脊髄性筋萎縮症3型
WordNet
- write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
- a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
- (biology) the taxonomic group whose characteristics are used to define the next higher taxon
- a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
- all of the tokens of the same symbol; "the word `element contains five different types of character"
- printed characters; "small type is hard to read"
- identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
- the 19th letter of the Roman alphabet (同)s
- writing done with a typewriter (同)typewriting
PrepTutorEJDIC
- 〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ
- sulfurの化学記号 / {略}South[ern]
UpToDate Contents
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English Journal
- 15-LO/15-HETE Mediated Vascular Adventitia Fibrosis via p38 MAPK-Dependent TGF-β.
- Zhang L, Li Y, Chen M, Su X, Yi D, Lu P, Zhu D.SourceDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang Province, People's Republic of China.
- Journal of cellular physiology.J Cell Physiol.2014 Feb;229(2):245-57. doi: 10.1002/jcp.24443.
- 15-Lipoxygenase/15-hydroxyeicosatetraenoic acid (15-LO/15-HETE) is known to modulate pulmonary vascular medial hypertrophy and intimal endothelial cells migration and angiogenesis after hypoxia. However, it is unclear whether 15-HETE affects the adventitia of the pulmonary arterial wall. We performe
- PMID 23982954
- GRP78 secreted by tumor cells stimulates differentiation of bone marrow mesenchymal stem cells to cancer-associated fibroblasts.
- Peng Y, Li Z, Li Z.SourceInstitute of Biotechnology, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan 030006, China.
- Biochemical and biophysical research communications.Biochem Biophys Res Commun.2013 Nov 1;440(4):558-63. doi: 10.1016/j.bbrc.2013.09.108. Epub 2013 Oct 7.
- Cancer-associated fibroblasts (CAFs), one type of tumor-associated stromal cells, have been shown to provide a favorable environment for the malignant tumor progression. Extensive reports have demonstrated that mesenchymal stem cells (MSCs) can function as precursors for CAFs. However, the mechanism
- PMID 24113381
- Clinical and skeletal muscle biopsy characteristics of 25 patients with floppy infant syndrome.
- Bing Q, Hu J, Li N, Shen HR, Zhao Z.AbstractAims: Floppy infant syndrome (FIS) comprises of a group of disorders with a common symptom of generalized hypotonia at birth or in early life, which causes diagnostic challenge. In the current work, we aimed to describe the clinical and histopathological characteristics of FIS to help improve the diagnosis of this condition. Methods: We collected information on the clinical characteristics, laboratory data, electrophysiological test results and detailed skeletal muscle biopsy histopathological features of 25 infants with FIS. We then discussed the final diagnoses and analyzed the neuromuscular features. Results: Among the 25 infants with FIS, there were 7 cases of spinal muscular atrophy (SMA), 4 cases of congenital muscular dystrophy (CMD) (3 cases of merosin-deficient CMD and 1 case of Ullrich CMD), 8 cases of congenital myopathy (2 cases of central core disease, 1 case each of nemaline myopathy and centronuclear myopathy, and 4 cases of congenital fiber-type disproportion), and 6 cases of metabolic myopathy (3 cases of lipid storage myopathy, 2 cases of Pompe's disease, and 1 case of Leigh's syndrome). The histopathological characteristics of muscle biopsy were found to be distinct for these subgroups. Conclusions: FIS is caused by a variety of neuromuscular disorders that have common clinical manifestations, including SMA, CMD, congenital myopathies and metabolic myopathies. Skeletal muscle biopsy is an essential tool for the definite and differential diagnoses of FIS, especially of neuromuscular origin.
- Clinical neuropathology.Clin Neuropathol.2013 November/December;32(6):471-479.
