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241 related items for PubMed ID: 7730575
1. [Prenatal diagnosis of homozygous pyruvate kinase deficiency]. Afriat R, Lecolier B, Prehu MO, Sauvanet E, Bercau G, Audit I, Galacteros F. J Gynecol Obstet Biol Reprod (Paris); 1995; 24(1):81-4. PubMed ID: 7730575 [Abstract] [Full Text] [Related]
3. Coexistence of congenital red cell pyruvate kinase and band 3 deficiency. Branca R, Costa E, Rocha S, Coelho H, Quintanilha A, Cabeda JM, Santos-Silva A, Barbot J. Clin Lab Haematol; 2004 Aug; 26(4):297-300. PubMed ID: 15279669 [Abstract] [Full Text] [Related]
4. [Chronic non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency in a Costa Rican family carrying hemoglobin C disease]. Chaves M, Vives-Corrons JL, Sáenz GF, Pujades MA, Briceño J, Colomer D. Sangre (Barc); 1990 Apr; 35(2):128-33. PubMed ID: 2363093 [Abstract] [Full Text] [Related]
13. Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study. Grace RF, Bianchi P, van Beers EJ, Eber SW, Glader B, Yaish HM, Despotovic JM, Rothman JA, Sharma M, McNaull MM, Fermo E, Lezon-Geyda K, Morton DH, Neufeld EJ, Chonat S, Kollmar N, Knoll CM, Kuo K, Kwiatkowski JL, Pospíšilová D, Pastore YD, Thompson AA, Newburger PE, Ravindranath Y, Wang WC, Wlodarski MW, Wang H, Holzhauer S, Breakey VR, Kunz J, Sheth S, Rose MJ, Bradeen HA, Neu N, Guo D, Al-Sayegh H, London WB, Gallagher PG, Zanella A, Barcellini W. Blood; 2018 May 17; 131(20):2183-2192. PubMed ID: 29549173 [Abstract] [Full Text] [Related]
19. Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations. Pissard S, Max-Audit I, Skopinski L, Vasson A, Vivien P, Bimet C, Goossens M, Galacteros F, Wajcman H. Br J Haematol; 2006 Jun 17; 133(6):683-9. PubMed ID: 16704447 [Abstract] [Full Text] [Related]