Results 171 to 180 of about 3,158 (217)
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Neuro-Chirurgie, 1995
The authors relate a clinical and radiological (X Ray and TDM tridimensional) study with an anthropological (dry skulls) study of plagiocephaly. The aim is to find with the aid of a physical examination, some anatomic parameters which permit to differentiate cranial asymmetry with coronal premature synostotic suture from functional deformation with ...
A, Czorny +5 more
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The authors relate a clinical and radiological (X Ray and TDM tridimensional) study with an anthropological (dry skulls) study of plagiocephaly. The aim is to find with the aid of a physical examination, some anatomic parameters which permit to differentiate cranial asymmetry with coronal premature synostotic suture from functional deformation with ...
A, Czorny +5 more
openaire +1 more source
2013
Purpose: Most cranial deformities in newborns are caused either by head position in the first weeks of life or premature closure of cranial sutures. Craniosynostosis is the process of premature sutural closure, taking place during a period of continuing...
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Purpose: Most cranial deformities in newborns are caused either by head position in the first weeks of life or premature closure of cranial sutures. Craniosynostosis is the process of premature sutural closure, taking place during a period of continuing...
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[Dolicocephaly and premature synostosis of the sagittal suture].
Zentralblatt fur Neurochirurgie, 1991Guided by the literature historical, racial, genetical and diagnostical aspects, likewise associated syndromes and malformations of dolichocephaly and premature sagittal synostosis are represented, also own clinical, roentgenological, pneum- and electroencephalographic findings of 57 patients.
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Skull morphology after early craniotomy in patients with premature synostosis of the coronal suture.
The Cleft palate journal, 1987The degree of normalization of the shape of the skull was studied in 12 craniosynostosis patients who had been treated with different types of craniotomies in infancy. Three diagnoses were represented: isolated bicoronal synostosis; Crouzon's syndrome; and Apert's syndrome; there were four subjects in each group.
H, Friede +4 more
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Premature Cranial Synostosis and Hypophosphatemic Rickets
Acta Paediatrica, 1984Peter Clemens +3 more
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49. Premature Synostosis of the Cranial Sutures
Acta Paediatrica, 1959M. SULAMAA, L. LAITINEN
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Craniofacial growth in premature craniofacial synostosis
Plastic and Reconstructive Surgery, 1983openaire +1 more source
THE PATHOGENESIS OF PREMATURE CRANIAL SYNOSTOSIS IN MAN
Cells Tissues Organs, 1959openaire +2 more sources