Results 1 to 10 of about 303,350 (158)

Nonlinear Relationship Between Macrocytic Anemia and Decompensated Hepatitis B Virus Associated Cirrhosis: A Population-Based Cross-Sectional Study

Frontiers in Pharmacology, 2021
Background: Mean corpuscular volume (MCV) is major used as an indicator for the differential diagnosis of anemia. Macrocytic anemia in decompensated cirrhosis is common.
Tian-Yu Zhao, Qing-Wei Cong, Fang Liu, Li-Ying Yao, Ying Zhu   +4 more
doaj   +2 more sources

Macrocytic anemia is associated with the severity of liver impairment in patients with hepatitis B virus-related decompensated cirrhosis: a retrospective cross-sectional study

BMC Gastroenterology, 2018
Background Macrocytic anemia is common in liver disease. However, its role in hepatitis B virus (HBV)-related decompensated cirrhosis remains unknown.
Jian Yang, Bin Yan, Lihong Yang, Huimin Li, Yajuan Fan, Feng Zhu, Jie Zheng, Xiancang Ma   +7 more
doaj   +2 more sources

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

Italian Journal of Pediatrics, 2023
Background Individuals with thiamine-responsive megaloblastic anemia (TRMA) mainly manifest macrocytic anemia, sensorineural deafness, ocular complications, and nonautoimmune diabetes.
Francesca Di Candia, Valentina Di Iorio, Nadia Tinto, Riccardo Bonfanti, Claudio Iovino, Francesco Maria Rosanio, Ludovica Fedi, Fernanda Iafusco, Francesca Arrigoni, Rita Malesci, Francesca Simonelli, Andrea Rigamonti, Adriana Franzese, Enza Mozzillo   +13 more
doaj   +2 more sources

Splenomegaly in a Patient with a History of Pernicious Anemia; the Potential Therapeutic Effects of B12 Therapy

Case Reports in Hematology, 2022
Splenomegaly is manifested by a variety of etiologies, one of which is macrocytic anemia. Macrocytic anemia has multiple causes in itself that include; folate (Vitamin B9) and Cobalamin (vitamin B12) deficiencies.
Alexis Lordi, Nida Ansari, Michael Maroules, Anusha Manjegowda   +3 more
doaj   +2 more sources

Hemi-Orolingual Angioedema in a Patient With VEXAS Syndrome. [PDF]

EJHaem
eJHaem, Volume 7, Issue 1, February 2026.
Suárez EU, Arquero-Portero T, Llamas-Sillero P.   +2 more
europepmc   +2 more sources

Digenic Functional B12 and Folate Defect Mimicking Myelodysplasia. [PDF]

Clin Case Rep
Proposed mechanistic model of mutation‐related outcomes. ABSTRACT A digenic defect involving CUBN and MTHFR produced functional B12/folate deficiency in a patient with pancytopenia and neurological signs, mimicking myelodysplasia. Genetic and metabolic screening revealed elevated methylmalonic acid/homocysteine, with rapid remission post‐parenteral B12.
Cluzeau T, Oussalah A, Silva Rodriguez M, Naïmi M.   +3 more
europepmc   +2 more sources

Macrocytic anemia, kidney dysfunction, and mortality in general population: Japan specific health checkup study [PDF]

Scientific Reports
Anemia and chronic kidney disease (CKD), which worsen bidirectionally, are associated with mortality in older adults. This study aimed to examine the association between CKD and the type of anemia and its impact on mortality in the general population ...
Yoichiro Otaki, Tetsu Watanabe, Tsuneo Konta, Masafumi Watanabe, Koichi Asahi, Kunihiro Yamagata, Shouichi Fujimoto, Kazuhiko Tsuruya, Ichiei Narita, Masato Kasahara, Yugo Shibagaki, Kunitoshi Iseki, Toshiki Moriyama, Masahide Kondo, Tsuyoshi Watanabe   +14 more
doaj   +2 more sources

COVID-19-Related Hematological Abnormalities Among Adults; A Cross-Sectional Study in a Resource-Limited Setting. [PDF]

Immun Inflamm Dis
ABSTRACT Background Alterations in hematological parameters in SARS‐CoV‐2 infection may contribute to disease severity and poor outcomes. This study reports the hematological profile of COVID‐19 patients. Methods This was a cross‐sectional study involving 169 confirmed COVID‐19 patients conducted at Sunyani Teaching Hospital between January and August,
Nkansah C, Osei-Boakye F, Appiah SK.
europepmc   +2 more sources

Imerslund-Gräsbeck syndrome presenting with a 12-year history of intermittent proteinuria and anemia: a case from the Middle East [PDF]

BMC Pediatrics
Background Imerslund-Gräsbeck Syndrome (IGS) is a rare autosomal recessive disorder characterized by selective cobalamin (vitamin B12) malabsorption and often accompanied by proteinuria.
Roonak Makrooni, Ramyar Rahimi Darehbagh, Avat Karimi, Borhan Moradveisi   +3 more
doaj   +2 more sources

Anemia Classification System Using Machine Learning

Informatics
In this study, a system was developed to predict anemia using blood count data and supervised learning algorithms. Anemia, a common condition characterized by low levels of red blood cells or hemoglobin, affects oxygenation and often causes symptoms ...
Jorge Gómez Gómez, Camilo Parra Urueta, Daniel Salas Álvarez, Velssy Hernández Riaño, Gustavo Ramirez-Gonzalez   +4 more
doaj   +2 more sources