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Items: 1 to 20 of 104

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. doi: 10.5581/1516-8484.20130037.

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.

PMID:
16840233
3.

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 Sep-Oct;77(5):381-3.

PMID:
1336469
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.

PMID:
17654075
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. Russian. No abstract available.

PMID:
959188
6.

Study of three families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish population: three homozygous cases.

de la Fuente-Gonzalo F, Baiget M, Badell I, Ricard P, Vinuesa L, Martínez-Nieto J, Ropero P, Villegas A, González FA, Díaz-Mediavilla J, Erythropathology Spanish Group.

Hemoglobin. 2012;36(6):526-32. doi: 10.3109/03630269.2012.733988. Epub 2012 Oct 24.

PMID:
23094635
7.

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.

PMID:
17486498
8.

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 4;14(22):5017-20.

PMID:
241397
9.

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.

PMID:
7338469
10.

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;2(7788):1170-2. No abstract available.

PMID:
4117593
11.

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.

PMID:
10335980
12.

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 15;83(4):1109-16.

13.

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. doi: 10.1080/03630260903058784.

PMID:
19657843
14.

Dominantly Inherited beta-Thalassemia.

Efremov GD.

Hemoglobin. 2007;31(2):193-207.

PMID:
17486503
15.

HB Les Andelys [alpha83(F4)LEU-->PRO]: a new moderately unstable variant.

Wajcman H, Promé D, Préhu C, Déon C, Riou J, Bouanga JC, Papassotiriou I, Lahary A, Galactéros F.

Hemoglobin. 1998 Mar;22(2):129-40.

PMID:
9576330
16.

Hemoglobin Debrousse (beta 96[FG3]Leu-->Pro): a new unstable hemoglobin with twofold increased oxygen affinity.

Lacan P, Kister J, Francina A, Souillet G, Galactéros F, Delaunay J, Wajcman H.

Am J Hematol. 1996 Apr;51(4):276-81.

17.

Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.

Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.

Blood Cells Mol Dis. 2000 Aug;26(4):276-84.

PMID:
11042028
18.
19.

Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama.

Prchal JT, Adler B, Wilson JB, Baysal E, Qin WB, Molchanova TP, Pobedimskaya DD, Kazanetz EG, Huisman TH.

Hemoglobin. 1995 May-Jul;19(3-4):151-64.

PMID:
7558871
20.

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. No abstract available.

PMID:
5085188
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