نتائج البحث

Reasons and experience for patients with amyotrophic lateral sclerosis using traditional Chinese medicine: a CARE-TCM based mixed method study.

• Authors : Jia Q; Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.; Institute for Brain Disorders, Beijing University of Chinese Medicine, Beijing, China.

Subjects: Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/drug therapy ; Medicine, Chinese Traditional*/Medicine, Chinese Traditional*/Medicine, Chinese Traditional*/methods; Humans

• Source: BMC complementary medicine and therapies [BMC Complement Med Ther] 2024 Jun 12; Vol. 24 (1), pp. 231. Date of Electronic Publication: 2024 Jun 12.Publisher: BioMed Central Country of Publication: England NLM ID: 101761232 Publication Model: Electronic Cited Medium: Internet ISSN: 2662-7671

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Mutation and clinical analysis of the CLCC1 gene in amyotrophic lateral sclerosis patients from Central South China.

• Authors : Tang L; Department of Neurology, Xiangya Hospital, Central South University, Jiangxi Hospital, National Regional Center for Neurological Diseases, Nanchang, P. R. China.; Department of Neurology, Xiangya Hospital, Central South University, Changsha, P. R. China.

Subjects: Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/genetics; Humans ; Mutation

• Source: Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2024 Jan; Vol. 11 (1), pp. 79-88. Date of Electronic Publication: 2023 Nov 02.Publisher: Wiley Periodicals, Inc on behalf of American Neurological Association Country of Publication: United States NLM ID: 101623278 Publication Model:

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Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China.

• Authors : Xu, Fanxi¹ (AUTHOR); Huang, Sen² (AUTHOR); Li, Xu-Ying^1,3 (AUTHOR)

• Source: BMC Medical Genomics. 8/5/2022, Vol. 15 Issue 1, p1-12. 12p.

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Natural history and remarkable psychiatric state of late‐onset amyotrophic lateral sclerosis in China.

• Authors : Huang, Sen^1,2 (AUTHOR); Zheng, Minying^1,2 (AUTHOR); Lin, Jianing^1,2 (AUTHOR)

• Source: Acta Neurologica Scandinavica. Jul2022, Vol. 146 Issue 1, p24-33. 10p.

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NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients.

• Authors : Manini, Arianna¹ (AUTHOR); Gagliardi, Delia¹ (AUTHOR); Meneri, Megi^1,2 (AUTHOR)

• Source: Scientific Reports. 2/23/2023, Vol. 13 Issue 1, p1-6. 6p.

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The distinct manifestation of young-onset amyotrophic lateral sclerosis in China.

• Authors : Lin, Jianing¹ (AUTHOR); Chen, Weineng¹ (AUTHOR); Huang, Pian¹ (AUTHOR)

• Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Feb2021, Vol. 22 Issue 1/2,

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A prospective study on split-hand index as a biomarker for the diagnosis of amyotrophic lateral sclerosis.

• Authors : Wang, Zhi-Li¹ (AUTHOR); Liu, Mingsheng¹ (AUTHOR); Cai, Zhengyi¹ (AUTHOR)

• Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Nov2020, Vol. 21 Issue 7/8,

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The protective role of pre-morbid type 2 diabetes in patients with amyotrophic lateral sclerosis: a center-based survey in China.

• Authors : Zhang, Linjing^1,2 (AUTHOR); Chen, Lu^1,2 (AUTHOR); Fan, Dongsheng^1,2,3 (AUTHOR)

• Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. May2020, Vol. 21 Issue 3/4,

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Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia.

• Authors : Yang X; Department of Neurology, Peking Union Medical College Hospital, 100730, Beijing, China.; Sun X

Subjects: Frontotemporal Dementia*/Frontotemporal Dementia*/Frontotemporal Dementia*/genetics ; Frontotemporal Dementia*/Frontotemporal Dementia*/Frontotemporal Dementia*/complications ; Frontotemporal Dementia*/Frontotemporal Dementia*/Frontotemporal Dementia*/epidemiology Amyotrophic lateral sclerosis 1

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Nov 07; Vol. 17 (1), pp. 404. Date of Electronic Publication: 2022 Nov 07.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

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Association of apolipoprotein E ε4 allele and amyotrophic lateral sclerosis in Chinese population.

• Authors : He D; Department of Neurology, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC), Beijing, China.; Shang L

Subjects: Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/epidemiology ; Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/genetics ; Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/Amyotrophic Lateral Sclerosis*/pathology

• Source: Amyotrophic lateral sclerosis & frontotemporal degeneration [Amyotroph Publisher: Taylor & Francis Country of Publication: England NLM ID: 101587185 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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