Results 141 to 150 of about 5,242 (165)

Partial splenectomy for hereditary spherocytosis: a multi-institutional review

Journal of Pediatric Surgery, 2011
Laura Cassidy, Elisabeth T Tracy, Frederick J Rescorla   +2 more
exaly  

Hematologically important mutations: Ankyrin variants in hereditary spherocytosis

Blood Cells, Molecules, and Diseases, 2005
Patrick Gallagher
exaly  

A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model

Intractable and Rare Diseases Research, 2015
Yazhou Cui, Jinxiang Han
exaly  

Adenosintriphosphatase activity in hereditary spherocytosis

Blut, 1967
L Mirčevová, V Brabec
exaly  

Combined ankyrin and spectrin deficiency in hereditary spherocytosis

Annals of Hematology, 1993
A Pekrun, S W Eber, Schröter W
exaly  

INCIDENCE OF HEREDITARY SPHEROCYTOSIS IN A POPULATION OF JAUNDICED NEONATES

Pediatric Hematology and Oncology, 2006
Saada Véronique, G Tchernia, Thérèse Cynober   +2 more
exaly  

Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders

International Journal of Laboratory Hematology, 2018
Isabel Badell, JOAN-LLUÍS Vives Corrons   +1 more
exaly  

Institutional experience with laparoscopic partial splenectomy for hereditary spherocytosis

Journal of Pediatric Surgery, 2010
Bethany J Slater, Sanjeev Dutta, Frandics P Chan   +2 more
exaly  

Advances in laboratory diagnosis of hereditary spherocytosis

Clinical Chemistry and Laboratory Medicine, 2017
exaly  

RED BLOOD CELL INDEXES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND β-THALASSEMIA COMBINATION

Pediatric Hematology and Oncology, 2002
Nejat Akar
exaly