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Volumn 19, Issue 4, 2007, Pages 414-417

Dental anomalies in neuropediatric disorders;Zahnanomalien in der neuropädiatrie

Author keywords

Ataxia; Dental anomalies; Epilepsy; Hypodontia; Neuropediatrics

Indexed keywords

ARTICLE; ATAXIA; CHILDHOOD DISEASE; EPILEPSY; GENETIC DISORDER; HUMAN; INCONTINENTIA PIGMENTI; NEUROLOGIC DISEASE; TOOTH MALFORMATION;

EID: 42049119403     PISSN: 09365931     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11825-007-0051-1     Document Type: Article
Times cited : (2)

References (16)
  • 1
    • 75449142022 scopus 로고
    • Bodenhoff J, Gorlin RJ (1963) Natal and neonatal teeth: Folklore and fact. Pediatrics 32: 1087-1093
    • (1963) Pediatrics , vol.32 , pp. 1087
    • Bodenhoff1
  • 2
    • 0035292149 scopus 로고    scopus 로고
    • Cunha RF, Boer FA, Torriani DD, Frossard WT (2001) Natal and neonatal teeth: review of the literature. Pediatr Dent 23: 158-162
    • (2001) Pediatr Dent , vol.23 , pp. 158
    • Cunha1
  • 3
    • 0141708025 scopus 로고    scopus 로고
    • Hadj-Rabia S, Froidevaux D, Bodak N et al. (2003) Clinical study of 40 cases of incontinentia pigmenti. Arch Dermatol 139: 1163-1170
    • (2003) Arch Dermatol , vol.139 , pp. 1163
    • Hadj-Rabia1
  • 4
    • 0016242848 scopus 로고
    • Kohlschutter A, Chappuis D, Meier C et al. (1974) Familial epilepsy and yellow teeth-a disease of the CNS associated with enamel hypoplasia. Helv Paediatr Acta 29: 283-294
    • (1974) Helv Paediatr Acta , vol.29 , pp. 283
    • Kohlschutter1
  • 5
    • 25144493747 scopus 로고    scopus 로고
    • Ku CL, Dupuis-Girod S, Dittrich AM et al. (2005) NEMO mutations in 2 unrelated boys with severe infections and conical teeth. Pediatrics 115: e615-e619
    • (2005) Pediatrics , vol.115 , pp. 615
    • Ku1
  • 6
    • 31944441372 scopus 로고    scopus 로고
    • Leung AK, Robson WL (2006) Natal teeth: a review. J Natl Med Assoc 98: 226-228
    • (2006) J Natl Med Assoc , vol.98 , pp. 226
    • Leung1
  • 7
    • 0036255381 scopus 로고    scopus 로고
    • Loddenkemper T, Grote K, Evers S et al. (2002) Neurological manifestations of the oculodentodigital dysplasia syndrome. J Neurol 249: 584-595
    • (2002) J Neurol , vol.249 , pp. 584
    • Loddenkemper1
  • 8
    • 0032732443 scopus 로고    scopus 로고
    • Nanni L, Ming JE, Bocian M et al. (1999) The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly. Hum Mol Genet 8: 2479-2488
    • (1999) Hum Mol Genet , vol.8 , pp. 2479
    • Nanni1
  • 9
    • 0037320927 scopus 로고    scopus 로고
    • Paznekas WA, Boyadjiev SA, Shapiro RE et al. (2003) Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia. Am J Hum Genet 72: 408-418
    • (2003) Am J Hum Genet , vol.72 , pp. 408
    • Paznekas1
  • 10
    • 33746810189 scopus 로고    scopus 로고
    • Richardson RJ, Joss S, Tomkin S et al. (2006) A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome. J Med Genet 43: e37
    • (2006) J Med Genet , vol.43 , pp. 37
    • Richardson1
  • 11
    • 0030294408 scopus 로고    scopus 로고
    • Roessler E, Belloni E, Gaudenz K et al. (1996) Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Nat Genet 14: 357-360
    • (1996) Nat Genet , vol.14 , pp. 357
    • Roessler1
  • 12
    • 15944387795 scopus 로고    scopus 로고
    • Theis M, Sohl G, Eiberger J, Willecke K (2005) Emerging complexities in identity and function of glial connexins. Trends Neurosci 28: 188-195
    • (2005) Trends Neurosci , vol.28 , pp. 188
    • Theis1
  • 13
    • 33845684652 scopus 로고    scopus 로고
    • Timmons M, Tsokos M, Asab MA et al. (2006) Peripheral and central hypomyelination with hypogonadotropic hypogonadism and hypodontia. Neurology 67: 2066-2069
    • (2006) Neurology , vol.67 , pp. 2066
    • Timmons1
  • 14
    • 3242693178 scopus 로고    scopus 로고
    • Uhlenberg B, Schuelke M, Ruschendorf F et al. (2004) Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease. Am J Hum Genet 75: 251-260
    • (2004) Am J Hum Genet , vol.75 , pp. 251
    • Uhlenberg1
  • 15
    • 20244380309 scopus 로고    scopus 로고
    • Wolf NI, Harting I, Boltshauser E et al. (2005) Leukoencephalopathy with ataxia, hypodontia, and hypomyelination. Neurology 64: 1461-1464
    • (2005) Neurology , vol.64 , pp. 1461
    • Wolf1
  • 16
    • 34548741364 scopus 로고    scopus 로고
    • Wolf NI, Harting I, Innes AM et al. (2007) Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy. Neuropediatrics 38: 64-70
    • (2007) Neuropediatrics , vol.38 , pp. 64
    • Wolf1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.