BBB syndrome

BBB症候群

WordNet

1. the 2nd letter of the Roman alphabet (同)b
2. the blood group whose red cells carry the B antigen (同)type_B, group B
3. a pattern of symptoms indicative of some disease
4. a complex of concurrent things; "every word has a syndrome of meanings"
5. a small pellet fired from an air rifle or BB gun (同)BB shot

PrepTutorEJDIC

1. (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
2. Better Business Bureau 商務改善協会

UpToDate Contents

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• 1. ディジョージ症候群：臨床的特徴および診断 digeorge syndrome clinical features and diagnosis
• 2. 症候群をきたす免疫不全症 syndromic immunodeficiencies
• 3. 心筋梗塞後の伝導異常 conduction abnormalities after myocardial infarction
• 4. 右脚ブロック right bundle branch block
• 5. 高用量メトトレキサートの治療使用および毒性 therapeutic use and toxicity of high dose methotrexate

English Journal

• Angiogenesis in refractory depression: A possible phenotypic target to avoid the blood brain barrier.

• Yamada MK1.
• Drug discoveries & therapeutics.Drug Discov Ther.2016 Feb 19. [Epub ahead of print]
• Major depressive syndrome (so-called depression) is a common but serious mental disease that causes low mood. Most patients are treatable, mainly because of high response rates for medicines such as selective serotonin-reuptake inhibitors (SSRIs). However, there are still a considerable number of pa
• PMID 26902903

• The MID1 protein is a central player during development and in disease.

• Winter J1, Basilicata MF2, Stemmler MP3, Krauss S4.
• Frontiers in bioscience (Landmark edition).Front Biosci (Landmark Ed).2016 Jan 1;21:664-82.
• Loss-of-function mutations in the MID1 gene cause a rare monogenic disorder, Opitz BBB/G syndrome (OS), which is characterized by malformations of the ventral midline. The MID1 gene encodes the MID1 protein, which assembles a large microtubule-associated protein complex. Intensive research over the
• PMID 26709798

• Punctate and curvilinear gadolinium enhancing lesions in the brain: a practical approach.

• Taieb G1, Duran-Peña A2, de Chamfleur NM3, Moulignier A4, Thouvenot E5, Allou T6, Lacour A7, Hoang-Xuan K2, Pelletier J8, Labauge P6.
• Neuroradiology.Neuroradiology.2015 Dec 23. [Epub ahead of print]
• INTRODUCTION: Cerebral punctate and curvilinear gadolinium enhancements (PCGE) correspond to opacification of small vessel lumen or its perivascular areas in case of blood-brain barrier (BBB) disruption. We will discuss the possible causes of intra-parenchymal central nervous system PCGE.METHODS: Ou
• PMID 26700824

Japanese Journal

• Case of polyhydramnios complicated by Opitz G/BBB syndrome

• TAJIMA Hiroko,ITOH Hiroaki,MOCHIZUKI Ayako,NAKAMURA Yuki,KOBAYASHI Yukiko,HIRAI Kyuya,SUZUKI Kazunao,SUGIHARA Kazuhiro,OHISHI Akira,OHZEKI Takehiko,KANAYAMA Naohiro
• The journal of obstetrics and gynaecology research 36(4), 876-881, 2010-08-01
• NAID 10031121711

• 妊娠中に羊水過多を来した Optiz G/BBB 症候群の1例

• 大石 彰,伊東 宏晃,岩島 覚
• 日本周産期・新生児医学会雑誌 = Journal of Japan Society of Perinatal and Neonatal Medicine 45(4), 1499-1504, 2009-12-20
• NAID 10029091740

• 神経系のバリアーシステム

• 神田 隆
• 山口医学 54(1), 5-11, 2005-02-28
• … 中枢神経では血液脳関門(Blood-brain barrier, BBB), 末梢神経では血液神経関門(Blood-nerve barrier, BNB)が神経系の内外を隔てるバリアーの実体であるが, 現在ではBBB, BNBは物質交換を妨げる単なる壁ではなく, 現在では神経系に対する物質透過を選択する能動的なシステムであると考えられている.臨床的な立場からは, BBB, BNBは炎症細胞や各種液性因子が神経実質内へと侵入する際の窓口であ …
• NAID 110002774445

Related Links

• Opitz G/BBB syndrome - Genetics Home Reference

Opitz G/BBB syndrome is a genetic condition that causes several abnormalities along the midline of the body. "G/BBB" represents the first letters of the last names of the families first diagnosed with this disorder and "Opitz" is the ...

• BBB syndrome - RightDiagnosis.com - Right Diagnosis

BBB syndrome symptoms, causes, diagnosis, and treatment information for BBB syndrome (Hypertelorism with esophageal abnormality and hypospadias) with alternative diagnoses, full-text book chapters, misdiagnosis, research ...

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★リンクテーブル★

リンク元	「BBB症候群」
関連記事	「B」「BBB」「BB」「syndrome」

「BBB症候群」

　　[★]

英

BBB syndrome

関

オピッツ症候群

「B」

　　[★]

• 気管分岐部下緑
• 補体のalternative pathwayに関わる蛋白質

• Mg2+存在下でC3, B, Dが反応してC3bBbとなり、これがC3転換酵素(C3bBb)あるいはC5転換酵素(C3bBb3b)を形成する。これらはP(properdin)と結合して活性化し、それぞれC3、C5を活性化する

　 　

「BBB」

　　[★]

• 脚ブロック bundle branch block
• 血液脳関門 blood-brain barrier

　

「BB」

　　[★]

• 緩衝塩基 buffer base

　

「syndrome」

　　[★]

• n.

• 症候群