These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
151 related articles for article (PubMed ID: 38970668)
1. Clinical spreading of muscle weakness in amyotrophic lateral sclerosis (ALS): a study in 910 patients. Ludolph AC; Dietrich J; Dreyhaupt J; Kassubek J; Del Tredici K; Rosenbohm A J Neurol; 2024 Aug; 271(8):5357-5367. PubMed ID: 38970668 [TBL] [Abstract][Full Text] [Related]
2. Different patterns of spreading direction and motor neurons involvement in a cohort of limb-onset amyotrophic lateral sclerosis patients from Southern Italy: Potential implication on disease course or progression? Milella G; Zoccolella S; Urso D; Nigro S; Tamburrino L; Gnoni V; Filardi M; Logroscino G Brain Behav; 2023 Jun; 13(6):e2899. PubMed ID: 37208847 [TBL] [Abstract][Full Text] [Related]
4. Cortical Thinning Pattern of Bulbar- and Spinal-onset Amyotrophic Lateral Sclerosis: a Surface-based Morphometry Study. Chen ZY; Liu MQ; Ma L Chin Med Sci J; 2018 Jun; 33(2):100-106. PubMed ID: 29976279 [TBL] [Abstract][Full Text] [Related]
5. Study of motor asymmetry in ALS indicates an effect of limb dominance on onset and spread of weakness, and an important role for upper motor neurons. Devine MS; Kiernan MC; Heggie S; McCombe PA; Henderson RD Amyotroph Lateral Scler Frontotemporal Degener; 2014 Dec; 15(7-8):481-7. PubMed ID: 24809721 [TBL] [Abstract][Full Text] [Related]
6. Spread Direction and Prognostic Factors in Limb-Onset Sporadic Amyotrophic Lateral Sclerosis. Hu F; Jin J; Jia R; Xiang L; Qi H; Chen X; Dang J Eur Neurol; 2016; 75(5-6):244-50. PubMed ID: 27165107 [TBL] [Abstract][Full Text] [Related]
7. Patterns of clinical and electrodiagnostic abnormalities in early amyotrophic lateral sclerosis. Simon NG; Lomen-Hoerth C; Kiernan MC Muscle Nerve; 2014 Dec; 50(6):894-9. PubMed ID: 24647900 [TBL] [Abstract][Full Text] [Related]
8. Time of symptoms beyond the bulbar region predicts survival in bulbar onset amyotrophic lateral sclerosis. He Z; Sun B; Feng F; Bai J; Wang H; Wang H; Yang F; Cui F; Huang X Neurol Sci; 2022 Mar; 43(3):1817-1822. PubMed ID: 34383162 [TBL] [Abstract][Full Text] [Related]
9. Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS. Gordon PH; Cheng B; Katz IB; Mitsumoto H; Rowland LP Neurology; 2009 Jun; 72(22):1948-52. PubMed ID: 19487653 [TBL] [Abstract][Full Text] [Related]
10. Onset and spreading patterns of lower motor neuron involvements predict survival in sporadic amyotrophic lateral sclerosis. Fujimura-Kiyono C; Kimura F; Ishida S; Nakajima H; Hosokawa T; Sugino M; Hanafusa T J Neurol Neurosurg Psychiatry; 2011 Nov; 82(11):1244-9. PubMed ID: 21921087 [TBL] [Abstract][Full Text] [Related]
11. [Clinical polymorphism of amyotrophic lateral sclerosis]. Kovrazhkina EA; Razinskaya OD; Gubsky LV Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(8):4-10. PubMed ID: 28884711 [TBL] [Abstract][Full Text] [Related]
12. Disease duration of progression is helpful in identifying isolated bulbar palsy of amyotrophic lateral sclerosis. Zhang H; Chen L; Tian J; Fan D BMC Neurol; 2021 Oct; 21(1):405. PubMed ID: 34686150 [TBL] [Abstract][Full Text] [Related]
14. Factors affecting longitudinal functional decline and survival in amyotrophic lateral sclerosis patients. Watanabe H; Atsuta N; Nakamura R; Hirakawa A; Watanabe H; Ito M; Senda J; Katsuno M; Izumi Y; Morita M; Tomiyama H; Taniguchi A; Aiba I; Abe K; Mizoguchi K; Oda M; Kano O; Okamoto K; Kuwabara S; Hasegawa K; Imai T; Aoki M; Tsuji S; Nakano I; Kaji R; Sobue G Amyotroph Lateral Scler Frontotemporal Degener; 2015 Jun; 16(3-4):230-6. PubMed ID: 25548957 [TBL] [Abstract][Full Text] [Related]
15. Relationship between Clinical Parameters and Brain Structure in Sporadic Amyotrophic Lateral Sclerosis Patients According to Onset Type: A Voxel-Based Morphometric Study. Kim HJ; de Leon M; Wang X; Kim HY; Lee YJ; Kim YH; Kim SH PLoS One; 2017; 12(1):e0168424. PubMed ID: 28095425 [TBL] [Abstract][Full Text] [Related]
16. Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study. Chiò A; Calvo A; Moglia C; Mazzini L; Mora G; J Neurol Neurosurg Psychiatry; 2011 Jul; 82(7):740-6. PubMed ID: 21402743 [TBL] [Abstract][Full Text] [Related]
17. What does the ALSFRS-R really measure? A longitudinal and survival analysis of functional dimension subscores in amyotrophic lateral sclerosis. Rooney J; Burke T; Vajda A; Heverin M; Hardiman O J Neurol Neurosurg Psychiatry; 2017 May; 88(5):381-385. PubMed ID: 27888187 [TBL] [Abstract][Full Text] [Related]
18. Dominant Heterogeneity of Upper and Lower Motor Neuron Degeneration to Motor Manifestation of Involved Region in Amyotrophic Lateral Sclerosis. Jin J; Hu F; Zhang Q; Chen Q; Li H; Qin X; Jia R; Kang L; Dang Y; Dang J Sci Rep; 2019 Dec; 9(1):20059. PubMed ID: 31882886 [TBL] [Abstract][Full Text] [Related]
19. [Analysis of disease progression rate and related factors in amyotrophic lateral sclerosis patients at initial visit]. Zhang JH; Wang HF; Yang F; He ZQ; Feng F; Li M; Bai JM; Wang HR; Huang XS Zhonghua Yi Xue Za Zhi; 2022 Jan; 102(3):222-227. PubMed ID: 35042292 [No Abstract] [Full Text] [Related]
20. Epidemiological and clinical features of amyotrophic lateral sclerosis in a Tunisian cohort. Kacem I; Sghaier I; Bougatef S; Nasri A; Gargouri A; Ajroud-Driss S; Gouider R Amyotroph Lateral Scler Frontotemporal Degener; 2020 Feb; 21(1-2):131-139. PubMed ID: 31858811 [No Abstract] [Full Text] [Related] [Next] [New Search]