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Items: 1 to 20 of 213

1.

Hereditary cranium bifidum and symmetric parietal foramina are the same entity.

Little BB, Knoll KA, Klein VR, Heller KB.

Am J Med Genet. 1990 Apr;35(4):453-8. Review.

PMID:
2185629
2.

Hereditary cranium bifidum persisting as enlarged parietal foramina (Catlin marks) on cephalometric radiographs.

Mupparapu M, Binder RE, Duarte F.

Am J Orthod Dentofacial Orthop. 2006 Jun;129(6):825-8.

PMID:
16769502
3.

Complete cranium bifidum without scalp abnormality. Case report.

Celik SE, Kara A.

J Neurosurg Pediatr. 2008 Mar;1(3):258-60. doi: 10.3171/PED/2008/1/3/258.

PMID:
18352774
4.

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.

Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, Hurst JA, Wall SA, Chrzanowska KH, Maxson RE Jr.

Nat Genet. 2000 Apr;24(4):387-90.

PMID:
10742103
5.

[Congenital absence of the parietal bones in a family].

Zabek M.

Wiad Lek. 1987 Jan 1;40(1):33-8. Polish. No abstract available.

PMID:
3590786
6.

[Cranium bifidum associated with unusual intracranial extension: MRI findings and possible pathogenesis. Case report].

Asano N, Oi S.

Neurol Med Chir (Tokyo). 1987 Nov;27(11):1114-9. Review. Japanese. No abstract available.

7.

Delayed membranous cranial ossification in a mother and child.

Gonzalez-del Angel A, Carnevale A, Takenaga R.

Am J Med Genet. 1992 Dec 1;44(6):786-9.

PMID:
1481847
8.

Prenatal sonographic appearance of foramina parietalia permagna.

Salamanca A, Gonzalez-Gomez F, Padilla MC, Motos MA, Zorrilla F, Sabatel RM.

Prenat Diagn. 1994 Aug;14(8):766-9.

PMID:
7991518
9.

[Foramina parietalia permagna. Familial occurrence in 3 generations].

Lipinski C, Stenzel K.

Neuropadiatrie. 1974 Nov;5(4):376-82. German. No abstract available.

PMID:
4480677
10.

[Giant parietal foramina. A surgical defect?].

Fasanelli S, Barbuti D, Di Rocco C, Moschini M.

Radiol Med. 1984 Sep;70(9):611-4. Italian.

PMID:
6536041
11.

Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes.

Kreiborg S, Marsh JL, Cohen MM Jr, Liversage M, Pedersen H, Skovby F, Børgesen SE, Vannier MW.

J Craniomaxillofac Surg. 1993 Jul;21(5):181-8.

PMID:
8360349
12.

Enlarged Parietal Foramina.

Wilkie AOM, Mavrogiannis LA.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2004 Mar 30 [updated 2012 Nov 08].

13.

Foramina parietalia permagna: report of nine cases in one family.

Kutilek S, Baxova A, Bayer M, Leiska A, Kozlowski K.

J Paediatr Child Health. 1997 Apr;33(2):168-70.

PMID:
9145364
14.

Hereditary enlarged parietal foramina (foramina parietalia permagna). Prenatal diagnosis, evolution and family study.

Rasore-Quartino A, Vignola G, Camera G.

Pathologica. 1985 Jul-Aug;77(1050):449-55. No abstract available.

PMID:
3834376
15.

Surgical management of foramina parietalia permagna.

Kortesis B, Richards T, David L, Glazier S, Argenta L.

J Craniofac Surg. 2003 Jul;14(4):538-44.

PMID:
12867871
16.

Parietal foramina clavicular hypoplasia. An autosomal dominant syndrome.

Golabi M, Carey J, Hall BD.

Am J Dis Child. 1984 Jun;138(6):596-9.

PMID:
6720648
17.

Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).

Cargile CB, McIntosh I, Clough MV, Rutberg J, Yaghmai R, Goodman BK, Chen XN, Korenberg JR, Thomas GH, Geraghty MT.

Am J Med Genet. 2000 Jun 19;92(5):328-35.

PMID:
10861662
18.

A novel locus for parietal foramina maps to chromosome 4q21-q23.

Chen G, Zhang D, Feng G, Liu W, He L.

J Hum Genet. 2003;48(8):420-4. Epub 2003 Aug 7.

PMID:
12905082
19.

Foramina parietalia permagna: the ins and outs.

Dharwal K.

Folia Morphol (Warsz). 2012 May;71(2):78-81.

PMID:
22648584
20.

Anomalous parietal suture mimicking skull fracture.

Tharp AM, Jason DR.

Am J Forensic Med Pathol. 2009 Mar;30(1):49-51. doi: 10.1097/PAF.0b013e3181859fd0.

PMID:
19237855
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