標(biāo)題: Titlebook: Genetic Counseling for Adult Neurogenetic Disease; A Casebook for Clini Jill S. Goldman Book 2015 Springer Science+Business Media New York [打印本頁] 作者: 快樂 時間: 2025-3-21 16:13
書目名稱Genetic Counseling for Adult Neurogenetic Disease影響因子(影響力)
書目名稱Genetic Counseling for Adult Neurogenetic Disease影響因子(影響力)學(xué)科排名
書目名稱Genetic Counseling for Adult Neurogenetic Disease網(wǎng)絡(luò)公開度
書目名稱Genetic Counseling for Adult Neurogenetic Disease網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Genetic Counseling for Adult Neurogenetic Disease被引頻次
書目名稱Genetic Counseling for Adult Neurogenetic Disease被引頻次學(xué)科排名
書目名稱Genetic Counseling for Adult Neurogenetic Disease年度引用
書目名稱Genetic Counseling for Adult Neurogenetic Disease年度引用學(xué)科排名
書目名稱Genetic Counseling for Adult Neurogenetic Disease讀者反饋
書目名稱Genetic Counseling for Adult Neurogenetic Disease讀者反饋學(xué)科排名
作者: incisive 時間: 2025-3-21 20:42
DFT - Diskrete Fourier-Transformationatomy, pathology, etiology, and genetics, none of which are perfect. Classification by genetic etiology is complicated by heterogeneity, in which many genes cause the same phenotype, as well as pleiotropy, in which mutations in a single gene can result in different phenotypes. Genetic counseling for作者: FLAX 時間: 2025-3-22 00:33 作者: exceed 時間: 2025-3-22 05:32 作者: Inkling 時間: 2025-3-22 10:26
The Loss of the Sleipner Condeep Platformor inherited. Classifications are made by age of onset, affected body part, whether it is primary, secondary or heredodegenerative, and by the presence or absence of other movement disorders. Numerous genes can cause dystonia, complicating testing and diagnosis. Inheritance patterns can be autosomal作者: 問到了燒瓶 時間: 2025-3-22 13:10
System of Organizing and Building DIISria, and, often, abnormal oculomotor control. Age of onset of these disorders ranges from infancy to late life, and may include many additional clinical features such as neuropathy, cognitive dysfunction, and parkinsonism. Genetic counseling is frequently complicated by the overlap in phenotypes, an作者: 問到了燒瓶 時間: 2025-3-22 18:01
Substanzmissbrauch und Substanzabh?ngigkeitmon causes of dementia is Alzheimer’s disease. Dementia may have associated motor symptoms that can develop before or after the cognitive dysfunction. This section reviews many of the genetic counseling issues, including complexity of family history with both sporadic and inherited forms of dementia作者: 人類學(xué)家 時間: 2025-3-23 00:32
Jürgen Margraf,Silvia Schneider, and .. Susceptibility genes such as APOE contribute to risk in a far larger number of cases. Predictive testing is available for the autosomal dominant genes, but is not recommended for risk genes as they are neither necessary nor sufficient to cause AD. Genetic testing is complicated by capacity 作者: GROSS 時間: 2025-3-23 02:42 作者: 團結(jié) 時間: 2025-3-23 08:10
https://doi.org/10.1007/978-3-642-84501-7a (FFI). Ten to fifteen percent of prion disease has a genetic etiology. Inherited forms of all 3 diseases are due to mutations in the . gene. The phenotype conferred by a specific mutation can be further modified by a polymorphism at codon 29. Additionally age of onset and symptom presentation cann作者: Stagger 時間: 2025-3-23 10:29
https://doi.org/10.1007/978-3-642-56761-2ke include age, gender, and ethnicity. Other risk factors for stroke, such as hypertension, high cholesterol, artherosclerosis, and obesity, are influenced by genetics. Genetic syndromes make up about 1?% of this risk. Genetic counseling should include a discussion of manageable environmental risk f作者: 無可非議 時間: 2025-3-23 16:51 作者: Pamphlet 時間: 2025-3-23 20:16 作者: 白楊 時間: 2025-3-24 01:42 作者: Between 時間: 2025-3-24 05:35 作者: 不斷的變動 時間: 2025-3-24 09:41
