125 related articles for article (PubMed ID: 23741194)
1. Hb Southampton [B106(G8)Leu→PRO, CTG→CCG] in a Uruguayan woman.
Pereira JA; López P; Costa FF; Sans M; Sonati Mde F
Rev Bras Hematol Hemoter; 2013; 35(2):146-7. PubMed ID: 23741194
[TBL] [Abstract][Full Text] [Related]
2. Hb Southampton [beta106(G8)Leu-->Pro, CTG-->CCG] in an Argentinean boy.
Eandi Eberle S; Noguera NI; Sciuccati G; Bonduel M; Díaz L; Staciuk R; Feliu-Torres A
Hemoglobin; 2006; 30(3):401-3. PubMed ID: 16840233
[TBL] [Abstract][Full Text] [Related]
3. Hb Southampton [β106(G8)Leu→Pro; HBB: c.320T>C] and Codons 41/42 (-TTCT; HBB: c.124_127delTTCT) in a Chinese Girl.
Liu J; Huang Y; Lei Y; Lai Y
Hemoglobin; 2017 Mar; 41(2):134-136. PubMed ID: 28580821
[TBL] [Abstract][Full Text] [Related]
4. Hb L'Aquila [beta106(G8)Leu-->Val, CTG-->GTG]: a novel thalassemic hemoglobin variant.
Amato A; Cappabianca MP; Ponzini D; Rinaldi S; Biagio PD; Foglietta E; Grisanti P; Mastropietro F
Hemoglobin; 2007; 31(3):375-8. PubMed ID: 17654075
[TBL] [Abstract][Full Text] [Related]
5. [A new case of the unstable hemoglobin Southampton--Casper(beta106) (G68) leucine--proline)].
Didkovskiĭ NA; Idel'son LI; Filippova AV; Lemann G
Probl Gematol Pereliv Krovi; 1976 Jun; 21(6):48-50. PubMed ID: 959188
[No Abstract] [Full Text] [Related]
6. Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies.
Gasperini D; Galanello R; Melis MA; Iannelli S; Giordano P; Bernini LF; Cao A
Haematologica; 1992; 77(5):381-3. PubMed ID: 1336469
[TBL] [Abstract][Full Text] [Related]
7. Isolation and functional characterization of hemoglobin Casper: beta106(G8) Leu replaced by Pro.
Wajcman H; Gacon G; Labie D; Koler RD; Jones RT
Biochemistry; 1975 Nov; 14(22):5017-20. PubMed ID: 241397
[TBL] [Abstract][Full Text] [Related]
8. Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln;
Su Q; Chen S; Wu L; Tian R; Yang X; Huang X; Chen Y; Peng Z; Chen J
Hemoglobin; 2019 Jan; 43(1):7-11. PubMed ID: 31084366
[TBL] [Abstract][Full Text] [Related]
9. Haemoglobin Southampton, 106 (G8) Leu leads to pro: an unstable variant producing severe haemolysis.
Hyde RD; Hall MD; Wiltshire BG; Lehmann H
Lancet; 1972 Dec; 2(7788):1170-2. PubMed ID: 4117593
[No Abstract] [Full Text] [Related]
10. The rare Hb Showa-Yakushiji [beta110(G12)Leu-->Pro, CTG-->CCG] in combination with an alpha gene triplication found in a Dutch patient during her first pregnancy examination.
Giordano PC; Addo-Daaku A; Sander MJ; van Rooijen-Nijdam I; van Delft P; Harteveld CL; Kok PJ
Hemoglobin; 2007; 31(2):167-71. PubMed ID: 17486498
[TBL] [Abstract][Full Text] [Related]
11. The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review.
Du L; Qin D; Wang J; Yao C; Zhu J; Guo H; Yuan T; Liang J; Yin A
Hematology; 2022 Dec; 27(1):258-262. PubMed ID: 35192774
[TBL] [Abstract][Full Text] [Related]
12. A new unstable hemoglobin, Hb Yokohama beta 31 (B13)Leu substituting for Pro, causing hemolytic anemia.
Nakatsuji T; Miwa S; Ohba Y; Hattori Y; Miyaji T; Hino S; Matsumoto N
Hemoglobin; 1981; 5(7-8):667-78. PubMed ID: 7338469
[TBL] [Abstract][Full Text] [Related]
13. Hb Chile [beta28(B10)Leu-->Met]: an unstable hemoglobin associated with chronic methemoglobinemia and sulfonamide or methylene blue-induced hemolytic anemia.
Hojas-Bernal R; McNab-Martin P; Fairbanks VF; Holmes MW; Hoyer JD; McCormick DJ; Kubik KS
Hemoglobin; 1999 May; 23(2):125-34. PubMed ID: 10335980
[TBL] [Abstract][Full Text] [Related]
14. A novel beta-globin mutation, beta Durham-NC [beta 114 Leu-->Pro], produces a dominant thalassemia-like phenotype.
de Castro CM; Devlin B; Fleenor DE; Lee ME; Kaufman RE
Blood; 1994 Feb; 83(4):1109-16. PubMed ID: 8111050
[TBL] [Abstract][Full Text] [Related]
15. Diagnostic Dilemma of Hb Perth [β32(B14)Leu→Pro; HBB: c.98T > C] in Mainland China.
Jiang H; Yan JM; Li J; Xie XM; Li DZ
Hemoglobin; 2016 Jun; 40(3):202-5. PubMed ID: 27117570
[TBL] [Abstract][Full Text] [Related]
16. Hemoglobin Casper G8 106 leu leads to pro: further evidence that hemoglobin mutations are not random.
Jones RT; Koler RD; Duerst M; Stocklen Z
Adv Exp Med Biol; 1972; 28():79-98. PubMed ID: 5085188
[No Abstract] [Full Text] [Related]
17. Hb Dartmouth [alpha66(E15)Leu-->Pro (alpha2) (CTG-->CCG)]: a novel alpha2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian alpha-thalassemia-1.
McBride KL; Snow K; Kubik KS; Fairbanks VF; Hoyer JD; Fairweather RB; Chaffee S; Edwards WH
Hemoglobin; 2001 Nov; 25(4):375-82. PubMed ID: 11791870
[TBL] [Abstract][Full Text] [Related]
18. Beta-thalassemia alleles and unstable hemoglobin types among Russian pediatric patients.
Cürük MA; Molchanova TP; Postnikov YuV ; Pobedimskaya DD; Liang R; Baysal E; Kolodey S; Smetanina NS; Tokarev YuN ; Rumyantsev AG
Am J Hematol; 1994 Aug; 46(4):329-32. PubMed ID: 8037185
[TBL] [Abstract][Full Text] [Related]
19. A dutch family with Hb Debrousse: severe anemia after parvovirus B19 infection.
van Balen P; van Wijnen M; Hogeman PH; Wittebol S
Hemoglobin; 2009; 33(3):269-73. PubMed ID: 19657843
[TBL] [Abstract][Full Text] [Related]
20. [Severe hemolytic anemia due to hemoglobin Southampton: case report].
Avalos Gómez V; Eandi Eberle S; Pepe C; Sciuccati G; García Rosolen N; Cervio C; Díaz L; Candás A; Bonduel M; Piazza G; Chaves D; Feliú Torres A
Arch Argent Pediatr; 2012 Oct; 110(5):e91-4. PubMed ID: 23070193
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
