WordNet
- (pathology) a waxy translucent complex protein resembling starch that results from degeneration of tissue
- a non-nitrogenous food substance consisting chiefly of starch; any substance resembling starch
- any pathology of the peripheral nerves
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- 1. アミロイドーシスの概要 overview of amyloidosis
- 2. 多発性神経障害の概要 overview of polyneuropathy
- 3. 免疫グロブリン軽鎖（AL）アミロイドーシス（原発性アミロイドーシス）の臨床像、検査所見、および診断 clinical presentation laboratory manifestations and diagnosis of immunoglobulin light chain al amyloidosis primary amyloidosis
- 4. アミロイド心筋症の臨床症状および診断 clinical manifestations and diagnosis of amyloid cardiomyopathy
- 5. アミロイド疾患の遺伝的要因 genetic factors in the amyloid diseases
English Journal
- miR-15b mediates oxaliplatin-induced chronic neuropathic pain through BACE1 down-regulation.
- Ito N1,2, Sakai A1, Miyake N3, Maruyama M1,4, Iwasaki H1,2, Miyake K3, Okada T3, Sakamoto A2, Suzuki H1.
- British journal of pharmacology.Br J Pharmacol.2017 Mar;174(5):386-395. doi: 10.1111/bph.13698. Epub 2017 Jan 23.
- BACKGROUND AND PURPOSE: Although oxaliplatin is an effective anti-cancer platinum compound, it can cause painful chronic neuropathy, and its molecular mechanisms are poorly understood. MicroRNAs (miRNAs) are small non-coding RNAs that negatively regulate gene expression in a sequence-specific manner
- PMID 28012171
- Clinical measures in transthyretin familial amyloid polyneuropathy.
- Coelho T1, Vinik A2, Vinik EJ2, Tripp T3, Packman J4, Grogan DR4.
- Muscle & nerve.Muscle Nerve.2017 Mar;55(3):323-332. doi: 10.1002/mus.25257. Epub 2016 Dec 16.
- INTRODUCTION: This observational, cross-sectional, single-center study aimed to identify instruments capable of measuring disease progression in transthyretin familial amyloid polyneuropathy (TTR-FAP).METHODS: The relationship between disease stage and Neuropathy Impairment Score-Lower Limbs (NIS-LL
- PMID 27422379
- Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathy.
- Cortese A1,2, Vegezzi E3,4, Lozza A1, Alfonsi E1, Montini A1, Moglia A1,5, Merlini G6, Obici L7.
- Journal of neurology, neurosurgery, and psychiatry.J Neurol Neurosurg Psychiatry.2017 Feb 10. pii: jnnp-2016-315262. doi: 10.1136/jnnp-2016-315262. [Epub ahead of print]
- PMID 28188196
Japanese Journal
- 家族性アミロイドポリニューロパチーの1孤発例に対するタファミジスの使用経験
- 日本老年医学会雑誌 54(1), 75-80, 2017
- NAID 130005394584
- 治療につながる末梢神経病理診断
- 神経治療学 33(3), 344-348, 2016
- NAID 130005279085
- 遺伝性ATTRアミロイドーシスの治療の現状と今後の展望
- 神経治療学 33(2), 163-166, 2016
- NAID 130005256645
Related Links
- Disorders of peripheral nerves are the most common neurological complications of systemic amyloidosis; an illness where a protein called amyloid is deposited in tissues and organs. Amyloidosis can affect peripheral sensory, motor ...
- 1. Mt Sinai J Med. 2012 Nov-Dec;79(6):733-48. doi: 10.1002/msj.21352. Amyloid neuropathies. Shin SC(1), Robinson-Papp J. Author information: (1)Mount Sinai School of Medicine, New York, NY, USA. Peripheral ...
Related Pictures
★リンクテーブル★
| リンク元 | 「amyloid polyneuropathy」「アミロイド神経障害」「アミロイドニューロパチー」 |
| 拡張検索 | 「familial amyloid neuropathy」 |
| 関連記事 | 「amyloid」「neuropathy」 |
「amyloid polyneuropathy」
アミロイド・リニューロパチー、アミロイド多発ニューロパチー、アミロイド多発神経障害
「アミロイド神経障害」
「アミロイドニューロパチー」
「familial amyloid neuropathy」
「amyloid」
「neuropathy」
- 同
- NARP