Memphis Regional Medical Program brings medicine to the people.

door Cox, J J
Gepubliceerd in 1973

Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome

door Holden, S T, Cox, J J, Kesterton, I, Thomas, N S, Carr, C, Woods, C G
Gepubliceerd in 2006

Mexiletine as a treatment for primary erythromelalgia: normalization of biophysical properties of mutant L858F Na(V)1.7 sodium channels

door Cregg, R, Cox, J J, Bennett, D L H, Wood, J N, Werdehausen, R
Gepubliceerd in 2014

The molecular landscape of ASPM mutations in primary microcephaly

door Nicholas, A K, Swanson, E A, Cox, J J, Karbani, G, Malik, S, Springell, K, Hampshire, D, Ahmed, M, Bond, J, Di Benedetto, D, Fichera, M, Romano, C, Dobyns, W B, Woods, C G
Gepubliceerd in 2009

A role for Piezo2 in EPAC1-dependent mechanical allodynia

door Eijkelkamp, N, Linley, J.E., Torres, J.M., Bee, L., Dickenson, A.H., Gringhuis, M., Minett, M.S., Hong, G.S., Lee, E., Oh, U., Ishikawa, Y., Zwartkuis, F.J., Cox, J.J., Wood, J.N.
Gepubliceerd in 2013