Results 71 to 80 of about 174,985 (199)

Megaloblastic Anemia with Malabsorption

, 2002
megaloblastic anemia with ...
Lawrence, Christine
core  

Elevated Hemoglobin A2: A Molecular Revisited, and Implications to β‐Thalassemia Screening

Journal of Clinical Laboratory Analysis, Volume 40, Issue 15, August 2026.
In Thailand, the Hb A2 cut‐off value for β‐thalassemia carrier has been changed from 4.0% to 3.6% since 2015. We examined the molecular basis of β‐thalassemia in a large cohort of Thai subjects with this change. The molecular basis of β‐thalassemia was updated, and a change in the Hb A2 cut‐off can alter this spectrum.
Kritsada Singha, Anupong Pansuwan, Hataichanok Srivorakun, Attawut Chaibunruang, Supawadee Yamsri, Wanicha Tepakhan, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen   +8 more
wiley   +1 more source

Megaloblastic and Iron Deficiency Anemia

, 2002
Megaloblastic and moderate iron deficiency anemia ...
Lawrence, Christine
core  

A Novel Mutation of SLC19A2 in a Chinese Zhuang Ethnic Family with Thiamine-Responsive Megaloblastic Anemia

Cellular Physiology and Biochemistry, 2018
Background/Aims: Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder resulting from mutations in SLC19A2, and is mainly characterized by megaloblastic anemia, diabetes, and progressive sensorineural hearing loss ...
Xiaoying Xian, Lin Liao, Wei Shu, Hongtao Li, Yuanyuan Qin, Jie Yan, Jianming Luo, Fa-Quan Lin   +7 more
doaj   +1 more source

Haematological and histopathological monitoring of monosodium glutamate–supplemented feeding in rainbow trout (Oncorhynchus mykiss): A possible modelling for a single health approach

Journal of Fish Biology, Volume 109, Issue 2, Page 839-848, August 2026.
Abstract The aim of this study was to investigate the potential effects of monosodium glutamate (MSG), a known flavour enhancer added to many ready‐to‐eat foods, as a feed additive in rainbow trout (Oncorhynchus mykiss). Evaluating the effects of MSG on aquatic organisms will fill the knowledge gap in this field by monitoring the haematological indices
Gonca Alak, Furkan Bedir, Aslı Çilingir Yeltekin, Serkan Yıldırım, Eylül Ecrin Ekiz, Nisa Gül Yiğit, Esat Mahmut Kocaman, Metin Kiliçlioğlu, Tuba Akbey, Elif Zeynep Özçelik, Koray Koşar, Muhammet Alaeddin Ekiz, Arzu Ucar, Ahmet Atmaca, Melihat Pilgi, Veysel Parlak, Muhammed Atamanalp   +16 more
wiley   +1 more source

Anemia megaloblástica aguda por inalação de óxido nitroso em doente com patologia autoimune múltipla.

Acta Médica Portuguesa, 2000
Although megaloblastic anemias are generally regarded as chronic conditions of insidious appearance, a megaloblastic state can arise over the course of only a few days due to acute folate or vitamin B12 deficiency.
L Barbosa, I Leal, A T Timóteo, T Matias   +3 more
doaj   +1 more source

Arrhythmia in thiamine responsive megaloblastic anemia syndrome [PDF]

, 2018
Thiamine responsive megaloblastic anemia syndrome (TRMAS) is a rare, autosomal recessive disorder characterized by megaloblastic anemia, diabetes mellitus, and progressive sensorineural deafness.
Argun, Mustafa, Mustafa Argun, Nihal Hatipoğlu, BAYKAN, Ali, Nazmi Narin, Sahin, Yavuz, HATİPOĞLU, Nihal, NARİN, Nazmi, AKIN, Leyla, Yavuz Şahin, Kurtoglu, Selim, Ali Baykan, Leyla Akın, Selim Kurtoğlu   +13 more
core   +1 more source

Megaloblastic anemia at the Mohamed VI University Hospital of Marrakech: About 132 cases

, 2023
Megaloblastic anemia is a common form of anemia that may be related to a vitamin B12 or B9 deficiency. It results from an abnormality of DNA synthesis and is diagnosed on the myelogram by a cellular gigantism of the medullary erythroblasts called ...
F-Z Rahali, S Rouhi, M Tarmidi, W Quiddi, F Bounani, I Ouahidi, S Sayagh   +6 more
core   +1 more source

Thiamine-Responsive Megaloblastic Anemia Syndrome: Long Term Follow-Up

, 2009
Thiamine-responsive megaloblastic anemia is a rare autosomal recessive disorder whose main symptoms are anemia, diabetes mellitus, and sensorineural deafness.
BORGNA, Caterina, S. Pedretti, AZZALLI, Milena, Stefania Pedretti, Caterina Borgna-Pignatti, Milena Azzalli   +5 more
core   +1 more source

Clinical and cytogenetic analysis of human anemias from Jammu region of Jammu and Kashmir state

Asian Journal of Transfusion Science, 2010
Background : Anemias are the blood disorders characterized by reduction in the number of circulating red blood cells, the amount of hemoglobin, or the volume of packed red cells in blood.
Upma, Kumar Parvinder, Raina T, Sharma Kuldeep, Gupta Subash   +4 more
doaj