Disease: Anemia- hereditary spherocytic hemolytic
- 2 CASES OF PORTAL HYPERTENSION OF RARE ETIOLOGY. 1. PORTAL THROMBOSIS AFTER SPLENECTOMY FOR CONGENITAL HEMOLYTIC JAUNDICE. 2. POSSIBLE CONGENITAL ATRESIA OF THE PORTAL VEIN IN A 10-YEAR-OLD CHILD
- A Bantu case of haemolytic anaemia resembling acholuric jaundice
- A biochemical lesion in congenital, nonobstructive, non-haemolytic jaundice
- A case of acute opisthorchiasis concurrent with chronic hereditary hemolytic anemia
- A defect in microsomal function in nonhemolytic acholuric jaundice
- A familial crisis in congenital acholuric jaundice
- A new simple approach for the determination of pyrimidine 5'-nucleotidase activity in human erythrocytes using an ELISA reader
- A Novel <em>de novo</em> Mutation in <em>ANK1</em> Gene Identified through Targeted Next-Generation Sequencing in a Neonate with Hereditary Spherocytosis
- A novel <em>SPTB</em> gene mutation in neonatal hereditary spherocytosis: A case report
- A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin
- Acholuric jaundice
- Apropos of neonatal icteric form of Minkowski-Chauffard disease
- Atypical Course of Hereditary Spherocytic Anemia With Severely Elevated Liver Enzymes
- Atypical hereditary corpuscular non-spherocytic hemolytic anemia
- Case report: A follow up of a major pelvic splenosis
- Case report: congenital hemolytic icterus during pregnancy
- Choledocholithiasis during a congenital non-microspherocytic hemolytic jaundice. Problems of diagnosis and therapy
- Cholelithiasis in congenital hemolytic jaundice
- Chronic haemolytic anaemia; a report of three cases of Cooley's anaemia and five cases of acholuric jaundice seen in Malaya with a discussion on the differential diagnosis
- Chronic haemolytic icterus resembling acholuric jaundice occurring in an African native
- Chronic ulcers of the leg associated with congenital hemolytic jaundice
- Clinical aspects and therapy of congenital hemolytic jaundice
- Clinical aspects of congenital hemolytic jaundice in children
- Clinical, hematological & therapeutic aspects of hereditary hemolytic anemias, excluding Minkowski-Chauffard disease
- COEXISTENCE OF HEREDITARY SPHEROCYTIC HEMOLYTIC ANEMIA AND SICKLE-CELL TRAIT. GENERAL REVIEW OF THE CASE
- Combined forms of congenital hemolytic jaundice and pernicious anemia
- Comparative hematological and clinical studies in patients with congenital hemolytic jaundice before and after splenectomy
- Compound Heterozygosity for <em>KLF1</em> Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review
- Congenital defect of the bile ducts associated with hemolytic jaundice & congenital hip luxation
- Congenital hemolytic icterus in a Negro family
- CONGENITAL HEMOLYTIC JAUNDICE CORRECTED BY SPLENECTOMY FOLLOWED TWENTY-SIX YEARS LATER BY BLEEDING TENDENCY, HEPATOMEGALY AND SUDDEN DEATH
- Congenital hemolytic jaundice in a Negro family
- Congenital hemolytic jaundice; a case report
- Congenital hemolytic jaundice; a case report with splenectomy in father and son
- Congenital non-spherocytic hemolytic jaundice with glucose-6-phosphate dehydrogenase deficiency. 2 cases
- Consensus document for the diagnosis and treatment of pyruvate kinase deficiency
- Crises in congenital spherocytic anaemia (acholuric jaundice)
- Diagnosing dehydrated hereditary stomatocytosis due to a <em>KCNN4</em> Gardos channel mutation: understanding challenges through study of a multi-generational family
- Dysmetabolic and enzymopenic congenital hemolytic jaundice of new individualization
- Effect of elective surgery on subjective health in veterans with chronic posttraumatic stress disorder
- Effects of <em>SPTA1</em> Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis
- Ektacytometry Analysis of Post-splenectomy Red Blood Cell Properties Identifies Cell Membrane Stability Test as a Novel Biomarker of Membrane Health in Hereditary Spherocytosis
- Extraction of large fluke living in bile duct of a patient with cholelithiasis and congenital hemolytic jaundice; first Belgian case of human distomiasis caused by Fasciola hepatica
- Familial acholuric jaundice with bone changes; treated by splenectomy
- First Belgian case of distomiasis caused by Fasciola hepatica discovered during operation on a patient with cholelithiasis and congenital hemolytic jaundice
- Haemolytic icterus (acholuric jaundice) congenital and acquired
- Haemolytic icterus (acholuric jaundice) congenital and acquired
