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Volumn 75, Issue 11, 2004, Pages 1648-1649

Epilepsy in one family with parietal foramina: An incidental finding?

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALX4 GENE; ARTICLE; CASE REPORT; CHILD; CLINICAL EXAMINATION; DISEASE ASSOCIATION; ELECTROENCEPHALOGRAM; EPILEPSY; FAMILY STUDY; FEMALE; GENE; GENE MUTATION; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SKULL MALFORMATION;

EID: 7244252891     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.2004.035733     Document Type: Article
Times cited : (11)

References (7)
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    • Currarino, G.1
  • 2
    • 0034074417 scopus 로고    scopus 로고
    • Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
    • Wilkie AO, Tang Z, Elanko N, et al. Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Nat Genet 2000;24:387-90.
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    • Wilkie, A.O.1    Tang, Z.2    Elanko, N.3
  • 3
    • 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, et al. The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). J Med Genet 2000;37:916-20.
    • (2000) J Med Genet , vol.37 , pp. 916-920
    • Wuyts, W.1    Cleiren, E.2    Homfray, T.3
  • 4
    • 0035158663 scopus 로고    scopus 로고
    • Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects
    • Mavrogiannis LA, Antonopoulou I, Baxova A, et al. Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. Nat Genet 2001;27:17-18.
    • (2001) Nat Genet , vol.27 , pp. 17-18
    • Mavrogiannis, L.A.1    Antonopoulou, I.2    Baxova, A.3
  • 5
    • 0000767102 scopus 로고
    • Seizures associated with the Catlin mark
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    • (1961) Neurology , vol.11 , pp. 345-348
    • Kyte Jr., W.C.1
  • 6
    • 0034029571 scopus 로고    scopus 로고
    • Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
    • Satokata I, Ma L, Ohshima H, et al. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet 2000;24:391 -5.
    • (2000) Nat Genet , vol.24 , pp. 391-395
    • Satokata, I.1    Ma, L.2    Ohshima, H.3
  • 7
    • 0034646234 scopus 로고    scopus 로고
    • Enlarged parietal foramina: Association with cerebral venous and cortical anomalies
    • Reddy AT, Hedlund GL, Percy AK. Enlarged parietal foramina: association with cerebral venous and cortical anomalies. Neurology 2000;54:1175-8.
    • (2000) Neurology , vol.54 , pp. 1175-1178
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.