標(biāo)題: Titlebook: Chorea; Causes and Managemen Federico E. Micheli,Peter A. LeWitt Book 2014 Springer-Verlag London 2014 chorea.choreiform disorder.cognitive [打印本頁] 作者: radionuclides 時(shí)間: 2025-3-21 18:14
書目名稱Chorea影響因子(影響力)
書目名稱Chorea影響因子(影響力)學(xué)科排名
書目名稱Chorea網(wǎng)絡(luò)公開度
書目名稱Chorea網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Chorea被引頻次
書目名稱Chorea被引頻次學(xué)科排名
書目名稱Chorea年度引用
書目名稱Chorea年度引用學(xué)科排名
書目名稱Chorea讀者反饋
書目名稱Chorea讀者反饋學(xué)科排名
作者: 悶熱 時(shí)間: 2025-3-21 21:42 作者: obnoxious 時(shí)間: 2025-3-22 03:07 作者: 強(qiáng)制性 時(shí)間: 2025-3-22 05:54
,Sydenham’s Chorea, its declining prevalence (particularly in developed countries), it is the most common explanation for acute onset of chorea in children. It is more common in girls than boys, and its features include chorea, decreased muscle tone, tics, and nonmovement disorder findings such as behavioral abnormali作者: Repetitions 時(shí)間: 2025-3-22 12:11
,Huntington’s Disease: Clinical Phenotypes and Therapeutics,rder. However, using disease models, and studies in human patients, great progress has been made in understanding the pathophysiology of HD. Research has led to the development of the first gene therapy approaches with promising results in HD model systems. This raises hopes that HD, a monogenetic f作者: dissent 時(shí)間: 2025-3-22 14:13 作者: dissent 時(shí)間: 2025-3-22 18:37
Huntington Disease and Huntington Disease-Like Syndromes: An Overview,on disease (HD). In addition there are disorders mimicking HD, the so-called HD-like syndromes, and molecular workup revealed that they account for about 1 % of suspected HD cases. The aim of this review is to summarize the main characteristics of these rare conditions in order to familiarize clinic作者: chance 時(shí)間: 2025-3-23 01:15
McLeod Syndrome,is and progressive striatal neurodegeneration. The so-called core NA syndromes include autosomal recessive chorea-acanthocytosis and X-linked McLeod syndrome. These two disorders have a Huntington disease-like phenotype consisting of a hyperkinetic, mostly choreatic, movement disorders, psychiatric 作者: anagen 時(shí)間: 2025-3-23 01:52 作者: Cardioversion 時(shí)間: 2025-3-23 09:11 作者: 很像弓] 時(shí)間: 2025-3-23 11:13
Aceruloplasminemia,mplete absence of ceruloplasmin ferroxidase activity due to a homozygous mutation of the ceruloplasmin gene. There is no apparent genotype-phenotype association. The diagnosis is based on the absence of serum ceruloplasmin, low serum iron concentration and high serum ferritin concentration, as well 作者: 聽覺 時(shí)間: 2025-3-23 17:16 作者: 遣返回國 時(shí)間: 2025-3-23 19:44
Chorea in Prion Diseases,onditions that occur in both humans and animals. Sporadic, acquired, and inherited forms of prion disease exist. One of the distinct characteristics of all human prion diseases is their clinical and pathological heterogeneity; however, there are clinical features that are common to all forms and the作者: Foolproof 時(shí)間: 2025-3-24 02:06
Inherited Metabolic Disorders Causing Chorea,arious and complex movement disorders, that can be seen in IMDs. Most of these conditions are rare and inherited and many of them manifest in childhood and adolescence and, less frequently, in adults .The term IMD can be used broadly to refer to almost any cellular process, including purine or pyrim作者: commute 時(shí)間: 2025-3-24 02:56 作者: BET 時(shí)間: 2025-3-24 09:33
Structural Causes of Chorea,he most frequent cause, with the vast majority of clinical symptoms remitting spontaneously with time.Post-traumatic chorea can present acutely or with significant delay from the time of initial injury, with the most effective treatment being evacuation of local hematomas, if present.Chorea from cer作者: SUE 時(shí)間: 2025-3-24 12:50 作者: Mobile 時(shí)間: 2025-3-24 17:01 作者: 暴發(fā)戶 時(shí)間: 2025-3-24 22:21
Psychogenic Chorea,ement disorders (PMDs)...: Neurologists and movement disorder specialists alike are frequently called upon to evaluate patients with bizarre movement disorders and suspected PMDs. The clinical evaluation and treatment of these disorders are frequently complex and time consuming. Psychogenic chorea i作者: 圓木可阻礙 時(shí)間: 2025-3-25 01:15
https://doi.org/10.1007/978-3-86226-453-7sive extrapyramidal deterioration and iron accumulation in the basal ganglia. Current therapeutic options include various symptomatic approaches, and new therapies are under consideration such as surgical approaches and chelating agents.作者: canvass 時(shí)間: 2025-3-25 06:22
