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PubPharm (109)
1
Treatment of Velopharyngeal Insufficiency Using Bilateral Myomucosal Buccinator Flaps
enthalten in:
Plastic and reconstructive surgery
| 2024
von
Raposo-Amaral, C.
|
Monte, T.
|
Raposo-Amaral, C.
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2
Discussion of "Does the Mutation Type Affect the Response to Cranial Vault Expansion in Children With Apert Syndrome?"
enthalten in:
The Journal of craniofacial surgery
| 2023
von
Raposo-Amaral, C.
|
Raposo-Amaral, C.
|
Ghizoni, E.
CommentOn: J Craniofac Surg. 2023 May 1;34(3):910-913. - PMID 36730527
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3
Apert Syndrome : Selection Rationale for Midface Advancement Technique
enthalten in:
Advances and technical standards in neurosurgery
| 2023
von
Raposo-Amaral, C.
|
Ghizoni, E.
|
Raposo-Amaral, C.
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4
Posterior Vault Distraction Outcomes in Patients With Severe Crouzon Syndrome Resulting from Ser347Cys and Ser354Cys Mutations
enthalten in:
The Journal of craniofacial surgery
| 2022
von
Raposo-Amaral, C.
|
Raposo-Amaral, C.
|
Adams, J.
| +1
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5
Apert Syndrome Outcomes : Comparison of Posterior Vault Distraction Osteogenesis Versus Fronto Orbital Advancement
enthalten in:
The Journal of craniofacial surgery
| 2022
von
Raposo-Amaral, C.
|
Oliveira, Y.
|
Raposo-Amaral, C.
| +1
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6
Functionality Assessment of Patients With Cleft Hands
enthalten in:
The Journal of craniofacial surgery
| 2022
von
Rosa, M.
|
do Monte, T.
|
Raposo-Amaral, C.
| +2
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7
An Extended 45-year Long-term Follow-up on a 1-13 Rare Facial Cleft Patient
enthalten in:
The Journal of craniofacial surgery
| 2021
von
Raposo-Amaral, C.
|
Oliveira, Y.
|
Denadai, R.
| +2
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8
Craniofrontonasal dysplasia : hypertelorism correction in late presenting patients
enthalten in:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
| 2021
von
Raposo-Amaral, C.
|
Resende, G.
|
Denadai, R.
| +2
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9
Treating Syndromic Craniosynostosis with Monobloc Facial Bipartition and Internal Distractor Devices : Destigmatizing the Syndromic Face
enthalten in:
Clinics in plastic surgery
| 2021
von
Raposo-Amaral, C.
|
Vieira, P.
|
Denadai, R.
| +2
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10
Severe craniolacunae and upper and lower extremity anomalies resulting from Crouzon syndrome, FGFR2 mutation, and Ser347Cys variant
enthalten in:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
| 2021
von
Raposo-Amaral, C.
|
Oliveira, Y.
|
Denadai, R.
| +2
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