Results 61 to 70 of about 5,131 (199)

Spherocytosis - 1

, 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

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

Prenatal Diagnosis, Volume 46, Issue 5-6, Page 780-818, May 2026.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa, Parisa Najjariasl, Faezeh Aghajani, Enaja V. Sambatur, Andrew Rodenbarger, Stephanie Guseh, Amy E. Roberts, Alireza A. Shamshirsaz   +7 more
wiley   +1 more source

Haemolysis and cation transport in hereditary spherocytosis. [PDF]

, 1971
Inherited forms of anaemia were only generally recognized at the turn of this century and Osler's textbook of Medicine (1893) lists only chlorosis and pernicious anaemia in his section on primary or essential anaemia.
Wiley, James Saville
core  

Cryohydrocytosis: When Cold Breaks the Membrane

American Journal of Hematology, Volume 101, Issue 6, Page 1217-1219, June 2026.
Athina Ntoumaziou, Mary Risinger, Yasmin Elgammal, Wenying Zhang, Theodosia A. Kalfa, Luke R. Smart   +5 more
wiley   +1 more source

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

Pregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld, Nicole Kasatkin, Bi Liu Yu, Milen Velinov, Justin S. Brandt, Elena Ashkinadze   +5 more
wiley   +1 more source

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

Paroxysmal Nocturnal Haemoglobinuria‐Associated Acute Cutaneous Thrombosis and Haemolysis in the Setting of Parvovirus B19 and Varicella Zoster Virus Infection

eJHaem, Volume 7, Issue 2, April 2026.
ABSTRACT A 28‐year‐old male with paroxysmal nocturnal haemoglobinuria (PNH) presented with headache, nasal bridge discomfort and haemoglobinuria. He developed a macular‐papular rash which rapidly progressed into purpura, necrosis and peri‐orbital oedema. Investigations demonstrated severe haemolytic anaemia and acute parvovirus B19 infection.
Louise J. Potter, Roochi Trikha, Shreyans Gandhi, Joanne Large, Tanya N. Basu, Jeanne Boissiere, Hannah Devine, Taku Sugai, Aushna Rasool, Austin Kulasekararaj   +9 more
wiley   +1 more source

Сlinical case of hemolytic anemia combined with secondary chronic pyelonephritis and intracellular infection in a 7-year-old child

Zdorovʹe Rebenka, 2017
Hemolytic anemias are group of diseases that are characterized by decreased lifetime of erythrocytes due to their accelerated destruction caused by membrane and enzymopathies of red blood cells, defects in globin synthesis or external factors such as ...
I.G. Samoylenko, V.V. Dolinsky, M.V. Karpovich, E.N. Pavlov, E.V. Tkachenko   +4 more
doaj   +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

A Case of Hereditary Spherocytosis Initially Manifested as an Aplastic Crisis Caused by Parvovirus B19 Infection

Clinical Pediatric Hematology-Oncology, 2020
Hereditary spherocytosis (HS) is the most common inherited red cell membrane disorder. Its main laboratory finding is anemia with reticulocytosis. However, in the case of an aplastic crisis, there may be no reticulocytosis, making the diagnosis of HS ...
Hyungsuk Jin, Ji Won Lee, Hee Young Ju, Hee Won Cho, Ju Kyung Hyun, Ki Woong Sung, Hong Hoe Koo, Hee-Jin Kim, Keon Hee Yoo   +8 more
doaj   +1 more source