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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
476 related items for PubMed ID: 10846232
41. Hemolytic anemias due to disorders of red cell membrane skeleton. Bossi D, Russo M. Mol Aspects Med; 1996 Apr; 17(2):171-88. PubMed ID: 8813717 [Abstract] [Full Text] [Related]
42. Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders. Da Costa L, Galimand J, Fenneteau O, Mohandas N. Blood Rev; 2013 Jul; 27(4):167-78. PubMed ID: 23664421 [Abstract] [Full Text] [Related]
47. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis. Agre P, Asimos A, Casella JF, McMillan C. N Engl J Med; 1986 Dec 18; 315(25):1579-83. PubMed ID: 3785322 [Abstract] [Full Text] [Related]
50. [Abnormal cation transport in erythrocyte membranes during congenital hemolytic anemia (author's transl)]. Bernard JF. Nouv Rev Fr Hematol Blood Cells; 1977 Dec 18; 18(1):117-37. PubMed ID: 142967 [Abstract] [Full Text] [Related]
51. The molecular basis of hereditary red cell membrane disorders. Delaunay J. Blood Rev; 2007 Jan 18; 21(1):1-20. PubMed ID: 16730867 [Abstract] [Full Text] [Related]
53. Disorders of red cell membrane skeleton: an overview. Palek J. Prog Clin Biol Res; 1984 Jan 18; 159():177-89. PubMed ID: 6382324 [No Abstract] [Full Text] [Related]
54. Red cell membrane skeletal defects in hereditary and acquired hemolytic anemias. Palek J, Lux SE. Semin Hematol; 1983 Jul 18; 20(3):189-224. PubMed ID: 6353590 [No Abstract] [Full Text] [Related]
55. Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis. Delaunay J, Alloisio N, Morle L, Baklouti F, Dalla Venezia N, Maillet P, Wilmotte R. Ann Genet; 1996 Jul 18; 39(4):209-21. PubMed ID: 9037349 [Abstract] [Full Text] [Related]
57. Red cell membrane protein phosphorylation in hemolytic anemias and muscular dystrophies. Tsung PK, Palek J. Muscle Nerve; 1980 Jul 18; 3(1):55-69. PubMed ID: 6246419 [Abstract] [Full Text] [Related]
58. Recent progress in research on red cell membrane disorders in Japan: pathogenesis of microspherocytosis in hereditary spherocytosis, sodium transport abnormalities in stomatocytosis, and homeo-adaptive compensatory mechanism for membrane fluidity in red cell membrane lipid abnormalities. Yawata Y. Nihon Ketsueki Gakkai Zasshi; 1983 Dec 18; 46(7):1426-40. PubMed ID: 6675403 [No Abstract] [Full Text] [Related]
59. Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis. Marík T, Kselíková M, Bíbr B, Brabec V, Lener J. Folia Haematol Int Mag Klin Morphol Blutforsch; 1983 Dec 18; 110(1):81-5. PubMed ID: 6192057 [Abstract] [Full Text] [Related]