J B Stephenson|A M Kerr - JoVE Visualize

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Clinical Dysmorphology|January 1, 1994

Syndromes associated with trichothiodystrophyJ L Tolmie, D de Berker, R Dawber, et al.

Journal of Brachial Plexus and Peripheral Nerve Injury|May 11, 2013

Cortical plasticity induced by different degrees of peripheral nerve injuries: a rat functional magnetic resonance imaging study under 9.4 TeslaRupeng Li, Patrick C Hettinger, Jacques A Machol, et al.

Archives of Disease in Childhood|June 23, 2001

Characterisation of breathing and associated central autonomic dysfunction in the Rett disorderP O Julu, A M Kerr, F Apartopoulos, et al.

Journal of the Neurological Sciences|November 1, 1988

Cytochrome oxidase deficiency: immunological studies of skeletal muscle mitochondrial fractionsI M Shepherd, M A Birch-Machin, M A Johnson, et al.

Human Genetics|November 10, 2001

Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexiaM I Rees, T M Lewis, B Vafa, et al.

Journal of Intellectual Disability Research : JIDR|January 25, 2003

Medical needs of people with intellectual disability require regular reassessment, and the provision of client- and carer-held reportsA M Kerr, D McCulloch, K Oliver, et al.

Neuropediatrics|February 1, 1997

Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.

Annals of Neurology|October 12, 2000

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variabilityL H Eunson, R Rea, S M Zuberi, et al.

Molecular Genetics and Metabolism|April 7, 1999

The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in ScotlandJ B Stephenson, N D Greene, K Y Leung, et al.

Brain : a Journal of Neurology|June 4, 1999

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsyS M Zuberi, L H Eunson, A Spauschus, et al.

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Showing results (71-80 of 85) with videos related to

Sort By:

Pageof 9

Clinical Dysmorphology|January 1, 1994

Syndromes associated with trichothiodystrophyJ L Tolmie, D de Berker, R Dawber, et al.

Journal of Brachial Plexus and Peripheral Nerve Injury|May 11, 2013

Cortical plasticity induced by different degrees of peripheral nerve injuries: a rat functional magnetic resonance imaging study under 9.4 TeslaRupeng Li, Patrick C Hettinger, Jacques A Machol, et al.

Archives of Disease in Childhood|June 23, 2001

Characterisation of breathing and associated central autonomic dysfunction in the Rett disorderP O Julu, A M Kerr, F Apartopoulos, et al.

Journal of the Neurological Sciences|November 1, 1988

Cytochrome oxidase deficiency: immunological studies of skeletal muscle mitochondrial fractionsI M Shepherd, M A Birch-Machin, M A Johnson, et al.

Human Genetics|November 10, 2001

Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexiaM I Rees, T M Lewis, B Vafa, et al.

Journal of Intellectual Disability Research : JIDR|January 25, 2003

Medical needs of people with intellectual disability require regular reassessment, and the provision of client- and carer-held reportsA M Kerr, D McCulloch, K Oliver, et al.

Neuropediatrics|February 1, 1997

Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.

Annals of Neurology|October 12, 2000

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variabilityL H Eunson, R Rea, S M Zuberi, et al.

Molecular Genetics and Metabolism|April 7, 1999

The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in ScotlandJ B Stephenson, N D Greene, K Y Leung, et al.

Brain : a Journal of Neurology|June 4, 1999

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsyS M Zuberi, L H Eunson, A Spauschus, et al.

Pageof 9