These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
27. [Occult hereditary spherocytosis in aplastic crisis of unknown cause]. Hansen JB; Ibsen JS; Pedersen G; Jensen S Ugeskr Laeger; 1993 Nov; 155(48):3928-30. PubMed ID: 8273201 [TBL] [Abstract][Full Text] [Related]
28. Hereditary Non-Spherocytic Hemolytic Anemia (HNSHA): Four Children with Rare Hereditary Red Cell Enzymopathies. Sivasankaran M; Reddy VK; Kumar V; Munirathnam D Indian Pediatr; 2021 Oct; 58(10):993-994. PubMed ID: 34636333 [No Abstract] [Full Text] [Related]
35. [Progress in research on red cell membrane disorders: from the genome to the postgenome era]. Yawata Y Rinsho Ketsueki; 2001 May; 42(5):343-51. PubMed ID: 11452448 [No Abstract] [Full Text] [Related]
36. Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management. Risinger M; Emberesh M; Kalfa TA Hematol Oncol Clin North Am; 2019 Jun; 33(3):373-392. PubMed ID: 31030808 [TBL] [Abstract][Full Text] [Related]
37. Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry. Vives-Corrons JL; Krishnevskaya E; Rodriguez IH; Ancochea A Int J Hematol; 2021 Feb; 113(2):163-174. PubMed ID: 33074480 [TBL] [Abstract][Full Text] [Related]
38. [Hereditary hemolytic anemias. (A review)]. Reimer EE Wien Med Wochenschr; 1972 May; 122(19):267-71. PubMed ID: 4558766 [No Abstract] [Full Text] [Related]
39. Hereditary hemolytic anemia due to erythrocyte enzyme deficiency. Miwa S Nihon Ketsueki Gakkai Zasshi; 1973 Oct; 36(5):573-61. PubMed ID: 4277504 [No Abstract] [Full Text] [Related]
40. Clinical symptoms and biochemical properties of three new glucosephosphate isomerase variants. Eber SW; Gahr M; Lakomek M; Prindull G; Schröter W Blut; 1986 Jul; 53(1):21-8. PubMed ID: 3719111 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]