Volume 29; Issue 3

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Hemoglobin
Volume 29; Issue 3

Hemoglobin

Volume 29; Issue 3

1

Two French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and Codon 127 [ C AG→ T AG (Gln→Stop])

Préhu, Claude, Pissard, Serge, Al-Sheikh, Maha, Le Niger, Catherine, Bachir, Dora, Galactéros, Fréderic, Wajcman, Henri

Journal:

Year:

2005

Language:

english

File:

PDF, 225 KB

english, 2005

2

In Vivo Action of Vanillin on Delay Time Determined by Magnetic Relaxation

García, Adolfo Fernández, Cabal, Carlos, Losada, Jorge, Álvarez, Eloy, Soler, Catalina, Otero, Josefina

Journal:

Year:

2005

Language:

english

File:

PDF, 213 KB

english, 2005

3

A Novel G γ A γ(δβ) 0 -Thalassemia with a 27 kb Deletion

Yamashiro, Yasuhiro, Hattori, Yukio, Okayama, Naoko, Shinoda, Emi, Suyama, Naomi, Tanaka, Tatehiko, Ohi, Shinji

Journal:

Year:

2005

Language:

english

File:

PDF, 456 KB

english, 2005

4

Compound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls

Edison, Eunice Sindhuvi, Shaji, Ramachandran V., Srivastava, Alok, Chandy, Mammen

Journal:

Year:

2005

Language:

english

File:

PDF, 337 KB

english, 2005

5

A Mutation of the β-Globin Gene Initiation Codon, A T G→A A G, Found in a French Caucasian Man

Lacan, Philippe, Aubry, Martine, Couprie, Nicole, Francina, Alain

Journal:

Year:

2005

Language:

english

File:

PDF, 242 KB

english, 2005

6

Clinical and Laboratory Effects of Hydroxyurea in Children and Adolescents with Sickle Cell Anemia: A Portuguese Hospital Study

Braga, Lígia Barbosa, Ferreira, Ana Cristina, Guimarães, Margarida, Nazário, Carlos, Pacheco, Paula, Miranda, Armandina, Picanço, Isabel, Seixas, Teresa, Rosado, Lino, Videira Amaral, João M.

Journal:

Year:

2005

Language:

english

File:

PDF, 127 KB

english, 2005

7

β-Thalassemia Due to a Novel Nonsense Mutation at Codon 37 (T G G→T A G) Found in an Afghanistani Family

Kornblit, Brian, Taaning, Pia, Birgens, Henrik

Journal:

Year:

2005

Language:

english

File:

PDF, 176 KB

english, 2005

8

Hb Oegstgeest [α104(G11)Cys → Ser (α1)]. A New Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype

Harteveld, Cornelis L., Rozendaal, Lieke, Blom, Nico A., Lo-A-Njoe, Shirley, Akkerman, Nicole, Arkestijn, Sandra, Van Delft, Peter, Giordano, Piero C.

Journal:

Year:

2005

Language:

english

File:

PDF, 119 KB

english, 2005

9

A Rare Association of α 0 -Thalassemia (– – SEA ) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand

Viprakasit, Vip, Chinchang, Worrawut, Glomglao, Waraporn, Tanphaichitr, Voravarn S

Journal:

Year:

2005

Language:

english

File:

PDF, 339 KB

english, 2005

10

Hyperbilirubinemia in Homozygous HbE Disease Is Associated with the UGT1A1 Gene Polymorphism

Edison, Eunice Sindhuvi, Shaji, Ramachandran V., Srivastava, Alok, Chandy, Mammen

Journal:

Year:

2005

Language:

english

File:

PDF, 147 KB

english, 2005

11

The First Case of Hb E-Saskatoon Associated with Hb Lepore-Baltimore Found in Spain

Ropero, Paloma, Murga, Maria José, González, Fernando A., Polo, Marta, Benavente, Celina, Salvador, María, Villegas, Ana

Journal:

Year:

2005

Language:

english

File:

PDF, 745 KB

english, 2005