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A K Nicholas

Showing results (1-10 of 6) with videos related to

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Pain|March 24, 2009
Two novel SCN9A mutations causing insensitivity to painK B Nilsen, A K Nicholas, C G Woods, et al.
Neuroreport|March 16, 2000
Does frontal lobe activation during retrieval reflect complexity of retrieved information?N M Hunkin, A R Mayes, S C Williams, et al.
The Journal of Clinical Endocrinology and Metabolism|January 7, 2016
A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital HypothyroidismO Koulouri, A K Nicholas, E Schoenmakers, et al.
Clinical Endocrinology|July 1, 2016
Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and IrelandA K Nicholas, S Jaleel, G Lyons, et al.
Behavioural Neurology|March 6, 2012
Storage of verbal associations is sufficient to activate the left medial temporal lobeA R Mayes, P A Gooding, N M Hunkin, et al.
Journal of Medical Genetics|November 26, 2008
The molecular landscape of ASPM mutations in primary microcephalyA K Nicholas, E A Swanson, J J Cox, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Pain|March 24, 2009
Two novel SCN9A mutations causing insensitivity to painK B Nilsen, A K Nicholas, C G Woods, et al.
Neuroreport|March 16, 2000
Does frontal lobe activation during retrieval reflect complexity of retrieved information?N M Hunkin, A R Mayes, S C Williams, et al.
The Journal of Clinical Endocrinology and Metabolism|January 7, 2016
A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital HypothyroidismO Koulouri, A K Nicholas, E Schoenmakers, et al.
Clinical Endocrinology|July 1, 2016
Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and IrelandA K Nicholas, S Jaleel, G Lyons, et al.
Behavioural Neurology|March 6, 2012
Storage of verbal associations is sufficient to activate the left medial temporal lobeA R Mayes, P A Gooding, N M Hunkin, et al.
Journal of Medical Genetics|November 26, 2008
The molecular landscape of ASPM mutations in primary microcephalyA K Nicholas, E A Swanson, J J Cox, et al.
Pageof 1