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Capecitabine combined with oxaliplatin (CapOx) in clinical practice: how significant is peripheral neuropathy?

Annals of oncology, 2010-08, Vol.21 (8), p.1657-1661

2010

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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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Genetic variation of CACNA1H in idiopathic generalized epilepsy

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

2004

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A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 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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Biosorption of heavy metals by Saccharomyces cerevisiae

Applied microbiology and biotechnology, 1995, Vol.42 (5), p.797-806

1995

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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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LGI1 mutations in temporal lobe epilepsies

Neurology, 2004-04, Vol.62 (7), p.1115

2004

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Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24

American journal of human genetics, 1998-10, Vol.63 (4), p.1108-1116

1998

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Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2

Nature genetics, 1995-05, Vol.10 (1), p.117-118

1995

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A de novo mutation in sporadic nocturnal frontal lobe epilepsy

Annals of neurology, 2000-08, Vol.48 (2), p.264-267

2000

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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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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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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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Surface meltstreams on the Amery Ice Shelf, East Antarctica

Annals of glaciology, 1998, Vol.27, p.177-181

Phillips, Helen A.

1998

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Bilateral leg amputation following chemoradiation for squamous carcinoma of the anus

Radiotherapy and oncology, 2004-10, Vol.73 (1), p.110-111

2004

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p53 mutations as a marker of malignancy in bladder washing samples from patients with bladder cancer

British journal of cancer, 2000-01, Vol.82 (1), p.136-141

2000

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The Role of the p53 Tumour Suppressor Gene in Human Breast Cancer

Clinical Oncology, 1999-01, Vol.11 (3), p.148-155

Phillips, H.A.

1999

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Pilot studies on the p53 gene in nipple aspirate fluid from patients with breast cancer

Breast cancer research and treatment, 2000-05, Vol.61 (2), p.139-143

2000

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Localization of craniosynostosis Adelaide type to 4p16

Human molecular genetics, 1995-04, Vol.4 (4), p.681-683

1995

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The treatment of bladder cancer in the elderly

Radiotherapy and oncology, 1998-03, Vol.46 (3), p.334

1998

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SSCP variants within the alpha 4 subunit of the neuronal nicotinic acetylcholine receptor gene

Clinical genetics, 1997-02, Vol.51 (2), p.135-136

1997

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Nipple aspirate fluid in relation to breast cancer

Breast (Edinburgh), 1999-08, Vol.8 (4), p.169-174

1999

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Keeping Up with New Legal Titles

Law Library Journal, 2006-04, Vol.98, p.409-849

2006

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Capecitabine combined with oxaliplatin (CapOx) in clinical practice: how significant is peripheral neuropathy?

Sodium-channel defects in benign familial neonatal-infantile seizures

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

Genetic variation of CACNA1H in idiopathic generalized epilepsy

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

Biosorption of heavy metals by Saccharomyces cerevisiae

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

LGI1 mutations in temporal lobe epilepsies

Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2

A de novo mutation in sporadic nocturnal frontal lobe epilepsy

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

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

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

Surface meltstreams on the Amery Ice Shelf, East Antarctica

Bilateral leg amputation following chemoradiation for squamous carcinoma of the anus

p53 mutations as a marker of malignancy in bladder washing samples from patients with bladder cancer

The Role of the p53 Tumour Suppressor Gene in Human Breast Cancer

Pilot studies on the p53 gene in nipple aspirate fluid from patients with breast cancer

Localization of craniosynostosis Adelaide type to 4p16

The treatment of bladder cancer in the elderly

SSCP variants within the alpha 4 subunit of the neuronal nicotinic acetylcholine receptor gene

Nipple aspirate fluid in relation to breast cancer

Keeping Up with New Legal Titles

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