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標題: Titlebook: Neuromuscular Disorders; A Comprehensive Revi Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Book 20181st edition Springer Nature Singa [打印本頁]

作者: Roosevelt    時間: 2025-3-21 19:50
書目名稱Neuromuscular Disorders影響因子(影響力)




書目名稱Neuromuscular Disorders影響因子(影響力)學科排名




書目名稱Neuromuscular Disorders網絡公開度




書目名稱Neuromuscular Disorders網絡公開度學科排名




書目名稱Neuromuscular Disorders被引頻次




書目名稱Neuromuscular Disorders被引頻次學科排名




書目名稱Neuromuscular Disorders年度引用




書目名稱Neuromuscular Disorders年度引用學科排名




書目名稱Neuromuscular Disorders讀者反饋




書目名稱Neuromuscular Disorders讀者反饋學科排名





作者: 是貪求    時間: 2025-3-21 21:50
Motor Neuron Diseases (Amyotrophic Lateral Sclerosis)xed; and can have different combinations of upper and lower motor neuron findings. These are usually sporadic in nature, while some forms can be familial. Amyotrophic lateral sclerosis (ALS) is common and active disorder of brain and spinal cord motor neurons. ALS is fundamentally a clinical diagnos
作者: MOTTO    時間: 2025-3-22 02:40

作者: 高興一回    時間: 2025-3-22 04:47

作者: START    時間: 2025-3-22 12:05
Acute Motor Axonal Neuropathyajor subtype of GBS. AMAN progresses more rapidly and has an earlier peak than demyelinating GBS; tendon reflexes are relatively preserved or even exaggerated, and autonomic dysfunction is rare. Molecular mimicry of human gangliosides by . lipo-oligosaccharides is believed to be the main pathophysio
作者: 石墨    時間: 2025-3-22 14:00

作者: SCORE    時間: 2025-3-22 19:50

作者: 無辜    時間: 2025-3-23 00:08
Post-polio Syndromeg over other areas. The involvement is restricted to the lower motor neuron. The condition needs to be differentiated from other causes of lower motor neuron diseases, and background of poliomyelitis is perhaps most important. While new cases of polio are not encountered in the modern times, individ
作者: 高談闊論    時間: 2025-3-23 03:58

作者: Camouflage    時間: 2025-3-23 05:38

作者: 紅潤    時間: 2025-3-23 12:47

作者: 撤退    時間: 2025-3-23 14:13

作者: 喚醒    時間: 2025-3-23 20:05

作者: dura-mater    時間: 2025-3-24 01:06
Congenital Muscular Dystrophies elevated serum creatine kinase levels and dystrophic pattern on the muscle biopsy. These can be characterised on the basis of biochemical defects (disorders of glycosylation, defects of structural proteins, proteins of endoplasmic reticulum and of the nucleus). Neuromuscular and non-neuromuscular c
作者: 傾聽    時間: 2025-3-24 03:10

作者: Serenity    時間: 2025-3-24 10:30

作者: Semblance    時間: 2025-3-24 14:01
Oculopharyngeal Muscular Dystrophyant and the course is slowly progressive; patients can go on to develop limb weakness later in the illness. Histology shows rimmed vacuoles and tubulofilamentous inclusions in the nuclei. Treatment is largely supportive.
作者: 拱墻    時間: 2025-3-24 17:34

作者: avulsion    時間: 2025-3-24 21:39

作者: minimal    時間: 2025-3-25 01:45

作者: 膠狀    時間: 2025-3-25 06:50

作者: 挑剔小責    時間: 2025-3-25 11:14
Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Patelare generally not available in the libraries of Western coun.Spectroscopic Data of Steroid Glycosides serves as an essential reference guide containing spectroscopic, physical and biological activity data of over 3500 steroid glycosides, offering the structures and the data of the naturally occurrin
作者: 含沙射影    時間: 2025-3-25 15:25

作者: 召集    時間: 2025-3-25 19:17

作者: 錯事    時間: 2025-3-25 20:22

作者: Fretful    時間: 2025-3-26 02:57

作者: 高興一回    時間: 2025-3-26 07:00
Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Patelare generally not available in the libraries of Western coun.Spectroscopic Data of Steroid Glycosides serves as an essential reference guide containing spectroscopic, physical and biological activity data of over 3500 steroid glycosides, offering the structures and the data of the naturally occurrin
作者: 聲音刺耳    時間: 2025-3-26 11:40