Methode und Kriterien der Auslegung,al accumulation diseases and others. Disorders affecting amino acids, carbohydrates or lipids will be emphasized. The main aspects regarding clinical approach to identify the underlying IMDs will be revised. The available genetic data will be shown, besides pathophysiological and treatment aspects of the more important IMDs.作者: NAVEN 時(shí)間: 2025-3-25 11:31
Neurodegeneration with Brain Iron Accumulation,sive extrapyramidal deterioration and iron accumulation in the basal ganglia. Current therapeutic options include various symptomatic approaches, and new therapies are under consideration such as surgical approaches and chelating agents.作者: Daily-Value 時(shí)間: 2025-3-25 12:17 作者: travail 時(shí)間: 2025-3-25 18:15 作者: 壓倒性勝利 時(shí)間: 2025-3-25 20:30 作者: 粗糙濫制 時(shí)間: 2025-3-26 02:29
Munich Studies on Innovation and Competitionfamilies have been reported and reviewed with typical or atypical symptoms. Since BHC is a nonprogressive condition and some patients respond favorably to some drugs, it is important to characterize it correctly in order to offer the best treatment options and give the right prognosis to the affected subject and relatives.作者: Locale 時(shí)間: 2025-3-26 08:06 作者: decipher 時(shí)間: 2025-3-26 10:47 作者: 美學(xué) 時(shí)間: 2025-3-26 16:14 作者: 聽覺 時(shí)間: 2025-3-26 20:08
Benign Hereditary Chorea,families have been reported and reviewed with typical or atypical symptoms. Since BHC is a nonprogressive condition and some patients respond favorably to some drugs, it is important to characterize it correctly in order to offer the best treatment options and give the right prognosis to the affected subject and relatives.作者: 葡萄糖 時(shí)間: 2025-3-26 22:59 作者: 色情 時(shí)間: 2025-3-27 02:43 作者: 鴿子 時(shí)間: 2025-3-27 09:02 作者: 肥料 時(shí)間: 2025-3-27 11:40
Kapitel 8: Weiterführende überlegungenians with them. While treatment remains symptomatic, advances have been made with genetic delineation. Hopefully with better understanding of their pathophysiology, we will also move towards mechanistic therapies.作者: CHIDE 時(shí)間: 2025-3-27 14:04
https://doi.org/10.1007/978-3-540-75516-6th other neurologic and extraneurologic symptoms. In these cases, family and clinical history, physical examination, and a specific set of ancillary studies such as genetic, neuroimaging, and biochemical studies will often enable a correct diagnosis.作者: zonules 時(shí)間: 2025-3-27 17:46
Huntington Disease and Huntington Disease-Like Syndromes: An Overview,ians with them. While treatment remains symptomatic, advances have been made with genetic delineation. Hopefully with better understanding of their pathophysiology, we will also move towards mechanistic therapies.作者: Self-Help-Group 時(shí)間: 2025-3-28 00:19
Chorea in Childhood,th other neurologic and extraneurologic symptoms. In these cases, family and clinical history, physical examination, and a specific set of ancillary studies such as genetic, neuroimaging, and biochemical studies will often enable a correct diagnosis.作者: electrolyte 時(shí)間: 2025-3-28 03:27
ical management of the different choreic disorders.Update on.Chorea: Causes and Management. provides a comprehensive and timely update for the wide variety of neurological conditions, both inherited and acquired, which result in this common hyperkinetic movement disorder..This book describes in deta作者: CHASE 時(shí)間: 2025-3-28 06:33 作者: Antarctic 時(shí)間: 2025-3-28 11:17
Chorea in Inherited Ataxias,ebellar ataxias (ARCAs), such as ataxia telangiectasia (more commonly), and Friedreich ataxia (more rarely). In the group of spinocerebellar ataxias (SCAs), chorea can be found more commonly in patients with SCA type 17, and in dentatorubral-pallidoluysian atrophy (DRPLA).作者: venous-leak 時(shí)間: 2025-3-28 17:52
Chorea-Acanthocytosis,levant clinical symptoms in the respective system. There is no cure for the disease, and treatment is purely symptomatic. Recent data hints towards chorein being involved in different kinase pathways and actin cytoskeleton disturbances. This book chapter tries to shed light into the clinical phenoty作者: 孵卵器 時(shí)間: 2025-3-28 21:24 作者: Homocystinuria 時(shí)間: 2025-3-29 00:27
