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182 related items for PubMed ID: 1987968
1. Hepatosplenomegaly as the only prenatal finding in a fetus with pyruvate kinase deficiency anemia. Ghidini A, Sirtori M, Romero R, Yarkoni S, Solomon L, Hobbins JC. Am J Perinatol; 1991 Jan; 8(1):44-6. PubMed ID: 1987968 [Abstract] [Full Text] [Related]
2. [Fetal hepatosplenomegaly in the third trimester: A sign of leukemia in fetuses with Down syndrome]. Fouché C, Ramos A, Esperandieu O, Briault S, Martin JG, Desroches A. J Gynecol Obstet Biol Reprod (Paris); 2010 Dec; 39(8):667-71. PubMed ID: 20692111 [Abstract] [Full Text] [Related]
3. Elevated delta OD 450 due to transient abnormal myelopoiesis in a Down syndrome fetus with hepatosplenomegaly on ultrasound. Mancuso A, Rijhsinghani A. Prenat Diagn; 2014 Mar; 34(3):299-301. PubMed ID: 24353262 [Abstract] [Full Text] [Related]
5. Erythrocyte pyruvate kinase deficiency. A case of severe congenital hemolytic anemia. O'Connor TA, Monzon CM, Clark FI. Mo Med; 1989 Feb; 86(2):92-4. PubMed ID: 2761512 [Abstract] [Full Text] [Related]
6. Fetal hepatosplenomegaly: an isolated sonographic sign of trisomy 21 in a case of myeloproliferative disorder. Hartung J, Chaoui R, Wauer R, Bollmann R. Ultrasound Obstet Gynecol; 1998 Jun; 11(6):453-5. PubMed ID: 9674095 [Abstract] [Full Text] [Related]
9. Fetal Splenomegaly: A Review. Moreira M, Brás R, Gonçalves D, Alencoão I, Inocêncio G, Rodrigues M, Braga J. Ultrasound Q; 2018 Mar; 34(1):32-33. PubMed ID: 29194292 [Abstract] [Full Text] [Related]
10. Prenatal ultrasound findings in a fetus diagnosed with Gaucher's disease (type 2) at birth. Rowlands S, Murray H. Prenat Diagn; 1997 Aug; 17(8):765-9. PubMed ID: 9267901 [Abstract] [Full Text] [Related]
11. Pyruvate kinase deficiency in a Somali cat in Australia. Mansfield CS, Clark P. Aust Vet J; 2005 Aug; 83(8):483-5. PubMed ID: 16119420 [Abstract] [Full Text] [Related]
12. Marked splenomegaly in fetal cytomegalovirus infection: detection supported by three-dimensional power Doppler ultrasound. Chaoui R, Zodan-Marin T, Wisser J. Ultrasound Obstet Gynecol; 2002 Sep; 20(3):299-302. PubMed ID: 12230458 [Abstract] [Full Text] [Related]
13. Prenatal diagnosis of 46,XX,DER(13;21)(Q10;Q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites. Chen CP, Tsai FJ, Chern SR, Chang TY, Hsu CY, Lin HH, Wang W. Taiwan J Obstet Gynecol; 2009 Mar; 48(1):84-7. PubMed ID: 19346201 [No Abstract] [Full Text] [Related]
16. Pyruvate kinase deficiency hemolytic anemia: two successful pregnancy outcomes. Fanning J, Hinkle RS. Am J Obstet Gynecol; 1985 Oct 01; 153(3):313-4. PubMed ID: 4050899 [Abstract] [Full Text] [Related]
17. [Congenital hemolytic anemia caused by pyruvate kinase variants (PK 'Kasumi')]. Katoh O, Fujimura K, Kuramoto A, Fujii H, Miwa S, Ohya T, Kajiyama G. Rinsho Ketsueki; 1988 Mar 01; 29(3):369-74. PubMed ID: 3294473 [No Abstract] [Full Text] [Related]
18. First reported case of prenatal diagnosis for pyruvate kinase deficiency in a Chinese family. So CC, Tang M, Li CH, Ha SY, Pissard S, Chan LC. Hematology; 2011 Nov 01; 16(6):377-9. PubMed ID: 22183074 [Abstract] [Full Text] [Related]