- Aims: Floppy infant syndrome (FIS) comprises of a group of disorders with a common symptom of generalized hypotonia at birth or in early life, which causes diagnostic challenge. In the current work, we aimed to describe the clinical and histopathological characteristics of FIS to help improve the di
- PMID 23743156
Japanese Journal
- 伊藤 万由里,斎藤 加代子,大澤 眞木子,ITO Mayuri,SAITO Kayoko,OSAWA Makiko
- 東京女子医科大学雑誌 83(E1), E52-E57, 2013-01-31
- … SMA)の臨床調査の結果を分析した.特定疾患治療研究事業の対象疾患への認定を目標として,全国の医療機関を対象に,郵送によるアンケート調査を施行した.回収率は34%であった.各施設から報告された患者総数は455例で,診療科別には,小児科365例,内科81例,整形外科5例,不明が4例であった.この結果から概算すると,通院中の推計患者数は741?1391人で,100,000人当たり0.5?1人となった.臨床調査の項目別アンケートの返信があった110 …
- NAID 110009559422
- Comparison of Test Methods for Detecting Metallo-β-Lactamase-Producing Gram-Negative Bacteria
- Hattori Tatsuya,Kawamura Kumiko,Arakawa Yoshichika
- Japanese Journal of Infectious Diseases 66(6), 512-518, 2013
- … Sodium mercaptoacetic acid (SMA) and EDTA were used as inhibitors for a double-disk synergy test (DDST), and antimicrobial agents, including ceftazidime (CAZ), imipenem, and meropenem (MEPM), along with the distance between the disks, were compared. … Among the six methods compared, DDST using the SMA disk showed the highest sensitivity (Se) and specificity (Sp). … A combination of CAZ and SMA successfully detected only MBL-producing isolates (Se, 87.5%; …
- NAID 130003390331
- 吉澤 真裕子,尾藤 利憲,椛島 利江子,吉木 竜太郎,中村 元信,戸倉 新樹
- Skin Cancer 27(3), 318-321, 2013
- … 再切除時の病理組織検査で，紡錘形の腫瘍細胞が密に錯綜して増殖する像がみられ，免疫組織化学的検討でdesmin，αSMAが陽性，CD34陰性であったことより皮膚平滑筋肉腫の診断に至った。 …
- NAID 130003378144
Related Links
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★リンクテーブル★
[★]
- 英
- spinal muscular atrophy, SMA
- 同？
- 脊髄進行性筋萎縮症 progressive spinal muscular atrophy
- 関
- 筋萎縮、運動ニューロン疾患, motor neuron disease, MND
運動ニューロン病
- BET.439
- 上位運動ニューロン and/or 下位運動ニューロンが選択的に傷害される疾患の総称
遺伝形式
原因遺伝子
症状
- 下位運動ニューロンの脱落・変性
- 近位筋優位の筋萎縮 ← 神経原性の筋萎縮なのに・・・ (cf. 筋萎縮)
参考
uptodate
- 1. [charged] 脊髄性筋萎縮症 - uptodate [1]
OMIM
- 1. SPINAL MUSCULAR ATROPHY, TYPE I; SMA1, Gene map locus 5q12.2-q13.3
- http://omim.org/entry/253300
- 2. SPINAL MUSCULAR ATROPHY, TYPE II; SMA2, Gene map locus 5q12.2-q13.3
- http://omim.org/entry/253550
- 3. SPINAL MUSCULAR ATROPHY, TYPE III; SMA3, Gene map locus 5q12.2-q13.3, 5q12.2-q13.3
- http://omim.org/entry/253400
- 4. SPINAL MUSCULAR ATROPHY, TYPE IV; SMA4, Gene map locus 5q12.2-q13.3
- http://omim.org/entry/271150
[★]
- 英
- motor neuron disease, MND
- 関
- 筋萎縮
運動ニューロン病(BET.439)
- 上位運動ニューロン and/or 下位運動ニューロンが選択的に傷害される疾患の総称
[★]
- (windows)ファイル内容表示(linux -> cat])
- ex. type report_20111118.jp.htm | php a.php > report_20111118.jp.jp.jp.html
- 関
- form、mode、pattern、type specimen、typed
[★]
[★]
[★]
- 関
- form、mode、pattern、type
[★]