메뉴 건너뛰기




Volumn 71, Issue 2, 2012, Pages 78-81

Foramina parietalia permagna: The ins and outs

Author keywords

Cranium bifidum; Enlarged parietal foramina; Familial; Parietal bone

Indexed keywords

ALX4 PROTEIN, HUMAN; DNA BINDING PROTEIN; TRANSCRIPTION FACTOR;

EID: 84865237227     PISSN: 00155659     EISSN: 16443284     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (24)
  • 1
    • 0000582294 scopus 로고
    • The emissary foramina of the cranium in man and the anthropoids
    • Boyd GI (1930) The emissary foramina of the cranium in man and the anthropoids. J Anat, 65: 108-121.
    • (1930) J Anat , vol.65 , pp. 108-121
    • Boyd, G.I.1
  • 2
    • 40449106604 scopus 로고    scopus 로고
    • Complete cranium bifidum without scalp abnormality: Case report
    • DOI 10.3171/PED/2008/1/3/258
    • Celik SE, Kara A (2008) Complete cranium bifidum without scalp abnormality. J Neurosurg Pediatr, 1: 258-260. (Pubitemid 351346518)
    • (2008) Journal of Neurosurgery: Pediatrics , vol.1 , Issue.3 , pp. 258-260
    • Celik, S.E.1    Kara, A.2
  • 3
    • 0038449055 scopus 로고
    • Congenital parietal foramina associated with faulty ossification of the clavicles
    • Eckstein HB, Hoare RD (1963) Congenital parietal foramina associated with faulty ossification of the clavicles. Br J Radiol; 36: 220-221.
    • (1963) Br J Radiol , vol.36 , pp. 220-221
    • Eckstein, H.B.1    Hoare, R.D.2
  • 4
    • 33747440750 scopus 로고    scopus 로고
    • Enlarged parietal foramina: MR imaging features in the fetus and neonate
    • Fink AM, Maixner W (2006) Enlarged parietal foramina: MR imaging features in the fetus and neonate. Am J Neuroradiol, 27: 1379-1381. (Pubitemid 44897662)
    • (2006) American Journal of Neuroradiology , vol.27 , Issue.6 , pp. 1379-1381
    • Fink, A.M.1    Maixner, W.2
  • 5
    • 0002537849 scopus 로고
    • "The catlin mark" the inheritance of an unusual opening in the parietal bone
    • Goldsmith WM (1922) "The catlin mark" the inheritance of an unusual opening in the parietal bone. J Hered, 13: 69-71.
    • (1922) J Hered , vol.13 , pp. 69-71
    • Goldsmith, W.M.1
  • 7
    • 40449086960 scopus 로고
    • On congenital and symmetrical perforation of both parietal bones
    • Greig DM (1892) On congenital and symmetrical perforation of both parietal bones. J Anat Physiol, 26: 187-191.
    • (1892) J Anat Physiol , vol.26 , pp. 187-191
    • Greig, D.M.1
  • 9
    • 84872208561 scopus 로고    scopus 로고
    • Huber cited by Rahilly et al. 1952 - [18]
    • Huber cited by Rahilly et al. 1952 - [18].
  • 10
    • 0014443035 scopus 로고
    • A concordant craniofacial dysostosis with Enlarged parietal Foramina in twins
    • Lehrer HZ, Familant JW (1969) A concordant craniofacial dysostosis with Enlarged parietal Foramina in twins. Radiology, 92: 127-129.
    • (1969) Radiology , vol.92 , pp. 127-129
    • Lehrer, H.Z.1    Familant, J.W.2
  • 12
    • 0025099424 scopus 로고
    • Enlarged parietal foramina and craniosynostosis in an American Indian child
    • Mann RW (1990) Enlarged parietal foramina and craniosynostosis in an American Indian child. Am J Rad, 154: 658. (Pubitemid 20071640)
    • (1990) American Journal of Roentgenology , vol.154 , Issue.3 , pp. 658
