Congenital Spherocytosis in Infancy [PDF]
Archives of Disease in Childhood, 1958 openaire +2 more sources
, 2014 Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. It is characterized by intermittent episodes of jaundice in the absence of hepatocellular disease or hemolysis.
이재희(조선대학교); 문경래(조선대학교)
core
Curing the “Incurable”: First Successful Hematopoietic Stem Cell Transplantation in Severe Hereditary Spherocytosis with Homozygous <i>SPTA1</i> Variant and Hepatic Fibrosis [PDF]
Turk J HaematolKoçak Göl D +6 more
europepmc +1 more source
Hereditary Hemolytic Spherocytosis in the Active-Duty Population: A Unique Case. [PDF]
CureusAhn D, Berenberg J.
europepmc +1 more source
New Thoughts on Hereditary Spherocytosis
, 1970 In addition to its accentuated pattern of rigidity at decreasing ATP/Ca ratios, the hereditary spherocyte poses a special challenge within the splenic pulp because of its shape.
Weed, Robert I.
core
Comorbidity of Dengue and Hereditary Spherocytosis in an 18-Year-Old Patient: A Case Report. [PDF]
CureusBecerra-Carrillo RI +4 more
europepmc +1 more source
Pediatric laparoscopic splenectomy using a repurposed sterile diathermy pouch as a retrieval bag: preliminary experience. [PDF]
BMC SurgZain M.
europepmc +1 more source
A novel heterozygous mutation in ANK1 solves a mystery of a patient with hyperbilirubinemia and splenomegaly. [PDF]
Pak J Med SciShi Y, Ou Y, Wu H.
europepmc +1 more source
Diagnostic Utility of Next-Generation Sequencing for Unconjugated Hyperbilirubinemia in Children. [PDF]
Pediatr Gastroenterol Hepatol NutrKim HJ.
europepmc +1 more source
Correction: Identification of a novel <i>ANK1</i> gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis. [PDF]
Front GenetXiong T +6 more
europepmc +1 more source