Red blood cell morphology
J Ford - International journal of laboratory hematology, 2013 - Wiley Online Library
The foundation of laboratory hematologic diagnosis is the complete blood count and review
of the peripheral smear. In patients with anemia, the peripheral smear permits interpretation …
of the peripheral smear. In patients with anemia, the peripheral smear permits interpretation …
Carrier screening for thalassemia and hemoglobinopathies in Canada
S Langlois, JC Ford, D Chitayat, VA Désilets… - Journal of obstetrics and …, 2008 - Elsevier
Objective To provide recommendations to physicians, midwives, genetic counsellors, and
clinical laboratory scientists involved in pre-conceptional or prenatal care regarding carrier …
clinical laboratory scientists involved in pre-conceptional or prenatal care regarding carrier …
Carrier testing for autosomal-recessive disorders
H Vallance, J Ford - Critical reviews in clinical laboratory sciences, 2003 - Taylor & Francis
The aim of carrier testing is to identify carrier couples at risk of having offspring with a
serious genetic (autosomal recessive) disorder. Carrier couples are offered genetic …
serious genetic (autosomal recessive) disorder. Carrier couples are offered genetic …
The role of molecular diagnostic testing for hemoglobinopathies and thalassemias
DE Sabath - International Journal of Laboratory Hematology, 2023 - Wiley Online Library
Hemoglobin disorders are among the most common genetic diseases worldwide. Molecular
diagnosis is helpful in cases where the diagnosis is uncertain and for genetic counseling …
diagnosis is helpful in cases where the diagnosis is uncertain and for genetic counseling …
Hematologic disorders and nonimmune hydrops fetalis
MO Arcasoy, PG Gallagher - Seminars in perinatology, 1995 - Elsevier
Hematologic disorders are implicated in approximately 10% to 27% of cases of nonimmune
hydrops fetalis. In almost all of these disorders, anemia leading to heart failure, edema …
hydrops fetalis. In almost all of these disorders, anemia leading to heart failure, edema …
An efficient method for generation of transgenic rats avoiding embryo manipulation
BS Pradhan, SS Majumdar - Molecular Therapy-Nucleic Acids, 2016 - cell.com
Although rats are preferred over mice as an animal model, transgenic animals are
generated predominantly using mouse embryos. There are limitations in the generation of …
generated predominantly using mouse embryos. There are limitations in the generation of …
Elevated zinc protoporphyrin associated with thalassemia trait and hemoglobin E
EA Graham, J Felgenhauer, JC Detter… - The Journal of pediatrics, 1996 - Elsevier
OBJECTIVE: Increased zinc protoporphyrin/heme (ZPP/H) ratio has been used in pediatrics
to screen for iron deficiency and lead poisoning. This study was conducted to determine …
to screen for iron deficiency and lead poisoning. This study was conducted to determine …
Binding of nitric oxide to thiols and hemes in hemoglobin H: implications for α-thalassemia and hypertension
PL Reddy, LJ Bowie, S Callistein - Clinical chemistry, 1997 - academic.oup.com
Our earlier studies suggested an association between α-thalassemia and hypertension. We
postulated that this association might involve trapping of the vasodilator nitric oxide (NO) by …
postulated that this association might involve trapping of the vasodilator nitric oxide (NO) by …
Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia
F Jiang, AP Ju, J Li, GL Chen, JY Zhou, XW Tang… - …, 2020 - Taylor & Francis
Abstract Hb Westmead (α122 (H5) His> Gln)(HBA2: c. 369C> G) is a common α-globin
variant causing α-thalassemia (α-thal) in Mainland China. In this study, we report the …
variant causing α-thalassemia (α-thal) in Mainland China. In this study, we report the …
The risk of α‐thalassaemia in offspring of β‐thalassaemia carriers in Hong Kong
YH Lam, A Ghosh, MHY Tang… - … Diagnosis: Published in …, 1997 - Wiley Online Library
Couples in whom one is heterozygous for α‐thalassaemia‐1 and the other is heterozygous
for β‐thalassaemia are assumed not to be at risk of having offspring with homozygous α …
for β‐thalassaemia are assumed not to be at risk of having offspring with homozygous α …