WordNet

readily reacting or replying to people or events or stimuli; showing emotion; "children are often the quickest and most responsive members of the audience"
containing or using responses; alternating; "responsive reading"; "antiphonal laughter" (同)antiphonal
a deficiency of red blood cells (同)anaemia
a lack of vitality (同)anaemia
abnormally large red blood cell present in pernicious anemia and folic acid deficiency
of or relating to megaloblasts
genus of terrestrial or lithophytic ferns having pinnatifid fronds; chiefly of tropical America (同)genus Anemia

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1. 大赤血球症 macrocytosis
2. 小児の栄養障害と関連した微量栄養素欠乏 micronutrient deficiencies associated with malnutrition in children
3. 鉄芽球性貧血の臨床的側面、診断、および治療 clinical aspects diagnosis and treatment of the sideroblastic anemias
4. 小児における後天性末梢性ニューロパチーの概要 overview of acquired peripheral neuropathies in children
5. 先天性および後天性鉄芽球性貧血の原因 causes of congenital and acquired sideroblastic anemias

Thiamine responsive megaloblastic anemia syndrome: a novel homozygous SLC19A2 gene mutation identified.

Mikstiene V1, Songailiene J1, Byckova J2, Rutkauskiene G3, Jasinskiene E4, Verkauskiene R4, Lesinskas E2, Utkus A1.
American journal of medical genetics. Part A.Am J Med Genet A.2015 Jul;167(7):1605-9. doi: 10.1002/ajmg.a.37015. Epub 2015 Feb 23.
Thiamine responsive megaloblastic anemia syndrome (TRMAS) is a rare autosomal recessive disorder especially in countries where consanguinity is uncommon. Three main features are characteristic of the disease - megaloblastic anemia, early onset deafness, and non-type I diabetes. TRMAS is a Mendelian
PMID 25707023

Fundus autofluorescence and optical coherence tomography findings in thiamine responsive megaloblastic anemia.

Ach T1, Kardorff R, Rohrschneider K.
Retinal cases & brief reports.Retin Cases Brief Rep.2015 Spring;9(2):114-6. doi: 10.1097/ICB.0000000000000106.
BACKGROUND: To report ophthalmologic fundus autofluorescence and spectral domain optical coherence tomography findings in a patient with thiamine responsive megaloblastic anemia (TRMA).METHODS: A 13-year-old girl with genetically proven TRMA was ophthalmologically (visual acuity, funduscopy, perimet
PMID 25383846

Angelousi A1, Larger E2.
Diabetes & metabolism.Diabetes Metab.2015 Feb;41(1):18-27. doi: 10.1016/j.diabet.2014.06.001. Epub 2014 Jul 17.
Anaemia in patients with diabetes, both type 1 and type 2, is a frequent clinical finding. The mechanisms of anaemia are multifactorial and often not very well understood. Iatrogenic causes, including oral antidiabetic drugs, ACE inhibitors and ARBs, and renal insufficiency are the major causes of a
PMID 25043174