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About 190 results

ALLMedicine™ Hemoglobin Electrophoresis Center

Research & Reviews  95 results

Comparison of methodologies to detect hemoglobinopathy carriers in a multi-ethnic sperm...
https://doi.org/10.1002/jgc4.1406
Journal of Genetic Counseling; Isley LJ, Chamberlain AK et. al.

Mar 31st, 2021 - An estimated 7% of the world's population are carriers for a hemoglobin disorder. Current guidelines recommend carrier screening by complete blood count, with follow-up hemoglobin electrophoresis or fractionation based on abnormal result or ethnic...

Acute Kidney Injury among Black Patients with Sickle Cell Trait and Sickle Cell Disease.
https://doi.org/10.2215/CJN.06960520
Clinical Journal of the American Society of Nephrology : ... Olaniran KO, Allegretti AS et. al.

Mar 2nd, 2021 - Sickle cell trait and sickle cell disease are associated with faster GFR decline compared with normal hemoglobin phenotypes. We sought to compare the AKI risk in sickle cell trait/disease to normal hemoglobin phenotypes and investigate the associa...

Hemoglobin C Trait Presenting with Bilateral Central Retinal Vein Occlusion.
https://doi.org/10.1097/ICB.0000000000001097
Retinal Cases & Brief Reports; Neuhouser AJ, Sanders RN et. al.

Nov 24th, 2020 - To report a case of bilateral sequential, CRVO in a man with newly diagnosed hemoglobin C trait. A 67-year-old man presented with a one-month history of declining visual acuity. He was diagnosed with left CRVO. Bilateral temporal retinal ischemia ...

Prenatal diagnosis of a rare β-thalassemia gene -90 (C>T) (HBB: c.-140 C>T) mutation a...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667371
Molecular Genetics & Genomic Medicine; Qian H, Huang J et. al.

Sep 4th, 2020 - Hemoglobin H (Hb H) disease can be caused by compound heterozygosity for two different mutations or from homozygotes for mutations, and conventional genetic methods may lead to misdiagnosis when Hb H disease is combined with a rare β-thalassemia. ...

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Clinicaltrials.gov  95 results

Comparison of methodologies to detect hemoglobinopathy carriers in a multi-ethnic sperm...
https://doi.org/10.1002/jgc4.1406
Journal of Genetic Counseling; Isley LJ, Chamberlain AK et. al.

Mar 31st, 2021 - An estimated 7% of the world's population are carriers for a hemoglobin disorder. Current guidelines recommend carrier screening by complete blood count, with follow-up hemoglobin electrophoresis or fractionation based on abnormal result or ethnic...

Acute Kidney Injury among Black Patients with Sickle Cell Trait and Sickle Cell Disease.
https://doi.org/10.2215/CJN.06960520
Clinical Journal of the American Society of Nephrology : ... Olaniran KO, Allegretti AS et. al.

Mar 2nd, 2021 - Sickle cell trait and sickle cell disease are associated with faster GFR decline compared with normal hemoglobin phenotypes. We sought to compare the AKI risk in sickle cell trait/disease to normal hemoglobin phenotypes and investigate the associa...

Hemoglobin C Trait Presenting with Bilateral Central Retinal Vein Occlusion.
https://doi.org/10.1097/ICB.0000000000001097
Retinal Cases & Brief Reports; Neuhouser AJ, Sanders RN et. al.

Nov 24th, 2020 - To report a case of bilateral sequential, CRVO in a man with newly diagnosed hemoglobin C trait. A 67-year-old man presented with a one-month history of declining visual acuity. He was diagnosed with left CRVO. Bilateral temporal retinal ischemia ...

Prenatal diagnosis of a rare β-thalassemia gene -90 (C>T) (HBB: c.-140 C>T) mutation a...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667371
Molecular Genetics & Genomic Medicine; Qian H, Huang J et. al.

Sep 4th, 2020 - Hemoglobin H (Hb H) disease can be caused by compound heterozygosity for two different mutations or from homozygotes for mutations, and conventional genetic methods may lead to misdiagnosis when Hb H disease is combined with a rare β-thalassemia. ...

see more →