Seok-Yong Choi,Hyunju Ro,Hankuil Yie, lower limb spasticity and weakness. HSPs are classified as pure/uncomplicated or complicated, and vary in symptoms, severity, age of onset, and genetic etiology. Over 50 loci have been associated with the HSPs and include autosomal dominant, autosomal recessive, and X-linked genes. Genetic counse作者: 尊重 時間: 2025-3-24 12:13 作者: 健談 時間: 2025-3-24 18:02 作者: DEMN 時間: 2025-3-24 21:59 作者: coddle 時間: 2025-3-25 02:17
Hardware: Das Interface mit dem ACIA 6551,otocol for predictive genetic testing for this disease has become the gold standard used for genetic counseling of other neurodegenerative diseases. The clinical characteristics of the disorder and its difficult genetic counseling issues, such as anticipation, reduced penetrant alleles, and the impact of predictive testing, are presented.作者: 無脊椎 時間: 2025-3-25 06:02
Jürgen Margraf,Silvia Schneiderant genes, but is not recommended for risk genes as they are neither necessary nor sufficient to cause AD. Genetic testing is complicated by capacity to consent, lack of treatment, the need to test an affected family member before predictive testing, and family disagreements about testing.作者: 培養(yǎng) 時間: 2025-3-25 08:49
https://doi.org/10.1007/978-3-642-84501-7notype conferred by a specific mutation can be further modified by a polymorphism at codon 29. Additionally age of onset and symptom presentation cannot always be predicted by the genotype. Genetic counseling for the prion disease must address these ambiguities and the impact of a rapidly progressive rare disease on family members.作者: 土產(chǎn) 時間: 2025-3-25 15:07 作者: 斑駁 時間: 2025-3-25 17:14 作者: Affluence 時間: 2025-3-25 20:29 作者: microscopic 時間: 2025-3-26 04:06 作者: TOXIN 時間: 2025-3-26 06:10
Book 2015d other practitioners. Because of the emotional and potentially life-altering impact of these diseases on the patient and family, counseling can be especially challenging..A rare hands-on guide to the subject, .Genetic Counseling for Adult Neurogenetic Disease. deals with core issues that differenti作者: CODE 時間: 2025-3-26 08:46
DFT - Diskrete Fourier-Transformation movement disorders is also complicated by having both Mendelian and multifactorial causes of disease. This section reviews the different types of movement disorders and the issues for genetic counseling.作者: Crater 時間: 2025-3-26 14:27 作者: Forehead-Lift 時間: 2025-3-26 18:14
The Loss of the Sleipner Condeep Platform dominant, autosomal recessive, or X-linked. Incomplete penetrance, imprinting, pleiotropic genes, and heterogeneous conditions are all seen. These genetic phenomena can present difficulties for genetic counseling. The most common genetic dystonias are presented in this chapter.作者: 內(nèi)閣 時間: 2025-3-26 23:52
System of Organizing and Building DIISticipation, inability to predict age of onset, and lack of treatment options. This chapter will focus on the autosomal dominant spinocerebellar ataxias (SCAs), autosomal recessive Friedreich ataxia, and X-linked Fragile X tremor ataxia syndrome.作者: Brain-Waves 時間: 2025-3-27 04:19
Substanzmissbrauch und Substanzabh?ngigkeit, the clinical overlap between dementias, distinction between autosomal dominant and risk genes, determining the capacity to consent to genetic testing, and the impact of predictive testing for a fatal, untreatable disease.作者: groggy 時間: 2025-3-27 05:26 作者: hauteur 時間: 2025-3-27 10:23 作者: Cleave 時間: 2025-3-27 14:22 作者: PRE 時間: 2025-3-27 20:09
