Results 271 to 280 of about 24,308 (321)

CRAO in Moyamoya Syndrome Associated With Southampton Hemoglobinopathy.

Ophthalmic Surgery Lasers and Imaging Retina, 2019
The authors present the first case of central retinal artery occlusion (CRAO) resulting from moyamoya syndrome secondary to Southampton hemoglobinopathy.
J. Ebert, Robert A. Sisk
semanticscholar   +1 more source

Hemoglobinopathies in the Sudan

Hemoglobin, 2008
In a prospective study, we evaluated hematological parameters in freshly obtained venous blood samples from 632 Sudanese patients attending the outpatient department at Khartoum Teaching Hospital, Khartoum, Sudan, in the period between March and July 2005. The patients were surveyed for full blood count (FBC) and hemoglobin (Hb) electrophoresis using a
Elderdery, A., Mohamed, B., Karsani, M., Ahmed, M., Knight, Gavin, Cooper, Alan   +5 more
openaire   +3 more sources

Hemoglobinopathies in the Neonate

NeoReviews
Hemoglobinopathies in neonates constitute a group of disorders influenced by genetic mutations in the human globin genes. They are often broadly categorized into quantitative defects or qualitative defects, though they are not mutually exclusive. In quantitative defects, the mutation causes insufficient production of a normal globin chain, which can ...
Katrina, Blankenhorn, Kaitlin, Strumph
openaire   +2 more sources

Anesthesia and Hemoglobinopathies

Anesthesiology Clinics, 2009
Hemoglobinopathies are diseases involving abnormalities of the structure or production of hemoglobin. Examples include sickle cell disease, the thalassemias, and rare hemoglobin variants producing cyanosis. Recent advances in the understanding of the consequences of hemoglobin dysfunction on nitric oxide signaling have led to a reassessment of the ...
openaire   +2 more sources

Sickle hemoglobinopathies

Current Opinion in Pediatrics, 1993
Neonatal screening for hemoglobinopathies, coupled with comprehensive medical care that includes parental education, prophylactic penicillin, and immunizations, has markedly reduced mortality from sickle hemoglobinopathies during infancy and early childhood.
openaire   +2 more sources

Successful mismatched hematopoietic stem cell transplantation for pediatric hemoglobinopathy by using ATG and post-transplant cyclophosphamide

Bone Marrow Transplantation, 2021
Lisa V. E. Oostenbrink, E. Pool, C. M. Jol-van der Zijde, A. Jansen-Hoogendijk, C. Vervat, A. V. van Halteren, R. Bredius, F. Smiers, M. V. van Tol, M. Schilham, A. Lankester, Alexander B. Mohseny   +11 more
semanticscholar   +1 more source

Hemoglobinopathies in India

Hemoglobin, 1981
Hemglobin variants, thalassemia, hereditary persistence of fetal herroglobin and compound disorders reported from India are listed in tabular form by state and population.In India, the heimglobinopathies occur in the midst of a uniqe genetic heterogeneity. The population of nearly 700 millim is divided into thousands of highly endogamus groups, many of
openaire   +2 more sources

Hemoglobinopathies in Yugoslavia

Hemoglobin, 1982
G D, Efremov, D, Juricić, N, Stojanovski   +2 more
openaire   +2 more sources

Hemoglobinopathies in Italy

Hemoglobin, 1982
M, Marinucci, G, Schilirò, G, Russo, L, Tentori   +3 more
openaire   +2 more sources

Hemoglobinopathies in Bulgaria

Hemoglobin, 1987
E S, Tasheva, S A, Toshkov, A M, Dobreva
openaire   +2 more sources