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24. Sporadic amyotrophic lateral sclerosis (SALS) - skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model. Shanmukha S; Narayanappa G; Nalini A; Alladi PA; Raju TR Dis Model Mech; 2018 Apr; 11(4):. PubMed ID: 29666144 [TBL] [Abstract][Full Text] [Related]
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30. Glycoprotein nonmetastatic melanoma protein B ameliorates skeletal muscle lesions in a SOD1G93A mouse model of amyotrophic lateral sclerosis. Nagahara Y; Shimazawa M; Tanaka H; Ono Y; Noda Y; Ohuchi K; Tsuruma K; Katsuno M; Sobue G; Hara H J Neurosci Res; 2015 Oct; 93(10):1552-66. PubMed ID: 26140698 [TBL] [Abstract][Full Text] [Related]
31. Spirituality and/or religious faith: A means for coping with the effects of amyotrophic lateral sclerosis/motor neuron disease? O'Brien MR; Clark D Palliat Support Care; 2015 Dec; 13(6):1603-14. PubMed ID: 25851240 [TBL] [Abstract][Full Text] [Related]
32. Cervical spinal cord and motor unit pathology in a canine model of SOD1-associated amyotrophic lateral sclerosis. Katz ML; Jensen CA; Student JT; Johnson GC; Coates JR J Neurol Sci; 2017 Jul; 378():193-203. PubMed ID: 28566164 [TBL] [Abstract][Full Text] [Related]
33. Adipose-derived stem cell conditioned medium impacts asymptomatic peripheral neuromuscular denervation in the mutant superoxide dismutase (G93A) transgenic mouse model of amyotrophic lateral sclerosis. Walker CL; Meadows RM; Merfeld-Clauss S; Du Y; March KL; Jones KJ Restor Neurol Neurosci; 2018; 36(5):621-627. PubMed ID: 30010155 [TBL] [Abstract][Full Text] [Related]
34. Distribution of the motor end-plates in the muscles of a sirenoid monster. Parízek J; Lipenská M Folia Morphol (Praha); 1978; 26(3):235-8. PubMed ID: 700533 [No Abstract] [Full Text] [Related]
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37. Normal development of muscle fibers and motor end plates in dystrophic mice. Burch TG; Law PK Exp Neurol; 1978 Feb; 58(3):570-4. PubMed ID: 620712 [No Abstract] [Full Text] [Related]
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