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

Year Number of Results
1962 1
1964 3
1965 3
1967 1
1968 2
1969 5
1970 1
1971 5
1972 1
1973 2
1974 7
1975 5
1977 5
1978 3
1979 4
1980 3
1981 2
1982 2
1983 4
1984 4
1985 6
1986 3
1987 2
1988 5
1989 3
1990 2
1991 6
1992 4
1993 3
1994 10
1995 5
1996 6
1997 3
1998 5
1999 9
2000 11
2001 7
2002 9
2003 5
2004 12
2005 11
2006 10
2007 9
2008 8
2009 4
2010 7
2011 10
2012 14
2013 11
2014 16
2015 13
2016 14
2017 12
2018 13
2019 12
2020 9
2021 18
2022 14
2023 12
2024 4

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364 results

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Page 1
Atypical Motor Neuron Disease variants: Still a diagnostic challenge in Neurology.
Pinto WBVR, Debona R, Nunes PP, Assis ACD, Lopes CG, Bortholin T, Dias RB, Naylor FGM, Chieia MAT, Souza PVS, Oliveira ASB. Pinto WBVR, et al. Rev Neurol (Paris). 2019 Apr;175(4):221-232. doi: 10.1016/j.neurol.2018.04.016. Epub 2019 Mar 4. Rev Neurol (Paris). 2019. PMID: 30846210 Review.
Motor neuron disease (MND) represents a wide and heterogeneous expanding group of disorders involving the upper or lower motor neurons, mainly represented by amyotrophic lateral sclerosis (ALS), primary lateral sclerosis, progressive muscular atrophy and progressive bulbar
Motor neuron disease (MND) represents a wide and heterogeneous expanding group of disorders involving the upper or lower motor neurons, main …
Differential diagnostic patterns of dysarthria.
Darley FL, Aronson AE, Brown JR. Darley FL, et al. J Speech Hear Res. 1969 Jun;12(2):246-69. doi: 10.1044/jshr.1202.246. J Speech Hear Res. 1969. PMID: 5808852 No abstract available.
Modified Erasmus GBS Respiratory Insufficiency Score: a simplified clinical tool to predict the risk of mechanical ventilation in Guillain-Barré syndrome.
Luijten LWG, Doets AY, Arends S, Dimachkie MM, Gorson KC, Islam B, Kolb NA, Kusunoki S, Papri N, Waheed W, Walgaard C, Yamagishi Y, Lingsma H, Jacobs BC; IGOS Consortium. Luijten LWG, et al. J Neurol Neurosurg Psychiatry. 2023 Apr;94(4):300-308. doi: 10.1136/jnnp-2022-329937. Epub 2022 Nov 25. J Neurol Neurosurg Psychiatry. 2023. PMID: 36428088
Independent predictors of MV were a shorter time from onset of weakness until admission, the presence of bulbar palsy and weakness of neck flexion and hip flexion. The modified EGRIS (mEGRIS) was based on these factors and accurately predicts the risk of MV with an …
Independent predictors of MV were a shorter time from onset of weakness until admission, the presence of bulbar palsy and weak …
Riboflavin in Neurological Diseases: A Narrative Review.
Plantone D, Pardini M, Rinaldi G. Plantone D, et al. Clin Drug Investig. 2021 Jun;41(6):513-527. doi: 10.1007/s40261-021-01038-1. Epub 2021 Apr 22. Clin Drug Investig. 2021. PMID: 33886098 Review.
Infant botulism: an underestimated threat.
Antonucci L, Locci C, Schettini L, Clemente MG, Antonucci R. Antonucci L, et al. Infect Dis (Lond). 2021 Sep;53(9):647-660. doi: 10.1080/23744235.2021.1919753. Epub 2021 May 8. Infect Dis (Lond). 2021. PMID: 33966588 Review.
The limited reporting of IB in many countries is probably due to diagnostic difficulties and nonspecific presentation. The onset is usually heralded by constipation, followed by bulbar palsy, and then by a descending bilateral symmetric paralysis; ultimately, palsy …
The limited reporting of IB in many countries is probably due to diagnostic difficulties and nonspecific presentation. The onset is usually …
Emergencies in motoneuron disease.
Finsterer J, Stöllberger C. Finsterer J, et al. Intern Emerg Med. 2017 Aug;12(5):641-650. doi: 10.1007/s11739-017-1644-6. Epub 2017 Mar 9. Intern Emerg Med. 2017. PMID: 28280980 Review.
Progressive supranuclear palsy.
Duvoisin RC, Golbe LI, Lepore FE. Duvoisin RC, et al. Can J Neurol Sci. 1987 Aug;14(3 Suppl):547-54. Can J Neurol Sci. 1987. PMID: 3315157 Review.
PSP has become familiar as a chronic progressive disorder with extrapyramidal rigidity, bradykinesia, gait impairment, bulbar palsy, dementia and a characteristic supranuclear ophthalmoplegia. ...
PSP has become familiar as a chronic progressive disorder with extrapyramidal rigidity, bradykinesia, gait impairment, bulbar pals
Benefit of high-dose oral riboflavin therapy in riboflavin transporter deficiency.
Fennessy JR, Cornett KMD, Burns J, Menezes MP. Fennessy JR, et al. J Peripher Nerv Syst. 2023 Sep;28(3):308-316. doi: 10.1111/jns.12587. Epub 2023 Aug 24. J Peripher Nerv Syst. 2023. PMID: 37537696 Review.
The domains that had the highest rates of response to riboflavin supplementation were gross motor function (93.3% improved), bulbar palsy (91.3%) and ataxia (90.0%). Improvements were also seen in limb muscle weakness, audiology, facial nerve palsy and respiratory f …
The domains that had the highest rates of response to riboflavin supplementation were gross motor function (93.3% improved), bulbar
Acute Bulbar Palsy and Ophtalmoplegia Associated With Anti-GT1a IgG Antibodies.
Brun G, Graber M, Mohr S, Béjot Y. Brun G, et al. Neurologist. 2022 Nov 1;27(6):348-349. doi: 10.1097/NRL.0000000000000407. Neurologist. 2022. PMID: 34967823
INTRODUCTION: Although several variants of Guillain-Barre syndrome (GBS) have been described, they are uncommon, and the atypical clinical presentation of patients makes the diagnosis challenging. This article reports a case of acute bulbar palsy plus (ABPp) syndrom …
INTRODUCTION: Although several variants of Guillain-Barre syndrome (GBS) have been described, they are uncommon, and the atypical clinical p …
Diagnostic challenges in ALS.
Belsh JM. Belsh JM. Neurology. 1999;53(8 Suppl 5):S26-30; discussion S35-6. Neurology. 1999. PMID: 10560634 Review.
The differential diagnosis must exclude nonmotor neuron diseases and other adult-onset motor neuron diseases with restricted presentations, e.g., progressive bulbar palsy (pure bulbar), progressive muscular atrophy (pure lower motor neuron) and primary lateral scler …
The differential diagnosis must exclude nonmotor neuron diseases and other adult-onset motor neuron diseases with restricted presentations, …
364 results