-
1
-
-
0032932817
-
Molecular basis of weak D phenotypes
-
Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood 1999 93 : 385 93.
-
(1999)
Blood
, vol.93
, pp. 385-93
-
-
Wagner, F.F.1
Gassner, C.2
Muller, T.H.3
Schonitzer, D.4
Schunter, F.5
Flegel, W.A.6
-
2
-
-
0034656006
-
Weak D alleles express distinct phenotypes
-
Wagner FF, Frohmajer A, Ladewig B, et al. Weak D alleles express distinct phenotypes. Blood 2000 95 : 2699 708.
-
(2000)
Blood
, vol.95
, pp. 2699-708
-
-
Wagner, F.F.1
Frohmajer, A.2
Ladewig, B.3
-
3
-
-
0036096390
-
Ammonia and Alzheimer's disease
-
Seiler N. Ammonia and Alzheimer's disease. Neurochem Int 2002 41 : 189 207.
-
(2002)
Neurochem Int
, vol.41
, pp. 189-207
-
-
Seiler, N.1
-
4
-
-
17044380221
-
Anti-D immunization by del red blood cells
-
Wagner T, Kormoczi GF, Buchta C, et al. Anti-D immunization by DEL red blood cells. Transfusion 2005 45 : 520 6.
-
(2005)
Transfusion
, vol.45
, pp. 520-6
-
-
Wagner, T.1
Kormoczi, G.F.2
Buchta, C.3
-
5
-
-
0029664458
-
The RoHar antigenic complex is associated with a limited number of D epitopes and alloanti-D production: A study of three unrelated persons and their families
-
Beckers EA, Porcelijn L, Ligthart P, et al. The RoHar antigenic complex is associated with a limited number of D epitopes and alloanti-D production: a study of three unrelated persons and their families. Transfusion 1996 36 : 104 8.
-
(1996)
Transfusion
, vol.36
, pp. 104-8
-
-
Beckers, E.A.1
Porcelijn, L.2
Ligthart, P.3
-
6
-
-
0029869605
-
The D antigen characteristic of RoHar is a partial D antigen
-
Wallace M, Lomas-Francis C, Tippett P. The D antigen characteristic of RoHar is a partial D antigen. Vox Sang 1996 70 : 169 72.
-
(1996)
Vox Sang
, vol.70
, pp. 169-72
-
-
Wallace, M.1
Lomas-Francis, C.2
Tippett, P.3
-
7
-
-
30844461438
-
Crawford: Investigation of a new low frequency red cell antigen (Abstract)
-
Cobb ML. Crawford: investigation of a new low frequency red cell antigen (Abstract). Transfusion 1980 20 : 631.
-
(1980)
Transfusion
, vol.20
, pp. 631
-
-
Cobb, M.L.1
-
8
-
-
33746136983
-
The RHCE allele ceCF: The molecular basis of Crawford (RH43)
-
Flegel WA, Wagner FF, Chen Q, et al. The RHCE allele ceCF: the molecular basis of Crawford (RH43). Transfusion 2006 46 : 1334 42.
-
(2006)
Transfusion
, vol.46
, pp. 1334-42
-
-
Flegel, W.A.1
Wagner, F.F.2
Chen, Q.3
-
9
-
-
0042334906
-
The RHCE allele ceRT: D epitope 6 expression does not require D-specific amino acids
-
Wagner FF, Ladewig B, Flegel WA. The RHCE allele ceRT: D epitope 6 expression does not require D-specific amino acids. Transfusion 2003 43 : 1248 54.
-
(2003)
Transfusion
, vol.43
, pp. 1248-54
-
-
Wagner, F.F.1
Ladewig, B.2
Flegel, W.A.3
-
10
-
-
33746348613
-
Outliers in RhD membrane integration are explained by variant RH haplotypes
-
Yu X, Wagner FF, Witter B, Flegel WA. Outliers in RhD membrane integration are explained by variant RH haplotypes. Transfusion 2006 46 : 1343 51.
