Guidelines for the diagnosis and management of hereditary spherocytosis.
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Bacterial Infections Following Splenectomy for Malignant and Nonmalignant Hematologic DiseasesProfiling individual human red blood cells using common-path diffraction optical tomographyHemolytic anemia in adults: main causes and diagnostic procedures.Short- and long-term risks of splenectomy for benign haematological disorders: should we revisit the indications?Anaesthetic management of a case of hereditary spherocytosis for splenectomy and cholecystectomy.Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis.Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis.Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type IIHereditary spherocytosis: evaluation of 68 children.Traditional laboratory measures of cardiovascular risk in hereditary spherocytosisCoinheritance of hereditary spherocytosis and reversibility of cirrhosis in a young female patient with hereditary hemochromatosisLaparoscopic splenectomy: present status and future perspective.The rule of four: a systematic approach to diagnosis of common pediatric hematologic and oncologic disorders.Hereditary hemolytic anemia in Korea from 2007 to 2011: A study by the Korean Hereditary Hemolytic Anemia Working Party of the Korean Society of Hematology.A new paradigm in the diagnosis of hereditary hemolytic anemia.Hereditary red cell membrane defects: diagnostic and clinical aspects.Hemolyzed specimens: a major challenge for emergency departments and clinical laboratories.Splenectomy for hereditary spherocytosis: complete, partial or not at all?Toward the harmonization of result presentation for the eosin-5'-maleimide binding test in the diagnosis of hereditary spherocytosis.Review of the Association between Splenectomy and Chronic Thromboembolic Pulmonary Hypertension.Evaluation of red cell membrane cytoskeletal disorders using a flow cytometric method in South iran.Recommendations regarding splenectomy in hereditary hemolytic anemias.Hereditary spherocytosis in children: profile and post-splenectomy outcome.An unusual febrile nonhemolytic reaction occurred after transfusion in a thalassemia major patient with asymptomatic Plasmodium falciparum infection.Anesthetic management of a patient with hereditary spherocytosis for laparoscopic cholecystectomy and splenectomy.Stability of eosin-5'-maleimide dye used in flow cytometric analysis for red cell membrane disorders.Laparoscopic splenectomy in children with benign hematological diseases: Leaving nothing behind policy.Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study.Flow cytometric osmotic fragility testing does reflect the clinical severity of hereditary spherocytosis.Causes and consequences of 93 fetuses with cardiomegaly in a tertiary center in Thailand.Clinico-hematological profile of hereditary spherocytosis: experience from a tertiary care center in North India.Hereditary spherocytosis with pregnancy — a case report.Flow cytometric analysis of patients with hereditary spherocytosis - an Indian scenario.A Daily Dose of 5 mg Folic Acid for 90 Days Is Associated with Increased Serum Unmetabolized Folic Acid and Reduced Natural Killer Cell Cytotoxicity in Healthy Brazilian Adults.Evaluation of OSMOCELLS, a new semi-automatic device for osmotic fragility assessment.Laparoscopic splenectomy in patients with hereditary spherocytosis: report on 12 consecutive cases.An ANK1 IVS3-2A>C mutation causes exon 4 skipping in two patients from a Chinese family with hereditary spherocytosis.Laparoscopic versus robotic subtotal splenectomy in hereditary spherocytosis. Potential advantages and limits of an expensive approach.Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
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P2860
Guidelines for the diagnosis and management of hereditary spherocytosis.
description
2004 nî lūn-bûn
@nan
2004 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Guidelines for the diagnosis and management of hereditary spherocytosis.
@ast
Guidelines for the diagnosis and management of hereditary spherocytosis.
@en
Guidelines for the diagnosis and management of hereditary spherocytosis.
@nl
type
label
Guidelines for the diagnosis and management of hereditary spherocytosis.
@ast
Guidelines for the diagnosis and management of hereditary spherocytosis.
@en
Guidelines for the diagnosis and management of hereditary spherocytosis.
@nl
prefLabel
Guidelines for the diagnosis and management of hereditary spherocytosis.
@ast
Guidelines for the diagnosis and management of hereditary spherocytosis.
@en
Guidelines for the diagnosis and management of hereditary spherocytosis.
@nl
P2093
P2860
P1476
Guidelines for the diagnosis and management of hereditary spherocytosis.
@en
P2093
General Haematology Task Force of the British Committee for Standards in Haematology
P H B Bolton-Maggs
P Tittensor
R F Stevens
P2860
P304
P356
10.1111/J.1365-2141.2004.05052.X
P407
P577
2004-08-01T00:00:00Z