Results 121 to 130 of about 163,269 (195)

A Case Report Highlighting the Significance of COVID-19 Unveiling Megaloblastic Anemia and Worsening Dementia in the Elderly. [PDF]

Cureus
Reddy P, Devarakonda PK, Gotlieb G, Moreno P.   +3 more
europepmc   +1 more source

Thiamine responsive megaloblastic Anemia and deafness: A rare case of Roger's syndrome with successful hearing rehabilitation by cochlear implantation. [PDF]

J Otol
Marfatia H, Sahai A, Narkhede K, Sharma M.   +3 more
europepmc   +1 more source

Megaloblastic anemia and bilateral disc edema: An enigma… Have we figured it out yet? [PDF]

Taiwan J Ophthalmol, 2020
Sethi HS, Naik M, Gandhi A.
europepmc   +1 more source

A Case Report and Literature Review on Dietary Practices and Megaloblastic Anemia in a Young Female: Unraveling the Impact of Nutrition on Hematological Health. [PDF]

Cureus
Dhande D, Dhok A, Anjankar A, Nagpure S.
europepmc   +1 more source

Modern Understanding OF the Role OF Immune Factors in the Development OF Megaloblastic Anemia: Literature Review

Megaloblastic anemia is a hematological disorder characterized by impaired DNA synthesis in erythroid precursor cells, leading to the formation of abnormally large but functionally deficient red blood cells. One of the primary causes of this condition is
Kurbonova, Z. C. (Zumrad), Babadzhanova, S. A. (Shaira), Ziyamutdinova, Z. K. (Zukhra), Abdullaeva, N. K. (Nozima)   +3 more
core  

[Pseudonormal Vit B(12) megaloblastic anemia misdiagnosed as Coombs-negative AIHA: a case report]. [PDF]

Zhonghua Xue Ye Xue Za Zhi
Zhu BC, Jiang XY, Zhang Y, Chen M, Wang W.   +4 more
europepmc   +1 more source

Thiamine-Responsive Megaloblastic Anemia Syndrome Mimicking Myelodysplastic Neoplasm.

Acta Haematol
Klötzer C, Schnabel F, Kubasch AS, Jentzsch M, Franke GN, Uhlig J, Faust H, Jauss RT, Oppermann H, Popp D, Metzeler KH, Lemke JR, Vučinić V, Platzbecker U.   +13 more
europepmc   +1 more source

Behind the Skin: A Rare Case of Scurvy-Associated Megaloblastic Anemia. [PDF]

Clin Med Insights Case Rep, 2019
Alhatem A, Cai D.
europepmc   +1 more source

A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia.

Blood, 2020
Svaton M, Skvarova Kramarzova K, Kanderova V, Mancikova A, Smisek P, Jesina P, Krijt J, Stiburkova B, Dobrovolny R, Sokolova J, Bakardjieva-Mihaylova V, Vodickova E, Rackova M, Stuchly J, Kalina T, Stary J, Trka J, Fronkova E, Kozich V.   +18 more
europepmc   +1 more source

Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine-responsive megaloblastic anemia in an Egyptian family. [PDF]

Mol Genet Genomic Med, 2019
Amr K, Pawlikowska P, Aoufouchi S, Rosselli F, El-Kamah G.   +4 more
europepmc   +1 more source