Detalhe da pesquisa
1.
Adrenal function in relation to cytokines and outcome in non-critically ill patients with COVID-19.
J Endocrinol Invest
; 47(3): 721-728, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37702927
2.
Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development.
Hum Reprod
; 38(12): 2526-2535, 2023 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37814912
3.
Liver function test abnormalities after traumatic brain injury: is hepato-biliary ultrasound a sensitive diagnostic tool?
Br J Anaesth
; 112(2): 298-303, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24067331
4.
Accuracy of T2 magnetic resonance assays as point-of-care methods in the intensive care unit.
J Hosp Infect
; 139: 240-248, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37392869
5.
Validation of recombinant Sendai virus in a non-natural host model.
Gene Ther
; 18(2): 182-8, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20962870
6.
Pre-clinical evaluation of three non-viral gene transfer agents for cystic fibrosis after aerosol delivery to the ovine lung.
Gene Ther
; 18(10): 996-1005, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21512505
7.
Carbapenem-resistant versus carbapenem-susceptible Acinetobacter baumannii bacteremia in a Greek intensive care unit: risk factors, clinical features and outcomes.
Infection
; 38(3): 173-80, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20224962
8.
PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol.
Reprod Biomed Online
; 19(3): 418-25, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19778490
9.
Prenatal and preimplantation diagnosis of hemoglobinopathies.
Int J Lab Hematol
; 40 Suppl 1: 74-82, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29741247
10.
Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).
J Cyst Fibros
; 15(2): 163-70, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26493493
11.
ICU-acquired bloodstream infections in critically ill patients with COVID-19.
J Hosp Infect
; 107: 95-97, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33217490
12.
Noninvasive prenatal diagnosis of beta-thalassaemia using individual fetal erythroblasts isolated from maternal blood after enrichment.
Prenat Diagn
; 27(13): 1228-32, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17987605
13.
Blastocyst biopsy versus cleavage stage biopsy and blastocyst transfer for preimplantation genetic diagnosis of beta-thalassaemia: a pilot study.
Hum Reprod
; 22(5): 1443-9, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17261575
14.
Birth of a healthy infant following trophectoderm biopsy from blastocysts for PGD of beta-thalassaemia major.
Hum Reprod
; 20(7): 1855-9, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15878929
15.
Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
Blood Cells Mol Dis
; 26(4): 276-84, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-11042028
16.
Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods.
Mol Hum Reprod
; 3(6): 523-8, 1997 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-9239742
17.
Molecular, haematological and clinical studies of a silent beta-gene C-->G mutation at 6 bp 3' to the termination codon (+1480 C-->G) in twelve Greek families.
Br J Haematol
; 103(1): 45-51, 1998 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-9792288
18.
Preimplantation genetic diagnosis in 10 couples at risk for transmitting beta-thalassaemia major: clinical experience including the initiation of six singleton pregnancies.
Prenat Diagn
; 19(13): 1217-22, 1999 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-10660958
19.
Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene.
Haematologica
; 86(4): 363-7, 2001 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11325640
20.
Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience.
Br J Haematol
; 111(3): 915-23, 2000 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11122156