Works by den Hollander, S.

Results: 36

Sonographically determined anomalies and outcome in 170 chromosomally abnormal fetuses.

Published in:

1995

By:

Wladimiroff, Juriy W.;
Bhaggoe, Wydia R.;
Kristelijn, Miranda;
Cohen-Overbeek, Titia E.;
Den Hollander, Nicolette S.;
Brandenburg, Helen;
Los, Frans J.;
Wladimiroff, J W;
Bhaggoe, W R;
Kristelijn, M;
Cohen-Overbeek, T E;
Den Hollander, N S;
Brandenburg, H;
Los, F J

Publication type:

journal article

Tackle Height and Tackle Success—An Analysis of 52,204 Tackle Events.

Published in:

European Journal of Sport Science, 2025, v. 25, n. 8, p. 1, doi. 10.1002/ejsc.70003

By:

Hendricks, S.;
Till, K.;
Scantlebury, S.;
Dalton‐Barron, N.;
den Hollander, S.;
Gill, N.;
Kemp, S.;
Kilding, A.;
Lambert, M.;
Mackreth, P.;
O'Reilly, J.;
Owen, C.;
Spencer, K.;
Stokes, K.;
Tee, J.;
Tucker, R.;
Vaz, L.;
Weaving, D.;
West, S. W.;
Dane, K.

Publication type:

Article

Sleep interventions in elite sport - a systematic review.

Published in:

South African Journal of Sports Medicine, 2025, v. 37, n. 1, p. 1, doi. 10.17159/2078-516X/2025/v37i1a18811

By:

Bilgoe, S. C.;
den Hollander, S.;
van Rensberg, D. C. Janse;
Hendricks, S.;
Kerkhoffs, G.;
Gouttebarge, V.

Publication type:

Article

Pain, impairment, medication use and health-related quality of life of retired professional rugby players.

Published in:

South African Journal of Sports Medicine, 2024, v. 36, n. 1, p. 1, doi. 10.17159/2078-516X/2024/v36i1a17651

By:

Roux, J. Le;
Janse van Rensburg, D. C.;
Hollander, S. den;
Kerkhoffs, G. M. M. J.;
Gouttebarge, V.

Publication type:

Article

Headers and concussions in elite female and male football: a pilot study.

Published in:

South African Journal of Sports Medicine, 2023, v. 35, n. 1, p. 1, doi. 10.17159/2078-516X/2023/v35i1a15236

By:

Hollander, S. Den;
Gouttebarge, V.

Publication type:

Article

Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.

Published in:

Nature Genetics, 2012, v. 44, n. 4, p. 379, doi. 10.1038/ng.2217

By:

Santen, Gijs W E;
Aten, Emmelien;
Sun, Yu;
Almomani, Rowida;
Gilissen, Christian;
Nielsen, Maartje;
Kant, Sarina G;
Snoeck, Irina N;
Peeters, Els A J;
Hilhorst-Hofstee, Yvonne;
Wessels, Marja W;
den Hollander, Nicolette S;
Ruivenkamp, Claudia A L;
van Ommen, Gert-Jan B;
Breuning, Martijn H;
den Dunnen, Johan T;
van Haeringen, Arie;
Kriek, Marjolein

Publication type:

Article

A Frame-Shift Mutation in the Type I Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Causing Blomstrand Lethal Osteochondrodysplasia.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 10, p. 3713, doi. 10.1210/jcem.84.10.6033

By:

KARPERIEN, MARCEL;
VAN DER HARTEN, HANS J.;
VAN SCHOOTEN, RON;
FARIH-SIPS, HETTY;
DEN HOLLANDER, NICOLETTE S.;
KNEPPERS, SANDER L. J.;
NIJWEIDE, PETER;
PAPAPOULOS, SOCRATES E.;
LÖWIK, CLEMENS W. G. M.

Publication type:

Article

Clinical presentation and risk factors of serious infections in children with Down syndrome treated for acute lymphoblastic leukemia.

Published in:

2016

By:

Ceppi, Francesco;
Stephens, Derek;
den Hollander, Barbara S.;
Krueger, Joerg;
Whitlock, James;
Sung, Lillian;
Hitzler, Johann

Publication type:

journal article

Successful use of indwelling tunneled catheters for the management of effusions in children with advanced cancer.

Published in:

Pediatric Blood & Cancer, 2014, v. 61, n. 6, p. 1007, doi. 10.1002/pbc.24902

By:

den Hollander, Barbara S.;
Connolly, Bairbre L.;
Sung, Lillian;
Rapoport, Adam;
Zwaan, C.M.;
Grant, Ronald M.;
Parra, Dimitri;
Temple, Michael J.

