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Epilepsia|December 17, 2009
Inhibition of long-term potentiation by valproic acid through modulation of cyclic AMPPishan Chang, Kate E Chandler, Robin S B Williams, et al.
Veterinary Journal (London, England : 1997)|May 1, 2007
The efficacy and tolerability of levetiracetam in pharmacoresistant epileptic dogsHolger A Volk, Lara A Matiasek, Alejandro Luján Feliu-Pascual, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Temple syndrome as a result of isolated hypomethylation of the 14q32 imprinted DLK1/MEG3 regionTracy A Briggs, Kemi Lokulo-Sodipe, Kate E Chandler, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 16, 2003
Plasticity of GABA(B) receptor-mediated heterosynaptic interactions at mossy fibers after status epilepticusKate E Chandler, Alessandra P Princivalle, Ruth Fabian-Fine, et al.
American Journal of Medical Genetics. Part A|September 26, 2017
De novo mutations in HNRNPU result in a neurodevelopmental syndromeT Michael Yates, Pradeep C Vasudevan, Kate E Chandler, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 11, 2016
Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disordersChristian de Goede, Wyatt W Yue, Guanhua Yan, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
CRTAP mutation in a patient with Cole-Carpenter syndromeMeena Balasubramanian, Rebecca C Pollitt, Kate E Chandler, et al.
European Journal of Human Genetics : EJHG|February 19, 2021
ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsyZerin Hyder, Wim Van Paesschen, Ataf Sabir, et al.
European Journal of Medical Genetics|June 15, 2020
Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformationsRajesh Madhu, Glenda M Beaman, Kate E Chandler, et al.
The British Journal of Dermatology|January 23, 2023
Biallelic TUFT1 variants cause woolly hair, superficial skin fragility and desmosomal defectsAdam Jackson, Celia Moss, Kate E Chandler, et al.
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