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Journal Abstract Search
132 related items for PubMed ID: 511585
1. Hb J Baltimore (beta 16 (A13) Gly leads to Asp) in association with beta-thalassemia in a Sicilian family. Musumeci S, Schilirò G, Fisher A, Musco A, Marinucci M, Mavilio F, Fontanarosa PP, Tentori L. Hemoglobin; 1979; 3(6):459-64. PubMed ID: 511585 [No Abstract] [Full Text] [Related]
2. First association in Spain of Hb J Baltimore alpha A2 beta 2 16 (A13) Gly replaced by Asp and beta o thalassemia. Romero C, Muñoz A, Fernández Fuertes I, Hernández-Jodra M, Navarro JL. Hemoglobin; 1982; 6(6):607-12. PubMed ID: 7161107 [No Abstract] [Full Text] [Related]
3. A new alkali-resistant hemoglobin alpha2J Oxford gammaF2 in a Sicilian baby girl with homozygous beta0 thalassemia. Schiliro G, Musumeci S, Pizzarelli G, Russo A, Marinucci M, Bruni E, Russo G. Blood; 1976 Nov; 48(5):639-51. PubMed ID: 10024 [Abstract] [Full Text] [Related]
4. Association of Hb S [beta 6(A3)Glu----Val] and Hb I-interlaken [alpha 15(A13)Gly----Asp] in a Sicilian man; review of the occurrence of Hb I-interlaken in Sicily. Schiliro G, Rizzari C, Testa R, Lo Faro F, Comisi FF, Russo A. Hemoglobin; 1989 Nov; 13(4):403-10. PubMed ID: 2666359 [No Abstract] [Full Text] [Related]
5. Occurrence of Hb J Paris in an Italian family and recombination studies on the free abnormal alpha-chain. Marinucci M, Mavilio F, Tentori L, Bestetti A. Hemoglobin; 1979 Nov; 3(6):465-9. PubMed ID: 511586 [No Abstract] [Full Text] [Related]
6. Globin chain synthesis in Hb J Baltimore-beta (+)-thalassemia. Ballas SK, Atwater J, Theriault C, Kim HC, Propst M. Am J Clin Pathol; 1981 Jun; 75(6):843-6. PubMed ID: 6167160 [Abstract] [Full Text] [Related]
7. Hemoglobin J Guantanamo [alpha 2 beta 2 128 (H6) Ala----Asp] in association with hemoglobin C and alpha-thalassemia in a family from Benin. Wajcman H, Baudin-Chich V, Kister J, Feo C, Gombaud-Saintonge G, Bohn B, Marden M, Pagnier J, Poyart C, Dodé C. Am J Hematol; 1988 Jul; 28(3):170-5. PubMed ID: 2841847 [Abstract] [Full Text] [Related]
8. A case of Hb J-Camaguey or alpha 2141(HC3)Arg----Gly beta 2 in a Chinese family. Xiong F, Yang KG, Liang CC, Huang YW, Wang RX, Zhang NJ. Hemoglobin; 1984 Jul; 8(4):397-9. PubMed ID: 6480361 [No Abstract] [Full Text] [Related]
9. Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family. Musumeci S, Schilirò G, Pizzarelli G, Tentori L, Marinucci M, Fontanarosa PP, Russo G. Hum Genet; 1979 Nov; 52(2):239-47. PubMed ID: 511180 [Abstract] [Full Text] [Related]
10. Haemoglobin J Rovigo 53 alpha (E-2) aspartic acid alanin. Araujo JT, Plowman D, Araujo RA, de Souza LF, Lehmann H. Rev Bras Pesqui Med Biol; 1980 Apr; 13(1-3):37-9. PubMed ID: 7414024 [Abstract] [Full Text] [Related]
11. Hemoglobin J-Baltimore (beta 16(A13)Gly----Asp): interference with the assay of HbA1c. Vandenesch F, Baklouti F, Francina A, Vianey-Liaud C, Bertrand A, Le Dévéhat C, Delaunay J. Clin Chim Acta; 1987 Sep 30; 168(2):121-8. PubMed ID: 3677411 [Abstract] [Full Text] [Related]
12. Hb-J-Georgia=Hb-J-Baltimore= 2 2 16 Gly leads to Asp. Wong SC, Bouver N, Wilson JB, Huisman TH. Clin Chim Acta; 1971 Dec 30; 35(2):521-2. PubMed ID: 5125343 [No Abstract] [Full Text] [Related]
13. Hb J-Calabria [beta 64(E8)Gly----Asp] found in a Japanese family. Harano T, Harano K, Imai K, Ohnishi T, Akabori T. Hemoglobin; 1989 Dec 30; 13(2):185-8. PubMed ID: 2737915 [No Abstract] [Full Text] [Related]
14. Hemoglobin J Rovigo (alpha53 Ala replaced by Asp) in association with beta-thalassemia. Moo-Penn WF, Jue DL, Baine RM. Hemoglobin; 1978 Dec 30; 2(5):443-5. PubMed ID: 31339 [No Abstract] [Full Text] [Related]
15. Influence of minicolumn procedure on apparent hemoglobin A1 in the presence of hemoglobin J-Baltimore. Jonah MH, Krauss JS, Mohorn PG. Clin Chem; 1983 Jul 30; 29(7):1444. PubMed ID: 6861356 [No Abstract] [Full Text] [Related]
16. [Hemoglobin J Baltimore 16 Gly leads to Asp in a young woman with cyanosis]. Lyonnais J, Richard MP. Union Med Can; 1981 May 30; 110(5):439-42. PubMed ID: 7256994 [No Abstract] [Full Text] [Related]
17. Double heterozygosis for Hb J Paris and beta-thalassemia. Marinucci M, Bruni E, Tentori L, De Sandre G, Vettore L. Hemoglobin; 1977 May 30; 1(6):595-8. PubMed ID: 914639 [No Abstract] [Full Text] [Related]
18. Hemoglobin QIndia, alpha 64 (E13) Asp replaced by His, and beta-thalassemia in a Canadian family. Schmidt RM, Bechtel KC, Moo-Penn WF. Am J Clin Pathol; 1976 Aug 30; 66(2):446-8. PubMed ID: 949043 [Abstract] [Full Text] [Related]
19. Identification of hemoglobin AC heterozygote status in a Malay family: a decision between hemoglobin electrophoresis and high performance liquid chromotography. Rosline H, Roshan TM, Ahmed SA, Ilunihayati I. Southeast Asian J Trop Med Public Health; 2007 May 30; 38(3):543-5. PubMed ID: 17877232 [Abstract] [Full Text] [Related]
20. A new fast-moving hemoglobin variant, Hb J-Tashikuergan alpha 19(AB1) Ala----Glu. Li HJ, Liu DX, Liu ZG, Li P, Li L, Chen J, Hou SZ. Hemoglobin; 1984 May 30; 8(4):391-5. PubMed ID: 6548207 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]