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Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.Human Genetics|June 1, 1997
Exclusion of the expansion of CAG/CTG repeats at thirteen loci on chromosome 12 as a candidate genetic mutation in scapuloperoneal spinal muscular atrophy with anticipationK Isozumi, R DeLong, J Kaplan, et al.American Journal of Medical Genetics|July 1, 1991
Penta X syndrome: a case report with review of the literatureR Kassai, I Hamada, H Furuta, et al.Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi = Zhonghua Laodong Weisheng Zhiyebing Zazhi = Chinese Journal of Industrial Hygiene and Occupational Diseases|October 10, 2019
[Analysis on social security of pneumoconiosis patients in two areas of Chongqing from 2006 to 2018]H X Deng, X X Wang, C J Qiu, et al.Bioscience, Biotechnology, and Biochemistry|November 1, 1995
Purification and some properties of S-Hemolysin produced by Streptomyces sp. strain no. A-6288K Suzuki, K Matsunaga, T Ehara, et al.Neurology|January 1, 1997
Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutaseT Juneja, M A Pericak-Vance, N G Laing, et al.The Journal of Physiology|April 14, 2011
Altered postnatal maturation of electrical properties in spinal motoneurons in a mouse model of amyotrophic lateral sclerosisK A Quinlan, J E Schuster, R Fu, et al.Journal of the Neurological Sciences|August 10, 2000
Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1M Said Ahmed, W Y Hung, J S Zu, et al.Human Genetics|April 1, 1991
Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPsH X Deng, K Abe, I Kondo, et al.Pageof 11