Tein I, DiMauro S, DeVivo DC. Tein I, et al. Adv Pediatr. 1990;37:77-117. Adv Pediatr. 1990. PMID: 2264536 Review.
The toxic group is also differentiated by a higher mortality rate and by the presence of additional clinical features, including ictal bulbar signs (8 of 18), encephalopathy (4 of 19), and seizures (2 of 7), as well as persistent cardiac abnormalities, developmental …
The toxic group is also differentiated by a higher mortality rate and by the presence of additional clinical features, including ictal bu …
Amyotrophic Lateral Sclerosis-Bulbar Dysfunction Index-Remote: Test-Retest and Interrater Reliability of Candidate Items.
Bouvier L, Green JR, Tapia CB, Tilton-Bolowsky V, Maffei MF, Fless Z, Seaver K, Huynh A, Gutz SE, Martino R, Abrahao A, Berry J, Zinman L, Yunusova Y. Bouvier L, et al. Am J Speech Lang Pathol. 2023 Aug 17;32(4S):1884-1900. doi: 10.1044/2023_AJSLP-22-00177. Epub 2023 Jul 26. Am J Speech Lang Pathol. 2023. PMID: 37494887 Free PMC article.
PURPOSE: The primary aim of this study was to establish the reliability of candidate items as a step in the development of the Amyotrophic Lateral Sclerosis-Bulbar Dysfunction Index-Remote (ALS-BDI-Remote), a novel tool being developed for the detection and monitoring of bulba …
PURPOSE: The primary aim of this study was to establish the reliability of candidate items as a step in the development of the Amyotrophic L …
Alexander's disease: clinical, pathologic, and genetic features.
Johnson AB, Brenner M. Johnson AB, et al. J Child Neurol. 2003 Sep;18(9):625-32. doi: 10.1177/08830738030180090901. J Child Neurol. 2003. PMID: 14572141 Review.
Juvenile cases often do not have megalencephaly and tend to have predominant pseudobulbar and bulbar signs. In both groups, characteristic magnetic resonance imaging findings have been described. ...
Juvenile cases often do not have megalencephaly and tend to have predominant pseudobulbar and bulbar signs. In both groups, ch …
Acoustic reflex patterns in amyotrophic lateral sclerosis.
Canale A, Albera R, Lacilla M, Canosa A, Albera A, Sacco F, Chiò A, Calvo A. Canale A, et al. Eur Arch Otorhinolaryngol. 2017 Feb;274(2):679-683. doi: 10.1007/s00405-016-4284-y. Epub 2016 Aug 30. Eur Arch Otorhinolaryngol. 2017. PMID: 27577043 Free article.
Patients were further divided in two groups: amyotrophic lateral sclerosis-bulbar (38 cases, with bulbar signs at evaluation) and amyotrophic lateral sclerosis-spinal (13 cases, without bulbar signs at evaluation). ...These results confirm the presence …
Patients were further divided in two groups: amyotrophic lateral sclerosis-bulbar (38 cases, with bulbar signs at evaluation) …
Polyneuritis cranialis: oculopharyngeal subtype of Guillain-Barré syndrome.
Wakerley BR, Yuki N. Wakerley BR, et al. J Neurol. 2015 Sep;262(9):2001-12. doi: 10.1007/s00415-015-7678-7. Epub 2015 Feb 26. J Neurol. 2015. PMID: 25712542 Review.
Mean number of cranial nerves involved was 6 (range, 3-10). 93% displayed ocular signs, 73% facial weakness or numbness and 87% bulbar signs. In 3 patients (20%), there was significant asymmetry. ...
Mean number of cranial nerves involved was 6 (range, 3-10). 93% displayed ocular signs, 73% facial weakness or numbness and 87% bulbar …
ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS.
Crockford C, Newton J, Lonergan K, Chiwera T, Booth T, Chandran S, Colville S, Heverin M, Mays I, Pal S, Pender N, Pinto-Grau M, Radakovic R, Shaw CE, Stephenson L, Swingler R, Vajda A, Al-Chalabi A, Hardiman O, Abrahams S. Crockford C, et al. Neurology. 2018 Oct 9;91(15):e1370-e1380. doi: 10.1212/WNL.0000000000006317. Epub 2018 Sep 12. Neurology. 2018. PMID: 30209236 Free PMC article.
The relationship between cognitive function and disease stage may be due to letter fluency impairment, whereas higher rates of all behavioral domains were seen in later King's stage. The presence of bulbar signs, but not site of onset, was significantly related to A …
The relationship between cognitive function and disease stage may be due to letter fluency impairment, whereas higher rates of all behaviora …
A preliminary study on self-care telemonitoring of dysarthria in spinal muscular atrophy.
Migliorelli L, Moccia S, Berardini D, Frontoni E, Coccia M, Villani L, Bandini A. Migliorelli L, et al. Annu Int Conf IEEE Eng Med Biol Soc. 2023 Jul;2023:1-4. doi: 10.1109/EMBC40787.2023.10340908. Annu Int Conf IEEE Eng Med Biol Soc. 2023. PMID: 38083694
Spinal muscular atrophy (SMA) is a rare neuromuscular disease which may cause impairments in oro-facial musculature. Most of the individuals with SMA present bulbar signs such as flaccid dysarthria which mines their abilities to speak and, as consequence, their psyc …
Spinal muscular atrophy (SMA) is a rare neuromuscular disease which may cause impairments in oro-facial musculature. Most of the individuals …
72 results