WordNet
- an impairment of health or a condition of abnormal functioning
- a hemoprotein composed of globin and heme that gives red blood cells their characteristic color; function primarily to transport oxygen from the lungs to the body tissues; "fish have simpler hemoglobin than mammals" (同)haemoglobin, Hb
- caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
- the 8th letter of the Roman alphabet (同)h
PrepTutorEJDIC
- (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
- 女性の話術芸人 =diseur
- ヘモグロビン,血色素
- 病気にかかった / 病的な,不健全な(morbid)
- hydrogenの化学記号
- 鉛筆の硬度 / 《俗》heroin
UpToDate Contents
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- 1. サラセミアの臨床症状および診断 clinical manifestations and diagnosis of the thalassemias
- 2. ヘモグロビン変異の概要 introduction to hemoglobin mutations
- 3. αサラセミアの病態生理 pathophysiology of alpha thalassemia
- 4. 骨髄異形成症候群の臨床症状および診断 clinical manifestations and diagnosis of the myelodysplastic syndromes
- 5. 幼児および小児における赤血球輸血の適応 indications for red blood cell transfusion in infants and children
English Journal
- Alpha-thalassemia X-linked intellectual disability syndrome identified by whole exome sequencing in two boys with white matter changes and developmental retardation.
- Lee JS1, Lee S2, Lim BC1, Kim KJ1, Hwang YS1, Choi M3, Chae JH4.
- Gene.Gene.2015 Sep 15;569(2):318-22. doi: 10.1016/j.gene.2015.04.075. Epub 2015 Apr 30.
- Alpha-thalassemia X-linked intellectual disability (ATRX) syndrome is a genetic syndrome caused by mutation of the ATRX gene associated with chromatin remodeling. Recently, a wide spectrum of brain MRI abnormalities and clinical manifestations has been recognized. We describe two male patients with
- PMID 25936994
- Genetic Inactivation of ATRX Leads to a Decrease in the Amount of Telomeric Cohesin and Level of Telomere Transcription in Human Glioma Cells.
- Eid R1, Demattei MV1, Episkopou H2, Augé-Gouillou C3, Decottignies A2, Grandin N1, Charbonneau M4.
- Molecular and cellular biology.Mol Cell Biol.2015 Aug 15;35(16):2818-30. doi: 10.1128/MCB.01317-14. Epub 2015 Jun 8.
- Mutations in ATRX (alpha thalassemia/mental retardation syndrome X-linked), a chromatin-remodeling protein, are associated with the telomerase-independent ALT (alternative lengthening of telomeres) pathway of telomere maintenance in several types of cancer, including human gliomas. In telomerase-pos
- PMID 26055325
- Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis.
- Herbaux C1,2, Duployez N3, Badens C4, Poret N5, Gardin C6, Decamp M7, Eclache V8, Daliphard S9, Murati A10, Cony-Makhoul P11, Cheze S12, Beve B13, Lacoste C4, Prebet T10, Hunault-Berger M14, Maloisel F15, Renneville A3, Figeac M5, Stamatoullas-Bastard A16, Bastard C16, Fenaux P13, Preudhomme C3, Rose C1; GFM (Groupe Francophone des Myelodysplasies).
- American journal of hematology.Am J Hematol.2015 Aug;90(8):737-8. doi: 10.1002/ajh.24073.
- Acquired α-thalassemia myelodysplastic syndrome (MDS) (ATMDS) is an acquired syndrome characterized by a somatic point mutation or splicing defect in the ATRX gene in patients with myeloid disorders, primarily MDS. In a large MDS patient series, the incidence of ATMDS was below 0.5%. But no large s
- PMID 26017030
Japanese Journal
- 特定健診対象者における歯周疾患スクリーニングテストとメタボリックシンドロームとの関連性
- 岩崎 正則,葭原 明弘,宮崎 秀夫
- 口腔衛生学会雑誌 61(5), 573-580, 2011-10-30
- 本研究の目的は特定健診対象者における歯周疾患スクリーニングテストとメタボリックシンドロームの関連を検討することである.2009,2010年度に本調査に参加した40〜74歳,488名を本研究対象とした.唾液中の潜血反応を利用した歯周疾患スクリーニングテストを行い,対象者を陽性群,陰性群に分けた.また特定健診の結果からメタボリックシンドローム判定項目である肥満,高血圧,高血糖,および脂質異常を定義した …
- NAID 110008761935
- 四川省〓川大地震の被災地における約1年後の妊婦・授乳婦および小児の栄養状態と改善方法(<緊急特集>災害栄養-ビタミン・ミネラルから食事と健康まで-III)
- 〓 士安,董 彩霞
- ビタミン 85(10), 519-530, 2011-10-25
- … the percentages of infants and young children suffered from the respiratory-infected disease and diarrhea within recent two weeks were up to 40.4% and 30.2%, respectively. … The hemoglobin concentrations in the 4 age groups were increased to the levels of 12.7, 11.4, 16.7 and 15.7 g/L compared to the baseline, respectively. …
- NAID 110008762035
Related Links
- Deletional and nondeletional Hb H disease Hb H disease is commonly caused by a deletion removing both α-globin genes on one chromosome 16, plus a deletion removing only a single α-globin gene on the other chromosome 16 ...
- hemoglobin H disease n. An inherited disease characterized by moderate anemia and red blood cell abnormalities, with red blood cells containing Bart's hemoglobin being replaced by cells containing hemoglobin H. Hemoglobin H ...
Related Pictures
★リンクテーブル★
| リンク元 | 「αサラセミア」「ヘモグロビンH病」 |
| 関連記事 | 「disease」「H」「hemoglobin」「hemoglobin H」 |
「αサラセミア」
- 英
- alpha thalassemia, alpha-thalassemia, α thalassemia, α-thalassemia. alpha-thalassaemia
- 関
- アルファサラセミア、α地中海貧血症、ヘモグロビンH症、α-サラセミア、サラセミア、hemoglobin H disease HbH病
- ヘモグロビンα鎖グロビンの合成障害による先天性貧血
「ヘモグロビンH病」
- 英
- hemoglobin H disease
- 関
- HbH、Hb H、ヘモグロビンH。αサラセミア
「disease」
- n.
- 疾患：illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
- 特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
- something that is very wrong with people's attitudes, way of life or with society.
- 注意
「H」
「hemoglobin」