標題: Titlebook: Atlas of Skeletal Muscle Pathology; Janice R. Anderson Book 1985 Janice R. Anderson 1985 inflammation.muscle.muscular dystrophy.pathology. [打印本頁] 作者: GUST 時間: 2025-3-21 18:11
書目名稱Atlas of Skeletal Muscle Pathology影響因子(影響力)
書目名稱Atlas of Skeletal Muscle Pathology影響因子(影響力)學科排名
書目名稱Atlas of Skeletal Muscle Pathology網絡公開度
書目名稱Atlas of Skeletal Muscle Pathology網絡公開度學科排名
書目名稱Atlas of Skeletal Muscle Pathology被引頻次
書目名稱Atlas of Skeletal Muscle Pathology被引頻次學科排名
書目名稱Atlas of Skeletal Muscle Pathology年度引用
書目名稱Atlas of Skeletal Muscle Pathology年度引用學科排名
書目名稱Atlas of Skeletal Muscle Pathology讀者反饋
書目名稱Atlas of Skeletal Muscle Pathology讀者反饋學科排名
作者: Simulate 時間: 2025-3-21 21:54
Denervation,re permanently deprived of its motor nerve supply gradually atrophies and shows internal disorganization. Neurogenic diseases can be conveniently divided into three groups according to the site of the primary pathological lesion: (1) anterior horn cell, (2) axon and (3) motor end plate. The distribu作者: 繁榮中國 時間: 2025-3-22 03:03 作者: 饒舌的人 時間: 2025-3-22 07:31 作者: 懸崖 時間: 2025-3-22 11:44
Peripheral Neuropathy, in many peripheral nerves. The causes are legion and include toxic inflammatory, metabolic and genetically determined conditions. There is usually impairment of both sensory and motor function, although one or other may dominate the clinical picture. Distal segments of the limbs are most severely a作者: Bouquet 時間: 2025-3-22 16:19 作者: OUTRE 時間: 2025-3-22 17:15 作者: menopause 時間: 2025-3-22 23:57
Other Forms of Muscular Dystrophy,ich shows changes of dystrophic nature very early in life. One distinctive type appears almost exclusive to the Japanese and seems to be one of the commonest causes of the floppy infant syndrome in Japan..作者: 誹謗 時間: 2025-3-23 01:55
Myotonia,a can also be elicited by percussion of the muscle. The phenomenon diminishes with both repetitive percussion or voluntary activity. EMG findings are characteristic. Insertion of the needle and voluntary contraction provoke bursts of repetitive activity, initially of high amplitude, but gradually di作者: 亂砍 時間: 2025-3-23 08:33 作者: HAVOC 時間: 2025-3-23 13:22 作者: Increment 時間: 2025-3-23 13:51
Inflammatory Myopathy II,ogical to consider polymyalgia rheumatica with this group, although genuine myositis is most unusual. Inclusion body myositis is also usually included with the inflammatory myopathies, but despite the name, its qualifications are rather slight.作者: 新娘 時間: 2025-3-23 21:11 作者: paleolithic 時間: 2025-3-24 02:13
Drug-induced Myopathies,syncratic and unpredictable. Clinical and histological findings are varied, but rarely unique and can resemble other neuromuscular diseases. The drug-induced myopathies described here are but a few well-recognized examples that illustrate the range of pathological reactions. Many other drugs have be作者: 東西 時間: 2025-3-24 04:20 作者: 厭倦嗎你 時間: 2025-3-24 07:45
Pipelining and Vector Processingich shows changes of dystrophic nature very early in life. One distinctive type appears almost exclusive to the Japanese and seems to be one of the commonest causes of the floppy infant syndrome in Japan..作者: Pamphlet 時間: 2025-3-24 11:27
Processor Organization and Performanceogical to consider polymyalgia rheumatica with this group, although genuine myositis is most unusual. Inclusion body myositis is also usually included with the inflammatory myopathies, but despite the name, its qualifications are rather slight.作者: VOK 時間: 2025-3-24 17:32
Processor Organization and Performance changes of systemic myopathies to a large extent reflect varying degrees of degeneration or regeneration and repair of skeletal muscle cells. Thus it is not surprising that the same abnormalities often appear in focal reactive lesions and can cause diagnostic difficulty if their fundamental nature is not appreciated.作者: ANA 時間: 2025-3-24 19:02
https://doi.org/10.1007/978-94-009-4866-2inflammation; muscle; muscular dystrophy; pathology; skeletal muscle; syndromes作者: Infantry 時間: 2025-3-25 02:44
978-94-010-8653-0Janice R. Anderson 1985作者: CERE 時間: 2025-3-25 04:56 作者: 蒙太奇 時間: 2025-3-25 11:02 作者: Grasping 時間: 2025-3-25 13:36
Processor Organization and PerformanceMuscle weakness is a symptom of several endocrine disturbances and is sometimes the presenting feature.作者: laxative 時間: 2025-3-25 18:13
General Cellular Reactions,Skeletal muscle is composed of highly adaptable cells, responding to physiological stimuli and alterations in the internal environment by both metabolic and structural changes. The same changes occur, and are sometimes very conspicuous, in muscle diseases.作者: 總 時間: 2025-3-25 20:27
Endocrine Myopathies,Muscle weakness is a symptom of several endocrine disturbances and is sometimes the presenting feature.作者: 數(shù)量 時間: 2025-3-26 00:53 作者: tenosynovitis 時間: 2025-3-26 05:47
Matthew N. O. Sadiku,Cajetan M. Akujuobire permanently deprived of its motor nerve supply gradually atrophies and shows internal disorganization. Neurogenic diseases can be conveniently divided into three groups according to the site of the primary pathological lesion: (1) anterior horn cell, (2) axon and (3) motor end plate. The distribu作者: 價值在貶值 時間: 2025-3-26 09:14
Pipelining and Vector Processingcell disease attributable to the cytopathic effects of the virus, but is unlikely to require diagnostic muscle biopsy. In the more chronic disorders pathological changes beginning in the nerve cell body are frequently followed by gradual ‘dying back’ of the axon. These diseases include the spinal mu作者: eulogize 時間: 2025-3-26 14:31
