Yanagihashi M, Hirayama T, Shibukawa M, Nagasawa J, Fujita K, Izumi Y
BMC Neurol. 2024; 24(1):282.
PMID: 39138414
PMC: 11320838.
DOI: 10.1186/s12883-024-03729-6.
Cai R, Yang J, Wu L, Liu Y, Wang X, Zheng Q
Orphanet J Rare Dis. 2024; 19(1):40.
PMID: 38308282
PMC: 10837960.
DOI: 10.1186/s13023-024-03057-5.
Mitsumoto H, Cheung K, Oskarsson B, Andrews H, Jang G, Andrews J
Trials. 2023; 24(1):449.
PMID: 37430314
PMC: 10332004.
DOI: 10.1186/s13063-023-07424-8.
De Marchi F, Saraceno M, Sarnelli M, Virgilio E, Cantello R, Mazzini L
Neurol Sci. 2023; 44(8):2795-2802.
PMID: 36949299
PMC: 10345066.
DOI: 10.1007/s10072-023-06751-7.
Donohue C, Carnaby G, Reilly M, Colquhoun R, Lacomis D, Garand K
eNeurologicalSci. 2023; 31:100452.
PMID: 36875937
PMC: 9982645.
DOI: 10.1016/j.ensci.2023.100452.
ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scale.
Maier A, Boentert M, Reilich P, Witzel S, Petri S, Grosskreutz J
Neurol Res Pract. 2022; 4(1):60.
PMID: 36522775
PMC: 9753252.
DOI: 10.1186/s42466-022-00224-6.
Analysis of routine blood parameters in patients with amyotrophic lateral sclerosis and evaluation of a possible correlation with disease progression-a multicenter study.
Hertel N, Kuzma-Kozakiewicz M, Gromicho M, Grosskreutz J, de Carvalho M, Uysal H
Front Neurol. 2022; 13:940375.
PMID: 35968316
PMC: 9364810.
DOI: 10.3389/fneur.2022.940375.
A Telehealth Intervention for Nutritional Counseling in Amyotrophic Lateral Sclerosis Patients.
De Marchi F, Serioli M, Collo A, Belotti E, Alloatti F, Biroli G
J Clin Med. 2022; 11(15).
PMID: 35893377
PMC: 9331838.
DOI: 10.3390/jcm11154286.
CNN-based severity prediction of neurodegenerative diseases using gait data.
Erdas C, Sumer E, Kibaroglu S
Digit Health. 2022; 8:20552076221075147.
PMID: 35111334
PMC: 8801640.
DOI: 10.1177/20552076221075147.
Discriminant ability of the 3-ounce water swallow test to detect aspiration in amyotrophic lateral sclerosis.
Donohue C, Gray L, Chapin J, Anderson A, DiBiase L, Wymer J
Neurogastroenterol Motil. 2021; 34(7):e14310.
PMID: 34936158
PMC: 10294259.
DOI: 10.1111/nmo.14310.
Measuring disease progression in primary lateral sclerosis.
Gilmore M, Elman L, Babu S, Andres P, Floeter M
Amyotroph Lateral Scler Frontotemporal Degener. 2021; 21(sup1):59-66.
PMID: 33602016
PMC: 7899091.
DOI: 10.1080/21678421.2020.1837179.
Detection of White Matter Ultrastructural Changes for Amyotrophic Lateral Sclerosis Characterization: A Diagnostic Study from Dti-Derived Data.
De Marchi F, Stecco A, Falaschi Z, Filippone F, Pasche A, Bebeti A
Brain Sci. 2020; 10(12).
PMID: 33339434
PMC: 7766961.
DOI: 10.3390/brainsci10120996.
Repeated Application of Autologous Bone Marrow-Derived Lineage-Negative Stem/Progenitor Cells-Focus on Immunological Pathways in Patients with ALS.
Baumert B, Sobus A, Golab-Janowska M, Paczkowska E, Luczkowska K, Roginska D
Cells. 2020; 9(8).
PMID: 32752182
PMC: 7463801.
DOI: 10.3390/cells9081822.
Umbilical Cord Mesenchymal Stem Cells in Amyotrophic Lateral Sclerosis: an Original Study.
Barczewska M, Maksymowicz S, Zdolinska-Malinowska I, Siwek T, Grudniak M
Stem Cell Rev Rep. 2020; 16(5):922-932.
PMID: 32725316
PMC: 7456414.
DOI: 10.1007/s12015-020-10016-7.
Clinical Measures of Bulbar Dysfunction in ALS.
Yunusova Y, Plowman E, Green J, Barnett C, Bede P
Front Neurol. 2019; 10:106.
PMID: 30837936
PMC: 6389633.
DOI: 10.3389/fneur.2019.00106.
Tollgate-based progression pathways of ALS patients.
Dalgic O, Erenay F, Pasupathy K, Ozaltin O, Crum B, Sir M
J Neurol. 2019; 266(3):755-765.
PMID: 30684209
DOI: 10.1007/s00415-019-09199-y.
Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis.
Eur J Hum Genet. 2018; 26(10):1537-1546.
PMID: 29955173
PMC: 6138692.
DOI: 10.1038/s41431-018-0177-4.
Increased Expressions of Plasma Galectin-3 in Patients with Amyotrophic Lateral Sclerosis.
Yan J, Xu Y, Zhang L, Zhao H, Jin L, Liu W
Chin Med J (Engl). 2016; 129(23):2797-2803.
PMID: 27900991
PMC: 5146785.
DOI: 10.4103/0366-6999.194656.
Association Between Dietary Intake and Function in Amyotrophic Lateral Sclerosis.
Nieves J, Gennings C, Factor-Litvak P, Hupf J, Singleton J, Sharf V
JAMA Neurol. 2016; 73(12):1425-1432.
PMID: 27775751
PMC: 5370581.
DOI: 10.1001/jamaneurol.2016.3401.
Reference Range of Respiratory Muscle Strength and Its Clinical Application in Amyotrophic Lateral Sclerosis: A Single-Center Study.
Park K, Kim R, Yang J, Oh J, Park S, Kim D
J Clin Neurol. 2016; 12(3):361-7.
PMID: 27449914
PMC: 4960222.
DOI: 10.3988/jcn.2016.12.3.361.