Publication type:

Article

Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 3, p. 239, doi. 10.1002/pd.551

By:

Wessels, Marja W.;
den Hollander, Nicolette S.;
Willems, Patrick J.

Publication type:

Article

The diagnostic performance of cytogenetic investigation in amniotic fluid cells and chorionic villi.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 13, p. 1150, doi. 10.1002/pd.194

By:

Los, Frans J.;
van den Berg, Cardi;
Wildschut, Hajo I. J.;
Brandenburg, Helen;
den Hollander, Nicolette S.;
Schoonderwaldt, Ernst M.;
Pijpers, Leen;
Jan H. Galjaard, Robert;
Van Opstal, Diane

Publication type:

Article

Early fetal anomaly scanning in a population at increased risk of abnormalities.

Published in:

Ultrasound in Obstetrics & Gynecology, 2002, v. 19, n. 6, p. 570, doi. 10.1046/j.1469-0705.2002.00649.x

By:

Den Hollander, N. S;
Wessels, M. W;
Niermeijer, M. F;
Los, F. J;
Wladimiroff, J. W

Publication type:

Article

Unilateral multicystic dysplastic kidney: a combined pre- and postnatal assessment.

Published in:

Ultrasound in Obstetrics & Gynecology, 2002, v. 19, n. 2, p. 180, doi. 10.1046/j.0960-7692.2001.00497.x

By:

van Eijk, L;
Cohen-Overbeek, T. E;
den Hollander, N. S;
Nijman, J. M;
Wladimiroff, J. W

Publication type:

Article

Early prenatal sonographic diagnosis and follow-up of Jeune syndrome.

Published in:

Ultrasound in Obstetrics & Gynecology, 2001, v. 18, n. 4, p. 378, doi. 10.1046/j.0960-7692.2001.00530.x

By:

Den Hollander, N. S.;
Robben, S. G. F.;
Hoogeboom, A. J. M.;
Niermeijer, M. F.;
Wladimiroff, J. W.

Publication type:

Article

Prenatal diagnosis of type A1 brachydactyly.

Published in:

Ultrasound in Obstetrics & Gynecology, 2001, v. 17, n. 6, p. 529, doi. 10.1046/j.1469-0705.2001.00428.x

By:

Den Hollander, N. S.;
Hoogeboom, A. J. M.;
Niermeijer, M. F.;
Wladimiroff, J. W.

Publication type:

Article

Clinomicrodactyly.

Published in:

Ultrasound in Obstetrics & Gynecology, 2000, v. 16, n. 2, p. 204, doi. 10.1046/j.1469-0705.2000.00205.x

By:

Den Hollander, N. S.

Publication type:

Article

In-utero diagnosis of mucopolysaccharidosis type VII in a fetus with an enlarged nuchal translucency.

Published in:

Ultrasound in Obstetrics & Gynecology, 2000, v. 16, n. 1, p. 87, doi. 10.1046/j.1469-0705.2000.00148.x

By:

Den Hollander, N. S.;
Kleijer, W. J.;
Schoonderwaldt, E. M.;
Los, F. J.;
Wladimiroff, J. W.;
Niermeijer, M. F.

Publication type:

Article

Early transvaginal ultrasonographic diagnosis of Beemer-Langer dysplasia: a report of two cases.

Published in:

Ultrasound in Obstetrics & Gynecology, 1998, v. 11, n. 4, p. 298, doi. 10.1046/j.1469-0705.1998.11040298.x

By:

den Hollander, N. S.;
H. J.;
Laudy, J. A. M.;
P.;
Wladimiroff, J. W.

Publication type:

Article

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.

Published in:

Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 65, doi. 10.1159/000184693

By:

Goobie, S.;
Knijnenburg, J.;
FitzPatrick, D.;
Sharkey, F. H.;
Lionel, A. C.;
Marshall, C. R.;
Azam, T.;
Shago, M.;
K. Chong;
Mendoza-Londono, R.;
den Hollander, N. S.;
Ruivenkamp, C.;
Maher, E.;
Tanke, H. J.;
Szuhai, K.;
Wintle, R. F.;
Scherer, S. W.

Publication type:

Article

Accuracy of abnormal karyotypes after the analysis of both short- and long-term culture of chorionic villi.

Published in:

Prenatal Diagnosis, 2000, v. 20, n. 12, p. 956, doi. 10.1002/1097-0223(200012)20:12<956::AID-PD956>3.0.CO;2-Y

By:

van den Berg, Cardi;
Van Opstal, Diane;
Brandenburg, Helen;
Wildschut, Hajo I. J.;
den Hollander, Nicolette S.;
Pijpers, Leen;
Jan H. Galjaard, Robert;
Los, Frans J.

