Results 91 to 100 of about 163,169 (213)

When B12 therapy fails: two case reports of intravenous vitamin B12 resistance in pernicious anemia

open access: yesKhyber Medical University Journal
BACKGROUND: Pernicious anemia is an autoimmune disorder causing vitamin B12 deficiency resulting from impaired absorption caused by intrinsic factor absence. Positive parietal cell and intrinsic factor antibodies confirm the diagnosis.
Zeeshan Shaikh   +5 more
doaj   +1 more source

Macrocytic Anemia: A Presenting Feature of VEXAS Syndrome

open access: yesAnnals of Internal Medicine: Clinical Cases
VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndrome is an X-linked multisystem inflammatory syndrome characterized by a combination of various clinical features, including myeloid dysplasia, sweet syndrome, relapsing polychondritis,
Indira Acharya   +2 more
doaj   +1 more source

Sanjad-Sakati syndrome with macrocytic anemia and failure to thrive: a case from South Jordan

open access: yes, 2018
Backgorund: Sanjad-Sakati syndrome (SSS) is a rare autosomal recessive disease caused by a deletion mutation (155–166del) in exon 3 of the TBCE gene on chromosome 1q42-43.
Salma A. Ajarmeh, Eyad M. Al Tamimi
core   +1 more source

My tummy hurts – a case report of abdominal pain and macrocytic anemia caused by hypothyroidism

open access: yes, 2018
A 6-year-old female presented with chronic intermittent abdominal pain for 1 year. She underwent extensive investigation, imaging and invasive procedures with multiple emergency room visits.
Neha Dayalani   +3 more
core   +1 more source

Multidisciplinary approach to anemia [PDF]

open access: yesRomanian 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

open access: yesMajallah-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
doaj  

Irreversible repression of DNA synthesis in Fanconi anemia cells is alleviated by the product of a novel cyclin-related gene [PDF]

open access: yes, 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
core  

How Important is Anemia for the Clinician?

open access: yes, 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
core   +1 more source

Anaemia focusing on macrocytic anaemia

open access: yes, 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
core  

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