    • Mann, R.W.1
  • 15
    • 0014873914 scopus 로고
    • Evolution of persistently enlarged parietal foramina
    • Murphy J, Gooding CA (1970) Evolution of persistently enlarged parietal foramina. Radiology, 97: 391-392.
    • (1970) Radiology , vol.97 , pp. 391-392
    • Murphy, J.1    Gooding, C.A.2
  • 16
    • 0029067515 scopus 로고
    • Aplasia cutis congenital and enlarged parietal foramina (Catlin marks)
    • Preis S, Engelbrecht V, Lenard HG (1995) Aplasia cutis congenital and enlarged parietal foramina (Catlin marks). Acta Paediatr, 84: 701-702.
    • (1995) Acta Paediatr , vol.84 , pp. 701-702
    • Preis, S.1    Engelbrecht, V.2    Lenard, H.G.3
  • 17
    • 0042604847 scopus 로고
    • Hereditary occrence of enlarged parietal foramina
    • cited by Hollender 1967 - [8]
    • Pepper OH, Pendergrass EP (1936) Hereditary occrence of enlarged parietal foramina. Am J Roentgenol Rad Therapy, 35: 1-8 (cited by Hollender 1967 - [8]).
    • (1936) Am J Roentgenol Rad Therapy , vol.35 , pp. 1-8
    • Pepper, O.H.1    Pendergrass, E.P.2
  • 18
    • 0344522622 scopus 로고
    • Foramina parietalia permagna
    • Rahilly RO, Twohig MJ (1952) Foramina parietalia permagna. Am J Radiol, 67: 551-561.
    • (1952) Am J Radiol , vol.67 , pp. 551-561
    • Rahilly, R.O.1    Twohig, M.J.2
  • 19
    • 0034646234 scopus 로고    scopus 로고
    • Enlarged parietal foramina: Association with cerebral venous and cortical anomalies
    • Reddy AT, Hedlund GL, Percy AK (2000) Neurology. Enlarged parietal foramina: association with cerebral venous and cortical anomalies. Neurology, 54: 1175-1178. (Pubitemid 30151864)
    • (2000) Neurology , vol.54 , Issue.5 , pp. 1175-1178
    • Reddy, A.T.1    Hedlund, G.L.2    Percy, A.K.3
  • 20
    • 0343745129 scopus 로고
    • Congenital perforations of the skull in relation to parietal bone
    • cited by Hollender 1967 - [8]
    • Robinsons RG (1962) Congenital perforations of the skull in relation to parietal bone. J Neurosurg, 19: 153 (cited by Hollender 1967 - [8]).
    • (1962) J Neurosurg , vol.19 , pp. 153
    • Robinsons, R.G.1
  • 21
    • 84872204239 scopus 로고    scopus 로고
    • Toldt cited by Rahilly et al. 1952 - [18]
    • Toldt cited by Rahilly et al. 1952 - [18].
  • 22
    • 0141679613 scopus 로고    scopus 로고
    • Parietal foramina are not synonymous with giant parietal foramina
    • DOI 10.1159/000072475
    • Tubbs RS, Smyth MD, Oakes WJ (2003) Parietal foramina are not synonymous with giant parietal foramina. Pediatr Neurosurg, 39: 216-217. (Pubitemid 37116990)
    • (2003) Pediatric Neurosurgery , vol.39 , Issue.4 , pp. 216-217
    • Tubbs, R.S.1    Smyth, M.D.2    Oakes, W.J.3
  • 24
    • 0034530307 scopus 로고    scopus 로고
    • The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)
    • Wuyts W, Cleiren E, Homfray T, Rasore-Quartino A, Vanhoenacker F, Van Hul W (2000) The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). Med Genet, 37: 916-920. (Pubitemid 32002887)
    • (2000) Journal of Medical Genetics , vol.37 , Issue.12 , pp. 916-920
    • Wuyts, W.1    Cleiren, E.2    Homfray, T.3    Rasore-Quartino, A.4    Vanhoenacker, F.5    Van Hul, W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.