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

American journal of human genetics, 2011-07, Vol.89 (1), p.67-81

2011

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Upper airway endoscopy to optimize obstructive sleep apnea treatment in Apert and Crouzon syndromes

Journal of cranio-maxillo-facial surgery, 2016-02, Vol.44 (2), p.191-196

2016

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

Plastic and reconstructive surgery. Global open, 2020-10, Vol.8 (10), p.e3204-e3204

2020

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Genetic Causes of Craniosynostosis: An Update

Molecular syndromology, 2019-02, Vol.10 (1-2), p.6-23

2019

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Intellectual, behavioral, and emotional functioning in children with syndromic craniosynostosis

Pediatrics (Evanston), 2014-06, Vol.133 (6), p.e1608

2014

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

Plastic and reconstructive surgery. Global open, 2019-09, Vol.7 (9), p.e2419-e2419

2019

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Secondary vault reconstruction after open or minimal invasive correction for unisutural, multisutural or syndromic craniosynostosis: A cohort study on the impact of diagnosis and type of initial surgical technique

Journal of plastic, reconstructive & aesthetic surgery, 2021-05, Vol.74 (5), p.1087-1092

2021

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Reducing social anxiety in adolescents distressed by a visible difference: Results from a randomised control trial of a web-based intervention

Body image, 2022-03, Vol.40, p.295-309

2022

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Guidelines for reconstruction of the eyelids and canthal regions

Journal of plastic, reconstructive & aesthetic surgery, 2010-09, Vol.63 (9), p.1420-1433

2010

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

American journal of human genetics, 2007-06, Vol.80 (6), p.1162-1170

2007

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Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability

American journal of human genetics, 2015-09, Vol.97 (3), p.378-388

2015

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

American journal of human genetics, 2009-05, Vol.84 (5), p.698-705

2009

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Venous hypertension in syndromic and complex craniosynostosis: The abnormal anatomy of the jugular foramen and collaterals

Journal of cranio-maxillo-facial surgery, 2015-04, Vol.43 (3), p.312-318

2015

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The formation of the foramen magnum and its role in developing ventriculomegaly and Chiari I malformation in children with craniosynostosis syndromes

Journal of cranio-maxillo-facial surgery, 2015-09, Vol.43 (7), p.1042-1048

2015

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Robin sequence: A European survey on current practice patterns

Journal of cranio-maxillo-facial surgery, 2015-10, Vol.43 (8), p.1626-1631

2015

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Eye and Orbital Anatomy in Metopic Synostosis

Plastic and reconstructive surgery. Global open, 2023-10, Vol.11 (10), p.e5303-e5303

2023

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Non-surgical and surgical interventions for airway obstruction in children with Robin Sequence

Journal of cranio-maxillo-facial surgery, 2016-12, Vol.44 (12), p.1871-1879

2016

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Adults with congenital or acquired facial disfigurement: Impact of appearance on social functioning

Journal of cranio-maxillo-facial surgery, 2012-12, Vol.40 (8), p.777-782

2012

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The Course and Interaction of Ventriculomegaly and Cerebellar Tonsillar Herniation in Crouzon Syndrome over Time

Plastic and reconstructive surgery. Global open, 2022-01, Vol.10 (1), p.e3979-e3979

2022

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Health-related quality of life in children and adolescents with syndromic craniosynostosis

Journal of plastic, reconstructive & aesthetic surgery, 2010-12, Vol.63 (12), p.1972-1981

2010

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Quality of life in children with robin sequence

International journal of pediatric otorhinolaryngology, 2016-07, Vol.86, p.98-103

2016

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Upper airway changes in syndromic craniosynostosis patients following midface or monobloc advancement: Correlation between volume changes and respiratory outcome

Journal of cranio-maxillo-facial surgery, 2012-04, Vol.40 (3), p.209-214

2012

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

American journal of human genetics, 2006-06, Vol.78 (6), p.999-1010

2006

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Orbital aspects following monobloc advancement in syndromic craniosynostosis

Journal of cranio-maxillo-facial surgery, 2013-10, Vol.41 (7), p.e146-e153

2013

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

Upper airway endoscopy to optimize obstructive sleep apnea treatment in Apert and Crouzon syndromes

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

Genetic Causes of Craniosynostosis: An Update

Intellectual, behavioral, and emotional functioning in children with syndromic craniosynostosis

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

Secondary vault reconstruction after open or minimal invasive correction for unisutural, multisutural or syndromic craniosynostosis: A cohort study on the impact of diagnosis and type of initial surgical technique

Reducing social anxiety in adolescents distressed by a visible difference: Results from a randomised control trial of a web-based intervention

Guidelines for reconstruction of the eyelids and canthal regions

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

Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability

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

Venous hypertension in syndromic and complex craniosynostosis: The abnormal anatomy of the jugular foramen and collaterals

The formation of the foramen magnum and its role in developing ventriculomegaly and Chiari I malformation in children with craniosynostosis syndromes

Robin sequence: A European survey on current practice patterns

Eye and Orbital Anatomy in Metopic Synostosis

Non-surgical and surgical interventions for airway obstruction in children with Robin Sequence

Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

Adults with congenital or acquired facial disfigurement: Impact of appearance on social functioning

The Course and Interaction of Ventriculomegaly and Cerebellar Tonsillar Herniation in Crouzon Syndrome over Time

Health-related quality of life in children and adolescents with syndromic craniosynostosis

Quality of life in children with robin sequence

Upper airway changes in syndromic craniosynostosis patients following midface or monobloc advancement: Correlation between volume changes and respiratory outcome

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

Orbital aspects following monobloc advancement in syndromic craniosynostosis

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