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Titlebook: Amyotrophic Lateral Sclerosis; Therapeutic, Psychol V. Cosi,Ann C. Kato,M. Poloni Book 1987 The Editor(s) (if applicable) and The Author(s)

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樓主: Debilitate
21#
發(fā)表于 2025-3-25 05:08:56 | 只看該作者
Die Lagerst?tten nutzbarer Mineralienen observable at the light microscopic level and were termed chromatolysis. In summary, the reaction is characterized by dissolution of the basophilic granules, rounding of the perikaryon, enlargement of the nucleolus, and dispersal of the Nissl substance. The latter corresponds to the disaggregatio
22#
發(fā)表于 2025-3-25 09:01:05 | 只看該作者
23#
發(fā)表于 2025-3-25 14:55:46 | 只看該作者
24#
發(fā)表于 2025-3-25 19:25:08 | 只看該作者
25#
發(fā)表于 2025-3-25 23:23:21 | 只看該作者
Zeichnende Aufnahmen und der Messtisch,idence from different sources has served to redirect attention towards such an involvement. Thus, early findings of a serum-borne neurotoxic factor in MND patients[l] have been confirmed by Roisen et al.[2], while Gurney and his colleagues[3,4] have reported the presence in MND sera of autoantibodie
26#
發(fā)表于 2025-3-26 02:33:59 | 只看該作者
27#
發(fā)表于 2025-3-26 06:35:03 | 只看該作者
Roh- und Augenscheins-Aufnahmen,re unable to demonstrate a cytotoxic effect of ALS sera on human central nervous system (CNS) cultures from 15 - 20 week old human foetuses, confirming the negative therapeutic effects obtained using plasma-exchange in affected patients[l]. We decided to study the effects of ALS-CSF on human foetal
28#
發(fā)表于 2025-3-26 11:28:16 | 只看該作者
https://doi.org/10.1007/978-3-642-51409-8ms of spinal muscular atrophy (SMA) or lateral sclerosis[1]; moreover its differentiation from hereditary ALS, phenocopies and exogenous similar syndromes is hardly possible except by the identification of the respective etiologies. A pathognomonic marker of primary sporadic ALS seems to be represen
29#
發(fā)表于 2025-3-26 15:28:09 | 只看該作者
30#
發(fā)表于 2025-3-26 17:25:11 | 只看該作者
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