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Annals of Surgery|December 29, 2004
Near-total splenectomy: a new technique for the management of hereditary spherocytosisGerhard A Stoehr, Urs G Stauffer, Stefan W Eber
British Journal of Haematology|August 6, 2003
Simultaneous (AC)n microsatellite polymorphism analysis and single-stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin-1 mutations in dominant hereditary spherocytosisRefik Ozcan, Petr Jarolim, Samuel E Lux, et al.
British Journal of Haematology|February 21, 2006
Immunogenicity of sequential pneumococcal vaccination in subjects splenectomised for hereditary spherocytosisGerhard A Stoehr, Markus A Rose, Stefan W Eber, et al.
British Journal of Haematology|February 21, 2006
Near-total splenectomy for hereditary spherocytosis: clinical prospects in relation to disease severityGerhard A Stoehr, Julian N Sobh, Jan Luecken, et al.
AJR. American Journal of Roentgenology|September 24, 2004
Radiographic and MRI features of deferiprone-related arthropathy of the knees in patients with beta-thalassemiaChristian J Kellenberger, Markus Schmugge, Traudel Saurenmann, et al.
Blood Advances|September 1, 2021
Health-related quality of life and fatigue in children and adults with pyruvate kinase deficiencyHanny Al-Samkari, Eduard J van Beers, D Holmes Morton, et al.
European Journal of Haematology|December 28, 2020
Comorbidities and complications in adults with pyruvate kinase deficiencyAudra N Boscoe, Yan Yan, Elizabeth Hedgeman, et al.
Pediatric Blood & Cancer|June 14, 2021
Pyruvate kinase deficiency in childrenSatheesh Chonat, Stefan W Eber, Susanne Holzhauer, et al.
The Lancet. Haematology|February 8, 2024
Diagnosis and management of pyruvate kinase deficiency: international expert guidelinesHanny Al-Samkari, Nadine Shehata, Kelly Lang-Robertson, et al.
Blood|March 18, 2018
Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History StudyRachael F Grace, Paola Bianchi, Eduard J van Beers, et al.
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