Publication type:

Article

Amniocentesis or chorionic villus sampling in multiple gestations? Experience with 500 cases.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 3, p. 234, doi. 10.1002/(SICI)1097-0223(199903)19:3<234::AID-PD516>3.0.CO;2-7

By:

van den Berg, Cardi;
Braat, Armando P. G.;
Van Opstal, Diane;
Halley, Dicky J. J.;
Kleijer, Wim J.;
den Hollander, Nicolette S.;
Brandenburg, Helen;
Pijpers, Leen;
Los, Frans J.

Publication type:

Article

Prenatally diagnosed fetal ventriculomegaly: prognosis and outcome.

Published in:

Prenatal Diagnosis, 1998, v. 18, n. 6, p. 557, doi. 10.1002/(SICI)1097-0223(199806)18:6<557::AID-PD303>3.0.CO;2-3

By:

Den Hollander, Nicolette S.;
Vinkesteijn, Astrid;
Schmitz-Van Splunder, Paula;
Catsman-Berrevoets, Coriene E.;
Wladimiroff, Juriy W.

Publication type:

Article

The efficacy of flecainide versus digoxin in the management of fetal supraventricular tachycardia.

Published in:

Prenatal Diagnosis, 1995, v. 15, n. 13, p. 1297, doi. 10.1002/pd.1970151309

By:

Frohn-Mulder, I. M.;
Stewart, P. A.;
Witsenburg, M.;
Den Hollander, N. S.;
Wladimiroff, J. W.;
Hess, J.

Publication type:

Article

The efficacy of flecainide versus digoxin in the management of fetal supraventricular tachycardia.

Published in:

1995

By:

Frohn-Mulder, I M;
Stewart, P A;
Witsenburg, M;
Den Hollander, N S;
Wladimiroff, J W;
Hess, J

Publication type:

journal article

Prenatal diagnosis of congenital diaphragmatic hernia: a retrospective analysis of 28 cases.

Published in:

1994

By:

Manni, M.;
Heydanus, R.;
Den Hollander, N. S.;
Stewart, P. A.;
de Vogelaere, Ch.;
Wladimiroff, J. W.;
De Vogelaere, C

Publication type:

journal article

CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis.

Published in:

2009

By:

Van Dijk, Fleur S.;
Nesbitt, Isabel M.;
Nikkels, Peter G. J.;
Dalton, Ann;
Bongers, Ernie M. H. F.;
van de Kamp, Jiddeke M.;
Hilhorst-Hofstee, Yvonne;
Den Hollander, Nicolette S.;
Lachmeijer, Augusta M. A.;
Marcelis, Carlo L.;
Tan-Sindhunata, Gita M. B.;
van Rijn, Rick R.;
Meijers-Heijboer, Hanne;
Cobben, Jan M.;
Pals, Gerard

Publication type:

Correction Notice

CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 12, p. 1560, doi. 10.1038/ejhg.2009.75

By:

Van Dijk, Fleur S.;
Nesbitt, Isabel M.;
Nikkels, Peter G. J.;
Dalton, Ann;
Bongers, Ernie M. H. F.;
van de Kamp, Jiddeke M.;
Hilhorst-Hofstee, Yvonne;
Den Hollander, Nicolette S.;
Lachmeijer, Augusta M. A.;
Marcelis, Carlo L.;
Tan-Sindhunata, Gita M. B.;
van Rijn, Rick R.;
Meijers-Heijboer, Hanne;
Cobben, Jan M.;
Pals, Gerard

Publication type:

Article

A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 11, p. 1394, doi. 10.1038/ejhg.2009.74

By:

Gijsbers, Antoinet C. J.;
Lew, Janet Y. K.;
Bosch, Cathy A. J.;
Schuurs-Hoeijmakers, Janneke H. M.;
van Haeringen, Arie;
den Hollander, Nicolette S.;
Kant, Sarina G.;
Bijlsma, Emilia K.;
Breuning, Martijn H.;
Bakker, Egbert;
Ruivenkamp, Claudia A. L.

Publication type:

Article

Pharmacological characterization of allosteric modulators: A case for chemokine receptors.

Published in:

Medicinal Research Reviews, 2024, v. 44, n. 5, p. 2291, doi. 10.1002/med.22043

By:

den Hollander, Lisa S.;
IJzerman, Adriaan P.;
Heitman, Laura H.

