Detalhe da pesquisa
1.
Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?
Ann Hematol
; 101(7): 1485-1491, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35459963
2.
Influence of diabetes and hypercholesterolemia on laboratory methods for hereditary spherocytosis diagnosis.
J Clin Lab Anal
; 36(3): e24248, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35080062
3.
Improvement of SCD morbimortality in children: experience in a remote area of an African country.
BMC Health Serv Res
; 21(1): 294, 2021 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33794895
4.
Detection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family.
Hemoglobin
; 43(2): 112-115, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31223040
5.
Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.
Br J Haematol
; 183(4): 648-660, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30334577
6.
Baseline hepcidin measurement in the differential diagnosis of anaemia for elderly patients and its correlation with the increment of transferrin saturation following an oral iron absorption test.
Clin Chem Lab Med
; 57(2): 250-258, 2018 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-30055098
7.
Recommendations regarding splenectomy in hereditary hemolytic anemias.
Haematologica
; 102(8): 1304-1313, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28550188
8.
Maternal serum markers in predicting successful outcome in expectant management of missed miscarriage.
Reprod Biomed Online
; 34(1): 98-103, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27692600
9.
Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience.
Clin Chem Lab Med
; 55(3): 394-402, 2017 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27559691
10.
Rare unstable and low oxygen affinity haemoglobin variant, Hb Hazebrouck, detected on Sysmex XN-9000.
Clin Chem Lab Med
; 60(5): e116-e118, 2022 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35075886
11.
Comparison of two assays measuring human chorionic gonadotrophin serum concentrations in pregnancy termination and trophoblastic or non-trophoblastic tumours.
Scand J Clin Lab Invest
; 77(8): 689-693, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29069923
12.
Hepcidin on 24-hour urine collection: preanalytical aspects and correlation with ferritin levels.
Scand J Clin Lab Invest
; 76(6): 454-9, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27284811
13.
Evaluation of the role of maternal serum high-sensitivity C-reactive protein in predicting early pregnancy failure.
Reprod Biomed Online
; 30(3): 268-74, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25596909
14.
Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment.
Pediatr Blood Cancer
; 62(11): 1956-61, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26173735
15.
Automated reticulocyte parameters for hereditary spherocytosis screening.
Ann Hematol
; 93(11): 1809-18, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24912770
16.
Serum and red blood cell folate testing for folate deficiency: new features?
Eur J Haematol
; 92(4): 354-9, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24351103
17.
Marked 25-hydroxyvitamin D deficiency is associated with poor prognosis in patients with alcoholic liver disease.
J Hepatol
; 59(2): 344-50, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23557869
18.
Limitations of serum values to estimate glomerular filtration rate during exercise.
Br J Sports Med
; 47(18): 1166-70, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22773320
19.
Differential diagnosis of lymphocytosis in routine laboratory practice: Contribution of lymphocyte parameters using the Sysmex-XN9000 haematology analyzer.
Int J Lab Hematol
; 45(5): 685-690, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37218119
20.
Sickle cell disease: embedding patient participation into an international conference can transform the role of lived experience.
Orphanet J Rare Dis
; 18(1): 341, 2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37908000