Results 101 to 110 of about 163,193 (205)
Multidisciplinary approach to anemia [PDF]
Romanian Journal of Military Medicine, 2015 Introduction: We present the case of a 65 years- old woman who was admitted with a severe macrocytic anemia Hb= 5.7g/dl and diffuse bone pain. Biologically she has moderate thrombocytopenia 35 000/µl, a hepatic cytolysis and cholestatic syndrome ...
Anca Ghiațău +4 more
doaj
Thiamine– Responsive Megaloblastic Anemia Syndrome
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2009 Thiamine Responsive megaloblastic anemia in DIDMOA (Wolfram) syndrome has an autosomal- recessive mode of inheritance . Megaloblastic anemia and sideroblastic anemia is accompanied by diabetes insipidus (DI), diabetes mellitus (DM) ,optic atrophy (OA ...
F Motavaselian +5 more
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Irreversible repression of DNA synthesis in Fanconi anemia cells is alleviated by the product of a novel cyclin-related gene [PDF]
, 1995 Primary fibroblasts from patients with the genetic disease Fanconi anemia, which are hypersensitive to cross-linking agents, were used to screen a cDNA library for sequences involved in their abnormal cellular response to a cross-linking challenge.
Digweed, M. +5 more
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How Important is Anemia for the Clinician?
, 2010 Anemia is defined as an insufficient red blood cell mass to adequately deliver oxygen to peripheral tissues. It is the most common problem in the community.
Turgut, Burhan
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Anaemia focusing on macrocytic anaemia
, 2016 The content of my thesis are macrocytic anaemia. I deal with overall issues of anaemia because it is a widespread disease. According to MCV, I divided individual anaemia into microcytic, normocytic and macrocytic.
ŠŤASTNÁ, Edita
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Severe Macrocytic Anemia Uncovering Pernicious Anemia and Early-Stage Gastric Adenocarcinoma: A Case Report. [PDF]
CureusHlupeni A +4 more
europepmc +1 more source
Machine learning models in predictive factors for megaloblastic character of macrocytic anemia. [PDF]
Leuk Res RepKechida M +9 more
europepmc +1 more source
A new disorder to keep in mind: VEXAS syndrome
Revista da Sociedade Portuguesa de Dermatologia e VenereologiaThe VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic), which has recently been described, is a monogenic autoinflammatory syndrome that primarily affects males and has its onset in adulthood.
Egídio Freitas +4 more
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A Case of Cobalamin Deficiency and Macrocytic Anemia Secondary to Sunitinib. [PDF]
Cureus, 2019 Reed JP, Chung J, Banerjee N.
europepmc +1 more source