Results 61 to 70 of about 45,554 (205)

Megaloblastic Anaemia (MA)

Hematology, 2005
Megaloblastic Anaemia (MA) is caused by retarded purine and pyrimidine (notably thymidylate) synthesis. Therefore DNA does not replicate, but RNA and protein (including haemoglobin) synthesis continues leading to typical cell changes, especially in rapidly dividing tissues such as the bone marrow, testicles, gastrointestinal and bronchial epithelia ...
openaire   +2 more sources

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

An extremely rare case of Rogers syndrome or thiamine responsive megaloblastic anemia

Indian Journal of Pathology and Microbiology
Rogers syndrome is an extremely rare autosomal recessive syndrome of which only 100 cases are known worldwide. It is characterized by thiamine-responsive megaloblastic anaemia, diabetes mellitus and sensorineural deafness.
Gurpreet Kaur, Ankur Ahuja, Arijit Sen, Paresh Singhal, Renjith Verghese   +4 more
doaj   +1 more source

Phenytoin Intake in Mothers Resulting in Early Onset Infantile Tremor Syndrome in Children: A Report of Two Cases [PDF]

Journal of Clinical and Diagnostic Research
Infantile Tremor Syndrome (ITS) is a complex neurological syndrome that affects exclusively breastfed infants, typically seen between 9 to 12 months of age.
Payal Mittal, Rohan Acharya, Dinkar Yadav, Kapil Bhalla, Shuchi Bhalla   +4 more
doaj   +1 more source

Evaluating Clinical Reasoning and Diagnostic Performance of Multimodal Large Language Models in Benign Hematology—A Comparative Analysis

International Journal of Imaging Systems and Technology, Volume 36, Issue 4, July 2026.
ABSTRACT Latest multimodal LLMs, capable of analyzing textual data and images. have potential application in decision support systems in diagnostics. Their performance and clinical reasoning abilities in benign hematology remain underexplored. This study evaluates and compares diagnostic performance and clinical reasoning of 3 LLM in classification of ...
Zahra Rashid Khan, Kamran Khan, Maham Nayab, Muhammad Usman Akram, Sundas Ali, Huma Abdul Shakoor, Ayesha Haque, Meeral Ahmed   +7 more
wiley   +1 more source

A Study on Megaloblastic Anaemia and Pancytopenia

, 2019
Background: Megaloblastic Anaemia and pancytopenia are common medical problems, Vitamin B12and folic acid deficiencies are common  causes for megaloblastic Anaemia.
Reddy, P Sashikanth, Srinivas, S
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Evaluation of the Usefulness of Machine Learning and Artificial Intelligence on Hyperspectral Images in the Diagnosis of Myelodysplastic Syndrome

Journal of Biophotonics, Volume 19, Issue 7, July 2026.
Hyperspectral imaging (350–1050 nm) captures spectral information beyond the visible range from bone marrow biopsy specimens. An HSI‐based AI system using machine learning achieved up to 97% accuracy in diagnosing and classifying MDS, outperforming a previous RGB‐based study.
Yasuo Ueda, Takafumi Ogawa, Akane Wada, Genshu Tate, Yuta Baba, Tetsuya Fukuda, Toshiko Yamochi   +6 more
wiley   +1 more source

Identification of transcobalamin deficiency with two novel mutations in the TCN2 gene in a Chinese girl with abnormal immunity: a case report

BMC Pediatrics, 2020
Background Transcobalamin (TC) transports vitamin B12 from blood into cells. TC II deficiency is a rare autosomal recessive disorder. It is characterized by failure to thrive, diarrhoea, pallor, anaemia, pancytopenia or agammaglobulinemia.
Shihong Zhan, Fangfang Cheng, Hailong He, Shaoyan Hu, Xing Feng   +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

Vitamin B12 deficiency--a major cause of megaloblastic anaemia in patients attending a tertiary care hospital [PDF]

, 2009
BACKGROUND: Folate and vitamin B12 deficiencies have been known to cause megaloblastic anaemia. Since the deficiencies of these two vitamins are very common in Pakistani population, it would be imperative to investigate their role in causing ...
Iqbal, Saira Perwaiz, Kakepoto, Ghulam Nabi, Iqbal, Saleem Perwaiz   +2 more
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