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Denervation drives mitochondrial dysfunction in skeletal muscle of octogenarians

The Journal of physiology, 2016-12, Vol.594 (24), p.7361-7379

2016

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Myometrial Defect in a Subsequent Pregnancy After Uterine Artery Embolization for Postpartum Hemorrhage, in the Absence of Leiomyomas or Previous Uterine Surgery

Journal of obstetrics and gynaecology Canada, 2020-02, Vol.42 (2), p.173-176

2020

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Survival in Medically Treated Patients with Homozygous β-Thalassemia

The New England journal of medicine, 1994-09, Vol.331 (9), p.574-578

1994

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Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus

Neurogenetics, 2009-07, Vol.10 (3), p.199-208

2009

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Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy

American journal of human genetics, 1993-06, Vol.52 (6), p.1164-1174

1993

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Characteristics of breast carcinomas missed by screening radiologists

Radiology, 1997-07, Vol.204 (1), p.131-135

1997

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Pre-injury status and adaptation following traumatic brain injury

Brain injury, 2002, Vol.16 (1), p.41-49

2002

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Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

Nature genetics, 1993-08, Vol.4 (4), p.393-397

1993

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Huntingtin Protein Colocalizes with Lesions of Neurodegenerative Diseases: An Investigation in Huntington's, Alzheimer's, and Pick's Diseases

Experimental neurology, 1998-04, Vol.150 (2), p.213-222

1998

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Dangerous Behaviour Preceding First Admissions for Schizophrenia

British journal of psychiatry, 1992-10, Vol.161 (4), p.501-505

1992

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Dentatorubral and pallidoluysian atrophy (DRPLA) Clinical and neuropathological findings in genetically confirmed north american and european pedigrees

Movement disorders, 1997-07, Vol.12 (4), p.519-530

1997

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Microsomal epoxide hydrolase gene polymorphism and susceptibility to colon cancer

British journal of cancer, 1999-01, Vol.79 (1), p.168-171

1999

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Successful mobilization of peripheral blood stem cells after addition of ancestim (stem cell factor) in patients who had failed a prior mobilization with filgrastim (granulocyte colony-stimulating factor) alone or with chemotherapy plus filgrastim

Bone marrow transplantation (Basingstoke), 2003-03, Vol.31 (5), p.371-378

2003

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Molecular analysis and clinical correlations of the Huntington's disease mutation

The Lancet (British edition), 1993-10, Vol.342 (8877), p.954-958

1993

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Partial Characterisation of Murine Huntingtin and Apparent Variations in the Subcellular Localisation of Huntingtin in Human, Mouse and Rat Brain

Human molecular genetics, 1996-04, Vol.5 (4), p.481-487

1996

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Clinical and genetic study of Friedreich ataxia in an Australian population

American journal of medical genetics, 1999-11, Vol.87 (2), p.168-174

1999

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Neuropathological diagnosis and CAG repeat expansion in Huntington's disease

Journal of neurology, neurosurgery and psychiatry, 1996-01, Vol.60 (1), p.78-81

1996

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Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine

Journal of the neurological sciences, 2004-12, Vol.227 (1), p.95-100

2004

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Discharge of the asthmatic patient

Clinical reviews in allergy & immunology, 2001-06, Vol.20 (3), p.341-356

2001

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Radiographic assessment of patellofemoral osteoarthritis

Annals of the rheumatic diseases, 1993-09, Vol.52 (9), p.655-658

1993

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Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci

Journal of medical genetics, 1999-03, Vol.36 (3), p.258-259

1999

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Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea

Journal of medical genetics, 1993-12, Vol.30 (12), p.1012-1013

1993

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Molecular diagnostic analysis for Huntington's disease: a prospective evaluation

Journal of neurology, neurosurgery and psychiatry, 1995-04, Vol.58 (4), p.496-498

1995

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The Charcot-Marie-Tooth syndrome: clinical aspects from a population study in South Wales, UK

Clinical genetics, 1994-03, Vol.45 (3), p.128-134

1994

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Cataract and myotonic dystrophy: the role of molecular diagnosis

British journal of ophthalmology, 1993-09, Vol.77 (9), p.579-583

1993

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Denervation drives mitochondrial dysfunction in skeletal muscle of octogenarians

Myometrial Defect in a Subsequent Pregnancy After Uterine Artery Embolization for Postpartum Hemorrhage, in the Absence of Leiomyomas or Previous Uterine Surgery

Survival in Medically Treated Patients with Homozygous β-Thalassemia

Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy

Characteristics of breast carcinomas missed by screening radiologists

Pre-injury status and adaptation following traumatic brain injury

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

Huntingtin Protein Colocalizes with Lesions of Neurodegenerative Diseases: An Investigation in Huntington's, Alzheimer's, and Pick's Diseases

Dangerous Behaviour Preceding First Admissions for Schizophrenia

Dentatorubral and pallidoluysian atrophy (DRPLA) Clinical and neuropathological findings in genetically confirmed north american and european pedigrees

Microsomal epoxide hydrolase gene polymorphism and susceptibility to colon cancer

Successful mobilization of peripheral blood stem cells after addition of ancestim (stem cell factor) in patients who had failed a prior mobilization with filgrastim (granulocyte colony-stimulating factor) alone or with chemotherapy plus filgrastim

Molecular analysis and clinical correlations of the Huntington's disease mutation

Partial Characterisation of Murine Huntingtin and Apparent Variations in the Subcellular Localisation of Huntingtin in Human, Mouse and Rat Brain

Clinical and genetic study of Friedreich ataxia in an Australian population

Neuropathological diagnosis and CAG repeat expansion in Huntington's disease

Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine

Discharge of the asthmatic patient

Radiographic assessment of patellofemoral osteoarthritis

Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci

Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation

The Charcot-Marie-Tooth syndrome: clinical aspects from a population study in South Wales, UK

Cataract and myotonic dystrophy: the role of molecular diagnosis

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