標(biāo)題: Titlebook: Amyotrophic Lateral Sclerosis; Therapeutic, Psychol V. Cosi,Ann C. Kato,M. Poloni Book 1987 The Editor(s) (if applicable) and The Author(s) [打印本頁(yè)] 作者: Debilitate 時(shí)間: 2025-3-21 18:37
書(shū)目名稱Amyotrophic Lateral Sclerosis影響因子(影響力)
作者: Militia 時(shí)間: 2025-3-21 21:14 作者: Gnrh670 時(shí)間: 2025-3-22 04:15 作者: Hyperopia 時(shí)間: 2025-3-22 06:46 作者: intuition 時(shí)間: 2025-3-22 12:04 作者: arrogant 時(shí)間: 2025-3-22 13:53
The Role of Axoplasmic Transport in the Restoration of Synaptic Transmission and in the Process of Sen 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作者: 合群 時(shí)間: 2025-3-22 19:40 作者: Intend 時(shí)間: 2025-3-22 23:30 作者: Minutes 時(shí)間: 2025-3-23 01:51
Human Spinal Cord Neurons in Culture as a Tool to Study Amyotrophic Lateral Sclerosis mouse anterior horn cultures[1-3]. In these experiments, morphological rather than biochemical criteria were used as an index of cytotoxicity. Since these results could not be repeated by other groups using the same assay system or another type of in vitro preparation[4-9], we decided to examine th作者: 修正案 時(shí)間: 2025-3-23 07:36
Autoimmune Involvement in Motor Neurone Diseaseidence 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作者: 蝕刻 時(shí)間: 2025-3-23 11:15 作者: resuscitation 時(shí)間: 2025-3-23 15:54 作者: ALIAS 時(shí)間: 2025-3-23 18:29
The Electromyographic, Physiopathogenetic Evaluation of Amyotrophic Lateral Sclerosisms 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作者: CORD 時(shí)間: 2025-3-24 01:58 作者: 廣口瓶 時(shí)間: 2025-3-24 04:16 作者: 真繁榮 時(shí)間: 2025-3-24 10:13
,Wünsche und Wege zur Verbesserung,’s disease. These include the occasional clinical association of the conditions in the same patient and the same family, the endemic foci of all three diseases, and the presence of changes of one disease in the central nervous system of some patients dying of another of these diseases. There are sev作者: 有特色 時(shí)間: 2025-3-24 13:54 作者: Eosinophils 時(shí)間: 2025-3-24 17:39
https://doi.org/10.1007/978-3-7091-2193-1myotubes from other species. In spite of an almost satisfactory morphological development with sarcomeric organization, the measure of biochemical parameters shows that this growth is arrested at an early stage of development. On the other hand, human myotubes contract occasionally but the reasons w作者: Debrief 時(shí)間: 2025-3-24 20:04
,Uranprovinzen und Uranvorr?te,ast with these more common cases, only a few familial cases occur with a pattern suggesting autosomal recessive inheritance. These genetic cases have recently stimulated research into the genetic dismetabolic conditions that could cause a phenotype similar to ALS or motor neuron diseases. In such fa作者: 顛簸下上 時(shí)間: 2025-3-25 02:54
Die Lagerst?tten nutzbarer Mineralientical, role in muscle regeneration after injury[1-9]. A concept of considerable stability and persistence of this structure or several components of it, has developed from studies principally in the frog that suggest it has major roles in the reinnervation of denervated adult muscle over and above a作者: Hormones 時(shí)間: 2025-3-25 05:08
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作者: DENT 時(shí)間: 2025-3-25 09:01 作者: MULTI 時(shí)間: 2025-3-25 14:55 作者: Nonconformist 時(shí)間: 2025-3-25 19:25 作者: Duodenitis 時(shí)間: 2025-3-25 23:23
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作者: Lyme-disease 時(shí)間: 2025-3-26 02:33 作者: projectile 時(shí)間: 2025-3-26 06:35
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 作者: liposuction 時(shí)間: 2025-3-26 11:28
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作者: dilute 時(shí)間: 2025-3-26 15:28 作者: Extort 時(shí)間: 2025-3-26 17:25 作者: Nucleate 時(shí)間: 2025-3-26 23:24 作者: 半圓鑿 時(shí)間: 2025-3-27 01:59 作者: 投射 時(shí)間: 2025-3-27 06:54
,Uranprovinzen und Uranvorr?te,While the article was in press, a new case with M-actyl-?- hexosaminidase B deficiency and progressive motor neuron disease has been reported by Hancock et al. (Biochem. Biophys. Res. Comm. 130:1185–1192, 1985).作者: 轉(zhuǎn)折點(diǎn) 時(shí)間: 2025-3-27 09:55 作者: GROG 時(shí)間: 2025-3-27 13:45
https://doi.org/10.1007/978-3-642-51409-8Amyotrophic lateral sclerosis (ALS) has been classified into sporadic and familial types[l]. The familial clustering does not imply a genetic mechanism but it seems a likely explanation in at least 5% of ALS cases.作者: 杠桿支點(diǎn) 時(shí)間: 2025-3-27 18:46
