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Pediatric craniopharyngiomas: classification and treatment according to the degree of hypothalamic involvement

Journal of neurosurgery, 2007-01, Vol.106 (1 Suppl), p.3-12

2007

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Posterior cranial vault expansion in the treatment of craniosynostosis. Comparison of current techniques

Child's nervous system, 2012-09, Vol.28 (9), p.1537-1544

2012

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Reduction of morbidity of the frontofacial monobloc advancement in children by the use of internal distraction

Plastic and reconstructive surgery (1963), 2007-09, Vol.120 (4), p.1009-1026

2007

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Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations

European journal of human genetics : EJHG, 2014-12, Vol.22 (12), p.1413-1416

2014

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Postoperative cognitive outcome for synostotic frontal plagiocephaly

Journal of neurosurgery, 2006-07, Vol.105 (1 Suppl), p.16-20

2006

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Failure of third ventriculostomy in the treatment of aqueductal stenosis in children

Journal of neurosurgery, 1999-03, Vol.90 (3), p.448

1999

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Papillomas and carcinomas of the choroid plexus in children

Journal of neurosurgery, 1998-03, Vol.88 (3), p.521

1998

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Postoperative Mental and Morphological Outcome for Nonsyndromic Brachycephaly

Plastic and reconstructive surgery (1963), 2002-07, Vol.110 (1), p.6-12

2002

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Prognosis for mental function in scaphocephaly

Journal of neurosurgery, 1995-09, Vol.83 (3), p.476

1995

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Pediatric craniofacial osteosynthesis and distraction using an ultrasonic-assisted pinned resorbable system: a prospective report with a minimum 30 months' follow-up

The Journal of craniofacial surgery, 2009-11, Vol.20 (6), p.2081-2086

2009

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Hydrocephalus and craniosynostosis

Journal of neurosurgery, 1998-02, Vol.88 (2), p.209

1998

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Exorbitism correction of faciocraniosynostoses by monobloc frontofacial advancement with distraction osteogenesis

The Journal of craniofacial surgery, 2007-03, Vol.18 (2), p.355-360

2007

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Benign cerebellar astrocytomas in children

Journal of neurosurgery, 1999-02, Vol.90 (2), p.265

1999

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Prognosis for mental function in Apert's syndrome

Journal of neurosurgery, 1996-07, Vol.85 (1), p.66

1996

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Successful use of biosorb osteofixation devices in 165 cranial and maxillofacial cases: a multicenter report

The Journal of craniofacial surgery, 2004-07, Vol.15 (4), p.692-701

2004

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Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome

European journal of human genetics : EJHG, 1999-01, Vol.7 (1), p.27-33

1999

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Unoperated Craniosynostosis Patients : Correction in Adulthood

Plastic and reconstructive surgery (1963), 2008-12, Vol.122 (6), p.1827-1838

2008

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Hypertelorism Correction: What Happens with Growth? Evaluation of a Series of 95 Surgical Cases

Plastic and reconstructive surgery (1963), 2012-03, Vol.129 (3), p.713-727

2012

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Chiari malformation in craniosynostosis

Child's nervous system, 2005-10, Vol.21 (10), p.889-901

2005

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Increased bone formation and osteoblastic cell phenotype in premature cranial suture ossification (craniosynostosis)

Journal of bone and mineral research, 1996-03, Vol.11 (3), p.401-407

1996

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Spring-assisted posterior skull expansion without osteotomies

Child's nervous system, 2012-09, Vol.28 (9), p.1545-1549

2012

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Anterior fronto-orbital remodeling for trigonocephay

Child's nervous system, 2012-09, Vol.28 (9), p.1369-1373

2012

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Scaphocephaly part II: Secondary coronal synostosis after scaphocephalic surgical correction

The Journal of craniofacial surgery, 2009-09, Vol.20 Suppl 2 (8), p.1843-1850

2009

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Focus session on the changing “epidemiology” of craniosynostosis (comparing two quinquennia: 1985-1989 and 2003-2007) and its impact on the daily clinical practice: a review from Necker Enfants Malades

Child's nervous system, 2009-07, Vol.25 (7), p.807-811

2009

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Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome

European journal of human genetics : EJHG, 2006-03, Vol.14 (3), p.289-298

2006

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Pediatric craniopharyngiomas: classification and treatment according to the degree of hypothalamic involvement

Posterior cranial vault expansion in the treatment of craniosynostosis. Comparison of current techniques

Reduction of morbidity of the frontofacial monobloc advancement in children by the use of internal distraction

Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations

Postoperative cognitive outcome for synostotic frontal plagiocephaly

Failure of third ventriculostomy in the treatment of aqueductal stenosis in children

Papillomas and carcinomas of the choroid plexus in children

Postoperative Mental and Morphological Outcome for Nonsyndromic Brachycephaly

Prognosis for mental function in scaphocephaly

Pediatric craniofacial osteosynthesis and distraction using an ultrasonic-assisted pinned resorbable system: a prospective report with a minimum 30 months' follow-up

Hydrocephalus and craniosynostosis

Exorbitism correction of faciocraniosynostoses by monobloc frontofacial advancement with distraction osteogenesis

Benign cerebellar astrocytomas in children

Prognosis for mental function in Apert's syndrome

Successful use of biosorb osteofixation devices in 165 cranial and maxillofacial cases: a multicenter report

Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome

Unoperated Craniosynostosis Patients : Correction in Adulthood

Hypertelorism Correction: What Happens with Growth? Evaluation of a Series of 95 Surgical Cases

Chiari malformation in craniosynostosis

Increased bone formation and osteoblastic cell phenotype in premature cranial suture ossification (craniosynostosis)

Spring-assisted posterior skull expansion without osteotomies

Anterior fronto-orbital remodeling for trigonocephay

Scaphocephaly part II: Secondary coronal synostosis after scaphocephalic surgical correction

Focus session on the changing “epidemiology” of craniosynostosis (comparing two quinquennia: 1985-1989 and 2003-2007) and its impact on the daily clinical practice: a review from Necker Enfants Malades

Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome

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