92 related articles for article (PubMed ID: 17712013)
1. Hemoglobin Hagley Park: a novel (alpha82Ala-->Thr) substitution identified in an infant with severe hemolytic anemia.
Brennan SO; Chan T; Beard M
Clin Chem; 2007 Sep; 53(9):1718-9. PubMed ID: 17712013
[No Abstract] [Full Text] [Related]
2. Familial hemolytic anemia due to Hb Sabine [beta 91(F7)Leu-->Pro] identified by polymerase chain reaction.
Hull D; Winter PC; McHale CM; Lappin TR; Mayne EE
Hemoglobin; 1998 May; 22(3):263-6. PubMed ID: 9629500
[No Abstract] [Full Text] [Related]
3. Coinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia.
Pedroso GA; Kimura EM; Santos MNN; Albuquerque DM; Ferruzzi JLH; Jorge SE; Costa FF; Saad STO; Sonati MF
Hemoglobin; 2017 May; 41(3):203-208. PubMed ID: 28670945
[TBL] [Abstract][Full Text] [Related]
4. Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.
Edward HL; Pisani LA; Rodriguez-Romero WE; Chaves-Villalobos J; Garcia-Quesada J; Harris NS; Luo HY; Steinberg MH; Forget BG; Chui DH
Hemoglobin; 2014; 38(6):381-4. PubMed ID: 25347256
[TBL] [Abstract][Full Text] [Related]
5. [Severe hemolytic anemia, caused by carriage of anomalous unstable hemoglobin Perth-Abraham Lincoln beta32 (B14) Leu---->Pro in a male patient of Russian nationality].
Idel'son LI; Spivak VA; Aseeva EA
Gematol Transfuziol; 1994; 39(5):11-4. PubMed ID: 7896021
[No Abstract] [Full Text] [Related]
6. Hemolytic anaemia due to unstable hemoglobin arising from spontaneous mutation--a case report.
Dash S; Menon S; Marwaha RK
Indian J Pathol Microbiol; 2006 Apr; 49(2):269-70. PubMed ID: 16933736
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Hemoglobin Hammersmith [beta42 (CD1) Phe --> Ser] in a Brazilian girl with congenital Heinz body hemolytic anemia.
Sonati MF; Kimura EM; Abreu CF; Oliveira DM; Pinheiro VR; Costa FF
Pediatr Blood Cancer; 2006 Nov; 47(6):855-6; author reply 857-8. PubMed ID: 16619220
[No Abstract] [Full Text] [Related]
10. Hb Mizuho [beta 68(E12)Leu----Pro]. Second occurrence identified in a Caucasian child with hemolytic anemia and dense erythrocyte inclusions.
Labotka RJ; Vida LN; Honig GR
Hemoglobin; 1990; 14(2):129-36. PubMed ID: 2272836
[TBL] [Abstract][Full Text] [Related]
11. Hb Jambol: a new hyperunstable hemoglobin causing severe hemolytic anemia.
Efremov GD; Simjanovska L; Plaseska-Karanfilska D; Stanojevic E; Petkov GH
Acta Haematol; 2007; 117(1):1-7. PubMed ID: 17095853
[TBL] [Abstract][Full Text] [Related]
12. Hemolytic anemia due to the unstable hemoglobin Wien: manifestations and long-term course in the largest pedigree identified to date.
Hilbert S; Voill-Glaninger A; Höller B; Minkov M
Haematologica; 2020 May; 105(5):e253-e255. PubMed ID: 32029504
[No Abstract] [Full Text] [Related]
13. 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]
14. Haemoglobinopathies and allied disorders.
WHO Chron; 1966 Nov; 20(11):407-11. PubMed ID: 5979644
[No Abstract] [Full Text] [Related]
15. Hemoglobin Hammersmith [beta 42(CD1) Phe --> Ser] causing severe hemolytic anemia in a Japanese girl.
Akiyama M; Murayama S; Yokoi K; Yanagisawa T; Hattori Y; Yamashiro Y; Eto Y; Fujisawa K
Pediatr Blood Cancer; 2006 Nov; 47(6):839-41. PubMed ID: 16078214
[TBL] [Abstract][Full Text] [Related]
16. Interaction between Hb S and Hb Hope in a Cuban family.
Martínez G; Colombo B
Hemoglobin; 1984; 8(5):519-22. PubMed ID: 6500990
[No Abstract] [Full Text] [Related]
17. First report of successful treatment for hemoglobin Bristol-Alesha by hemopoietic stem cell transplantation.
Li S; Chen K; Huang C; Zhang N; Jiang H; Jiang S
Ann Hematol; 2022 Mar; 101(3):617-619. PubMed ID: 34851438
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary anemia: genetic basis, clinical characteristics, diagnosis and treatment. WHO Workgroup].
Bull World Health Organ; 1983; 61(2):179-98. PubMed ID: 6345012
[No Abstract] [Full Text] [Related]
19. Clinical presentation of the hemoglobin Youngstown variant in a Chinese family.
Huang Y; Wang M; Yu C; Lei Y; Lai Y; Liu R
Ann Hematol; 2016 Oct; 95(11):1925-7. PubMed ID: 27515425
[No Abstract] [Full Text] [Related]
20. Anemia and hydrops in a fetus with homozygous hemoglobin constant spring.
Charoenkwan P; Sirichotiyakul S; Chanprapaph P; Tongprasert F; Taweephol R; Sae-Tung R; Sanguansermsri T
J Pediatr Hematol Oncol; 2006 Dec; 28(12):827-30. PubMed ID: 17164653
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
