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Pachygyria (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Pachygyria" in English language version.

refsWebsite
Global rank English rank
7doi.org
2nd place
2nd place
7nih.gov
4th place
4th place
4semanticscholar.org
11th place
8th place

doi.org

  • Guerrini R (2005). "Genetic malformations of the cerebral cortex and epilepsy". Epilepsia. 46 (Suppl 1): 32–37. doi:10.1111/j.0013-9580.2005.461010.x. PMID 15816977.
  • Guerrini R, Marini C (2006). "Genetic malformations of cortical development". Exp Brain Res. 173 (2): 322–333. doi:10.1007/s00221-006-0501-z. PMID 16724181. S2CID 12482656.
  • Dobyns WB, Truwit CL (1995). "Lissencephaly and other malformations of cortical development: 1995 update". Neuropediatrics. 26 (3): 132–147. doi:10.1055/s-2007-979744. PMID 7477752. S2CID 260238199.
  • Cardoso C, Leventer RJ, Matsumoto N, et al. (2000). "The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene". Hum. Mol. Genet. 9 (20): 3019–3028. doi:10.1093/hmg/9.20.3019. PMID 11115846.
  • Kato M, Dobyns WB (2003). "Lissencephaly and the molecular basis of neuronal migration". Hum. Mol. Genet. 12 Spec No 1 (90001): R89–96. doi:10.1093/hmg/ddg086. PMID 12668601.
  • Pieh C, Goebel HH, Engle EC, Gottlob I (2003). "Congenital fibrosis syndrome associated with central nervous system abnormalities". Graefes Arch. Clin. Exp. Ophthalmol. 241 (7): 546–553. doi:10.1007/s00417-003-0703-z. PMID 12819981. S2CID 25436215.
  • Ozawa H, Takayama C, Nishida A, Nagai T, Nishimura G, Higurashi M (2005). "Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type II". Brain Dev. 27 (3): 237–240. doi:10.1016/j.braindev.2004.06.007. PMID 15737708. S2CID 26150025.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Guerrini R (2005). "Genetic malformations of the cerebral cortex and epilepsy". Epilepsia. 46 (Suppl 1): 32–37. doi:10.1111/j.0013-9580.2005.461010.x. PMID 15816977.
  • Guerrini R, Marini C (2006). "Genetic malformations of cortical development". Exp Brain Res. 173 (2): 322–333. doi:10.1007/s00221-006-0501-z. PMID 16724181. S2CID 12482656.
  • Dobyns WB, Truwit CL (1995). "Lissencephaly and other malformations of cortical development: 1995 update". Neuropediatrics. 26 (3): 132–147. doi:10.1055/s-2007-979744. PMID 7477752. S2CID 260238199.
  • Cardoso C, Leventer RJ, Matsumoto N, et al. (2000). "The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene". Hum. Mol. Genet. 9 (20): 3019–3028. doi:10.1093/hmg/9.20.3019. PMID 11115846.
  • Kato M, Dobyns WB (2003). "Lissencephaly and the molecular basis of neuronal migration". Hum. Mol. Genet. 12 Spec No 1 (90001): R89–96. doi:10.1093/hmg/ddg086. PMID 12668601.
  • Pieh C, Goebel HH, Engle EC, Gottlob I (2003). "Congenital fibrosis syndrome associated with central nervous system abnormalities". Graefes Arch. Clin. Exp. Ophthalmol. 241 (7): 546–553. doi:10.1007/s00417-003-0703-z. PMID 12819981. S2CID 25436215.
  • Ozawa H, Takayama C, Nishida A, Nagai T, Nishimura G, Higurashi M (2005). "Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type II". Brain Dev. 27 (3): 237–240. doi:10.1016/j.braindev.2004.06.007. PMID 15737708. S2CID 26150025.

semanticscholar.org

api.semanticscholar.org