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

Year Number of Results
1971 1
1973 1
1974 2
1979 2
1980 1
1981 1
1982 1
1983 1
1984 1
1985 3
1986 3
1987 2
1989 2
1990 1
1991 1
1994 3
1995 1
1996 2
1997 2
1998 3
1999 2
2000 2
2003 2
2004 3
2005 4
2006 3
2007 3
2008 3
2009 3
2010 2
2011 4
2012 4
2013 1
2014 2
2015 4
2016 2
2017 3
2018 1
2019 5
2020 4
2021 6
2022 3
2023 2
2024 1

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91 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 bul …
Motor neuron disease (MND) represents a wide and heterogeneous expanding group of disorders involving the upper or lower motor neurons, main …
Recent advances in riboflavin transporter RFVT and its genetic disease.
Jin C, Yonezawa A. Jin C, et al. Pharmacol Ther. 2022 May;233:108023. doi: 10.1016/j.pharmthera.2021.108023. Epub 2021 Oct 15. Pharmacol Ther. 2022. PMID: 34662687 Review.
These patients commonly present with bulbar palsy, hearing loss, muscle weakness, and respiratory symptoms in infancy or later in childhood. A decrease in plasma riboflavin levels has been observed in several cases. Recent studies on knockout mice and patient-derived cells …
These patients commonly present with bulbar palsy, hearing loss, muscle weakness, and respiratory symptoms in infancy or later in childhood. …
Clinical Features of Isolated Bulbar Palsy of Amyotrophic Lateral Sclerosis in Chinese Population.
Zhang HG, Chen L, Tang L, Zhang N, Fan DS. Zhang HG, et al. Chin Med J (Engl). 2017 Aug 5;130(15):1768-1772. doi: 10.4103/0366-6999.211538. Chin Med J (Engl). 2017. PMID: 28748847 Free PMC article.
BACKGROUND: Progressive bulbar palsy (PBP) is a classic phenotype of bulbar onset amyotrophic lateral sclerosis (ALS) with more rapid progression and worse prognosis. ...Significant differences were noted in sex ratio, onset age, ALSFRS-R score, upper …
BACKGROUND: Progressive bulbar palsy (PBP) is a classic phenotype of bulbar onset amyotrophic lateral sclerosis (ALS) w …
Facial onset sensory and motor neuronopathy (FOSMN syndrome): Cases series and systematic review.
Hu N, Zhang L, Yang X, Fu H, Cui L, Liu M. Hu N, et al. Neurol Sci. 2023 Jun;44(6):1969-1978. doi: 10.1007/s10072-023-06703-1. Epub 2023 Mar 3. Neurol Sci. 2023. PMID: 36864244 Review.
RESULTS: We identified a total of 71 cases, including 4 cases from our database and 67 ones from online searching. A predominance of male was observed [44 (62.0%)] with median onset age of 53 (range: 7-75) years old. ...
RESULTS: We identified a total of 71 cases, including 4 cases from our database and 67 ones from online searching. A predominance of male wa …
Rehabilitation for postpolio sequelae.
Khan F. Khan F. Aust Fam Physician. 2004 Aug;33(8):621-4. Aust Fam Physician. 2004. PMID: 15373379 Review.
Diagnosis can be complicated particularly in nonparalytic cases of poliomyelitis. Disabilities in PPS may not be obvious to the observer but significantly affect the quality of life of the PPS patient. ...
Diagnosis can be complicated particularly in nonparalytic cases of poliomyelitis. Disabilities in PPS may not be obvious to the observer …
Clinical Profile and Predictors of Mechanical Ventilation in Guillain-Barre Syndrome in North Indian Children.
Tiwari I, Alam A, Kanta C, Koonwar S, Garg RK, Pandey S, Jain A, Kumar R. Tiwari I, et al. J Child Neurol. 2021 May;36(6):453-460. doi: 10.1177/0883073820978020. Epub 2020 Dec 17. J Child Neurol. 2021. PMID: 33331796
Logistic regression revealed older age, history of predisposing illness, lower MRC sum at presentation, and bulbar palsy as independent predictors of mechanical ventilation. CONCLUSIONS: The most common electrophysiological subtype in northern Indian children is acute moto …
Logistic regression revealed older age, history of predisposing illness, lower MRC sum at presentation, and bulbar palsy as independent p …
Outcomes of Neonatal Bulbar Weakness.
Baudon JJ, Renault F, Flores-Guevara R, Vazquez MP. Baudon JJ, et al. Pediatrics. 2016 Jan;137(1). doi: 10.1542/peds.2015-3004. Epub 2015 Dec 11. Pediatrics. 2016. PMID: 26659817
RESULTS: Of 175 patients, 73% had developmental disorders, 25% suffered from acquired brain damage, and 2% had no apparent underlying disorders. Motor or mental impairment was observed in 71%; death occurred in 16%. Outcomes were not significantly different when comparing …
RESULTS: Of 175 patients, 73% had developmental disorders, 25% suffered from acquired brain damage, and 2% had no apparent underlying disord …
Clinical predictors and electrodiagnostic characteristics in patients with Guillain-Barre syndrome with respiratory failure: a retrospective, matched case-control study.
Charoentanyarak K, Singjam A, Saengsuwan J. Charoentanyarak K, et al. PeerJ. 2022 Feb 10;10:e12930. doi: 10.7717/peerj.12930. eCollection 2022. PeerJ. 2022. PMID: 35186497 Free PMC article.
The data showed that patients with respiratory failure had higher GBS disability scores, lower motor power (3) of the hip flexors and ankle dorsiflexors, and experienced facial and bulbar palsy. In the multivariate analysis, the significant predictive factors were b …
The data showed that patients with respiratory failure had higher GBS disability scores, lower motor power (3) of the hip flexors and …
Prevalence of multimorbidity and its impact on survival in people with motor neuron disease.
Glasmacher SA, Kearns PKA, Larraz J, Stirland L, Mehta AR, Newton J, Weir CJ, Chandran S, Pal S; CARE-MND Consortium. Glasmacher SA, et al. Eur J Neurol. 2021 Aug;28(8):2756-2765. doi: 10.1111/ene.14940. Epub 2021 Jun 15. Eur J Neurol. 2021. PMID: 34036680
People with amyotrophic lateral sclerosis, primary lateral sclerosis, progressive muscular atrophy, or progressive bulbar palsy were included. We fitted latent class regression models incorporating comorbidities (class indicators), age, sex, and bulbar onset …
People with amyotrophic lateral sclerosis, primary lateral sclerosis, progressive muscular atrophy, or progressive bulbar p …
The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives.
Bosch AM, Stroek K, Abeling NG, Waterham HR, Ijlst L, Wanders RJ. Bosch AM, et al. Orphanet J Rare Dis. 2012 Oct 29;7:83. doi: 10.1186/1750-1172-7-83. Orphanet J Rare Dis. 2012. PMID: 23107375 Free PMC article. Review.
Abnormalities in plasma flavin levels and/or plasma acylcarnitine profiles were observed in some but not in all patients, and also patients with normal plasma flavin levels and acylcarnitine profiles demonstrated a striking clinical improvement on riboflavin supplementatio …
Abnormalities in plasma flavin levels and/or plasma acylcarnitine profiles were observed in some but not in all patients, and also pa …
91 results