-
(2006)
Transfusion
, vol.46
, pp. 1343-51
-
-
Yu, X.1
Wagner, F.F.2
Witter, B.3
Flegel, W.A.4
-
11
-
-
34250671892
-
Blood group genotyping in Germany
-
Flegel WA. Blood group genotyping in Germany. Transfusion 2007 47 (Suppl 47S 53S.
-
(2007)
Transfusion
, vol.47
-
-
Flegel, W.A.1
-
12
-
-
1842364688
-
Incidence of D category VI among du donors in the USA
-
Beck ML, Harding J. Incidence of D category VI among Du donors in the USA. Transfusion 1991 31 (Suppl 25.
-
(1991)
Transfusion
, vol.31
, pp. 25
-
-
Beck, M.L.1
Harding, J.2
-
13
-
-
0020530949
-
Fatal hemolytic disease of a newborn due to anti-D in an Rh-positive du variant mother
-
Lacey PA, Caskey CR, Werner DJ, Moulds JJ. Fatal hemolytic disease of a newborn due to anti-D in an Rh-positive Du variant mother. Transfusion 1983 23 : 91 4.
-
(1983)
Transfusion
, vol.23
, pp. 91-4
-
-
Lacey, P.A.1
Caskey, C.R.2
Werner, D.J.3
Moulds, J.J.4
-
14
-
-
0038307181
-
Probability of anti-D development in D- patients receiving D+ RBCs
-
Frohn C, Dumbgen L, Brand J-M, Gorg S, Luhm J, Kirchner H. Probability of anti-D development in D- patients receiving D+ RBCs. Transfusion 2003 43 : 893 8.
-
(2003)
Transfusion
, vol.43
, pp. 893-8
-
-
Frohn, C.1
Dumbgen, L.2
Brand, J.-M.3
Gorg, S.4
Luhm, J.5
Kirchner, H.6
-
16
-
-
0031671377
-
The VS and V blood group polymorphisms in Africans: A serologic and molecular analysis
-
Daniels GL, Faas BH, Green CA, et al. The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis. Transfusion 1998 38 : 951 8.
-
(1998)
Transfusion
, vol.38
, pp. 951-8
-
-
Daniels, G.L.1
Faas, B.H.2
Green, C.A.3
-
17
-
-
0031037853
-
Rh haplotypes that make e but not hrB usually make VS
-
Reid ME, Storry JR, Issitt PD, et al. Rh haplotypes that make e but not hrB usually make VS. Vox Sang 1997 72 : 41 4.
-
(1997)
Vox Sang
, vol.72
, pp. 41-4
-
-
Reid, M.E.1
Storry, J.R.2
Issitt, P.D.3
-
18
-
-
33750491143
-
Molecular characterization of GYPB and RH in donors in the American Rare Donor Program
-
Vege S, Westhoff CM. Molecular characterization of GYPB and RH in donors in the American Rare Donor Program. Immunohematology 2006 22 : 143 7.
-
(2006)
Immunohematology
, vol.22
, pp. 143-7
-
-
Vege, S.1
Westhoff, C.M.2
-
19
-
-
0036892762
-
Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: Identification and transfusion safety
-
Noizat-Pirenne F, Lee K, Pennec PY, et al. Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety. Blood 2002 100 : 4223 31.
-
(2002)
Blood
, vol.100
, pp. 4223-31
-
-
Noizat-Pirenne, F.1
Lee, K.2
Pennec, P.Y.3
-
20
-
-
0028473702
-
To match or not to match: The question for chronically transfused patients with sickle cell anemia
-
Ness PM. To match or not to match: the question for chronically transfused patients with sickle cell anemia. Transfusion 1994 34 : 558 60.
-
(1994)
Transfusion
, vol.34
, pp. 558-60
-
-
Ness, P.M.1
-
21
-
-
0034858110
-
Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: A multicenter transfusion trial
-
Vichinsky EP, Luban NL, Wright E, et al. Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial. Transfusion 2001 41 : 1086 92.
-
(2001)
Transfusion
, vol.41
, pp. 1086-92
-
-
Vichinsky, E.P.1
Luban, N.L.2
Wright, E.3
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