Results 61 to 70 of about 296,651 (276)

The emerging roles of ribosome biogenesis in craniofacial development. [PDF]

, 2014
Neural crest cells (NCCs) are a transient, migratory cell population, which originates during neurulation at the neural folds and contributes to the majority of tissues, including the mesenchymal structures of the craniofacial skeleton.
Ross, Adam P, Zarbalis, Konstantinos S
core   +2 more sources

Evaluation of mean corpuscular volume among anemic people with HIV in North America following ART initiation

AIDS Research and Therapy
Background Anemia is common and associated with increased morbidity among people with HIV (PWH). Classification of anemia using the mean corpuscular volume (MCV) can help investigate the underlying causative factors of anemia.
Raynell Lang, Sally B. Coburn, M. John Gill, Amy C. Justice, Jennifer Grossman, Kelly A. Gebo, Michael A. Horberg, Angel M. Mayor, Michael J. Silverberg, Kathleen A. McGinnis, Brenna Hogan, Richard D. Moore, Keri N. Althoff, for the North American AIDS Cohort Collaboration on Research, Design (NA-ACCORD) of the International Epidemiologic Databases to Evaluate AIDS (IeDEA)   +13 more
doaj   +1 more source

Gastroesophageal resection and anastomosis in a dog with a caudal oesophageal leiomyoma with subsequent fluoroscopic oesophagram

Veterinary Record Case Reports, EarlyView.
Abstract This case report describes the clinical presentation, diagnostic evaluation, surgical technique and postoperative treatment of a 10‐year‐old castrated male mixed breed dog that was presented for lethargy and hyporexia with pale mucous membranes, a heart murmur and melena. Bloodwork demonstrated a regenerative anaemia, and a computed tomography
Kara Anderson, Laura Selmic, Julie Byron, Arin Cox, Hunter J. Piegols   +4 more
wiley   +1 more source

Megaloblastic Anemia in a Patient with Addison’s Disease: A Case Report [PDF]

International Journal of Hematology-Oncology and Stem Cell Research, 2010
Primary adrenal insufficiency (Addison’s disease) is due to adrenocortical disease. This study is about a 40 year old man who had been referred to a hematologist who assessed him for anemia. He  had been affected by a periodic paresthesia one month prior
Shahrbanou Keyhanian, Zahra Fotokian, Mohammad Mansour Saravi, Houman Ghoreyshi   +3 more
doaj   +1 more source

Case Report: Adenosine kinase deficiency diagnosed 10 years after liver transplantation: Novel phenotypic insights

Frontiers in Pediatrics, 2022
Adenosine kinase (ADK) deficiency is a rare inborn error of methionine and adenosine metabolism. So far, a total of 27 patients with ADK deficiency have been reported.
Patryk Lipiński, Elżbieta Ciara, Dorota Jurkiewicz, Maciej Pronicki, Elżbieta Jurkiewicz, Anna Bogdańska, Rafał Płoski, Irena Jankowska   +7 more
doaj   +1 more source

Mapping VEXAS‐associated and rare UBA1 variants in the United Kingdom: Insights from patient cohorts and the general population

British Journal of Haematology, EarlyView.
VEXAS syndrome is a late‐onset inflammatory disorder with rheumatological and haematological features. Epidemiological studies of VEXAS syndrome so far have been limited. Analysis of various UK cohorts estimates the incidence of VEXAS to be 1.51/100 000, or 171 new cases in the population of men over the age of 50 who are being investigated for myeloid
Ana Martinez Rodriguez, Leon Chang, Dorota Rowczenio, Alexandra Smith, Ebun Omoyinmi, James A. Poulter, Andrew McGregor, Sebastian Francis, Roochi Trikha, Adam Al‐Hakim, Kar Lok Kong, David G. Kent, Helen Lachmann, Austin Kulasekararaj, Catherine Cargo, Sinisa Savic   +15 more
wiley   +1 more source

Orotic Aciduria [PDF]

, 2018
Orotic acid is an intermediate found in the pathway for pyrimidine synthesis. The mitochondrial enzyme dihydroorotate dehydrogenase (DHODH) catalyzes the production of orotic acid by the conversion of the compound dihydroorotate to orotic acid.
Fonteh, Aliah L
core   +1 more source

Anemia [PDF]

, 2009
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of ...
Brill, John
core   +1 more source

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

Journal of Clinical Investigation, 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.
Vijay G. Sankaran, Vijay G. Sankaran, Jacob C. Ulirsch, Jacob C. Ulirsch, Vassili Tchaikovskii, Leif S. Ludwig, Aoi Wakabayashi, Aoi Wakabayashi, S. Kadirvel, R. C. Lindsley, Rafael Bejar, Rafael Bejar, Jiahai Shi, S. Lovitch, David F. Bishop, D. Steensma   +15 more
semanticscholar   +1 more source

Magnitude and morphological types of anemia differ by age among under five children: A facility-based study

Heliyon, 2022
Background: World Health Organization recently acknowledged the proportion of anemia attributable to iron deficiency among under-five children could be lower than the previously assumed 50%.
Anteneh Omer, Dejene Hailu, Gezahegn Nigusse, Afework Mulugeta   +3 more
doaj