101 related articles for article (PubMed ID: 9668571)
1. Homozygous hemoglobin constant spring with normal electrophoresis. A possible cause for under-diagnosis.
Krishnamurti L; Little JA
Ann N Y Acad Sci; 1998 Jun; 850():415-9. PubMed ID: 9668571
[No Abstract] [Full Text] [Related]
2. Homozygous Constant Spring: the first case described in the west.
Noguera NI; González FA; Ropero P; Anguita E; Milani AC; Villegas A
Haematologica; 2000 Jun; 85(6):667-9. PubMed ID: 10870130
[No Abstract] [Full Text] [Related]
3. Hb A2 Yokoshima, alpha(2)delta(2)25(B7)Gly----Asp, a new delta chain variant found in a Japanese family.
Ohba Y; Igarashi M; Tsukahara M; Nakashima M; Sanada C; Ami M; Arai Y; Miyaji T
Hemoglobin; 1985; 9(6):613-5. PubMed ID: 3841531
[No Abstract] [Full Text] [Related]
4. [Hemolytic anemia due to anomalous unstable hemoglobin Buenos Aires].
Rumiantseva IuV; Surin VL; Smetanina NS; Pliasunova SA; Blokhina LV; Kolodeĭ SV; Zhirkova LV
Ter Arkh; 2003; 75(7):78-81. PubMed ID: 12934488
[No Abstract] [Full Text] [Related]
5. Homozygous Hb Sallanches [alpha104(G11)Cys-->Tyr] in a Pakistani child with Hb H disease.
Waye JS; Walker L; Chui DH; Lafferty J; Kirby M
Hemoglobin; 2000 Nov; 24(4):355-7. PubMed ID: 11186268
[No Abstract] [Full Text] [Related]
6. A family with hemoglobin Hirosaki.
Tanaka Y; Matsui K; Matsuda K; Shinohara K; Haranob K
Int J Hematol; 2005 Aug; 82(2):124-6. PubMed ID: 16146843
[TBL] [Abstract][Full Text] [Related]
7. Asymmetric hybrids between hemoglobin Alberta (alpha 2 beta 2 101 Glu replaced by Gly) and hemoglobins A, A2 or F1 in different liganded states.
Harasym CA; Stinson RA
Clin Biochem; 1980 Apr; 13(2):95-8. PubMed ID: 6156029
[TBL] [Abstract][Full Text] [Related]
8. Unstable hemoglobin Rush [beta 101(G3) Glu>Gln, HBB:c.304G>C] in a Brazilian family with moderate hemolytic anemia.
Silva MR; Sendin SM; Velloso-Rodrigues C; Belisário AR; D'Ávila TS; Lyra LR; Viana MB
Ann Hematol; 2012 Jul; 91(7):1091-6. PubMed ID: 22273838
[TBL] [Abstract][Full Text] [Related]
9. The first Japanese case of Hb Santa Ana, an unstable abnormal hemoglobin, identified rapidly by electrospray ionization mass spectrometry.
Miyazaki A; Nakanishi T; Kishikawa M; Shimizu A; Jozaki K; Yonezawa T
Intern Med; 1997 May; 36(5):365-70. PubMed ID: 9213176
[TBL] [Abstract][Full Text] [Related]
10. Homozygous hemoglobin S with concomitant hemoglobin G-Philadelphia: a diagnostic challenge.
Racsa L; Mitui M; Park JY; Timmons CF; Luu HS; Rogers ZR; Park JY
Pediatr Blood Cancer; 2014 Oct; 61(10):1899-900. PubMed ID: 24777785
[No Abstract] [Full Text] [Related]
11. Hemoglobin A2 quantification by capillary zone electrophoresis.
Shihabi ZK; Hinsdale ME; Daugherty HK
Electrophoresis; 2000 Mar; 21(4):749-52. PubMed ID: 10733216
[TBL] [Abstract][Full Text] [Related]
12. Clinical Course of Homozygous Hemoglobin Constant Spring in Pediatric Patients.
Komvilaisak P; Jetsrisuparb A; Fucharoen G; Komwilaisak R; Jirapradittha J; Kiatchoosakun P
J Pediatr Hematol Oncol; 2018 Jul; 40(5):409-412. PubMed ID: 29668548
[TBL] [Abstract][Full Text] [Related]
13. Hemoglobinopathies in a hospital population in Vancouver.
Gray GR; Marion RB
Can Med Assoc J; 1978 Oct; 119(7):701-4. PubMed ID: 709469
[TBL] [Abstract][Full Text] [Related]
14. Model mice for Presbyterian hemoglobinopathy (Asn(beta108)-->Lys) confer hemolytic anemia with altered oxygen affinity and instability of Hb.
Suzuki Y; Shimizu T; Sakai H; Tamaki M; Koizumi Ki; Kuriyama T; Tsuchida E; Koseki H; Shirasawa T
Biochem Biophys Res Commun; 2002 Jul; 295(4):869-76. PubMed ID: 12127975
[TBL] [Abstract][Full Text] [Related]
15. Hydrops fetalis associated with homozygosity for hemoglobin Taybe (alpha 38/39 THR deletion) in newborn triplets.
Arnon S; Tamary H; Dgany O; Litmanovitz I; Regev R; Bauer S; Dolfin T; Yacobovich J; Wolach B; Jaber L
Am J Hematol; 2004 Jul; 76(3):263-6. PubMed ID: 15224363
[TBL] [Abstract][Full Text] [Related]
16. Analysis of the gamma chains in a homozygote for HPFH Negro type and in three related heterozygotes.
Guerrasio A; Acquaye CT; Oldham JH; Sartoris ML; Camaschella C; Saglio G; Mazza U
Acta Haematol; 1980; 63(3):146-50. PubMed ID: 6155042
[TBL] [Abstract][Full Text] [Related]
17. [Clinical aspects, diagnosis and treatment of hereditary hemolytic anemia caused by carrier state of unstable hemoglobin].
Idel'son LI; Didkovskiĭ NA
Ter Arkh; 1976; 48(8):120-7. PubMed ID: 1024290
[No Abstract] [Full Text] [Related]
18. A severe hemolytic anemia related to a new case of hemoglobin Perth (Abraham Lincoln) in a French patient.
Rousseaux J; Nuyts JP; Demouveau G; Dautrevaux M
Hemoglobin; 1980; 4(1):89-93. PubMed ID: 6153383
[No Abstract] [Full Text] [Related]
19. Hemoglobin Hammersmith (beta 42 (CD1) Phe replaced by Ser) associated with severe hemolytic anemia.
Rahbar S; Feagler RJ; Beutler E
Hemoglobin; 1981; 5(1):97-105. PubMed ID: 6259091
[TBL] [Abstract][Full Text] [Related]
20. Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches.
Warang P; Nair S; Nadkarni A; Ghosh K; Colah RB
Hemoglobin; 2010; 34(1):45-8. PubMed ID: 20113287
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]