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Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential, membrane integrity, sperm motility and in vitro fertilization in bovine epididymal sperm

Reproduction in domestic animals, 2017-04, Vol.52 (2), p.257-263

2017

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Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

Annals of neurology, 2000-10, Vol.48 (4), p.647-656

2000

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Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopes

Archives of disease in childhood, 2005-12, Vol.90 (12), p.1283-1287

2005

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Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism

Journal of medical genetics, 2003-03, Vol.40 (3), p.183-187

2003

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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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Increased chromosomal radiosensitivity in breast cancer patients: a comparison of two assays

International journal of radiation biology, 1999, Vol.75 (1), p.1-10

SCOTT, D.

1999

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Gratification disorder (“infantile masturbation”): a review

Archives of disease in childhood, 2004-03, Vol.89 (3), p.225-226

2004

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Caregiver characteristics and economic cost of home-based care: a case study of Maun and Gumare villages in North West District, Botswana

Chronic illness, 2013-03, Vol.9 (1), p.3-15

2013

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Cardiac pacing for severe childhood neurally mediated syncope with reflex anoxic seizures

Heart (British Cardiac Society), 1999-12, Vol.82 (6), p.721-725

1999

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Cataplexy in the Prader–Willi syndrome

Archives of disease in childhood, 2002-08, Vol.87 (2), p.170-170

2002

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Occupational asthma in the city of São Paulo, 1995-2000, with special reference to gender analysis

American journal of industrial medicine, 2003-06, Vol.43 (6), p.611-617

2003

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Detection of Individual Differences in Radiation-Induced Apoptosis of Peripheral Blood Lymphocytes in Normal Individuals, Ataxia Telangiectasia Homozygotes and Heterozygotes, and Breast Cancer Patients after Radiotherapy

Radiation research, 2000-05, Vol.153 (5), p.570-578

2000

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Impression formation from intellectual and social traits: Evidence for behavioural adaptation and cognitive processing

British journal of social psychology, 2000-12, Vol.39 (4), p.537-554

2000

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The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)

Journal of medical genetics, 1995-11, Vol.32 (11), p.881-884

1995

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The Prader-Willi syndrome

Archives of disease in childhood, 1994-01, Vol.70 (1), p.58-63

1994

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Analysis of Reproductive Isolation Between Sibling Species Anopheles albitarsis sensu stricto and Anopheles deaneorum, Two Malaria Vectors Belonging to the Albitarsis Complex (Diptera: Culicidae)

Journal of medical entomology, 2004-09, Vol.41 (5), p.888-893

2004

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Clinical presentation, haematological indices and management of children with severe and uncomplicated malaria in Douala, Cameroon

Pakistan journal of biological sciences, 2008-10, Vol.11 (20), p.2401-2406

2008

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Heritability of chromosomal radiosensitivity in breast cancer patients: a pilot study with the lymphocyte micronucleus assay

International journal of radiation biology, 2000, Vol.76 (12), p.1617-1619

Burrill, J. B. P. Barber, S. A. Roberts, B. Bulman, D. Scott, W.

2000

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Anoxic seizures: self‐terminating syncopes

Epileptic disorders, 2001-01, Vol.3 (1), p.3-6

Stephenson, John B.P.

2001

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Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues

Journal of medical genetics, 1994-01, Vol.31 (1), p.41-44

1994

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"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome

Journal of medical genetics, 1998-02, Vol.35 (2), p.94-98

1998

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Genetic aspects of tuberous sclerosis in the west of Scotland

Journal of medical genetics, 1989-01, Vol.26 (1), p.28-31

1989

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Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families

Journal of neurology, neurosurgery and psychiatry, 1996-12, Vol.61 (6), p.616-620

1996

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Diagnosis in Prader-Willi syndrome

Archives of disease in childhood, 1994-11, Vol.71 (5), p.441-442

1994

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SEIZURES AND INTELLECTUAL DISABILITY ASSOCIATED WITH TUBEROUS SCLEROSIS COMPLEX IN THE WEST OF SCOTLAND

Developmental medicine and child neurology, 1992-09, Vol.34 (9), p.766-774

1992

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Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential, membrane integrity, sperm motility and in vitro fertilization in bovine epididymal sperm

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopes

Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism

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

Increased chromosomal radiosensitivity in breast cancer patients: a comparison of two assays

Gratification disorder (“infantile masturbation”): a review

Caregiver characteristics and economic cost of home-based care: a case study of Maun and Gumare villages in North West District, Botswana

Cardiac pacing for severe childhood neurally mediated syncope with reflex anoxic seizures

Cataplexy in the Prader–Willi syndrome

Occupational asthma in the city of São Paulo, 1995-2000, with special reference to gender analysis

Detection of Individual Differences in Radiation-Induced Apoptosis of Peripheral Blood Lymphocytes in Normal Individuals, Ataxia Telangiectasia Homozygotes and Heterozygotes, and Breast Cancer Patients after Radiotherapy

Impression formation from intellectual and social traits: Evidence for behavioural adaptation and cognitive processing

The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)

The Prader-Willi syndrome

Analysis of Reproductive Isolation Between Sibling Species Anopheles albitarsis sensu stricto and Anopheles deaneorum, Two Malaria Vectors Belonging to the Albitarsis Complex (Diptera: Culicidae)

Clinical presentation, haematological indices and management of children with severe and uncomplicated malaria in Douala, Cameroon

Heritability of chromosomal radiosensitivity in breast cancer patients: a pilot study with the lymphocyte micronucleus assay

Anoxic seizures: self‐terminating syncopes

Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues

"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome

Genetic aspects of tuberous sclerosis in the west of Scotland

Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families

Diagnosis in Prader-Willi syndrome

SEIZURES AND INTELLECTUAL DISABILITY ASSOCIATED WITH TUBEROUS SCLEROSIS COMPLEX IN THE WEST OF SCOTLAND

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