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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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Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine

Brain research, 2011-03, Vol.1378, p.119-124

2011

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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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Further Investigation of the Predictors of Outcome Following First Schizophrenic Episodes

British journal of psychiatry, 1990-08, Vol.157 (2), p.182-189

1990

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PAK3 mutation in nonsyndromic X-linked mental retardation

Nature genetics, 1998-09, Vol.20 (1), p.25-30

1998

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Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

Neurogenetics, 2012-02, Vol.13 (1), p.97-101

2012

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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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Bevacizumab Diminishes Experimental Autoimmune Encephalomyelitis by Inhibiting Spinal Cord Angiogenesis and Reducing Peripheral T-Cell Responses

Journal of neuropathology and experimental neurology, 2012-11, Vol.71 (11), p.983-999

2012

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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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Growth and clinical course of children with Crohn's disease

Gut, 1993-07, Vol.34 (7), p.939-943

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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Failed upregulation of TFAM protein and mitochondrial DNA in oxidatively deficient fibers of chronic obstructive pulmonary disease locomotor muscle

Skeletal muscle, 2016-02, Vol.6 (10), p.10-10, Article 10

2016

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The effects of recreational sport on VO2peak, VO2 kinetics and submaximal exercise performance in males and females

European journal of applied physiology, 2013, Vol.113 (1), p.259-266

2013

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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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A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

Journal of medical genetics, 2003-07, Vol.40 (7), p.515-519

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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A population genomics overview of the neuronal nitric oxide synthase (nNOS) gene and its relationship to migraine susceptibility

Cellular and molecular biology (Noisy-le-Grand, France), 2005-09, Vol.51 (3), p.285

2005

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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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Mitochondrial DNA depletion: Prevalence in a pediatric population referred for neurologic evaluation

Pediatric neurology, 1996-04, Vol.14 (3), p.203-210

1996

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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

Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine

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

Further Investigation of the Predictors of Outcome Following First Schizophrenic Episodes

PAK3 mutation in nonsyndromic X-linked mental retardation

Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

Pre-injury status and adaptation following traumatic brain injury

Bevacizumab Diminishes Experimental Autoimmune Encephalomyelitis by Inhibiting Spinal Cord Angiogenesis and Reducing Peripheral T-Cell Responses

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

Growth and clinical course of children with Crohn's disease

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

Failed upregulation of TFAM protein and mitochondrial DNA in oxidatively deficient fibers of chronic obstructive pulmonary disease locomotor muscle

The effects of recreational sport on VO2peak, VO2 kinetics and submaximal exercise performance in males and females

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

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

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

A population genomics overview of the neuronal nitric oxide synthase (nNOS) gene and its relationship to migraine susceptibility

Clinical and genetic study of Friedreich ataxia in an Australian population

Mitochondrial DNA depletion: Prevalence in a pediatric population referred for neurologic evaluation

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