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Pike MG

References (2)

Title : Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters - Harrison_2011_Am.J.Med.Genet.A_155A_2826
Author(s) : Harrison V , Connell L , Hayesmoore J , McParland J , Pike MG , Blair E
Ref : American Journal of Medicine Genet A , 155A :2826 , 2011
Abstract : Harrison_2011_Am.J.Med.Genet.A_155A_2826
ESTHER : Harrison_2011_Am.J.Med.Genet.A_155A_2826
PubMedSearch : Harrison_2011_Am.J.Med.Genet.A_155A_2826
PubMedID: 21964664

Title : Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies - Robb_2011_Neuromuscul.Disord_21_379
Author(s) : Robb SA , Sewry CA , Dowling JJ , Feng L , Cullup T , Lillis S , Abbs S , Lees MM , Laporte J , Manzur AY , Knight RK , Mills KR , Pike MG , Kress W , Beeson D , Jungbluth H , Pitt MC , Muntoni F
Ref : Neuromuscular Disorders , 21 :379 , 2011
Abstract : Robb_2011_Neuromuscul.Disord_21_379
ESTHER : Robb_2011_Neuromuscul.Disord_21_379
PubMedSearch : Robb_2011_Neuromuscul.Disord_21_379
PubMedID: 21440438