A Proposal for the Interpretation of Serum IGF-I Concentration as Part of Laboratory Screening in Children with Growth Failure

por Wit, Jan M., Bidlingmaier, Martin, de Bruin, Christiaan, Oostdijk, Wilma
Publicado 2020

Vitamin D Deficiency in Pediatric Fracture Patients: Prevalence, Risk Factors, and Vitamin D Supplementation

por Gorter, Erwin A., Oostdijk, Wilma, Felius, Abraham, Krijnen, Pieta, Schipper, Inger B.
Publicado 2016

Improved growth with growth hormone treatment in children after hematopoietic stem cell transplantation

por Hoekx, Carlijn A., Bresters, Dorine, le Cessie, Saskia, Oostdijk, Wilma, Hannema, Sabine E.
Publicado 2022

Pituitary Adenoma Apoplexy in an Adolescent: A Case Report and Review of the Literature

por Zijlker, Hero, Schagen, Sebastian, Wit, Jan Maarten, Biermasz, Nienke, van Furth, Wouter, Oostdijk, Wilma
Publicado 2017

A mathematical model for predicting the adult height of girls with idiopathic central precocious puberty: A European validation

por Lemaire, Pierre, Duhil de Bénazé, Gwénaëlle, Mul, Dick, Heger, Sabine, Oostdijk, Wilma, Brauner, Raja
Publicado 2018

IGSF1 deficiency syndrome: A newly uncovered endocrinopathy

por Joustra, Sjoerd D., van Trotsenburg, A. S. Paul, Sun, Yu, Losekoot, Monique, Bernard, Daniel J., Biermasz, Nienke R., Oostdijk, Wilma, Wit, Jan M.
Publicado 2013

Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome

por Hulle, Severine Van, Craen, Margarita, Callewaert, Bert, Joustra, Sjoerd, Oostdijk, Wilma, Losekoot, Monique, Wit, Jan Maarten, Turgeon, Marc Olivier, Bernard, Daniel J., Schepper, Jean De
Publicado 2016

The diagnostic work up of growth failure in secondary health care; An evaluation of consensus guidelines

por Grote, Floor K, Oostdijk, Wilma, De Muinck Keizer-Schrama, Sabine MPF, van Dommelen, Paula, van Buuren, Stef, Dekker, Friedo W, Ketel, Arnoldus G, Moll, Henriette A, Wit, Jan M
Publicado 2008

Successful Growth Hormone Therapy in Cornelia de Lange Syndrome

por de Graaf, Michael, Kant, Sarina G, Wit, Jan Maarten, Redeker, Egbert Johan Willem, Santen, Gijs Willem Eduard, Verkerk, Annemieke Johanna Maria Henriëtta, Uitterlinden, André Gerardus, Losekoot, Monique, Oostdijk, Wilma
Publicado 2017

Screening rules for growth to detect celiac disease: A case-control simulation study

por van Dommelen, Paula, Grote, Floor K, Oostdijk, Wilma, Keizer-Schrama, Sabine MPF de Muinck, Boersma, Bart, Damen, Gerard M, Csizmadia, Cassandra G, Verkerk, Paul H, Wit, Jan M, van Buuren, Stef
Publicado 2008

Referral patterns of children with poor growth in primary health care

por Grote, Floor K, Oostdijk, Wilma, De Muinck Keizer-Schrama, Sabine MPF, Dekker, Friedo W, van Dommelen, Paula, van Buuren, Stef, Lodder-van der Kooij, Adry M, Verkerk, Paul H, Wit, Jan Maarten
Publicado 2007

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

por Bertko, Eleonore, Klammt, Jürgen, Dusatkova, Petra, Bahceci, Mithat, Gonc, Nazli, ten Have, Louise, Kandemir, Nurgun, Mansmann, Georg, Obermannova, Barbora, Oostdijk, Wilma, Pfäffle, Heike, Rockstroh-Lippold, Denise, Schlicke, Marina, Tuzcu, Alpaslan Kemal, Pfäffle, Roland
Publicado 2017

Phenotypic characterization of patients with deletions in the 3’-flanking SHOX region

por Kant, Sarina G., Broekman, Sander J., de Wit, Caroline C., Bos, Marloes, Scheltinga, Sitha A., Bakker, Egbert, Oostdijk, Wilma, van der Kamp, Hetty J., van Zwet, Erik W., van der Hout, Annemieke H., Wit, Jan M., Losekoot, Monique
Publicado 2013