,Huntington’s Disease: Molecular Pathogenesis and New Therapeutic Perspectives, synaptic signaling. Notably, not all the effects of mutant HTT are cell autonomous. The present review focuses on the molecular pathogenesis of HD and the current state of therapeutic development for the treatment of HD. We review the preclinical and clinical development molecular therapies targeti作者: 吹牛大王 時(shí)間: 2025-3-29 06:24 作者: Painstaking 時(shí)間: 2025-3-29 07:36 作者: reaching 時(shí)間: 2025-3-29 14:34
Chorea in Prion Diseases,nt that a diagnosis of prion disease is considered if HD gene testing is negative. This chapter aims to give a general overview of the clinical features, investigations, and pathophysiology of the human prion diseases, accompanied by representative case reports of patients seen at the NHS National P作者: 隱語 時(shí)間: 2025-3-29 16:05 作者: ANT 時(shí)間: 2025-3-29 22:57
Chorea: A Surgical Approach,. However, in the absence of high level of scientific evidence, the surgical approach for treating chorea still remains empirical. Several other experimental approaches (such as cellular transplantation and delivery of neurotrophic factors) have showed promising results when applied to animal models作者: 悲痛 時(shí)間: 2025-3-30 00:19
Psychogenic Chorea,ific diagnostic criteria for psychogenic chorea, we can use the available criteria already published for PMD. Treatment should be implemented in an organized process where the diagnosis has to be informed clearly to the patient and the family; a treatment plan should be explained including a psychia作者: LAP 時(shí)間: 2025-3-30 06:51 作者: 微枝末節(jié) 時(shí)間: 2025-3-30 08:32 作者: 一個(gè)姐姐 時(shí)間: 2025-3-30 14:55 作者: Minatory 時(shí)間: 2025-3-30 19:48
https://doi.org/10.1007/978-3-322-97036-7degeneration is not known, the association of the acanthocytic membrane abnormality with selective striatal degeneration suggests a common pathogenetic pathway. Useful diagnostic laboratory tests, besides blood smears to detect acanthocytosis, encompass determination of serum creatine kinase, since 作者: 笨拙的我 時(shí)間: 2025-3-31 00:27
https://doi.org/10.1007/978-3-86226-453-7taxia, involuntary movement (dystonia, chorea, and tremors), Parkinsonism, and cognitive dysfunction correspond to the regions of iron deposition in the brain. The neuropathological process extends beyond the basal ganglia to the cerebral cortex with time. Patients with aceruloplasminemia usually pr作者: 星星 時(shí)間: 2025-3-31 02:33
Methode und Kriterien der Auslegung,nt that a diagnosis of prion disease is considered if HD gene testing is negative. This chapter aims to give a general overview of the clinical features, investigations, and pathophysiology of the human prion diseases, accompanied by representative case reports of patients seen at the NHS National P作者: immunity 時(shí)間: 2025-3-31 07:35
Die Regelungen des Forschungsprotokolls, such instances, the diagnosis is more troublesome and a careful search for drug intake should be done..In this chapter, the main causes of drug-induced choreas are analyzed as well as their possible therapeutic approaches.作者: affect 時(shí)間: 2025-3-31 11:05
https://doi.org/10.1007/978-3-540-75516-6. However, in the absence of high level of scientific evidence, the surgical approach for treating chorea still remains empirical. Several other experimental approaches (such as cellular transplantation and delivery of neurotrophic factors) have showed promising results when applied to animal models作者: Lobotomy 時(shí)間: 2025-3-31 17:06
Methode und Kriterien der Auslegung,ific diagnostic criteria for psychogenic chorea, we can use the available criteria already published for PMD. Treatment should be implemented in an organized process where the diagnosis has to be informed clearly to the patient and the family; a treatment plan should be explained including a psychia作者: 邪惡的你 時(shí)間: 2025-3-31 19:36
sychologists, specialists in medical genetics, clinical and basic researchers in neurosciences, and generalist clinical physicians with an interest in movement disorders..978-1-4471-7042-6978-1-4471-6455-5作者: COST 時(shí)間: 2025-3-31 22:13
,A Clinician’s Approach to Chorea, of etiologies, including acquired and genetic causes. The workup of a patient with chorea often depends on the “company” that this movement disorder keeps. Various forms of laboratory testing can enhance a clinical diagnosis.作者: AGATE 時(shí)間: 2025-4-1 04:41
https://doi.org/10.1007/978-1-4471-6455-5chorea; choreiform disorder; cognitive impairment; dyskinesia; hyperkinesia; movement disorder作者: 廣告 時(shí)間: 2025-4-1 09:27 作者: Carcinogen 時(shí)間: 2025-4-1 14:06