Pipelining and Vector Processingcle weakness. Pearn. has defined seven separate SMA syndromes on a clinical and genetic basis, of which acute infantile and chronic childhood SMA form the majority. In recent years adult onset SMA has been identified as a major cause of the limb girdle syndrome.. The carrier frequency for one of the作者: scrape 時間: 2025-3-26 18:03
Overview of Computer Organization in many peripheral nerves. The causes are legion and include toxic inflammatory, metabolic and genetically determined conditions. There is usually impairment of both sensory and motor function, although one or other may dominate the clinical picture. Distal segments of the limbs are most severely a作者: Irremediable 時間: 2025-3-27 00:30 作者: 現(xiàn)存 時間: 2025-3-27 04:44
Pipelining and Vector Processinginexorably progressive condition. Other forms, largely distinguished by selective muscle involvement, e.g. oculopharyngeal and facioscapulohumeral dystrophy, are more variable in their rate of progression. Many theories of causation have at some time held sway, including vascular and neural hypothes作者: 是突襲 時間: 2025-3-27 05:41 作者: 壓碎 時間: 2025-3-27 10:00 作者: 行業(yè) 時間: 2025-3-27 14:20
Processor Organization and Performanceve muscle weakness. They are often familial but quite distinct from both the progressive muscular dystrophies and the severely disabling spinal muscular atrophies. Congenital myopathies are characterized by histochemical type 1 fibre predominance and by a variety of peculiar structural changes withi作者: 打算 時間: 2025-3-27 20:13 作者: 你不公正 時間: 2025-3-28 01:04 作者: Fecundity 時間: 2025-3-28 05:32
Overview of Computer Organizationsuch as the abnormal permeability of the cell membrane in Duchenne dystrophy, are unknown. The mode of action of various drugs and hormones is not well defined. There is, however, a sizeable group of myopathies where a fundamental biochemical defect, often a specific enzyme deficiency, has been iden作者: 鑒賞家 時間: 2025-3-28 10:05 作者: lethargy 時間: 2025-3-28 10:51
Processor Organization and Performance changes of systemic myopathies to a large extent reflect varying degrees of degeneration or regeneration and repair of skeletal muscle cells. Thus it is not surprising that the same abnormalities often appear in focal reactive lesions and can cause diagnostic difficulty if their fundamental nature 作者: CURL 時間: 2025-3-28 18:01
Other Forms of Muscular Dystrophy,ich shows changes of dystrophic nature very early in life. One distinctive type appears almost exclusive to the Japanese and seems to be one of the commonest causes of the floppy infant syndrome in Japan..作者: menopause 時間: 2025-3-28 22:50 作者: largesse 時間: 2025-3-29 00:56
Focal Lesions, changes of systemic myopathies to a large extent reflect varying degrees of degeneration or regeneration and repair of skeletal muscle cells. Thus it is not surprising that the same abnormalities often appear in focal reactive lesions and can cause diagnostic difficulty if their fundamental nature is not appreciated.作者: 衣服 時間: 2025-3-29 03:22 作者: 低能兒 時間: 2025-3-29 09:04
ned to promote ‘spot‘ histological diagnoses. I mystique and to describe and illustrate the basic have aimed to provide a guide to pathological reactions reactions of muscle cells. of muscle which will be useful to the practising histo- Interpretation of the biopsy depends not only upon pathologist and all st978-94-010-8653-0978-94-009-4866-2作者: 欺騙手段 時間: 2025-3-29 15:23 作者: seruting 時間: 2025-3-29 15:35 作者: conifer 時間: 2025-3-29 22:31 作者: Lipoprotein 時間: 2025-3-30 02:27 作者: Interim 時間: 2025-3-30 06:47
Myasthenia,nts, clinical manifestations remain limited to the extra-ocular muscles, although EMG investigation will reveal more widespread abnormalities. It is suggested that if the disease has been localized for a year, further progression is unlikely.. In chronic disease temporary muscle weakness may give wa作者: Grasping 時間: 2025-3-30 09:21
Congenital Myopathies, and which disorders to include can perhaps be solved by borrowing Brooke’s title of ‘Congenital (more or less) muscle diseases’.. The myopathies described in this chapter all have distinctive morphological features, but whilst they may be suspected clinically they can only be identified with certai作者: 軟弱 時間: 2025-3-30 13:23
https://doi.org/10.1007/978-3-319-25811-9e site for biopsy and secondly to handle the specimen correctly. Rough treatment of the fresh specimen, or misguided fixation, can destroy important diagnostic clues and introduce spectacular artifacts (Figures 1.1 and 1.2).作者: Limited 時間: 2025-3-30 19:48 作者: 大溝 時間: 2025-3-30 22:57
Technical Methods and Normal Parameters,e site for biopsy and secondly to handle the specimen correctly. Rough treatment of the fresh specimen, or misguided fixation, can destroy important diagnostic clues and introduce spectacular artifacts (Figures 1.1 and 1.2).作者: 不來 時間: 2025-3-31 00:51
Peripheral Neuropathy, provided some large, fast conducting axons remain. Changes in the muscle biopsy are usually most severe when there is axonal degeneration. The pathological spectrum is covered by two categories, the chronic, hereditary peripheral neuropathies and acute acquired postinfective neuropathy.作者: homeostasis 時間: 2025-3-31 05:22
