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searching for Hemoglobinopathy 9 found (40 total)

alternate case: hemoglobinopathy

Hemoglobin D (3,748 words) [view diff] exact match in snippet view article find links to article

7860/JCDR/2017/27816.10114. PMC 5535424. PMID 28764232. Randolph, Tim R. (2020), "Hemoglobinopathies (structural defects in hemoglobin)", Rodak's Hematology, Elsevier
Mazandaran University of Medical Sciences (358 words) [view diff] exact match in snippet view article find links to article
Health Sciences Research in Region 1 Plant and animal products health Hemoglobinopathy Research Institute MazUMS has published 1674 scientific articles in
Spherocytosis (948 words) [view diff] exact match in snippet view article find links to article
15 November 2010. Thoma J, Kutter D, Casel S, et al. (2005). "HbSC hemoglobinopathy suspected by chest x-ray and red blood cell morphology". Acta Clin
UDP glucuronosyltransferase 1 family, polypeptide A1 (1,653 words) [view diff] exact match in snippet view article find links to article
polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients". PLOS ONE. 8 (10): e77681. Bibcode:2013PLoSO...877681A. doi:10
Pythiosis (2,007 words) [view diff] exact match in snippet view article find links to article
pre-existing medical condition, usually associated with thalassemic hemoglobinopathy. Prognosis is poor to guarded and treatments include aggressive surgical
Hemoglobin subunit alpha (1,147 words) [view diff] exact match in snippet view article find links to article
[alpha15(A13)Gly→Arg (alpha1) (GGT→CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect". Hemoglobin. 26 (1): 77–81. doi:10
NT5C3 (1,670 words) [view diff] exact match in snippet view article find links to article
linked to the conversion of hemoglobin E disease into an unstable hemoglobinopathy-like disease. NT5C3 is identical to p36, a previously identified
Newborn screening (8,018 words) [view diff] exact match in snippet view article find links to article
under the broad category of hemoglobinopathies. Worldwide, it is estimated that 7% of the population may carry a hemoglobinopathy with clinical significance
Phaedon Fessas (1,879 words) [view diff] exact match in snippet view article find links to article
that made him internationally known. His special interest were the hemoglobinopathies, with a major focus on thalassemia. He studied and described the pathological