Publication type:

Article

Lethal/Severe Osteogenesis Imperfecta in a Large Family: A Novel Homozygous Mutation and Bone Histological Findings.

Published in:

Pediatric & Developmental Pathology, 2011, v. 14, n. 3, p. 228, doi. 10.2350/10-03-0806-CR.1

By:

VAN DIJK, FLEUR S.;
NIKKELS, PETER G. J.;
DEN HOLLANDER, NICOLETTE S.;
NESBITT, ISABEL M.;
VAN RIJN, RICK R.;
COBBEN, JAN M.;
PALS, GERARD

Publication type:

Article

Implementing routine medical and mental health screening in children and adolescents with inflammatory bowel disease.

Published in:

Journal of Pediatric Gastroenterology & Nutrition, 2025, v. 81, n. 1, p. 43, doi. 10.1002/jpn3.70039

By:

van Dalen, Marije;
van Gaalen, Martha A. C.;
Favejee, Marein M.;
den Hollander–Ardon, Monique S.;
Dulfer, Karolijn;
de Ridder, Lissy;
Escher, Johanna C.

Publication type:

Article

EHMT1 mosaicism in apparently unaffected parents is associated with autism spectrum disorder and neurocognitive dysfunction.

Published in:

Molecular Autism, 2018, v. 9, p. 1, doi. 10.1186/s13229-018-0193-9

By:

de Boer, Anneke;
Vermeulen, Karlijn;
Egger, Jos I. M.;
Janzing, Joost G. E.;
de Leeuw, Nicole;
Veenstra-Knol, Hermine E.;
den Hollander, Nicolette S.;
van Bokhoven, Hans;
Staal, Wouter;
Kleefstra, Tjitske

Publication type:

Article

Clinical and molecular characterization of patients with YWHAG‐related epilepsy.

Published in:

Epilepsia (Series 4), 2024, v. 65, n. 5, p. 1439, doi. 10.1111/epi.17939

By:

Cetica, Valentina;
Pisano, Tiziana;
Lesca, Gaetan;
Marafi, Dana;
Licchetta, Laura;
Riccardi, Florence;
Mei, Davide;
Chung, Hon‐yin B.;
Bayat, Allan;
Balasubramanian, Meena;
Lowenstein, Daniel H.;
Endzinienė, Milda;
Alotaibi, Maha;
Villeneuve, Nathalie;
Jacobs, Julia;
Isidor, Bertrand;
Solazzi, Roberta;
den Hollander, Nicolette S.;
Marjanovic, Dragan;
Rougeot‐Jung, Christelle

Publication type:

Article

X-chromosome duplications in males with mental retardation: pathogenic or benign variants?

Published in:

Clinical Genetics, 2011, v. 79, n. 1, p. 71, doi. 10.1111/j.1399-0004.2010.01438.x

By:

Gijsbers, A. C. J.;
Den Hollander, N. S.;
Helderman-van de Enden, A. T. J. M.;
Schuurs-Hoeijmakers, J. H. M.;
Vijfhuizen, L.;
Bijlsma, E. K.;
Van Haeringen, A.;
Hansson, K. B. M.;
Bakker, E.;
Breuning, M. H.;
Ruivenkamp, C. A. L.

Publication type:

Article

Recurrent Duplications of 17q12 Associated with Variable Phenotypes.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3038, doi. 10.1002/ajmg.a.37351

By:

Mitchell, Elyse;
Douglas, Andrew;
Kjaegaard, Susanne;
Callewaert, Bert;
Vanlander, Arnaud;
Janssens, Sandra;
Yuen, Amy Lawson;
Skinner, Cindy;
Failla, Pinella;
Alberti, Antonino;
Avola, Emanuela;
Fichera, Marco;
Kibaek, Maria;
Digilio, Maria C.;
Hannibal, Mark C.;
den Hollander, Nicolette S.;
Bizzarri, Veronica;
Renieri, Alessandra;
Mencarelli, Maria Antonietta;
Fitzgerald, Tomas

Publication type:

Article

Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 8, p. 1884, doi. 10.1002/ajmg.a.37076

By:

Tan, Ratna N. G. B.;
Witlox, Ruben S. G. M.;
Hilhorst‐Hofstee, Yvonne;
Peeters‐Scholte, Cacha M. P. C. D.;
den Hollander, Nicolette S.;
Ruivenkamp, Claudia A. L.;
Hoffer, Mariëtte J.V.;
Hansson, Kerstin B.;
van Roosmalen, Mark J.;
Kloosterman, Wigard P.;
Santen, Gijs W. E.

Publication type:

Article