Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis

por Mathijssen, Irene M.J.
Publicado en J Craniofac Surg (2015)

Introduction to Updated Guideline on Treatment and Management of Craniosynostosis

por Mathijssen, Irene M.J.
Publicado en J Craniofac Surg (2021)

Updated Guideline on Treatment and Management of Craniosynostosis

por Mathijssen, Irene M.J.
Publicado en J Craniofac Surg (2021)

Genetic Causes of Craniosynostosis: An Update

por Goos, Jacqueline A.C., Mathijssen, Irene M.J.
Publicado en Mol Syndromol (2019)

Is Cortical Complexity Development Affected By Syndromic Craniosynostosis?

por Wilson, Alexander T., Vrooman, Henri A., Mathijssen, Irene M. J.
Publicado en Plast Reconstr Surg Glob Open (2020)

Health-related problems and quality of life in patients with syndromic and complex craniosynostosis

por de Jong, Tim, Maliepaard, Marianne, Bannink, Natalja, Raat, Hein, Mathijssen, Irene M. J.
Publicado 2012

Assessing Nonacceptance of the Facial Appearance in Adult Patients After Complete Treatment of Their Rare Facial Cleft

por van den Elzen, Marijke E. P., Versnel, Sarah L., Duivenvoorden, Hugo J., Mathijssen, Irene M. J.
Publicado 2012

Testing for Implicit Gender Bias among Plastic Surgeons

por Bucknor, Alexandra, Ngaage, Ledibabari M., Taylor, Kirsten J., Kamali, Parisa, Rakhorst, Hinne A., Mathijssen, Irene M. J., Furnas, Heather
Publicado en Plast Reconstr Surg Glob Open (2021)

Intracranial Hypertension and Cortical Thickness in Syndromic Craniosynostosis

por Wilson, Alexander T., den Ottelander, Bianca K., de Goederen, Robbin G., Dremmen, Marjolein H. G., Vrooman, Henri A., Mathijssen, Irene M. J.
Publicado en Plast Reconstr Surg Glob Open (2019)

Using Perfusion Contrast for Spatial Normalization of ASL MRI Images in a Pediatric Craniosynostosis Population

por de Planque, Catherine A., Mutsaerts, Henk J. M. M., Keil, Vera C., Erler, Nicole S., Dremmen, Marjolein H. G., Mathijssen, Irene M. J., Petr, Jan
Publicado en Front Neurosci (2021)

Management and outcomes of obstructive sleep apnea in children with Robin sequence, a cross-sectional study

por van Lieshout, Manouk J.S., Joosten, Koen F.M., Koudstaal, Maarten J., van der Schroeff, Marc P., Dulfer, Karolijn, Mathijssen, Irene M.J., Wolvius, Eppo B.
Publicado en Clin Oral Investig (2016)

Cortical Thickness in Crouzon–Pfeiffer Syndrome: Findings in Relation to Primary Cranial Vault Expansion

por Wilson, Alexander T., de Planque, Catherine A., Yang, Sumin S., Tasker, Robert C., van Veelen, Marie-Lise C., Dremmen, Marjolein H.G., Vrooman, Henri A., Mathijssen, Irene M.J.
Publicado en Plast Reconstr Surg Glob Open (2020)

Improvement in Sleep Architecture is associated with the Indication of Surgery in Syndromic Craniosynostosis

por de Goederen, Robbin, Joosten, Koen F.M., den Ottelander, Bianca K., van der Oest, Mark J.W., Bröker-Schenk, Els M.M., van Veelen, Marie-Lise C., Wolvius, Eppo B., Versnel, Sarah L., Tasker, Robert C., Mathijssen, Irene M.J.
Publicado en Plast Reconstr Surg Glob Open (2019)

Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure

por Oussoren, Esmee, Mathijssen, Irene M. J., Wagenmakers, Margreet, Verdijk, Rob M., Bredero-Boelhouwer, Hansje H., van Veelen-Vincent, Marie-Lise C., van der Meijden, Jan C., van den Hout, Johanna M. P., Ruijter, George J. G., van der Ploeg, Ans T., Langeveld, Mirjam
Publicado en J Inherit Metab Dis (2018)

Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene

por Twigg, Stephen R.F., Versnel, Sarah L., Nürnberg, Gudrun, Lees, Melissa M., Bhat, Meenakshi, Hammond, Peter, Hennekam, Raoul C.M., Hoogeboom, A. Jeannette M., Hurst, Jane A., Johnson, David, Robinson, Alexis A., Scambler, Peter J., Gerrelli, Dianne, Nürnberg, Peter, Mathijssen, Irene M.J., Wilkie, Andrew O.M.
Publicado 2009

Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth

por Nieminen, Pekka, Morgan, Neil V., Fenwick, Aimée L., Parmanen, Satu, Veistinen, Lotta, Mikkola, Marja L., van der Spek, Peter J., Giraud, Andrew, Judd, Louise, Arte, Sirpa, Brueton, Louise A., Wall, Steven A., Mathijssen, Irene M.J., Maher, Eamonn R., Wilkie, Andrew O.M., Kreiborg, Sven, Thesleff, Irma
Publicado 2011

RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity

por Jenkins, Dagan , Seelow, Dominik , Jehee, Fernanda S. , Perlyn, Chad A. , Alonso, Luís G. , Bueno, Daniela F. , Donnai, Dian , Josifiova, Dragana , Mathijssen, Irene M. J. , Morton, Jenny E. V. , Ørstavik, Karen Helene , Sweeney, Elizabeth , Wall, Steven A. , Marsh, Jeffrey L. , Nürnberg, Peter , Passos-Bueno, Maria Rita , Wilkie, Andrew O. M. 
Publicado 2007

The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

por Twigg, Stephen R. F., Matsumoto, Kazuya, Kidd, Alexa M. J., Goriely, Anne, Taylor, Indira B., Fisher, Richard B., Hoogeboom, A. Jeannette M., Mathijssen, Irene M. J., Lourenço, M. Teresa, Morton, Jenny E. V., Sweeney, Elizabeth, Wilson, Louise C., Brunner, Han G., Mulliken, John B., Wall, Steven A., Wilkie, Andrew O. M.
Publicado 2006

A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis

por Goos, Jacqueline A C, Vogel, Walter K, Mlcochova, Hana, Millard, Christopher J, Esfandiari, Elahe, Selman, Wisam H, Calpena, Eduardo, Koelling, Nils, Carpenter, Evan L, Swagemakers, Sigrid M A, van der Spek, Peter J, Filtz, Theresa M, Schwabe, John W R, Iwaniec, Urszula T, Mathijssen, Irene M J, Leid, Mark, Twigg, Stephen R F
Publicado en Hum Mol Genet (2019)

Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12‐Related Craniosynostosis

por Goos, Jacqueline A.C., Fenwick, Aimee L., Swagemakers, Sigrid M.A., McGowan, Simon J., Knight, Samantha J.L., Twigg, Stephen R.F., Hoogeboom, A. Jeannette M., van Dooren, Marieke F., Magielsen, Frank J., Wall, Steven A., Mathijssen, Irene M.J., Wilkie, Andrew O.M., van der Spek, Peter J., van den Ouweland, Ans M.W.
Publicado en Hum Mutat (2016)