Overview of Movement Disorders movement disorders is also complicated by having both Mendelian and multifactorial causes of disease. This section reviews the different types of movement disorders and the issues for genetic counseling.作者: obsession 時間: 2025-3-27 22:57 作者: 休閑 時間: 2025-3-28 05:52
Dystonia dominant, autosomal recessive, or X-linked. Incomplete penetrance, imprinting, pleiotropic genes, and heterogeneous conditions are all seen. These genetic phenomena can present difficulties for genetic counseling. The most common genetic dystonias are presented in this chapter.作者: 彩色 時間: 2025-3-28 10:20
Ataxiaticipation, inability to predict age of onset, and lack of treatment options. This chapter will focus on the autosomal dominant spinocerebellar ataxias (SCAs), autosomal recessive Friedreich ataxia, and X-linked Fragile X tremor ataxia syndrome.作者: byline 時間: 2025-3-28 11:15 作者: 過去分詞 時間: 2025-3-28 17:41 作者: hematuria 時間: 2025-3-28 19:08 作者: ungainly 時間: 2025-3-29 00:31 作者: perjury 時間: 2025-3-29 05:09 作者: 尊嚴 時間: 2025-3-29 10:35
Alzheimer Diseaseant genes, but is not recommended for risk genes as they are neither necessary nor sufficient to cause AD. Genetic testing is complicated by capacity to consent, lack of treatment, the need to test an affected family member before predictive testing, and family disagreements about testing.作者: 劇毒 時間: 2025-3-29 11:59
Prion Diseasenotype conferred by a specific mutation can be further modified by a polymorphism at codon 29. Additionally age of onset and symptom presentation cannot always be predicted by the genotype. Genetic counseling for the prion disease must address these ambiguities and the impact of a rapidly progressive rare disease on family members.作者: omnibus 時間: 2025-3-29 16:33 作者: 深淵 時間: 2025-3-29 20:56 作者: 禍害隱伏 時間: 2025-3-30 02:10 作者: 道學(xué)氣 時間: 2025-3-30 05:37 作者: 很像弓] 時間: 2025-3-30 09:36
Book 2015t, plus guidelines for asking, and answering, pertinent questions. The major concentration, however, is on genetic counseling issues and case histories illustrating these issues. As an added dimension, the accompanying .videos depict representative issues and challenges in genetic counseling for spe作者: 發(fā)源 時間: 2025-3-30 13:08 作者: 斷言 時間: 2025-3-30 17:43
Overview of Movement Disordersatomy, pathology, etiology, and genetics, none of which are perfect. Classification by genetic etiology is complicated by heterogeneity, in which many genes cause the same phenotype, as well as pleiotropy, in which mutations in a single gene can result in different phenotypes. Genetic counseling for作者: ONYM 時間: 2025-3-30 23:14 作者: Madrigal 時間: 2025-3-31 03:06
Parkinson Diseaseeristics, parkinsonism, may also be found in related diseases known as the Parkinson’s plus disorders and may be a component of numerous Mendelian conditions. The variety of inheritance patterns in familial parkinsonism includes autosomal dominant, autosomal recessive, autosomal dominant with reduce作者: Parameter 時間: 2025-3-31 06:23 作者: Cholecystokinin 時間: 2025-3-31 11:25 作者: 被告 時間: 2025-3-31 13:43
Overview of the Dementiasmon causes of dementia is Alzheimer’s disease. Dementia may have associated motor symptoms that can develop before or after the cognitive dysfunction. This section reviews many of the genetic counseling issues, including complexity of family history with both sporadic and inherited forms of dementia作者: CORD 時間: 2025-3-31 18:12
Alzheimer Disease, and .. Susceptibility genes such as APOE contribute to risk in a far larger number of cases. Predictive testing is available for the autosomal dominant genes, but is not recommended for risk genes as they are neither necessary nor sufficient to cause AD. Genetic testing is complicated by capacity 作者: 削減 時間: 2025-3-31 22:57
