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Genetic variation of CACNA1H in idiopathic generalized epilepsy

Annals of neurology, 2004-04, Vol.55 (4), p.595-596

2004

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The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene

Journal of human genetics, 2004-06, Vol.49 (6), p.308-311

2004

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Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

Epilepsia (Copenhagen), 2003-04, Vol.44 (4), p.613-617

2003

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Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12

Epilepsia (Copenhagen), 2004-09, Vol.45 (9), p.1054-1060

2004

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Sodium-channel defects in benign familial neonatal-infantile seizures

The Lancet (British edition), 2002-09, Vol.360 (9336), p.851-852

2002

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CHRNB2 Is the Second Acetylcholine Receptor Subunit Associated with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

American journal of human genetics, 2001-01, Vol.68 (1), p.225-231

2001

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Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability

Epilepsia (Copenhagen), 2008-12, Vol.49 (12), p.2125-2129

2008

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Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore

Molecular pharmacology, 2008-08, Vol.74 (2), p.379-391

2008

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A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

Nature genetics, 1995-10, Vol.11 (2), p.201-203

1995

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Bringing German to Life: Creative activities for 5-11

1, 2015

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Bringing French to Life: Creative activities for 5-11

1, 2015

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Bringing Spanish to Life: Creative activities for 5-11

1, 2015

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Jumpstart! Spanish and Italian: Engaging Activities for Ages 7-12

1st edition., 2014

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Jumpstart! French and German: Engaging Activities for Ages 7-12

1, 2014

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Living Languages: An Integrated Approach to Teaching Foreign Languages in Primary Schools

1, 2013

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Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel β1 subunit gene SCN1B

Nature genetics, 1998, Vol.19 (4), p.366-370

1998

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Febrile seizures and generalized epilepsy associated with a mutation in the Na + -channel ß1 subunit gene SCN1B

Nature genetics, 1998-08, Vol.19 (4), p.366-370

1998

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Incidence and origin of null alleles in the (AC)n microsatellite markers

American journal of human genetics, 1993-05, Vol.52 (5), p.922-927

1993

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Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2

Annals of neurology, 1998-12, Vol.44 (6), p.890-899

1998

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Human Nocturnal Frontal Lobe Epilepsy: Pharmocogenomic Profiles of Pathogenic Nicotinic Acetylcholine Receptor Î²-Subunit Mutations outside the Ion Channel Pore

Molecular pharmacology, 2008-08, Vol.74 (2), p.379

2008

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Setting the Scene

Jumpstart! Spanish and Italian, 2014, p.1-18

1, 2014

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Exploring Stories

Jumpstart! Spanish and Italian, 2014, p.125-149

1, 2014

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Using Flashcards

Jumpstart! Spanish and Italian, 2014, p.19-28

1, 2014

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Using Songs

Jumpstart! Spanish and Italian, 2014, p.101-124

1, 2014

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On Your Feet

Jumpstart! Spanish and Italian, 2014, p.46-66

1, 2014

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Genetic variation of CACNA1H in idiopathic generalized epilepsy

The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene

Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12

Sodium-channel defects in benign familial neonatal-infantile seizures

CHRNB2 Is the Second Acetylcholine Receptor Subunit Associated with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability

Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore

A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

Bringing German to Life: Creative activities for 5-11

Bringing French to Life: Creative activities for 5-11

Bringing Spanish to Life: Creative activities for 5-11

Jumpstart! Spanish and Italian: Engaging Activities for Ages 7-12

Jumpstart! French and German: Engaging Activities for Ages 7-12

Living Languages: An Integrated Approach to Teaching Foreign Languages in Primary Schools

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel β1 subunit gene SCN1B

Febrile seizures and generalized epilepsy associated with a mutation in the Na + -channel ß1 subunit gene SCN1B

Incidence and origin of null alleles in the (AC)n microsatellite markers

Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2

Human Nocturnal Frontal Lobe Epilepsy: Pharmocogenomic Profiles of Pathogenic Nicotinic Acetylcholine Receptor Î²-Subunit Mutations outside the Ion Channel Pore

Setting the Scene

Exploring Stories

Using Flashcards

Using Songs

On Your Feet

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