常染色体優性パーキソニズム
- 関
- autosomal recessive juvenile Parkinson disease、autosomal recessive juvenile parkinsonism、autosomal recessive parkinsonism、experimental parkinsonism、juvenile Parkinson disease、juvenile parkinsonism、MPTP-induced experimental parkinsonism、parkinsonian disorder、parkinsonian syndrome、parkinsonism
WordNet
- exercising influence or control; "television plays a dominant role in molding public opinion"; "the dominant partner in the marriage"
- (music) the fifth note of the diatonic scale
- (of genes) producing the same phenotype whether its allele is identical or dissimilar
- of or relating to an autosome; "autosomal gene"
PrepTutorEJDIC
- 『支配的な』,最も有力な / (位置が)群を抜いて高い,そびえ立つ / (手・目など左右のいずれかが)力のある / (遺伝で)優性の / (音階で)第5度音の,属音の / (遺伝の)優性形質 / 第5度音,属音
UpToDate Contents
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English Journal
- L-dopa co-drugs in nanostructured lipid carriers: A comparative study.
- Cortesi R1, Esposito E2, Drechsler M3, Pavoni G2, Cacciatore I4, Sguizzato M2, Di Stefano A4.
- Materials science & engineering. C, Materials for biological applications.Mater Sci Eng C Mater Biol Appl.2017 Mar 1;72:168-176. doi: 10.1016/j.msec.2016.11.060. Epub 2016 Nov 18.
- This paper describes the production and characterization of nanostructured lipid carriers (NLC) containing four different levodopa (LD) co-drugs (PD), named PDA (3,4-diacetyloxy-LD-caffeic acid co-drug), PDB (lipoic acid-dopamine co-drug), PDC (lipoic acid-3,4-diacetoxy-dopamine co-drug), and PDD (d
- PMID 28024573
- Distinct patterns of imprecise consonant articulation among Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
- Tykalova T1, Rusz J2, Klempir J3, Cmejla R1, Ruzicka E4.
- Brain and language.Brain Lang.2017 Feb;165:1-9. doi: 10.1016/j.bandl.2016.11.005. Epub 2016 Nov 25.
- Distinct speech characteristics that may aid in differentiation between Parkinson's disease (PD), progressive supranuclear palsy (PSP) and multiple system atrophy (MSA) remain tremendously under-explored. Here, the patterns and degree of consonant articulation deficits across voiced and voiceless st
- PMID 27894006
- Non-motor and Extracerebellar Features in Spinocerebellar Ataxia Type 2.
- Pedroso JL1, Braga-Neto P2,3, Escorcio-Bezerra ML2, Abrahão A2, de Albuquerque MV2, Filho FM2, de Souza PV2, de Rezende Pinto WB2, Borges FR Jr4, Saraiva-Pereira ML5, Jardim LB6, Barsottini OG2.
- Cerebellum (London, England).Cerebellum.2017 Feb;16(1):34-39. doi: 10.1007/s12311-016-0761-5.
- Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant degenerative disease. Pathological studies have demonstrated not only cerebellar and brainstem atrophy, but substantia nigra, motoneurons, basal ganglia, thalamus, and peripheral nerves involvement. These findings may explain non-motor an
- PMID 26825292
- Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria.
- Gagliardi M1, Iannello G2, Colica C3, Annesi G3, Quattrone A2.
- Neurobiology of aging.Neurobiol Aging.2017 Feb;50:169.e5-169.e6. doi: 10.1016/j.neurobiolaging.2016.10.022. Epub 2016 Oct 21.
- Parkinson's disease (PD) is the most common form of degenerative Parkinsonism with a prevalence of 1% of those older than 65 years. PD is characterized by the combination of slowness of movement (bradykinesia), muscular rigidity, resting tremor, and postural instability. Recently, using a genome-w
- PMID 27839905
Japanese Journal
- A novel A792D mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids characterized by slow progression
- パーキンソン症候群と多発ニューロパチーを呈し,<i>POLG1</i>遺伝子変異をみとめた家族性進行性外眼筋麻痺の1家系
- 家族性パーキンソニズム--PARK8パーキンソニズムを中心に
Related Links
- 1. Ann Neurol. 1992 Sep;32(3):312-20. Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration. Wszolek ZK, Pfeiffer RF, Bhatt MH, Schelper RL, Cordes M, Snow BJ, Rodnitzky RL ...
- Recently, several genes for parkinsonism have been identified. Among them, familial Parkinson's disease (PD) could be assigned for PARK disorders. PARK disorder ... Autosomal dominant Parkinsonism: its etiologies and ...
- 1. Neuron. 2004 Nov 18;44(4):601-7. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan M, Uitti RJ, Calne ...
Related Pictures
★リンクテーブル★
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- 英
- autosomal dominant parkinsonism
- 関
- パーキンソニズム、パーキンソン症候群、若年性パーキンソニズム、常染色体劣性若年性パーキンソニズム、若年性パーキンソン病、実験的パーキソニズム、常染色体劣性若年性パーキンソン病、パーキンソン病様症状、MPTP誘発実験的パーキンソニズム、常染色体劣性遺伝パーキンソニズム
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常染色体劣性若年性パーキンソニズム、常染色体劣性遺伝性若年性パーキンソニズム
- 関
- autosomal dominant parkinsonism、autosomal recessive juvenile Parkinson disease、autosomal recessive parkinsonism、experimental parkinsonism、juvenile Parkinson disease、juvenile parkinsonism、MPTP-induced experimental parkinsonism、parkinsonian disorder、parkinsonian syndrome、parkinsonism
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常染色体劣性若年性パーキンソン病、常染色体劣性若年性Parkinson病
- 関
- autosomal dominant parkinsonism、autosomal recessive juvenile parkinsonism、autosomal recessive parkinsonism、experimental parkinsonism、juvenile Parkinson disease、juvenile parkinsonism、MPTP-induced experimental parkinsonism、parkinsonian disorder、parkinsonian syndrome、parkinsonism
[★]
若年性パーキンソン病、若年性Parkinson病
- 関
- autosomal dominant parkinsonism、autosomal recessive juvenile Parkinson disease、autosomal recessive juvenile parkinsonism、autosomal recessive parkinsonism、experimental parkinsonism、juvenile parkinsonism、MPTP-induced experimental parkinsonism、parkinsonian disorder、parkinsonian syndrome、parkinsonism
[★]
常染色体劣性遺伝パーキンソニズム
- 関
- autosomal dominant parkinsonism、autosomal recessive juvenile Parkinson disease、autosomal recessive juvenile parkinsonism、experimental parkinsonism、juvenile Parkinson disease、juvenile parkinsonism、MPTP-induced experimental parkinsonism、parkinsonian disorder、parkinsonian syndrome、parkinsonism
[★]
- 優性の、優位な、顕性の、優占の、支配的な、ドミナントな
- 関
- dominance、dominantly、manifest、overt、predominance、predominant、predominantly、predominately、prevailing、superior、superiorly
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- 関
- autosomally、autosome
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パーキンソン症候群