Zobrazeno 1 - 10
of 380
pro vyhledávání: '"Giordano PC"'
Autor:
Ivaldi, G, Barberio, G, Caruso, V, Caldini, A, Mosca, A, Russo, Giovanna, Leone, D, Mancini, R, Zaninotto, M, Zanolli, Fa, Giordano, Pc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4731::198a30643642ce2f4d570d5fc4bc983c
http://hdl.handle.net/20.500.11769/20102
http://hdl.handle.net/20.500.11769/20102
Association of XmnI (-158 γG) Polymorphism and Response to Hydroxyurea in Omani S/S and S/β Patients
Publikováno v:
Journal of Genetics and Genome Research. 1
Objective: To describe the effect of Hydroxyurea (HU) treatment in Omani Sickle Cell Disease (SCD) patients with different beta-globin gene cluster haplotypes. Materials and methods: A total of 52 cases treated with HU were enrolled in this study. Re
BACKGROUND: Hemoglobin (Hb) Groene Hart [alpha119 (H2)Pro-->Ser (alpha1)], also known as Hb Bernalda, is a nondeletional alpha-thalassemic Hb variant that is frequent in southern Italy and North Africa. This variant is not supposed to be produced in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______166::b5fbb57c548217c18640386357f8383c
https://hal.archives-ouvertes.fr/hal-00315195
https://hal.archives-ouvertes.fr/hal-00315195
Autor:
Harteveld, Cl, Versteegh, Fg, Vanleer, Eh, Starreveld, Js, Kok, Pj, Vanrooijen-Nijdam, I., Vandelft, P., Zanella-Cleon, I., Becchi, M., Wajcman, H., Giordano, Pc
We report a new hemoglobin (Hb) variant found in a 6-year-old girl of Moroccan origin, living in the Dutch city of Gouda. The child was referred because of microcytic and hypochromic parameters. A normal zinc protoporphyirin (ZPP) value excluded iron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______166::0957d2dd01053d845bae2e8bb77a6889
https://hal.archives-ouvertes.fr/hal-00315124
https://hal.archives-ouvertes.fr/hal-00315124
Publikováno v:
Haematologica, 90(4), 551-552. Ferrata Storti Foundation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::375549df8765d4e70abd9a507b6f9e78
https://pure.eur.nl/en/publications/95ecc981-0baa-43ff-8247-c11315766969
https://pure.eur.nl/en/publications/95ecc981-0baa-43ff-8247-c11315766969
Publikováno v:
Haematologica, 90, 551-552. Ferrata Storti Foundation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::8828536e3e38b3db46d449c613c60a57
https://pure.eur.nl/en/publications/00fff143-6ed6-4d9c-ac45-f19023c8c952
https://pure.eur.nl/en/publications/00fff143-6ed6-4d9c-ac45-f19023c8c952
Autor:
Harteveld, CL, van Delft, P, Wijermans, PW, Klunne, Mies, Weegenaar, J, Losekoot, M, Giordano, PC
Publikováno v:
British Journal of Haematology, 120, 364-366. Wiley-Blackwell Publishing Ltd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::70f0903629faa5a355e97e4637dd38d1
https://pure.eur.nl/en/publications/632cdbd7-036a-4e2c-9804-46afa2e49ed1
https://pure.eur.nl/en/publications/632cdbd7-036a-4e2c-9804-46afa2e49ed1
Akademický článek
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In this report we describe a case of Hb H disease due to the interaction of the - -((MED I)) deletion with a new alpha(+)-thalassemia determinant. The molecular analysis of the proband’s genomic DNA was carried out by polymerase chain reaction ampl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a250af2e3ee9aeed272aeb8d9714321b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3052390
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3052390
Autor:
Giordano, PC, Harteveld, CL, Bernini, LF, Doorduijn, Jeanette, Geenen, AA, Kok, PJM, Versteegh, FGA
Publikováno v:
Hemoglobin, 23(2), 193-195. Informa Healthcare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::36ac90a4287b00ab90d4abe3b9c41770
https://pure.eur.nl/en/publications/f219b340-3691-44d6-87b7-d539c5a5043f
https://pure.eur.nl/en/publications/f219b340-3691-44d6-87b7-d539c5a5043f