Results 101 to 110 of about 12,229 (218)

Arrhythmia in thiamine responsive megaloblastic anemia syndrome

open access: yesThe Turkish Journal of Pediatrics, 2018
Thiamine responsive megaloblastic anemia syndrome (TRMAS) is a rare, autosomal recessive disorder characterized by megaloblastic anemia, diabetes mellitus, and progressive sensorineural deafness.
Mustafa Argun   +6 more
doaj   +1 more source

How do you evaluate macrocytosis without anemia? [PDF]

open access: yes, 2008
Start with a detailed history, paying particular attention to medications and alcohol use (strength of recommendation [SOR]: B, prospective cohort studies). Blood testing can include a peripheral smear, evaluation for vitamin deficiencies (especially B12
Hitchcock, Kristin   +2 more
core  

An interesting case of anemia [PDF]

open access: yes, 2014
Cobalamin (Vitamin B12) deficiency can result in abnormalities in all cell lines which normalize after cobalamin replacement. Moreover, Andres et al. reported hematological findings in 201 consecutive patients with vitamin B12 deficiency 2. Approximately
Chastain, Veronica   +2 more
core  

An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment. [PDF]

open access: yesItal J Pediatr, 2023
Di Candia F   +13 more
europepmc   +1 more source

Mechanism of megaloblastic anemia combined with hemolysis. [PDF]

open access: yesBioengineered, 2021
Wu Q   +5 more
europepmc   +1 more source

Flow cytometry-detected changes in megaloblastic anemia secondary to cobalamin deficiency. [PDF]

open access: yesColomb Med (Cali), 2023
Briones V   +5 more
europepmc   +1 more source

The Value of Duodenal Biopsies in the Evaluation of Megaloblastic Anemia. [PDF]

open access: yesJ Lab Physicians, 2021
Nasrin NN   +2 more
europepmc   +1 more source

Hypermucoviscous Klebsiella pneumoniae liver abscess in a previously healthy Burmese male [PDF]

open access: yes, 2014
We report the case of a 38 year-old previously healthy Burmese man who presented with abdominal pain, headache, myalgia, and back pain. He was found to have leukocytosis, transaminitis, hyperbilirubinemia, and evidence of systemic inflammation.
Katta, Natraj, Levasseur, Victoria
core  

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