Baylor College of Medicine

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Chapters and Other Publications

Developmental Neurogenetics Laboratory

Click on the Expand plus sign sign to list the book chapters and other publications by year. Then click on the link for details of that publication.

<2021

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  • Aiba I, Noebels J. The genetic borderland of migraine and epilepsy. In: Dalkara T, Moskowitz MA, editors. Neurobiological basis of migraine. Wiley-Blackwell; 2017. p. 209-231.
  • Goldman AM, Buchanan G, Aiba I, Noebels JL. SUDEP animal models. In: Pitkänen A, Buckmaster PS, Galanopoulou AS, Moshé SL, editors. Models of seizures and epilepsy. Academic Press; 2017. p. 1007-1018.
  • Krishnan V, Benatar M, Drislane FW. Cognitive manifestations of focal status epilepticus. In: Drislane FW, Kaplan PW, editors. Status epilepticus: A clinical perspective. 2nd ed. Springer Sciences; 2017. p. 259-274.
  • Krishnan V, Chang BS, Schomer DL. Normal EEG in wakefulness and sleep: Adults and elderly. In: Schomer DL, Lopes da Silva FH, editors. Niedermeyer's electroencephalography: Basic principles, clinical applications, and related fields. 7th ed. Oxford: Oxford University Press; 2017. p. 202-228.
  • Krishnan V, Chang BS, Schomer DL. The application of EEG to epilepsy in adults and elderly. In: Schomer DL, Lopes da Silva FH, editors. Niedermeyer's electroencephalography: Basic principles, clinical applications, and related fields. 7th ed. Oxford: Oxford University Press; 2017. p. 521-535.
  • Goldman A, Maheshwari A. Genetics of clinical epilepsy practice. In: Haneef Z, Maheshwari A, editors. A concise manual of epilepsy. 2nd ed. CreateSpace Publishing; 2016. p. 144-155.
  • Holmes GL, Noebels JL. The epilepsy spectrum: Targeting future research challenges. In: Holmes GL, Noebels JL, editors. Epilepsy: The biology of a spectrum disorder. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 2016. p. 439-450.
  • Noebels JL. Single-gene determinants of epilepsy comorbidity. In: Holmes GL, Noebels JL, editors. Epilepsy: The biology of a spectrum disorder. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 2016. p. 331-344.
  • Maheshwari A, Noebels JL. Monogenic models of absence epilepsy: Windows into the complex balance between inhibition and excitation in thalamocortical microcircuits. In: Steinlein OK, editor. Genetics of epilepsy. Progress in brain research. Vol. 213. Amsterdam: Elsevier; 2014. p. 223-252. Available from: https://www.sciencedirect.com/science/article/pii/B9780444633262000120.
  • Noebels JL. The voltage-gated calcium channel and absence epilepsy. In: Noebels J, Avoli M, Rogawski M, Olsen R, Delgado-Escueta A, editors. Jasper's basic mechanisms of the epilepsies. 4th ed. New York: Oxford University Press; 2012. p. 702-13.
  • Goldman A. Basic mechanisms of SUDEP. In: Chapman D, Panelli R, Hanna J, Jeffs T, editors. Sudden unexpected death in epilepsy: continuing the global conversation. Camberwell, Australia: Epilepsy Australia, Epilepsy Bereaved & SUDEP Aware; 2011.
  • Noebels JL. Genes and the biology of complex epilepsy phenotypes. In: Avanzini G, Noebels J, editors. Genetics of epilepsy and genetic epilepsies. Montrouge, France: John Libbey Eurotext; 2009. p. 23-30.
  • Noebels JL. Spontaneous epileptic mutations in the mouse. In: Pitkanen A, Schwartzkroin PA, Moshe SL, editors. Models of seizures and epilepsy. Boston: Elsevier Academic Press; 2006. p. 223-232.
  • Noebels JL. Sodium channel gene expression and epilepsy. In: Novartis Foundation , editor. Sodium channels and neuronal hyperexcitability. New York: John Wiley & Sons, LTD.; 2002. p. 109-123.
  • Noebels JL. Genetic and phenotypic heterogeneity of inherited spike-and-wave epilepsies. In: Malafosse A, Genton P, Hirsch E, Marescaux C, Broglin D, Bernasconi R, editors. Idiopathic generalized epilepsies: Clinical, experimental and genetic aspects. London: John Libbey; 1994. p. 215-225.