Latest papers

Antiphospholipid antibodies in a family with dehydrated hereditary stomatocytosis.

Molecular basis of pyrimidine 5'-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutations.

Pediatric blood and marrow transplantation: state of the science.

[Recurrence of thromboembolic disease after splenectomy for hereditary xerocytosis].

Diagnosis and management of congenital haemolytic anaemia.

Hemoglobin Hagley Park: a novel (alpha82Ala-->Thr) substitution identified in an infant with severe hemolytic anemia.

A case of portal vein thrombosis after laparoscopy-assisted splenectomy and cholecystectomy in a child

Hemoglobin SE disease: a concise review.

Pyruvate kinase deficiency: the genotype-phenotype association.

Pyruvate kinase deficiency.

Severe hypertriglyceridemia in an infant with red cell pyruvate kinase deficiency.

[Anemia, this time without iron deficiency].

Haemolytic disease of the newborn.

Hereditary pyropoikilocytosis: a rare but potentially severe form of congenital hemolytic anemia.

The molecular basis of hereditary red cell membrane disorders.

Hb Jambol: a new hyperunstable hemoglobin causing severe hemolytic anemia.

Pyruvate kinase deficiency: Correlation between enzyme activity, extent of hemolytic anemia and protection against malaria in independent mouse mutants

Anemia and hydrops in a fetus with homozygous hemoglobin constant spring.

Hemoglobin Hammersmith [beta 42(CD1) Phe --> Ser] causing severe hemolytic anemia in a Japanese girl.

Severe conjugated hyperbilirubinaemia and neonatal haemolysis.