UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Recommendations regarding splenectomy in hereditary hemolytic anemias

Haematologica (Roma), 2017-08, Vol.102 (8), p.1304-1313

2017

Volltextzugriff (PDF)

Sickle cell disease: embedding patient participation into an international conference can transform the role of lived experience

Orphanet journal of rare diseases, 2023-11, Vol.18 (1), p.1-341, Article 341

2023

Volltextzugriff (PDF)

Haemoglobinopathies in Europe: health & migration policy perspectives

Orphanet journal of rare diseases, 2014-07, Vol.9 (1), p.97-97, Article 97

2014

Volltextzugriff (PDF)

Expert Services for Rare Anaemias across Europe

Thalassemia reports, 2013-03, Vol.3 (11), p.e30

Gulbis, Beatrice

2013

Volltextzugriff (PDF)

Influence of diabetes and hypercholesterolemia on laboratory methods for hereditary spherocytosis diagnosis

Journal of clinical laboratory analysis, 2022-03, Vol.36 (3), p.e24248-n/a

2022

Volltextzugriff (PDF)

Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: the Belgian experience

Blood, 2005-04, Vol.105 (7), p.2685-2690

2005

Volltextzugriff (PDF)

Persistent high-risk behavior and escalating HIV, syphilis and hepatitis B incidences among men who have sex with men living in Bangui, Central African Republic

The Pan African medical journal, 2018, Vol.29 (132), p.132-132

2018

Volltextzugriff (PDF)

Evaluation of maternal serum biomarkers in predicting outcome of successful expectant management of tubal ectopic pregnancies

European journal of obstetrics & gynecology and reproductive biology, 2020-07, Vol.250, p.61-65

2020

Volltextzugriff (PDF)

Evaluation of two automated and three rapid lateral flow immunoassays for the detection of anti-SARS-CoV-2 antibodies

Journal of clinical virology, 2020-07, Vol.128, p.104413-104413, Article 104413

2020

Volltextzugriff (PDF)

Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment

Pediatric blood & cancer, 2015-11, Vol.62 (11), p.1956-1961

2015

Volltextzugriff (PDF)

Recommendations for Pregnancy in Rare Inherited Anemias

HemaSphere, 2020-08, Vol.4 (4), p.e446-n/a

2020

Volltextzugriff (PDF)

Differential diagnosis of lymphocytosis in routine laboratory practice: Contribution of lymphocyte parameters using the Sysmex-XN9000 haematology analyzer

International journal of laboratory hematology, 2023-10, Vol.45 (5), p.685-690

2023

Volltextzugriff (PDF)

Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?

Annals of hematology, 2022-07, Vol.101 (7), p.1485-1491

2022

Volltextzugriff (PDF)

Transfer of folic acid inside the first-trimester gestational sac and the effect of maternal smoking

American journal of obstetrics and gynecology, 2007-07, Vol.197 (1), p.58.e1-58.e6

2007

Volltextzugriff (PDF)

Study of FibroTest and hyaluronic acid biological variation in healthy volunteers and comparison of serum hyaluronic acid biological variation between chronic liver diseases of different etiology and fibrotic stage using confidence intervals

Clinical biochemistry, 2015-07, Vol.48 (10-11), p.652-657

2015

Volltextzugriff (PDF)

Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience

Clinical chemistry and laboratory medicine, 2017-03, Vol.55 (3), p.394

2017

Volltextzugriff (PDF)

Improvement of SCD morbimortality in children: experience in a remote area of an African country

BMC health services research, 2021-04, Vol.21 (1), p.294-294, Article 294

2021

Volltextzugriff (PDF)

Serum and red blood cell folate testing for folate deficiency: new features?

European journal of haematology, 2014-04, Vol.92 (4), p.354-359

2014

Volltextzugriff (PDF)

Rare unstable and low oxygen affinity haemoglobin variant, Hb Hazebrouck, detected on Sysmex XN-9000

Clinical chemistry and laboratory medicine, 2022-04, Vol.60 (5), p.e116-e118

2022

Volltextzugriff (PDF)

Hepcidin-25: Measurement by LC–MS/MS in serum and urine, reference ranges and urinary fractional excretion

Clinica chimica acta, 2013-08, Vol.423, p.99-104

2013

Volltextzugriff (PDF)

Evaluation of the role of maternal serum high-sensitivity C-reactive protein in predicting early pregnancy failure

Reproductive biomedicine online, 2015-03, Vol.30 (3), p.268-274

2015

Volltextzugriff (PDF)

Osmotic gradient ektacytometry: A tool for more than just hereditary haemolytic anaemia

International journal of laboratory hematology, 2023-04, Vol.45 (2), p.e36-e38

2023

Volltextzugriff (PDF)

Newborn screening for sickle cell disease in Kisangani, Democratic Republic of the Congo: an update

Hematology (Luxembourg), 2023-12, Vol.28 (1), p.2213043-2213043

2023

Volltextzugriff (PDF)

1 – 25 von 165

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(158)
Mit Volltextzugriff
(136)

Publikationsform

Artikel
(162)
Webseiten
(2)
Berichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(104)
Life Sciences & Biomedicine
(103)
Humans
(102)
Female
(61)
Biological And Medical Sciences
(45)
Pregnancy
(35)
Male
(33)
Adult
(31)
Medical Sciences
(31)
Hematology
(27)
Obstetrics & Gynecology
(23)
Infant, Newborn
(22)
Sickle Cell Disease
(20)
Medical Laboratory Technology
(16)
Coelomic Fluid
(15)
Fundamental And Applied Biological Sciences. Psychology
(15)
Child
(14)
Middle Aged
(14)
Gestational Age
(13)
Pediatrics
(13)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Recommendations regarding splenectomy in hereditary hemolytic anemias

Sickle cell disease: embedding patient participation into an international conference can transform the role of lived experience

Haemoglobinopathies in Europe: health & migration policy perspectives

Expert Services for Rare Anaemias across Europe

Influence of diabetes and hypercholesterolemia on laboratory methods for hereditary spherocytosis diagnosis

Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: the Belgian experience

Persistent high-risk behavior and escalating HIV, syphilis and hepatitis B incidences among men who have sex with men living in Bangui, Central African Republic

Evaluation of maternal serum biomarkers in predicting outcome of successful expectant management of tubal ectopic pregnancies

P1427: RARE ANAEMIA DISORDERS EUROPEAN EPIDEMIOLOGICAL PLATFORM (RADEEP): DISTRIBUTION OF PATIENTS AFFECTED BY RADS IN EUROPE

Evaluation of two automated and three rapid lateral flow immunoassays for the detection of anti-SARS-CoV-2 antibodies

Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment

Recommendations for Pregnancy in Rare Inherited Anemias

Differential diagnosis of lymphocytosis in routine laboratory practice: Contribution of lymphocyte parameters using the Sysmex-XN9000 haematology analyzer

Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?

Transfer of folic acid inside the first-trimester gestational sac and the effect of maternal smoking

Study of FibroTest and hyaluronic acid biological variation in healthy volunteers and comparison of serum hyaluronic acid biological variation between chronic liver diseases of different etiology and fibrotic stage using confidence intervals

Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience

Improvement of SCD morbimortality in children: experience in a remote area of an African country

Serum and red blood cell folate testing for folate deficiency: new features?

Rare unstable and low oxygen affinity haemoglobin variant, Hb Hazebrouck, detected on Sysmex XN-9000

Hepcidin-25: Measurement by LC–MS/MS in serum and urine, reference ranges and urinary fractional excretion

Time for Change? The Why, What and How of Promoting Innovation to Tackle Rare Diseases – Is It Time to Update the EU’s Orphan Regulation? And if so, What Should be Changed?

Evaluation of the role of maternal serum high-sensitivity C-reactive protein in predicting early pregnancy failure

Osmotic gradient ektacytometry: A tool for more than just hereditary haemolytic anaemia

Newborn screening for sickle cell disease in Kisangani, Democratic Republic of the Congo: an update

Suchergebnisse filtern