122 related articles for article (PubMed ID: 8450301)
1. Unstable haemoglobin causing haemolytic anaemia: de novo mutation in Sweden identified by PCR.
Landin B; Astrom M
J Intern Med; 1993 Mar; 233(3):299-302. PubMed ID: 8450301
[TBL] [Abstract][Full Text] [Related]
2. A family with haemolytic anaemia and three beta-globins: the deletion in haemoglobin Atlanta-Coventry (beta 75 Leu----Pro, 141 Leu deleted) is not present at the nucleotide level.
George PM; Myles T; Williamson D; Higuchi R; Symmans WA; Brennan SO
Br J Haematol; 1992 May; 81(1):93-8. PubMed ID: 1520631
[TBL] [Abstract][Full Text] [Related]
3. Haemoglobin Köln as de novo mutations in Sweden: diagnosis by PCR and specific enzymatic cleavage.
Landin B; Fröstad B; Brune M; Ljung R
Eur J Haematol; 1994 Mar; 52(3):156-61. PubMed ID: 8168595
[TBL] [Abstract][Full Text] [Related]
4. Hb Vanvitelli: A new unstable α-globin chain variant causes undiagnosed chronic haemolytic anaemia when co-inherited with deletion - α
Casale M; Cozzolino F; Scianguetta S; Pucci P; Monaco V; Sanchez G; Santoro C; Rubino R; Cannata M; Perrotta S
Clin Biochem; 2019 Dec; 74():80-85. PubMed ID: 31493379
[TBL] [Abstract][Full Text] [Related]
5. Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [beta122 (GH5) Phe-->Ser], a probable case of germ line mutation, and Hb Olinda [beta22 (B4) - 25 (B7)], a deletion of a 12 base-pair sequence.
Bezerra MA; Albuquerque DM; Santos MN; Kimura EM; Jorge SE; Oliveira DM; Domingues BL; Peres JC; Araújo AS; Costa FF; Sonati MF
Eur J Haematol; 2009 Oct; 83(4):378-82. PubMed ID: 19527272
[TBL] [Abstract][Full Text] [Related]
6. Homozygous haemoglobin Constant Spring: a need for revision of concept.
Pootrakul P; Winichagoon P; Fucharoen S; Pravatmuang P; Piankijagum A; Wasi P
Hum Genet; 1981; 59(3):250-5. PubMed ID: 7327587
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl.
van den Berg HM; Bruin MC; Batelaan D; van Delft P; van Zwieten R; Roos D; Harteveld CL; Bernini LF; Giordano PC
Hemoglobin; 1999 May; 23(2):135-44. PubMed ID: 10335981
[TBL] [Abstract][Full Text] [Related]
9. Severe hemolytic anemia associated with the homozygous state for an unstable hemoglobin variant (Hb Bushwick).
Srivastava P; Kaeda JS; Roper D; Vulliamy TJ; Buckley M; Luzzatto L
Blood; 1995 Sep; 86(5):1977-82. PubMed ID: 7655024
[TBL] [Abstract][Full Text] [Related]
10. Haemoglobin Tunis-Bizerte: a new alpha 1 globin 129 Leu-->Pro unstable variant with thalassaemic phenotype.
Darbellay R; Mach-Pascual S; Rose K; Graf J; Beris P
Br J Haematol; 1995 May; 90(1):71-6. PubMed ID: 7786798
[TBL] [Abstract][Full Text] [Related]
11. Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.
Wilson JB; Webber BB; Kutlar A; Reese AL; McKie VC; Lutcher CL; Felice AE; Huisman TH
Hemoglobin; 1989; 13(6):557-66. PubMed ID: 2606724
[TBL] [Abstract][Full Text] [Related]
12. Haemoglobin Lleida: a new alpha 2-globin variant (12 bp deletion) with mild thalassaemic phenotype.
Ayala S; Colomer D; Pujades A; Aymerich M; Vives Corrons JL
Br J Haematol; 1996 Sep; 94(4):639-44. PubMed ID: 8826886
[TBL] [Abstract][Full Text] [Related]
13. Haemoglobin Leiden in a South African negro. A case report.
Perlman MM; Wiltshire BG; Stevens K; Cassel R; Lehmann H
S Afr Med J; 1981 Apr; 59(15):537-40. PubMed ID: 7221756
[TBL] [Abstract][Full Text] [Related]
14. Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia.
Pobedimskaya DD; Molchanova TP; Streichman S; Huisman TH
Am J Hematol; 1994 Nov; 47(3):198-202. PubMed ID: 7942784
[TBL] [Abstract][Full Text] [Related]
15. Unstable-haemoglobin haemolytic anaemia.
Brostrom K
Acta Paediatr Scand; 1976 May; 65(3):397-400. PubMed ID: 1274572
[TBL] [Abstract][Full Text] [Related]
16. Hb A
Lederer CW; Pavlou E; Tanteles GA; Evangelidou P; Sismani C; Kolnagou A; Sitarou M; Christou S; Hadjigavriel M; Kleanthous M
Hematology; 2017 Jun; 22(5):304-309. PubMed ID: 28007020
[TBL] [Abstract][Full Text] [Related]
17. Hb Sun Prairie: A rare cause of chronic hemolysis in an Indian patient.
Jain A; Prasad P; Chaudhry S; Gupta DK; Saluja S
Hematol Oncol Stem Cell Ther; 2021 Sep; 14(3):257-259. PubMed ID: 32199931
[TBL] [Abstract][Full Text] [Related]
18. Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual.
Pu J; Zhang L; Wei X; Xu X
Hemoglobin; 2018 May; 42(3):184-188. PubMed ID: 30277086
[TBL] [Abstract][Full Text] [Related]
19. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
[TBL] [Abstract][Full Text] [Related]
20. Haemoglobin Manukau beta 67[E11] Val-->Gly: transfusion-dependent haemolytic anaemia ameliorated by coexisting alpha thalassaemia.
Fay KC; Brennan SO; Costello JM; Potter HC; Williamson DA; Trent RJ; Ockelford PA; Boswell DR
Br J Haematol; 1993 Oct; 85(2):352-5. PubMed ID: 8280608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]