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Journal Abstract Search

208 related items for PubMed ID: 18352774

  • 1. Complete cranium bifidum without scalp abnormality. Case report.
    Celik SE, Kara A.
    J Neurosurg Pediatr; 2008 Mar; 1(3):258-60. PubMed ID: 18352774
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  • 3. A case of an extremely large accessory bone with unusual sutures and foramina parietalia permagna in multiple premature craniosynostoses.
    Hanninger SE, Schwabegger AH.
    J Craniomaxillofac Surg; 2012 Oct; 40(7):555-8. PubMed ID: 22075323
    [Abstract] [Full Text] [Related]

  • 4. 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. PubMed ID: 2185629
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  • 6. [Skull fracture or bipartite parietal bone].
    Angonèse A, Sonnaert M, Rassart A, Gauquier N, Cavatorta E.
    Arch Pediatr; 2010 Apr; 17(4):391-3. PubMed ID: 20202802
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  • 8. 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. PubMed ID: 16769502
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  • 9. Squamosal suture craniosynostosis in Muenke syndrome.
    Doumit GD, Sidaoui J, Meisler E, Papay FA.
    J Craniofac Surg; 2014 Mar; 25(2):429-31. PubMed ID: 24448525
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  • 10. Surgical treatment of aplasia cutis congenita of the scalp associated with bilateral coronal synostosis.
    Komuro Y, Yanai A, Seno H, Ichida M, Inoue M, Miyajima M, Arai H, Sato K.
    J Craniofac Surg; 2002 Jul; 13(4):513-9. PubMed ID: 12140414
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  • 11. Large parietal midline defect with unusual ridge-like structure at the rim and persistent falcine sinus.
    Yang CA, Peng SS, Hsieh WS, Tsao PN, Chen CY, Chou HC.
    Childs Nerv Syst; 2013 Jul; 29(7):1069-72. PubMed ID: 23559396
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  • 12. Modeling of scaphocephaly using superelastic titanium-nickel rings: a preliminary report.
    Kobus K, Wegrzyn M, Lekston Z, Morawiec H, Drugacz J.
    J Craniofac Surg; 2007 May; 18(3):504-10. PubMed ID: 17538309
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  • 13. [Congenital cutaneous aplasia of the scalp. Apropos of 4 cases].
    Laumonier F, Varlet F, Favier T, Berthelot J, Pouplard F.
    Chir Pediatr; 1990 May; 31(2):106-12. PubMed ID: 2268948
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  • 14. [Mother and son with enlarged parietal foramina, persistent fetal vein, and ALX4 mutation].
    Morita M, Nanba E, Adachi K, Ohno K.
    No To Hattatsu; 2016 May; 48(3):205-8. PubMed ID: 27349084
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  • 16. The sequence in appearance and disappearance of impressiones gyrorum cerebri and cerebelli.
    Grgurević L, Vinter I, Jalsovec D, Krmpotić-Nemanić J.
    Coll Antropol; 2004 Dec; 28(2):849-55. PubMed ID: 15666620
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  • 18. Meningomyelocele associated with cranium bifidum: rare coexistence of two major malformations.
    Anegawa S, Hayashi T, Torigoe R, Hashimoto T.
    Childs Nerv Syst; 1993 Aug; 9(5):278-81. PubMed ID: 8252518
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  • 19. Congenital cavernous hemangioma of the calvaria. Case report.
    Vural M, Acikalin MF, Adapinar B, Atasoy MA.
    J Neurosurg Pediatr; 2009 Jan; 3(1):41-5. PubMed ID: 19119903
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  • 20. [Massive lytic osteodystrophy or Gorham-Stout disease of the craniomaxillofacial area].
    Oujilal A, Lazrak A, Benhalima H, Boulaich M, Amarti A, Saidi A, Kzadri M.
    Rev Laryngol Otol Rhinol (Bord); 2000 Jan; 121(4):255-60. PubMed ID: 11233709
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