- Hematological and molecular analysis of patients with G6PD deficiency revealed coexistent hereditary spherocytosis and alpha thalassemia
- Hemochromatosis and Minkowski-Chauffard disease
- Hemolytic anemia in a big family; thirteen cases of Minkowski-Chauffard disease in one family
- Hereditary Elliptocytosis
- HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA. A STUDY OF RED-CELL CARBOHYDRATE METABOLISM IN TWELVE CASES OF PYRUVATE-KINASE DEFICIENCY
- Hereditary non-spherocytic hemolytic anemia
- Hereditary Non-Spherocytic Hemolytic Anemia (HNSHA): Four Children with Rare Hereditary Red Cell Enzymopathies
- Hereditary non-spherocytic hemolytic anemia (jaundice)
- Hereditary non-spherocytic hemolytic anemia of the pyruvate-kinase deficient type
- Hereditary spherocytosis (congenital hemolytic jaundice): pathogenesis of the hemolytic crisis
- Hereditary spherocytosis diagnosed with extremely low glycated hemoglobin compared to plasma glucose levels
- Hypoplasia of the internal carotid artery: a rare cause of cerebral ischemic stroke in children
- Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing
- Insane in the membrane: A case of hereditary spherocytic pyropoikilocytosis
- Metabolism and disposition of C14-bilirubin in congenital non-hemolytic jaundice
- Minkowski-Chauffard disease
- MINKOWSKI-CHAUFFARD DISEASE (APROPOS OF 8 CASES)
- Minkowski-Chauffard disease & gravidopuerperal state; hemolytic attack & splenectomy at the fifth month of pregnancy
- Minkowski-Chauffard disease complicated by neoplastic obstructive jaundice
- Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature
- Neonatal icteric form of Minkowski-Chauffard disease
- Neonatal jaundice as a sign of Minkowski-Chauffard disease
- Neonatal jaundice disclosing Minkowski-Chauffard disease
- Non-spherocytic hereditary hemolytic anemia, with thrombopenia. An unclassifiable case with enzymatic study
- NON-SPHEROCYTIC HEREDITARY HEMOLYTIC ANEMIA. GENERALITIES ON ITS HISTORY AND DIAGNOSTIC CONDITIONS
- Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the <em>HK1</em> gene causing severe haemolytic anaemia with developmental delay in an Indian family
- Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosis
- ON THE DIFFERENTIAL DIAGNOSIS OF HEREDITARY NON-SPHEROCYTIC HEMOLYTIC ANEMIAS
- Paterson-Plummer-Vinson Syndrome in a Case of Familial Acholuric Jaundice
- Phase Angle: Could Be an Easy Tool to Detect Low-Grade Systemic Inflammation in Adults Affected by Prader-Willi Syndrome?
- Primary carcinoma of the gall-bladder in a patient with congenital hemolytic jaundice
- Prolonged Exposure Therapy for Post-traumatic Stress Disorder
- Pyruvate kinase activator: A major breakthrough in the world of Hematology
- Pyruvate Kinase Deficiency
- Rapid Identification of Biallelic <em>SPTB</em> Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure
- Red Blood Cell Metabolism in Pyruvate Kinase Deficient Patients
- Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants
- Relations between congenital hemolytic jaundice, thalassemia, and pregnancy
- Resistant anaemia; a note on the differential diagnosis of pernicious anaemia and familial acholuric jaundice
- Skeletal age in Cooley's disease and in congenital hemolytic jaundice
- Skeletal changes in Minkowski-Chauffard congenital hemolytic jaundice
- Spherocytosis in Newborn Secondary to Novel Heterozygous Mutation in <em>SPTB</em> Gene: Case Report
- Studies in the mechanism of hemolysis in congenital hemolytic jaundice; (hereditary spherocytosis)
- STUDIES OF CONGENITAL NON-HEMOLYTIC JAUNDICE WITH C14-BILIRUBIN
- Studies on the destruction of red blood cells. IX. Quantitative methods for determining the osmotic and mechanical fragility of red cells in the peripheral blood and splenic pulp; the mechanism of increased hemolysis in hereditary spherocytosis (congenita
- Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
- TGA/Chemometric Test Is Able to Detect the Presence of a Rare Hemoglobin Variant Hb Bibba
- The influence of the spleen on the osmotic behavior and the longevity of red cells in hereditary spherocytosis (congenital hemolytic jaundice); a case study
- The mechanism of blood destruction in congenital hemolytic jaundice
- The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiency
- The variable manifestations of disease in pyruvate kinase deficiency and their management
- Utility of Cryohemolysis Test in the Diagnosis of Hereditary Spherocytosis
- When HbA1c is unreliable : a case report of hereditary spherocytosis