Results 61 to 70 of about 8,139 (212)

Codocytosis in the Dog: 345 Cases (2020–2022)

Veterinary Clinical Pathology, EarlyView.
ABSTRACT Introduction Codocytes, or target cells, are a morphologic variation of erythrocytes characterized by increased membrane surface area relative to volume. In dogs, codocytosis is frequently noted on blood smear evaluation, but its clinical significance remains poorly understood. Objectives To characterize the clinical conditions associated with
Sarena M. Krojanker, Maria Jaramillo, Brad D. Cingolani, Floyd L. Williams Jr., Priscila B. S. Serpa, Andrew D. Woolcock   +5 more
wiley   +1 more source

Differential diagnosis of macrocytic anemias - literature review [PDF]

, 2018
Author: Zdeněk Kepka Thesis title: Differential diagnosis of macrocytic anemias - literature review Type of assignment: Bachelor's thesis Charles University, Faculty of Pharmacy in Hradec Králové Branch of study: Healthcare Laboratory Assistant (ZDLB ...
Kepka, Zdeněk
core  

X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation

, 2015
Macrocytic anemia with abnormal erythropoiesis is a common feature of megaloblastic anemias, congenital dyserythropoietic anemias, and myelodysplastic syndromes. Here, we characterized a family with multiple female individuals who have macrocytic anemia.
Ludwig, L.S., Ulirsch, J.C., Tchaikovskii, V., Shi, J., Wakabayashi, A., Lindsley, R.C., Bejar, R., Sankaran, V.G., Bishop, D.F., Lovitch, S.B., Steensma, D.P., Kadirvel, S.   +11 more
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Morphological patterns of anemia among children aged 6 to 59 months attending Maputo Central Hospital, Maputo City Province, Mozambique

, 2023
Publisher Copyright: © (2023), (European Publishing). All Rights Reserved.Background and Objective: Globally, childhood anemia is a public health concern as it leads to poor health, physical and mental growth retardations, and increased risk of morbidity
Craveiro, Isabel, Cane, Réka Maulide, Keita, Youssouf, Varandas, Luís   +3 more
core   +1 more source

Delayed Gastric Bleeding in a Patient With Chronic Myeloid Leukemia: A Case of Post‐Biopsy Bleeding

DEN Open, Volume 7, Issue 1, April 2027.
The presence of underlying conditions, particularly malignancies such as myeloproliferative disorders, may increase the risk of delayed bleeding following gastric mucosal biopsy, and similar cases warrant careful accumulation and evaluation in future. ABSTRACT A 76‐year‐old man was referred to our hospital for evaluation of anemia.
Yoko Kosaka, Hiromichi Yamane, Hidekazu Nakanishi, Nagio Takigawa   +3 more
wiley   +1 more source

Combined nutritional anemia coexisting with microcytic anemia

, 2013
Objective: Iron deficiency is a leading cause of microcytic anemia for children. On the other hand, B12 deficiency, which is a relatively rare event than iron deficiency, coexists with macrocytic anemia.
Saygi, Semra, Demirbilek, HÜSEYİN, Soker, Murat, Aliosmanoglu, Cigdem, Yildirim, Aysen Turedi   +4 more
core   +1 more source

A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome.

, 2010
The identification of the genes associated with chromosomal translocation breakpoints has fundamentally changed understanding of the molecular basis of hematological malignancies.
Lane, AL, Holmes, LR, McKenzie, AN, Barlow, J., Warren, AJ, Hewett, D., Lorenzo-Abalde, S., Pannell, R., Middleton, A., Drynan, LF, Lane, A., Boultwood, J., Lorenzo-Abalde, S, Jolin, HE, Pannell, R, Wong, S., Wainscoat, J., Holmes, L., Wong, SH, McKenzie, A., Wainscoat, JS, Boultwood, Jacqueline, Barlow, JL, Drynan, L., Middleton, AJ, Jolin, H., Boultwood, J, Hewett, DR, Warren, A.   +28 more
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Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source

Neuropathy caused by B12 deficiency in a patient with ileal tuberculosis: A case report

Journal of Medical Case Reports, 2008
Introduction Vitamin B12 deficiency can result in macrocytic anemia. Neurologic abnormalities of B12 deficiency include sensory deficits, loss of deep tendon reflexes, movement disorders, neuropsychiatric changes and seizures.
Toosi Taraneh, Shahi Farhad, Afshari Ali, Roushan Nader, Kermanshahi Marjan   +4 more
doaj   +1 more source

First Revision of the Guidelines for the Diagnosis and Management of Remethylation Disorders

Journal of Inherited Metabolic Disease, Volume 49, Issue 4, July 2026.
ABSTRACT This guideline summarizes diagnostic and therapeutic approaches based on a systematic literature review and evidence evaluation using the GRADE methodology. Given the limited high‐quality data, expert consensus was additionally obtained through a modified Delphi process.
Giorgia Olivieri, Andrea Bordugo, Birute Burnyte, Alessandro Costetti, Maria‐Luz Couce, Luisa Diogo, Francois Feillet, D. Sean Froese, Benedetta Greco, Jean‐Louis Gueant, Luciana Hannibal, Friederike Hörster, Viktor Kožich, Giancarlo La Marca, Irini Manoli, Fanny Mochel, Lorenzo Orazi, Belén Pérez, Manuel Schiff, Bernd C. Schwahn, Ida Schwartz, Karolina M. Stepien, Jolanta Sykut‐Cegielska, Trine Tangeraas, Rolf H. Zetterström, Carlo Dionisi‐Vici, Martina Huemer   +26 more
wiley   +1 more source