SCOPUS 정보 검색 플랫폼

Journal of Neurosurgery: Pediatrics

Volumn 10, Issue 4, 2012, Pages 310-314

Bilateral endoscopic craniectomies in the treatment of an infant with Apert syndrome: Case report

(2) Jimenez, David F a Barone, Constance M a

a University of Texas Health Science Center at San Antonio (United States)

Author keywords

Apert syndrome; Congenital deformity; Coronal craniosynostosis; Cranial orthosis; Craniectomy; Endoscopy

Indexed keywords

ACROCEPHALOSYNDACTYLY; ANTERIOR FONTANEL; ARTICLE; BRACHYCEPHALY; CASE REPORT; CRANIAL ORTHOSIS; CRANIECTOMY; CRANIOFACIAL SYNOSTOSIS; EXOPHTHALMOS; FEMALE; HELMET; HUMAN; INFANT; MIDFACE HYPOPLASIA; NEUROENDOSCOPY; NOSE RECONSTRUCTION; ORTHOSIS; OSTEOTOMY; PRIORITY JOURNAL; RIGID ENDOSCOPE;

ACROCEPHALOSYNDACTYLIA; CRANIOTOMY; EXOPHTHALMOS; FEMALE; FRONTAL BONE; HUMANS; IMAGING, THREE-DIMENSIONAL; INFANT; NEUROENDOSCOPY; ORTHOTIC DEVICES; TOMOGRAPHY, X-RAY COMPUTED; TREATMENT OUTCOME;

EID: 84868339134 PISSN: 19330707 EISSN: 19330715 Source Type: Journal
DOI: 10.3171/2012.7.PEDS11281 Document Type: Article

Times cited : (21)

References (9)

1
- 0016736856
- Trapezoidocephaly, midfacial hypoplasia and cartilage abnormalities with multiple synostoses and skeletal fractures
- Antley R, Bixler D: Trapezoidocephaly, midfacial hypoplasia and cartilage abnormalities with multiple synostoses and skeletal fractures. Birth Defects Orig Artic Ser 11:397-401, 1975
- (1975) Birth Defects Orig Artic Ser , vol.11 , pp. 397-401
- Antley, R.¹ Bixler, D.²

2
- 0000003824
- De L'acrocéphalosyndactylie
- Apert E: De L'acrocéphalosyndactylie. Bull Soc Med Paris 23:1310-1330, 1906
- (1906) Bull Soc Med Paris , vol.23 , pp. 1310-1330
- Apert, E.¹

3
- 0006659266
- Two sisters showing malformations of the skull and other congenital abnormalities
- Carpenter G: Two sisters showing malformations of the skull and other congenital abnormalities. Rep Soc Study Dis Child (London) 1:110-118, 1901
- (1901) Rep Soc Study Dis Child (London) , vol.1 , pp. 110-118
- Carpenter, G.¹

4
- 0001956946
- Eine eigenartige familiäre Entwicklungsstörung. (Akrocephalosyndaktylie, Dysostosis craniofacilalis und hypertelorismus)
- Chotzen F: Eine eigenartige familiäre Entwicklungsstörung. (Akrocephalosyndaktylie, Dysostosis Craniofacilalis und Hypertelorismus). Monatsschrift Kinderheilkd 55:97-122, 1932
- (1932) Monatsschrift Kinderheilkd , vol.55 , pp. 97-122
- Chotzen, F.¹

5
- 0001326304
- Dysostose craniofaciale héréditaire
- Crouzon O: Dysostose craniofaciale héréditaire. Bull Soc Med Paris 33:1037-1044, 1912
- (1912) Bull Soc Med Paris , vol.33 , pp. 1037-1044
- Crouzon, O.¹

6
- 77649086944
- Multiple-suture nonsyndromic craniosynostosis: Early and effective management using endoscopic techniques. Clinical article
- Jimenez DF, Barone CM: Multiple-suture nonsyndromic craniosynostosis: Early and effective management using endoscopic techniques. Clinical article. J Neurosurg Pediatr 5: 223-231, 2010
- (2010) J Neurosurg Pediatr , vol.5 , pp. 223-231
- Jimenez, D.F.¹ Barone, C.M.²

7
- 2842580997
- Associated deformities of the head and hands
- Pfeiffer RA: Associated deformities of the head and hands. Birth Defects Orig Artic Ser 5:18-34, 1969
- (1969) Birth Defects Orig Artic Ser , vol.5 , pp. 18-34
- Pfeiffer, R.A.¹

8
- 0000008683
- Dominant erbliche akrocephalosyndaktylie
- Pfeiffer RA: Dominant erbliche akrocephalosyndaktylie. Z Kinderheilkd 90:301-320, 1964
- (1964) Z Kinderheilkd , vol.90 , pp. 301-320
- Pfeiffer, R.A.¹

9
- 0001636485
- Ein Beitrag zum turmschädel problem (Pathogenese, Erblichkeit und Symptologie)
- Saethre H: Ein Beitrag zum turmschädel problem (Pathogenese, Erblichkeit und Symptologie). Dtsch Z Nervenheilkd 17:533-555, 1931
- (1931) Dtsch Z Nervenheilkd , vol.17 , pp. 533-555
- Saethre, H.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.