AddendumWhile the article was in press, a new case with M-actyl-?- hexosaminidase B deficiency and progressive motor neuron disease has been reported by Hancock et al. (Biochem. Biophys. Res. Comm. 130:1185–1192, 1985).作者: antiquated 時(shí)間: 2025-3-27 22:03
The Pathogenetic Role of Metals in Motor Neuron Disease — The Participation of AluminumAmong possible causative factors, an association of metal(s) and motor neuron disease (MND) has been repeatedly reported since Aran’s description on lead intoxication with amyotrophy in 1850[1].作者: 創(chuàng)作 時(shí)間: 2025-3-28 04:48 作者: 彩色的蠟筆 時(shí)間: 2025-3-28 09:19 作者: 斜 時(shí)間: 2025-3-28 13:58
https://doi.org/10.1007/978-3-7091-2193-1 that their cell bodies and dendrites are located within the central neurous system, whereas their axons constitute part of the peripheral nerves. The distal endings of the motor neurons in the motor end plates are unprotected by the blood-brain and blood-nerve barriers, and are therefore directly exposed to various substances in the blood.作者: COST 時(shí)間: 2025-3-28 18:30 作者: 允許 時(shí)間: 2025-3-28 19:46 作者: 不開(kāi)心 時(shí)間: 2025-3-28 23:37 作者: 吞吞吐吐 時(shí)間: 2025-3-29 05:07
Roh- und Augenscheins-Aufnahmen,vival in culture, factors which influence substrate attachment and neurite outgrowth, and factors which influence biochemical differentiation[1]. The biological role in vivo of only one, NGF (nerve growth factor), has received experimental support[2].作者: LAIR 時(shí)間: 2025-3-29 08:54
Zeichnende Aufnahmen und der Messtisch, 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 autoantibodies to a muscle-derived growth factor for spinal neurones.作者: 法律 時(shí)間: 2025-3-29 11:34 作者: 煉油廠 時(shí)間: 2025-3-29 17:46 作者: ETHER 時(shí)間: 2025-3-29 20:56 作者: Jacket 時(shí)間: 2025-3-30 02:47 作者: 外形 時(shí)間: 2025-3-30 06:57
Cytotoxicity of Serum from Amyotrophic Lateral Sclerosis Patients on Spinal Cord Cells in Cultured explants[1-3]. Other workers could not confirm such findings[4-6]. The potential significance of such a possibility and the discrepancy between the results of these studies have motivated us to address the same question, with some difference in the employed techniques as described below.作者: 知道 時(shí)間: 2025-3-30 08:42 作者: 過(guò)于平凡 時(shí)間: 2025-3-30 14:52
Roh- und Augenscheins-Aufnahmen,sensitive assay for trophic factors and toxic substances of clinical relevance. ALS-CSF induces a significant glial cell proliferation in vitro. Indirect immunofluorescence techniques were used to identify the atroglial proliferating cells.作者: 獎(jiǎng)牌 時(shí)間: 2025-3-30 17:33 作者: 得意人 時(shí)間: 2025-3-30 21:58 作者: DEFT 時(shí)間: 2025-3-31 02:42
ALS Cerebrospinal Fluid Enhances Human Foetal Astroglial Cell Proliferation ,sensitive assay for trophic factors and toxic substances of clinical relevance. ALS-CSF induces a significant glial cell proliferation in vitro. Indirect immunofluorescence techniques were used to identify the atroglial proliferating cells.作者: 假 時(shí)間: 2025-3-31 07:59 作者: 休戰(zhàn) 時(shí)間: 2025-3-31 11:35
Polygonmessung und die Bussolen,e effects of control and disease serum on human spinal cord neurons in culture. This preparation was recently developed and characterized in our laboratory[10]. Here we describe some of the properties of these cells and the effects of serum from ALS patients on their biochemical properties.作者: Flinch 時(shí)間: 2025-3-31 15:00
Die Lagerst?tten nutzbarer Mineralienon of acetylcholine receptors (AChRs) in the absence of the nerve[12,13]. Using much the same experimental paradigm, these same authors conclude that the same or different molecules, ‘stably’ attached to the synaptic basal lamina, regulate or ‘direct’ the accumulation of acetylcholinesterase (AChE), again at original synaptic sites[14].作者: TRUST 時(shí)間: 2025-3-31 18:21
Roh- und Augenscheins-Aufnahmen,tomy’[2]; (b) axons of responsive neurons are capable of transporting NGF in a retrograde manner from the nerve terminal to the cell body[3]; and (c) levels of NGF in target organs correlate with the density of sympathetic innervation[4]. NGF, however, has no known action on spinal motor neurons.作者: 禮節(jié) 時(shí)間: 2025-3-31 22:23 作者: PANEL 時(shí)間: 2025-4-1 05:12
