Giordano PC - Search Results

1

The disappearance of fetal and donor red blood cells in alloimmunised pregnancies: a reappraisal.

Egberts J, van Kamp IL, Kanhai HH, Meerman RH, Giordano PC, Gravenhorst JB. Egberts J, et al. Among authors: giordano pc. Br J Obstet Gynaecol. 1997 Jul;104(7):818-24. doi: 10.1111/j.1471-0528.1997.tb12026.x. Br J Obstet Gynaecol. 1997. PMID: 9236647

2

Prenatal diagnosis of homozygous alpha zero-thalassemia by an immunological method.

Bernini LF, Kanhai HH, Losekoot M, Giordano P, Harteveld CL. Bernini LF, et al. Ann N Y Acad Sci. 1994 Sep 7;731:193-6. doi: 10.1111/j.1749-6632.1994.tb55769.x. Ann N Y Acad Sci. 1994. PMID: 7944118 No abstract available.

3

Exploring the use of expanded erythroid cells for autologous transfusion for anemia of prematurity.

Khodabux CM, van Hensbergen Y, Slot MC, Bakker-Verweij M, Giordano PC, Brand A. Khodabux CM, et al. Among authors: giordano pc. Transfusion. 2013 Dec;53(12):3230-9. doi: 10.1111/trf.12169. Epub 2013 Mar 22. Transfusion. 2013. PMID: 23521158

4

Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.

Losekoot M, Fodde R, Gerritsen EJ, van de Kuit I, Schreuder A, Giordano PC, Vossen JM, Bernini LF. Losekoot M, et al. Among authors: giordano pc. Blood. 1991 Feb 15;77(4):861-7. Blood. 1991. PMID: 1704267 Free article.

5

A novel polyadenylation signal mutation in the alpha 2-globin gene causing alpha thalassaemia.

Harteveld CL, Losekoot M, Haak H, Heister GA, Giordano PC, Bernini LF. Harteveld CL, et al. Among authors: giordano pc. Br J Haematol. 1994 May;87(1):139-43. doi: 10.1111/j.1365-2141.1994.tb04883.x. Br J Haematol. 1994. PMID: 7947237

6

Hb Utrecht [alpha 2 129(H12)Leu-->Pro], a new unstable alpha 2-chain variant associated with a mild alpha-thalassaemic phenotype.

Harteveld CL, Giordano PC, Losekoot M, Heister JG, Batelaan D, van Delft P, Bruin MC, Bernini LF. Harteveld CL, et al. Among authors: giordano pc. Br J Haematol. 1996 Sep;94(3):483-5. doi: 10.1046/j.1365-2141.1996.d01-1828.x. Br J Haematol. 1996. PMID: 8790146

7

alpha-thalassaemia as a result of a novel splice donor site mutation of the alpha1-globin gene.

Harteveld CL, Beijer C, van Delft P, Zanardini R, Bernini LF, Giordano PC. Harteveld CL, et al. Among authors: giordano pc. Br J Haematol. 2000 Sep;110(3):694-8. doi: 10.1046/j.1365-2141.2000.02225.x. Br J Haematol. 2000. PMID: 10997982 Free article.

8

Atypical HbH disease in a Surinamese patient resulting from a combination of the -SEA and -alpha 3.7 deletions with HbC heterozygosity.

Giordano PC, Harteveld CL, Michiels JJ, Terpstra W, Batelaan D, van Delft P, Plug RJ, van der Wielen MJ, Losekoot M, Bernini LF. Giordano PC, et al. Br J Haematol. 1997 Mar;96(4):801-5. doi: 10.1046/j.1365-2141.1997.d01-2093.x. Br J Haematol. 1997. PMID: 9074424 Free article.

9

An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch families.

Harteveld CL, Heister JG, Giordano PC, Batelaan D, von Delft P, Haak HL, Wijermans PW, Losekoot M, Bernini LF. Harteveld CL, et al. Among authors: giordano pc. Br J Haematol. 1996 Dec;95(3):461-6. doi: 10.1046/j.1365-2141.1996.d01-1926.x. Br J Haematol. 1996. PMID: 8943885

10

A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutation.

Giordano PC, Harteveld CL, Haak HL, Batelaan D, van Delft P, Plug RJ, Emonts M, Zanardini R, Bernini LF. Giordano PC, et al. Br J Haematol. 1998 Nov;103(2):370-6. doi: 10.1046/j.1365-2141.1998.00999.x. Br J Haematol. 1998. PMID: 9827907 Free article.

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