PAPSS2 Deficiency Causes Androgen Excess via Impaired DHEA Sulfation—In Vitro and in Vivo Studies in a Family Harboring Two Novel PAPSS2 Mutations

por Oostdijk, Wilma, Idkowiak, Jan, Mueller, Jonathan W., House, Philip J., Taylor, Angela E., O'Reilly, Michael W., Hughes, Beverly A., de Vries, Martine C., Kant, Sarina G., Santen, Gijs W. E., Verkerk, Annemieke J. M. H., Uitterlinden, André G., Wit, Jan M., Losekoot, Monique, Arlt, Wiebke
Publicado 2015

A bone overgrowth disorder due to a gain-of-function mutation in the kinase homology domain of guanylyl cyclase B, the receptor for CNP

por Kuhn, Michaela, Premsler, Thomas, Yang, Ruey-Bing, Mueller, Thomas D, Gaßner, Birgit, Oberwinkler, Heike, Hannema, Sabine E, van Duyvenvoorde, Hermine A, Roelfsema, Ferdinand, Santen, Gijs WE, Prickett, Timothy, Kant, Sarina G, Verkerk, Annemieke JMH, Uitterlinden, André G, Espiner, Eric, Ruivenkamp, Claudia AL, Oostdijk, Wilma, Pereira, Alberto M, Losekoot, Monique, Wit, Jan M
Publicado 2013

Mutations in TBL1X Are Associated With Central Hypothyroidism

por Heinen, Charlotte A., Losekoot, Monique, Sun, Yu, Watson, Peter J., Fairall, Louise, Joustra, Sjoerd D., Zwaveling-Soonawala, Nitash, Oostdijk, Wilma, van den Akker, Erica L. T., Alders, Mariëlle, Santen, Gijs W. E., van Rijn, Rick R., Dreschler, Wouter A., Surovtseva, Olga V., Biermasz, Nienke R., Hennekam, Raoul C., Wit, Jan M., Schwabe, John W. R., Boelen, Anita, Fliers, Eric, van Trotsenburg, A. S. Paul
Publicado 2016

IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory Hyperfunction

por Joustra, Sjoerd D, Roelfsema, Ferdinand, van Trotsenburg, A S Paul, Schneider, Harald J, Kosilek, Robert P, Kroon, Herman M, Logan, John G, Butterfield, Natalie C, Zhou, Xiang, Toufaily, Chirine, Bak, Beata, Turgeon, Marc-Olivier, Brûlé, Emilie, Steyn, Frederik J, Gurnell, Mark, Koulouri, Olympia, Le Tissier, Paul, Fontanaud, Pierre, Duncan Bassett, J H, Williams, Graham R, Oostdijk, Wilma, Wit, Jan M, Pereira, Alberto M, Biermasz, Nienke R, Bernard, Daniel J, Schoenmakers, Nadia
Publicado 2019

Response to Letter to the Editor: “IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory Hyperfunction”

por Joustra, Sjoerd D, Roelfsema, Ferdinand, van Trotsenburg, A S Paul, Schneider, Harald J, Kosilek, Robert P, Kroon, Herman M, Logan, John G, Butterfield, Natalie C, Zhou, Xiang, Toufaily, Chirine, Bak, Beata, Turgeon, Marc-Olivier, Brûlé, Emilie, Steyn, Frederik J, Gurnell, Mark, Koulouri, Olympia, Le Tissier, Paul, Fontanaud, Pierre, Bassett, J H Duncan, Williams, Graham R, Oostdijk, Wilma, Wit, Jan M, Pereira, Alberto M, Biermasz, Nienke R, Bernard, Daniel J, Schoenmakers, Nadia
Publicado 2020

Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement

por Sun, Yu, Bak, Beata, Schoenmakers, Nadia, van Trotsenburg, A.S. Paul, Oostdijk, Wilma, Voshol, Peter, Cambridge, Emma, White, Jacqueline K., le Tissier, Paul, Gharavy, S. Neda Mousavy, Martinez-Barbera, Juan P., Stokvis-Brantsma, Wilhelmina H., Vulsma, Thomas, Kempers, Marlies J., Persani, Luca, Campi, Irene, Bonomi, Marco, Beck-Peccoz, Paolo, Zhu, Hongdong, Davis, Timothy M.E., Hokken-Koelega, Anita C.S., Del Blanco, Daria Gorbenko, Rangasami, Jayanti J., Ruivenkamp, Claudia A.L., Laros, Jeroen F.J., Kriek, Marjolein, Kant, Sarina G., Bosch, Cathy A.J., Biermasz, Nienke R., Appelman-Dijkstra, Natasha M., Corssmit, Eleonora P., Hovens, Guido C.J., Pereira, Alberto M., den Dunnen, Johan T., Wade, Michael G., Breuning, Martijn H., Hennekam, Raoul C., Chatterjee, Krishna, Dattani, Mehul T., Wit, Jan M., Bernard, Daniel J.
Publicado 2012