Works matching AU LOUTRADI, APHRODITE

Results: 9

Subclinical autonomic dysfunction in patients with beta-thalassemia.

Published in:

2012

By:

Stamboulis, Elefterios;
Vlachou, Nikoleta;
Voumvourakis, Konstantinos;
Andrikopoulou, Athina;
Arvaniti, Chrisa;
Tsivgoulis, Athanasios;
Athanasiadis, Dimitrios;
Tsiodras, Sotirios;
Tentolouris, Nikolaos;
Triantafyllidi, Heleni;
Drossou-Servou, Marouso;
Loutradi-Anagnostou, Aphrodite;
Tsivgoulis, Georgios

Publication type:

Letter

Prenatal Diagnosis of Thalassemia and of the Sickle Cell Syndromes in Greece<sup>a</sup>.

Published in:

Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 226, doi. 10.1111/j.1749-6632.1990.tb24310.x

By:

LOUKOPOULOS, DIMITRIS;
HADJI, ANNA;
PAPADAKIS, MANOS;
KARABABA, PHOTINI;
SINOPOULOU, KLIO;
BOUSSIOU, MARINA;
KOLLIA, PANAGOULA;
XENAKIS, MATHILDE;
ANTSAKLIS, ARIS;
MESOGHITIS, SPYRIDON;
LOUTRADI, APHRODITE;
FESSAS, PHAEDON

Publication type:

Article

Prenatal Diagnosis of Thalassemia Intermedia: Is It Justified?

Published in:

Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 521, doi. 10.1111/j.1749-6632.1990.tb24351.x

By:

KOLLIA, PANAGOULA;
VOSKARIDOU, ERSI;
ROMBOS, JOHN;
LOUTRADI, APHRODITE;
MARINAKIS, THEODOROS;
FESSAS, PHAEDON;
LOUKOPOULOS, DIMITRIS

Publication type:

Article

Bone resorption is increased in young adults with thalassaemia major.

Published in:

British Journal of Haematology, 2001, v. 112, n. 1, p. 36, doi. 10.1046/j.1365-2141.2001.02549.x

By:

Voskaridou, Ersi;
Kyrtsonis, Maria-Christina;
Terpos, Evangelos;
Skordili, Maroussa;
Theodoropoulos, Ilias;
Bergele, Angeliki;
Diamanti, Evanthia;
Kalovidouris, Angelos;
Loutradi, Aphrodite;
Loukopoulos, Dimitris

Publication type:

Article

'Silent'β-thalassaemia caused by a 'silent'β-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia.

Published in:

British Journal of Haematology, 1982, v. 51, n. 4, p. 577, doi. 10.1111/j.1365-2141.1982.tb02821.x

By:

Fessas, Phaedon;
Loukopoulos, Dimitris;
Loutradi-Anagnostou, Aphrodite;
Komis, George

Publication type:

Article

A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotes.

Published in:

Journal of Molecular Medicine, 2002, v. 80, n. 4, p. 243, doi. 10.1007/s00109-001-0312-4

By:

Papadakis, Manoussos N.;
Patrinos, George P.;
Tsaftaridis, Panayotis;
Loutradi-Anagnostou, Aphrodite

Publication type:

Article

A Unique Thalassaemic Syndrome: Homozygous α-Thalassaemia + Homozygous β-Thalassaemia.

Published in:

British Journal of Haematology, 1978, v. 39, n. 3, p. 377, doi. 10.1111/j.1365-2141.1978.tb01109.x

By:

Loukopoulos, Dimitris;
Loutradi, Aphrodite;
Fessas, Phaedon

Publication type:

Article

Hydroxyurea Therapy in Thalassemia<sup>a</sup>.

Published in:

Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 120, doi. 10.1111/j.1749-6632.1998.tb10469.x

By:

LOUKOPOULOS, DIMITRIS;
VOSKARIDOU, ERSI;
STAMOULAKATOU, ALEXANDRA;
PAPASSOTIRIOU, YANNIS;
KALOTYCHOU, VASILIKI;
LOUTRADI, APHRODITE;
COZMA, GABRIEL;
TSIARTA, HELENI;
PAVLIDES, NIKOS

Publication type:

Article

Aγ-haplotypes: A new group of genetic markers for thalassemic mutations inside the 5′ regulatory region of the human Aγ-globin gene.

Published in:

American Journal of Hematology, 2001, v. 66, n. 2, p. 99, doi. 10.1002/1096-8652(200102)66:2<99::AID-AJH1024>3.0.CO;2-9

By:

Patrinos, George P.;
Kollia, Panagoula;
Papapanagiotou, Elisavet;
Loutradi-Anagnostou, Aphrodite;
Loukopoulos, Dimitris;
Papadakis, Manoussos N.

Publication type:

Article