Volume 32; Issue 3

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Hemoglobin
Volume 32; Issue 3

Hemoglobin

Volume 32; Issue 3

1

Results of the National Program for Prevention of β-Thalassemia Major in the Iranian Province of Mazandaran

Khorasani, Ghasemali, Kosaryan, Mehrnoosh, Vahidshahi, Koorosh, Shakeri, Sepideh, Nasehi, Mohamad Mehdi

Journal:

Year:

2008

Language:

english

File:

PDF, 138 KB

english, 2008

2

Association of Hb Q-Thailand with Heterozygous Hb E in a Chinese Patient

Li, Dongzhi, Liao, Can, Li, Jian, Xie, Xingmei, Zhong, Huizhu

Journal:

Year:

2008

Language:

english

File:

PDF, 470 KB

english, 2008

3

A +8 (C→T) Mutation within the 5′ Untranslated Region of β-Globin Down-Regulates the mRNA Transcription

Van de Water, Neil, Tan, Tina, Chan, George, Cole, Nyree, Browett, Peter

Journal:

Year:

2008

Language:

english

File:

PDF, 252 KB

english, 2008

4

THE Hb S/β + -Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele

Schmugge, Markus, Waye, John S., Basran, Raveen K., Zurbriggen, Karin, Frischknecht, Hannes

Journal:

Year:

2008

Language:

english

File:

PDF, 89 KB

english, 2008

5

Compound Heterozygosity for Hb S [β6(A3)Glu→Val, G A G→G T G] and a New Thalassemic Mutation [β132(H10)Lys→Term, A AA→ T AA] Detected in a Family from West Africa

Frischknecht, Hannes, Troxler, Heinz, Greiner, Jeanette, Hengartner, Heinz, Dutly, Fabrizio

Journal:

Year:

2008

Language:

english

File:

PDF, 207 KB

english, 2008

6

Molecular Spectrum of β-Thalassemia Mutations in Northwestern Iran

Hosseinpour Feizi, Mohammad A., Hosseinpour Feizi, Abbas A., Pouladi, Nasser, Haghi, Mehdi, Azarfam, Parvin

Journal:

Year:

2008

Language:

english

File:

PDF, 152 KB

english, 2008

7

Frameshift Mutation in the α2-Globin Gene Causing α + -Thalassemia: Codon 49 (−GC)

Eng, Barry, Waye, John S.

Journal:

Year:

2008

Language:

english

File:

PDF, 598 KB

english, 2008

8

Molecular Basis of α-Thalassemia in Algeria

Mesbah-Amroun, Hamida, Rouabhi, Fatiha, Ducrocq, Rolande, Elion, Jacques

Journal:

Year:

2008

Language:

english

File:

PDF, 95 KB

english, 2008

9

Hb Jeddah [α68(E17)Asn→His (α1)]: A Newly Recognized α Chain Variant, Seen in Combination with Hb S [β6(A3)Glu→Val], and Found in Three Separate Families of Middle Eastern Origin

Markley, Karra M., Elkhalifa, Mohamed, Maini, Archana, Hoyer, James D.

Journal:

Year:

2008

Language:

english

File:

PDF, 181 KB

english, 2008

10

An Estimation of the Incidence and Demographic Picture of the Major Hemoglobinopathies in Belgium (From a Confidential Inquiry)

Gulbis, Béatrice, Ferster, Alice, Vermylen, Christiane, Dresse, Marie-Françoise, Vanderfaeillie, Anna, Delannoy, André, Labarque, Veerle, Philippet, Pierre, Kentos, Alain, Sztern, Bernard, Deprijck, B

Journal:

Year:

2008

Language:

english

File:

PDF, 124 KB

english, 2008

11

Hb Agrinio [α29(B10)Leu→Pro (α2)] in Combination with – – MED I Results in a Severe Form of Hb H Disease

Felekis, Xenia, Phylactides, Marios, Drousiotou, Anthi, Christou, Sotiroulla, Kyrri, Andreani, Kyriakou, Kyriakos, Kalogerou, Eleni, Christopoulos, George, Kleanthous, Marina

Journal:

Year:

2008

Language:

english

File:

PDF, 219 KB

english, 2008

12

Analyses of Expression of Cytoglobin by Immunohistochemical Studies in Human Tissues

Shigematsu, Akio, Adachi, Yasushi, Matsubara, Junko, Mukaide, Hiromi, Koike-Kiriyama, Naoko, Minamino, Keizo, Shi, Ming, Yanai, Seiji, Imamura, Masahiro, Taketani, Shigeru, Ikehara, Susumu

Journal:

Year:

2008

Language:

english

File:

PDF, 917 KB

english, 2008

13

Hemoglobinopathies in the Sudan

Elderdery, Abozer Y., Mohamed, Babiker A., Karsani, Mubarak E., Ahmed, Mohamed H., Knight, Gavin, Cooper, Alan J.

Journal:

Year:

2008

Language:

english

File:

PDF, 71 KB

english, 2008