Results
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81.
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Algorithm for the Management of Intracranial Hypertension in Children with Syndromic Craniosynostosis. [electronic resource] by
- Spruijt, Bart
- Joosten, Koen F M
- Driessen, Caroline
- Rizopoulos, Dimitris
- Naus, Nicole C
- van der Schroeff, Marc P
- Wolvius, Eppo B
- van Veelen, Marie-Lise C
- Tasker, Robert C
- Mathijssen, Irene M J
Producer: 20151019
In:
Plastic and reconstructive surgery vol. 136
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82.
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83.
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84.
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Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome. [electronic resource] by
- Fenwick, Aimee L
- Goos, Jacqueline A C
- Rankin, Julia
- Lord, Helen
- Lester, Tracy
- Hoogeboom, A Jeannette M
- van den Ouweland, Ans M W
- Wall, Steven A
- Mathijssen, Irene M J
- Wilkie, Andrew O M
Producer: 20141104
In:
BMC medical genetics vol. 15
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85.
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Surgical Correction of Craniofacial Microsomia: Evaluation of Interventions in 565 Patients at Three Major Craniofacial Units. [electronic resource] by
- Pluijmers, Britt I
- Caron, Cornelia J J M
- van de Lande, Lara S
- Schaal, Sontje
- Mathijssen, Irene M
- Wolvius, Eppo B
- Bulstrode, Neil
- Evans, Robert D
- Padwa, Bonnie L
- Koudstaal, Maarten J
- Dunaway, David J
Producer: 20190522
In:
Plastic and reconstructive surgery vol. 143
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86.
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87.
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On the origin of bitemporal hollowing. [electronic resource] by
- van der Meulen, Jacques J N M
- Willemsen, Joep
- van der Vlugt, Joris
- Nazir, Patricia R N
- Hilling, Denise
- Mathijssen, Irene M J
- Ongkosuwito, Edwin
- van Adrichem, Leon N A
- Vaandrager, Michiel J M
- Hovius, Steven E R
Producer: 20090820
In:
The Journal of craniofacial surgery vol. 20
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88.
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Improvement in Sleep Architecture is associated with the Indication of Surgery in Syndromic Craniosynostosis. [electronic resource] by
- 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
Publication details: Plastic and reconstructive surgery. Global open Sep 2019
In:
Plastic and reconstructive surgery. Global open vol. 7
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89.
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Papilledema in patients with Apert, Crouzon, and Pfeiffer syndrome: prevalence, efficacy of treatment, and risk factors. [electronic resource] by
- Bannink, Natalja
- Joosten, Koen F M
- van Veelen, Marie-Lise C
- Bartels, Marjolijn C
- Tasker, Robert C
- van Adrichem, Léon N A
- van der Meulen, Jacques J N M
- Vaandrager, J Michiel
- de Jong, Tjeerd H R
- Mathijssen, Irene M J
Producer: 20080418
In:
The Journal of craniofacial surgery vol. 19
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90.
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Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure. [electronic resource] by
- 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
Producer: 20191104
In:
Journal of inherited metabolic disease vol. 41
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91.
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Cerebral blood flow in children with syndromic craniosynostosis: cohort arterial spin labeling studies. [electronic resource] by
- Doerga, Priya N
- Lequin, Maarten H
- Dremmen, Marjolein H G
- den Ottelander, Bianca K
- Mauff, Katya A L
- Wagner, Matthias W
- Hernandez-Tamames, Juan A
- Versnel, Sarah L
- Joosten, Koen F M
- van Veelen, Marie-Lise C
- Tasker, Robert C
- Mathijssen, Irene M J
Publication details: Journal of neurosurgery. Pediatrics 04 2020
In:
Journal of neurosurgery. Pediatrics vol. 25
Availability: No items available.
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92.
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Inactivation of IL11 signaling causes craniosynostosis, delayed tooth eruption, and supernumerary teeth. [electronic resource] by
- 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
Producer: 20110919
In:
American journal of human genetics vol. 89
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93.
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Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. [electronic resource] by
- 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
Producer: 20090609
In:
American journal of human genetics vol. 84
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94.
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Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome. [electronic resource] by
- Florisson, Joyce M G
- Mathijssen, Irene M J
- Dumee, Belinda
- Hoogeboom, Jeannette A M
- Poddighe, Pino J
- Oostra, Ben A
- Frijns, Jean Pierre
- Koster, Linda
- de Klein, Annelies
- Eussen, Bert
- de Vries, Bert B A
- Swagemakers, Sigrid
- van der Spek, Peter J
- Verkerk, Annemieke J M H
Producer: 20130701
In:
American journal of medical genetics. Part A vol. 161A
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95.
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International importance of robust breast device registries. [electronic resource] by
- Cooter, Rodney D
- Barker, Shane
- Carroll, Sean M
- Evans, Gregory R D
- von Fritschen, Uwe
- Hoflehner, Helmut
- Le Louarn, Claude
- Lumenta, David B
- Mathijssen, Irene M J
- McNeil, John
- Mulgrew, Stephen
- Mureau, Marc A M
- Perks, Graeme
- Rakhorst, Hinne
- Randquist, Charles
- Topaz, Moris
- Verheyden, Charles
- de Waal, John
Producer: 20150417
In:
Plastic and reconstructive surgery vol. 135
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96.
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The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males. [electronic resource] by
- 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
- Lourenco, M Teresa
- Morton, Jenny E V
- Sweeney, Elizabeth
- Wilson, Louise C
- Brunner, Han G
- Mulliken, John B
- Wall, Steven A
- Wilkie, Andrew O M
Producer: 20060630
In:
American journal of human genetics vol. 78
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97.
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RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity. [electronic resource] by
- Jenkins, Dagan
- Seelow, Dominik
- Jehee, Fernanda S
- Perlyn, Chad A
- Alonso, Luis G
- Bueno, Daniela F
- Donnai, Dian
- Josifova, Dragana
- Josifiova, Dragana
- Mathijssen, Irene M J
- Morton, Jenny E V
- Orstavik, Karen Helene
- Sweeney, Elizabeth
- Wall, Steven A
- Marsh, Jeffrey L
- Nurnberg, Peter
- Passos-Bueno, Maria Rita
- Wilkie, Andrew O M
Producer: 20070626
In:
American journal of human genetics vol. 80
Availability: No items available.
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98.
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A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis. [electronic resource] by
- 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
Producer: 20210831
In:
Human molecular genetics vol. 28
Availability: No items available.
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99.
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Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12-Related Craniosynostosis. [electronic resource] by
- 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
Producer: 20171215
In:
Human mutation vol. 37
Availability: No items available.
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100.
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Muenke syndrome: long-term outcome of a syndrome-specific treatment protocol. [electronic resource] by
- den Ottelander, Bianca K
- de Goederen, Robbin
- van Veelen, Marie-Lise C
- van de Beeten, Stephanie D C
- Lequin, Maarten H
- Dremmen, Marjolein H G
- Loudon, Sjoukje E
- Telleman, Marieke A J
- de Gier, Henriëtte H W
- Wolvius, Eppo B
- Tjoa, Stephen T H
- Versnel, Sarah L
- Joosten, Koen F M
- Mathijssen, Irene M J
Publication details: Journal of neurosurgery. Pediatrics 10 2019
In:
Journal of neurosurgery. Pediatrics vol. 24
Availability: No items available.
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