Hemoglobin SE disease in Hatay, in the southern part of Turkey

Autor: Can Acipayam, Gonul Oktay, Gul Ilhan, Mehmet Akif Çürük

Publikováno v: Thalassemia Reports, Vol 5, Iss 1 (2015)

Double heterozygosity for hemoglobin (Hb) E and S, known as HbSE disease, is a rare, clinically benign condition involving mild hemolysis. Only 25 cases have been reported to date. The current literature generally associates HbSE with a benign clinic

Externí odkaz: https://doaj.org/article/a0677222feb94ff2b2b0f72a36589e43

Determination of βS haplotypes in patients with sickle-cell anemia in the state of Rio Grande do Norte, Brazil

Autor: Thales Allyrio Araújo de Medeiros Fernandes, Tereza Maria Dantas de Medeiros, Ivanise Marina Moretti Rebecchi, Fernando Ferreira Costa, Elza Miyuki Kimura, Maria de Fátima Sonati, Édvis Santos Soares Serafim, Waleska Rayane Dantas Bezerra de Medeiros, Cynthia Hatsue Kitayama Cabral

Publikováno v: Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 34, Issue: 3, Pages: 421-424, Published: 22 JUL 2011
Genetics and Molecular Biology v.34 n.3 2011
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 34, Iss 3, Pp 421-424 (2011)

β(S) haplotypes were studied in 47 non-related patients with sickle-cell anemia from the state of Rio Grande do Norte, Brazil. Molecular analysis was conducted by PCR/RFLP using restriction endonucleases XmnI, HindIII, HincII and HinfI to analyze si

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a009196b1f8c1d1bc70bd2127e772f
https://doi.org/10.1590/s1415-47572011005000027

ßS-Haplotypes in sickle cell anemia patients from Salvador, Bahia, Northeastern Brazil

Autor: G.C. Bomfim, A. Pontes, Elisângela Vitória Adorno, Angela A. D. Zanette, M.G. dos Reis, A. Albuquerque, Elves Anderson Pires Maciel, Marilda Souza Goncalves, M.F. Dupuit, I. Cerqueira, Isa Menezes Lyra, G. Bomfim, G.B. Fernandes

Publikováno v: Brazilian Journal of Medical and Biological Research, Vol 36, Iss 10, Pp 1283-1288 (2003)
Brazilian Journal of Medical and Biological Research v.36 n.10 2003
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Volume: 36, Issue: 10, Pages: 1283-1288, Published: OCT 2003

BetaS-Globin haplotypes were studied in 80 (160 betaS chromosomes) sickle cell disease patients from Salvador, Brazil, a city with a large population of African origin resulting from the slave trade from Western Africa, mainly from the Bay of Benin.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96c1b2799775b9d5679cf9b54dd63242
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2003001000001

Brazilian Journal of Medical and Biological Research

Autor: Gonçalves, Marilda Souza, Bomfim, Gilberto Cafezeiro, Maciel, Elves Anderson Pires, Siqueira, Isadora Cristina de, Adorno, Elisângela Vitória, Albuquerque, Arlete Barreto Lins de, Fernandes, Gilênio Borges, Reis, Mitermayer Galvão dos, Lyra, Isa Menezes, Zanette, Angela Maria Dias, Pontes, Angela Maria de Carvalho, Dupuit, Marie France, Bomfim, Glória

Publikováno v: Repositório Institucional da UFBA
Universidade Federal da Bahia (UFBA)
instacron:UFBA

p. 1283-1288 Submitted by Ana Valéria de Jesus Moura (anavaleria_131@hotmail.com) on 2011-10-13T12:24:29Z No. of bitstreams: 1 4526.pdf: 585067 bytes, checksum: cb0d25b2f356bbb59ad509d85a02d8a8 (MD5) Made available in DSpace on 2011-10-13T12:24:29Z

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::43e16a9f5a1dc1e5b9556a447fee68b8
http://www.repositorio.ufba.br/ri/handle/ri/3290

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