نتایج جستجو برای: hemoglobin hb

تعداد نتایج: 66164  

2016
Keith Quirolo Elliott Vichinsky

Each year, an estimated 300,000 infants are born with either of the two most common hemoglobinopathies: the sickle cell diseases or the thalassemias. These inherited diseases are the most prevalent monogenetic disorders worldwide. Sickle cell disease makes up 85% of the total infants, and thalassemias the remaining 15%. It is increasingly apparent that sickle cell disease and thalassemia have b...

Journal: :Analytical chemistry 2000
C L Gatlin J K Eng S T Cross J C Detter J R Yates

Amino acid sequence variations resulting from single-nucleotide polymorphisms (SNPs) were identified using a novel mass spectrometric method. This method obtains 99+% protein sequence coverage for human hemoglobin in a single LC-microspray tandem mass spectrometry (microLC-MS/MS) experiment. Tandem mass spectrometry data was analyzed using a modified version of the computer program SEQUEST to i...

2016
F. B. Lepira E. K. Sumaili P. K. Kayembe N. M. Nseka

Objective: To assess the relationship between SCT, hemoglobin levels and anemia in CKD black patients. Method: A post-hoc analysis of data from 188 patients, enrolled in a cross-sectional study of sickle cell trait (SCT) and chronic kidney disease (CKD), was performed to assess the relationship between SCT, hemoglobin (Hb) levels and anemia defined as Hb < 12 g/dl in men and <11 g/dl in women. ...

2005
A. M. Dozy B. E. HORTON

By T. H. J. HUISMAN, A. M. Dozy, B. E. HORTON AND J. B. WILsON T HE EXISTENCE of variants of normal human fetal hemoglobin ( HbFor a2y2 ) has been suggested in different reports in the literature. Variants of fetal hemoglobin with abnormal a-polypeptide chains have been described5 ”5 and some are well characterized.’0 Only one abnormality, namely the electrophoretically fast moving hemoglobin v...

Journal: :The Southeast Asian journal of tropical medicine and public health 2003
Pimlak Charoenkwan Pattra Thanarattanakorn Siriporn Chaovaluksakul Somjai Sittipreechacharn Rattika Sae-Tang Torpong Sanguansermsri

We report a case of beta-thalassemia/Hb Tak compound heterozygote. The 7 year-old Thai boy presented with plethora since birth. Hemoglobin electrophoresis showed a major band between Hb A2 and Hb F and absent Hb A. DNA sequencing study demonstrated an AC insertion at the terminal codon of the beta-globin gene. The clinical feature of polycythemia reflected a high oxygen affinity of Hb Tak.

Journal: :nephro-urology monthly 0
mohammad mahdi sagheb shiraz nephrourology research center, shiraz university of medical sciences, shiraz, ir iran mohammad amin fallahzadeh shiraz nephrourology research center, shiraz university of medical sciences, shiraz, ir iran; shiraz nephrourology research center, shiraz university of medical sciences, zand avenue, shiraz, ir iran. tel: +98-7136466976, fax: +98-71 36474298 alireza moaref department of cardiology, shiraz university of medical sciences, shiraz, ir iran mohammad hossein fallahzadeh shiraz nephrourology research center, shiraz university of medical sciences, shiraz, ir iran banafshe dormanesh department of pediatrics, aja university of medical sciences, tehran, ir iran

patients and methods in this cross-sectional study, the hemoglobin levels of 52 patients with end-stage renal disease were measured before and after hemodialysis. the required erythropoietin doses and the differences in cost were calculated based on the hemoglobin levels before and after hemodialysis. a model to predict the adjusted erythropoietin dosages based on post-hemodialysis hemoglobin l...

2016
Yasemin Işık Balcı Şule Ünal Fatma Gümrük

Conflict of Interest: The authors of this paper have no conflicts of interest, including specific financial interests, relationships, and/or affiliations relevant to the subject matter or materials included. References 1. Harteveld CL, Higgs DR. Alpha-thalassaemia. Orphanet J Rare Dis 2010;5:13. 2. Blackwell RQ, Jim RT, Tan TG, Weng MI, Liu CS, Wang CL. Hemoglobin G Waimanalo: alpha-64 Asp lead...

Journal: :Medical Principles and Practice 2008

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Benjamin P Luchsinger Eric N Rich Andrew J Gow Elizabeth M Williams Jonathan S Stamler David J Singel

Previous studies of the interactions of NO with human hemoglobin have implied the predominance of reaction channels that alternatively eliminate NO by converting it to nitrate, or tightly complex it on the alpha subunit ferrous hemes. Both channels could effectively quench NO bioactivity. More recent work has raised the idea that NO groups can efficiently transfer from the hemes to cysteine thi...

Journal: :Sao Paulo medical journal = Revista paulista de medicina 1999
J Rosenblit C R Abreu L N Szterling J M Kutner N Hamerschlak P Frutuoso T R Paiva O C Ferreira

CONTEXT The hemoglobin (Hb) level is the most-used parameter for screening blood donors for the presence of anemia, one of the most-used methods for measuring Hb levels is based on photometric detection of cyanmetahemoglobin, as an alternative to this technology, HemoCue has developed a photometric method based on the determination of azide metahemoglobin. OBJECTIVE To evaluate the performanc...

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