作者: 辮子帶來幫助    時間: 2025-3-26 14:05

作者: PALMY    時間: 2025-3-26 19:16

作者: 鐵砧    時間: 2025-3-26 21:18

作者: orient    時間: 2025-3-27 04:14
Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Pateler 3500 steroid glycosides, offering the structures and the data of the naturally occurring glycosides of steroids. All compounds are arranged according to the structure of the aglycone, and, in its own class, according to the increasing molecular weight, making Spectroscopic Data of Steroid Glycosi
作者: elastic    時間: 2025-3-27 06:09

作者: 極少    時間: 2025-3-27 12:28
Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Patelare generally not available in the libraries of Western coun.Spectroscopic Data of Steroid Glycosides serves as an essential reference guide containing spectroscopic, physical and biological activity data of over 3500 steroid glycosides, offering the structures and the data of the naturally occurrin
作者: handle    時間: 2025-3-27 15:21

作者: Servile    時間: 2025-3-27 20:14
Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Pateler 3500 steroid glycosides, offering the structures and the data of the naturally occurring glycosides of steroids. All compounds are arranged according to the structure of the aglycone, and, in its own class, according to the increasing molecular weight, making Spectroscopic Data of Steroid Glycosi
作者: 欺騙手段    時間: 2025-3-27 23:26
Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Patelare generally not available in the libraries of Western coun.Spectroscopic Data of Steroid Glycosides serves as an essential reference guide containing spectroscopic, physical and biological activity data of over 3500 steroid glycosides, offering the structures and the data of the naturally occurrin
作者: GRAIN    時間: 2025-3-28 03:40

作者: Paraplegia    時間: 2025-3-28 07:23

作者: Musket    時間: 2025-3-28 12:51

作者: Adenocarcinoma    時間: 2025-3-28 17:40
Book 20181st editioners disorder characteristics, clinical differentiating points, relevant investigations and their interpretation, available genetic testing, best management approaches and counselling. Illustrative cases provide valuable insights, while extensive tables and illustrations mean that information can be rapidly found..
作者: 挫敗    時間: 2025-3-28 20:19

作者: BUOY    時間: 2025-3-29 00:37
Motor Neuron Diseases (Amyotrophic Lateral Sclerosis)ial. Amyotrophic lateral sclerosis (ALS) is common and active disorder of brain and spinal cord motor neurons. ALS is fundamentally a clinical diagnosis, supported by neurophysiological testing. There are no cures for ALS, but there are evidence-based guidelines for standards of care.
作者: 凹槽    時間: 2025-3-29 05:46

作者: BILIO    時間: 2025-3-29 07:35

作者: 扔掉掐死你    時間: 2025-3-29 14:13

作者: Circumscribe    時間: 2025-3-29 18:06

作者: GRE    時間: 2025-3-29 19:58

作者: 中國紀念碑    時間: 2025-3-30 00:12
Congenital Muscular Dystrophiessorders of glycosylation, defects of structural proteins, proteins of endoplasmic reticulum and of the nucleus). Neuromuscular and non-neuromuscular clinical features form an important part of the diagnostic evaluation. MRI of the muscles and brain and muscle immunocytochemistry can provide diagnostic information.
作者: 禍害隱伏    時間: 2025-3-30 07:01
Congenital Myopathiesd congenital fibre-type disproportion constitute majority of this group. Muscle biopsy plays an important role in diagnosis and classification of congenital myopathies. Therapy is usually supportive and directed bulbar dysfunction, respiratory distress and joint contractures.
作者: palpitate    時間: 2025-3-30 08:12
Book 20181st editionive cases..Treating neuromuscular disorders?calls for a sound, step-by-step clinical approach based on differential diagnosis and laboratory investigations. Yet to date, there has been no single, compact book that offers all the relevant information related to the management of these disorders.. .Th
作者: FIN    時間: 2025-3-30 13:27
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作者: 小隔間    時間: 2025-3-30 19:48

作者: 不愿    時間: 2025-3-30 21:30
Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. A case based learning of neuromuscular disorders.Description of key differential clinical points.Analysis of investigation in clinical context.Guidance for genetic tests.Comprehensive management guide




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