Results 41 to 50 of about 6,512 (195)

Spherocytosis - 2

, 2014
This image from a peripheral blood smear demonstrates increased spherocytosis and polychromasia seen in either hereditary spherocytosis or autoimmune hemolytic anemia (AIHA)
Fraser, Marion
core   +1 more source

Spherocytosis - 4

, 2014
This image from a peripheral blood smear demonstrates increased spherocytosis and polychromasia seen in either hereditary spherocytosis or autoimmune hemolytic anemia (AIHA)
Fraser, Marion
core   +1 more source

Spherocytosis - 5

, 2018
An image from a peripheral blood smear demonstrating marked spherocytosis and polychromasia in hereditary spherocytosis (100X oil immersion).
Kwon, Gloria
core   +1 more source

Spherocytosis - 5

, 2014
A peripheral blood smear picture showing spherocytosis and polychromasia under 50X ...
Fraser, Marion
core   +1 more source

Transcriptomic signatures reveal systemic adaptations and immune modulation in response to training and competitive racing in horses

Equine Veterinary Journal, EarlyView.
Abstract Background The molecular mechanisms underlying adaptation to physical exertion and racing stress in horses remain incompletely understood. Peripheral blood transcriptomics offers a minimally invasive method to monitor systemic responses to exercise and identify biomarkers of adaptation or overload. Objectives To evaluate transcriptomic changes
Izabela Dąbrowska, Jowita Grzędzicka‐Agko, Paula Kiełbik, Michał Trela, Olga Witkowska‐Piłaszewicz   +4 more
wiley   +1 more source

Resolving a Complex Neonatal Phenotype by Rapid Trio Whole‐Genome Sequencing: A De Novo 11q14.3–q22.3 Deletion and a Splicing‐Altering Synonymous ANK1 Variant

Journal of Clinical Laboratory Analysis, EarlyView.
Clinical utility of trio WGS and time metrics in a neonate with congenital anomalies and hemolytic anemia. ABSTRACT Background Neonates with complex and evolving phenotypes often lack sufficiently specific clinical features to guide targeted genetic testing.
Hyun‐Woo Lee, Ja‐Hyun Jang, Beom Hee Lee, Hee‐Jeong Youk, Eun Sun Kim, Kee Hyun Cho, Yun Sil Chang, Heui Seung Jo, Mi‐Ae Jang   +8 more
wiley   +1 more source

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

Prenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell, Samantha Stover, Nora Gibson, Timothy Olson, James Connelly, Matthew Grace, Jennifer Andrews   +6 more
wiley   +1 more source

Bilateral macular hemorrhage in a patient with COVID-19

American Journal of Ophthalmology Case Reports, 2020
Purpose: We report a case of a patient with a known hereditary spherocytosis who developed a bilateral macular hemorrhage in concurrence with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-related respiratory syndrome.
Rossella D'Aloisio, Vincenzo Nasillo, Matteo Gironi, Rodolfo Mastropasqua   +3 more
doaj   +1 more source

Cross Sectional Study of Prenatal Diagnosis Uptake Among Individuals With Genetic Conditions

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Prenatal diagnostic genetic testing allows for early identification of significant fetal conditions and enables informed decision‐making regarding management options. The aim of this study was to assess prenatal testing practice among individuals with genetic conditions.
Ebunoluwa Ojo, Roni Zemet, Allyson Nevins, Katherine Abraham, April D. Adams   +4 more
wiley   +1 more source

Herediter spherocytosis a marosvásárhelyi gyermekhematológia osztály tapasztalatában = Hereditary spherocytosis in the experience of two pediatric clinics from Targu Mures [PDF]

, 2019
Absztrakt: Bevezetés: A herediter spherocytosis egy öröklött heterogén tünetcsoport, melyre jellemző a kis átmérőjű, gömb alakú vörösvértestek jelenléte a perifériás kenetben haemolysissel ...
Papp, Zsuzsanna Erzsébet, Adrienne Mária Horváth, Mihaela Chincesan, Kelemen, Izabella, Izabella Kelemen, Horváth, Adrienne Mária, Zsuzsanna Erzsébet Papp, Chincesan, Mihaela   +7 more
core   +1 more source