Craniostenosi: Neuro e Splancnocranio

Abstract

Keywords

craniostenosis craniofacial malformations spiral TC 3D reconstructions

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References

Bellussi

Miele

: Ricostruzioni tridimensionali mediante tomografia computerizzata spirale nello studio delle craniostenosi. Esperienza preliminare e considerazioni tecniche. Radiol Med 94: 579–582, 1997.

Benson

Oliverio

: Primary craniosynostosis: Imaging features. Am J Radiol 166: 697–703, 1996.

Brueton

van Herwerden

: The mapping of a gene for craniosynostosis: Evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p. Med Genet 29: 681–685, 1992.

Cohen

Jr : Etiopathogenesis of craniosynostosis. Neurosurg-Clin-N-Am 2(3): 507–513; 1042–3680, 1991.

Craven

Naik

: Multispiral three-dimensional computed tomography in the investigation of craniosynostosis: Technique optimization. Br J Radiol 68: 724–730, 1995.

Darling

Byrd

: Three-dimensional Computed Tomography imaging in the evaluation of craniofacial abnormalities. J National Med Assoc 86: 676–680, 1994.

Denis

Genitori

: Ocular findings in Trigonocephaly. Graefes Arch Clin Exp Ophthalmol 232(12): 728–733, 1994.

Di Rocco

Velardi

: Nosographic identification and classification of plagiocephaly. Child's Nerv Sist 4: 9–15, 1988.

Fernbach

Naidich

: Radiological evaluation of craniosynostosis. In: Cohen

Jr. Craniosynostosis, diagnosis, evaluation and management. Raven Press, New York 1986: 191–214.

10.

Freeman

Barkowf

: Craniostenosis: Rewiew of the literature and report of thirty-four cases. Pediatrics 30: 57–70, 1962.

11.

Genitori

Zanon

: The skull base in plagiocephaly. Child's Nerv Syst 10: 217–223, 1994.

12.

Heiken

Brink

: Spiral (helical) CT. Radiology 189: 647–656, 1993.

13.

Hui

Joyner

: A mouse model of Greig cephalopolysyndactyly syndrome: The extra-toes mutation contains an intragenic deletion of the Gli3 gene. Nature Genet 3: 241–246, 1993.

14.

Levy

: Three-dimensional craniocervical helical CT: Is isotropic imaging possible? Radiology 197: 645–648, 1995.

15.

Mathijssen

IMJ

Vaandrager

: The role of bone centers in the pathogenesis of craniosynostosis: An embryologic approach using CT measurements in isolated craniosynostosis and Apert and Crouzon syndromes. Plastic and Reconstructive Surgery 98(1): 17–26, 1996.

16.

Muenke

Schell

: A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome. Nature Genet 8: 269–274, 1994.

17.

Naidich

Zimmermann

: Midface: Embryology and congenital lesions. In: Som

Curtin

: Head and neck imaging 3th ed. Mosby-Year Book, Inc., St. Louis (MO) 1996: 45–47.

18.

Posnick

Bite

: Indirect intracranial volume masurements using CT Scans. Plastic and Recostructive Surgery 89(1): 34–45, 1992.

19.

Preston

Post

: A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10. Nature Genet 7: 149–153, 1994.

20.

Reardon

Winter

: Mutations in the fibroblast growth receptor 2 gene cause Crouzon syndrome. Nature Genet 8: 98–103, 1994.

21.

Tartaro

Larici

: Ottimizzazione e accuratezza diagnostica della Tomografia Computerizzata con tecnica spirale tridimensionale nello studio della craniostenosi. La Radiologia Medica (in stampa).

22.

Vannier

Pilgram

: Craniosynostosis: Diagnostic value of three-dimensional CT. Presentation. Am J Neuroradiol 15: 1861–1869, 1994.

23.

Virchow

: Über den Cretinismus, namentlich in Franken, und über pathol-ogische Schädelforamen. Ver Phys Med Ges Würzburg 2: 230–241, 1852.

24.

Vortkamp

Gessler

: GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families. Nature 352: 539–540, 1991.

25.

Wilkie

AOM

Slaney

: Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genet 9: 165–172, 1995.