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Publications by Xiqiang Dang
Genetic Diagnosis and Pathogenic Analysis of an Atypical Hereditary Spherocytosis Combined With UGT1A1 Partial Deficiency: A Case Report
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Related publications
Partial Splenic Embolization in a Child With Hereditary Spherocytosis
European Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Blood Cell Parameters for Screening and Diagnosis of Hereditary Spherocytosis
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Ascertaining Genetic Carriers of Hereditary Spherocytosis by Statistical Analysis of Multiple Laboratory Tests*
Journal of Clinical Investigation
Medicine
Open-Heart Surgery Using a Centrifugal Pump: A Case of Hereditary Spherocytosis
Journal of Cardiothoracic Surgery
Cardiology
Cardiovascular Medicine
Medicine
Pulmonary
Respiratory Medicine
Surgery
Anaesthetic Management of a Case of Hereditary Spherocytosis for Splenectomy and Cholecystectomy.
Journal of Evolution of Medical and Dental Sciences
Hereditary Spherocytosis; New Guidelines
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Combined Dystonia With Self-Mutilation in PTPS Deficiency: A Case Report
Movement Disorders Clinical Practice
Neurology
Woman Presenting With Chronic Iron Deficiency Anemia Associated With Hereditary Hemorrhagic Telangiectasia: A Case Report
Drug, Healthcare and Patient Safety
Health Policy
Pharmacology
Recombinant Erythropoietin in Infants With Hereditary Spherocytosis
Pediatric Research
Child Health
Pediatrics
Perinatology