Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""Lannoo L"" wg kryterium: Autor


Tytuł :
OC151: Pattern recognition by less experienced examiners and use of mathematical models to discriminate between static ultrasound images of benign and malignant adnexal masses.
Autorzy :
Van Holsbeke, C.
Lannoo, L.
Mesens, T.
de Jonge, E.
Valentin, L.
Jurkovic, D.
Yazbek, J.
Holland, T.
Timmerman, D.
Daemen, A.
Pokaż więcej
Temat :
ABSTRACTS
ULTRASONIC imaging
ADNEXAL diseases
Źródło :
Ultrasound in Obstetrics & Gynecology; Aug2008, Vol. 32 Issue 3, p292-292, 1p
Czasopismo naukowe
Tytuł :
Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?
Autorzy :
Lannoo L; Department of Development and Regeneration, Division Woman and Child, Clinical Department Obstetrics and Gynaecology, University Hospital Leuven, KULeuven, Leuven, Belgium.
Lenaerts L; Department of Gynaecological Oncology, KULeuven, Leuven, Belgium.
Van Den Bogaert K; Department of Human Genetics, KULeuven, Leuven, Belgium.
Che H; Department of Human Genetics, KULeuven, Leuven, Belgium.
Brison N; Department of Human Genetics, KULeuven, Leuven, Belgium.
Devriendt K; Department of Human Genetics, KULeuven, Leuven, Belgium.
Amant F; Department of Gynaecological Oncology, KULeuven, Leuven, Belgium.; Center for Gynecological Oncology Amsterdam, Academic Medical Centre Amsterdam, University of Amsterdam, The Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, the Netherlands.
Vermeesch JR; Department of Human Genetics, KULeuven, Leuven, Belgium.
Van Calsteren K; Department of Development and Regeneration, Division Woman and Child, Clinical Department Obstetrics and Gynaecology, University Hospital Leuven, KULeuven, Leuven, Belgium.
Pokaż więcej
Źródło :
Prenatal diagnosis [Prenat Diagn] 2021 Sep; Vol. 41 (10), pp. 1264-1272. Date of Electronic Publication: 2021 Aug 26.
Typ publikacji :
Journal Article; Review
Czasopismo naukowe
Tytuł :
Outcome of publicly funded nationwide first-tier noninvasive prenatal screening.
Autorzy :
Van Den Bogaert K; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium.
Lannoo L; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
Brison N; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium.
Gatinois V; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium.
Baetens M; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
Blaumeiser B; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.; Center for Medical Genetics, University Hospital Antwerp, Edegem, Belgium.
Boemer F; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
Bourlard L; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
Bours V; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
De Leener A; Center for Human Genetics, Université Catholique de Louvain, Brussels, Belgium.
De Rademaeker M; Center for Medical Genetics, University Hospital Antwerp, Edegem, Belgium.
Désir J; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
Dheedene A; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
Duquenne A; Center for Human Genetics, Université Catholique de Louvain, Brussels, Belgium.
Fieremans N; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
Fieuw A; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
Gatot JS; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
Grisart B; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
Janssens K; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
Janssens S; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
Lederer D; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
Marichal A; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
Menten B; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
Meunier C; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
Palmeira L; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
Pichon B; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
Sammels E; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
Smits G; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
Sznajer Y; Center for Human Genetics, Université Catholique de Louvain, Brussels, Belgium.
Vantroys E; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
Devriendt K; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium.
Vermeesch JR; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium. .
Pokaż więcej
Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Jun; Vol. 23 (6), pp. 1137-1142. Date of Electronic Publication: 2021 Feb 09.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Disorders*/diagnosis
Chromosome Disorders*/epidemiology
Chromosome Disorders*/genetics
Down Syndrome*/diagnosis
Down Syndrome*/epidemiology
Down Syndrome*/genetics
Noninvasive Prenatal Testing*
Aneuploidy ; Female ; Humans ; Pregnancy ; Prenatal Diagnosis ; Trisomy
Czasopismo naukowe
Tytuł :
Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations.
Autorzy :
van Riel M; Department of Human Genetics, Katholieke Universiteit Leuven, Leuven, the Center for Human Genetics and the Department of Obstetrics and Gynecology, Universitair Ziekenhuis Leuven, Leuven, the Center for Medical Genetics, Universitair Ziekenhuis Gent, Ghent, the Center for Medical Genetics, Universitair Ziekenhuis Antwerpen, Antwerp, the Center for Medical Genetics, Universiteit Antwerpen, Antwerp, the Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, the Center for Human Genetics, Université Libre de Bruxelles, Brussels, the Center for Human Genetics, Université Catholique de Louvain, Brussels, the Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, the Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, and the Department of Obstetrics, Women's Clinic, Universitair Ziekenhuis Gent, Ghent, Belgium.
Brison N
Baetens M
Blaumeiser B
Boemer F
Bourlard L
Bulk S
De Leener A
Désir J
Devriendt K
Dheedene A
Duquenne A
Fieremans N
Fieuw A
Gatot JS
Grisart B
Janssens S
Khudashvili N
Lannoo L
Marichal A
Meunier C
Palmeira L
Parijs I
Pichon B
Roets E
Sammels E
Smits G
Suenaert M
Sznajer Y
Van den Bogaert K
Vancoillie L
Vandeputte L
Vantroys E
Vermeesch JR
Janssens K
Pokaż więcej
Źródło :
Obstetrics and gynecology [Obstet Gynecol] 2021 Jun 01; Vol. 137 (6), pp. 1102-1108.
Typ publikacji :
Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
MeSH Terms :
Fetal Resorption*/diagnosis
Fetal Resorption*/genetics
Noninvasive Prenatal Testing*
Pregnancy, Multiple*
Down Syndrome/*diagnosis
Trisomy 13 Syndrome/*diagnosis
Trisomy 18 Syndrome/*diagnosis
Amniocentesis ; Amnion/diagnostic imaging ; Cell-Free Nucleic Acids/analysis ; Chorion/diagnostic imaging ; Diagnostic Errors ; False Negative Reactions ; Female ; Genome, Human ; Humans ; Pregnancy ; Pregnancy, Quadruplet ; Pregnancy, Triplet ; Pregnancy, Twin ; Retrospective Studies ; Sensitivity and Specificity ; Trisomy
Czasopismo naukowe
Tytuł :
Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies.
Autorzy :
Lenaerts L; Department of Oncology, KU Leuven, Herestraat 49, Leuven, Belgium.
Brison N; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.
Maggen C; Department of Oncology, KU Leuven, Herestraat 49, Leuven, Belgium.
Vancoillie L; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.
Che H; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.
Vandenberghe P; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.; Hematology, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.
Dierickx D; Department of Oncology, KU Leuven, Herestraat 49, Leuven, Belgium.; Hematology, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.
Michaux L; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.
Dewaele B; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.
Neven P; Department of Oncology, KU Leuven, Herestraat 49, Leuven, Belgium.; Gynaecology and Obstetrics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.
Floris G; Pathology, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Imaging & Pathology, KU Leuven, Herestraat 49, Leuven, Belgium.
Tousseyn T; Pathology, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Imaging & Pathology, KU Leuven, Herestraat 49, Leuven, Belgium.
Lannoo L; Gynaecology and Obstetrics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Department of Development and Regeneration, KU Leuven, Herestraat 49, Leuven, Belgium.
Jatsenko T; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.
Bempt IV; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.
Van Calsteren K; Gynaecology and Obstetrics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Department of Development and Regeneration, KU Leuven, Herestraat 49, Leuven, Belgium.
Vandecaveye V; Radiology, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Imaging & Pathology, KU Leuven, Herestraat 49, Leuven, Belgium.
Dehaspe L; Genomics Core facility, KU Leuven, Herestraat 49, Leuven, Belgium.
Devriendt K; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.
Legius E; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.
Bogaert KVD; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.
Vermeesch JR; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Department of Human Genetics, KU Leuven, Herestraat 49, Leuven, Belgium.; Genomics Core facility, KU Leuven, Herestraat 49, Leuven, Belgium.
Amant F; Department of Oncology, KU Leuven, Herestraat 49, Leuven, Belgium.; Gynaecology and Obstetrics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Academic Medical Centers Amsterdam-University of Amsterdam and The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, Netherlands.
Pokaż więcej
Źródło :
EClinicalMedicine [EClinicalMedicine] 2021 May 13; Vol. 35, pp. 100856. Date of Electronic Publication: 2021 May 13 (Print Publication: 2021).
Typ publikacji :
Journal Article
Czasopismo naukowe

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies