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Self-management of overactive bladder at home using transcutaneous tibial nerve stimulation: a qualitative study of women's experiences

BMC women's health, 2021-10, Vol.21 (1), p.374-374, Article 374

2021

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Clinical and anatomical heterogeneity in autistic spectrum disorder: a structural MRI study

Psychological medicine, 2010-07, Vol.40 (7), p.1171-1181

2010

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Brain morphometry volume in autistic spectrum disorder: a magnetic resonance imaging study of adults

Psychological medicine, 2009-02, Vol.39 (2), p.337-346

2009

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The phenotypic and genetic assessment of antithrombin deficiency

International journal of laboratory hematology, 2011-06, Vol.33 (3), p.227-237

2011

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Short-term effects of severe dietary carbohydrate-restriction advice in Type 2 diabetes-a randomized controlled trial

Diabetic medicine, 2006-01, Vol.23 (1), p.15-20

2006

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Urethral bulking agents: a retrospective review of primary versus salvage procedure outcomes

World journal of urology, 2021-06, Vol.39 (6), p.2107-2112

2021

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Esophageal tolerance to high-dose stereotactic ablative radiotherapy

Diseases of the esophagus, 2012-09, Vol.25 (7), p.623-629

2012

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Congenital macrothrombocytopenia is a heterogeneous disorder in India

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-07, Vol.22 (4), p.570-582

2016

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The interactive effect of acute ovarian suppression and the cholinergic system on visuospatial working memory in young women

Psychoneuroendocrinology, 2010-08, Vol.35 (7), p.987-1000

2010

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Novel platelet membrane glycoprotein VI dimorphism is a risk factor for myocardial infarction

Circulation (New York, N.Y.), 2001-09, Vol.104 (13), p.1459-1463

2001

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A Case Study of Delayed Action PIR Urinal-Controls in a University Setting and Their Impact before, during and after COVID-19

Sustainability, 2022-11, Vol.14 (23), p.15506

2022

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Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

Journal of thrombosis and haemostasis, 2015-04, Vol.13 (4), p.643-650

2015

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Intrinsic gray-matter connectivity of the brain in adults with autism spectrum disorder

Proceedings of the National Academy of Sciences - PNAS, 2013-08, Vol.110 (32), p.13222-13227

2013

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The interactive effect of the cholinergic system and acute ovarian suppression on the brain: An fMRI study

Hormones and behavior, 2009, Vol.55 (1), p.41-49

2009

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Prevalence of antithrombin deficiency in the healthy population

British journal of haematology, 1994-05, Vol.87 (1), p.106-112

1994

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A novel mutation in the P2Y12 receptor and a function‐reducing polymorphism in protease‐activated receptor 1 in a patient with chronic bleeding

Journal of thrombosis and haemostasis, 2014-05, Vol.12 (5), p.716-725

2014

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Dietary carbohydrates and insulin sensitivity: a review of the evidence and clinical implications

The American journal of clinical nutrition, 1997-11, Vol.66 (5), p.1072-1085

1997

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Supplementary active optics for illumination within an adaptive optics system

Journal of modern optics, 2011-11, Vol.58 (19-20), p.1716-1728

2011

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Volumes of Medial Temporal Lobe Structures in Patients with Alzheimer’s Disease and Mild Cognitive Impairment (and in Healthy Controls)

Biological psychiatry (1969), 1998, Vol.43 (1), p.60-68

1998

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Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S

Blood, 2000-03, Vol.95 (6), p.1935-1941

2000

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Interactive effects of age and hypertension on volumes of brain structures

Stroke (1970), 1997-07, Vol.28 (7), p.1410-1417

1997

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Clinical-dosimetric relationship between lacrimal gland dose and ocular toxicity after intensity-modulated radiotherapy for sinonasal tumours

British journal of radiology, 2013-12, Vol.86 (1032), p.20130459

2013

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The GPIa C807T dimorphism associated with platelet collagen receptor density is not a risk factor for myocardial infarction

British journal of haematology, 1999-09, Vol.106 (3), p.771-776

1999

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The functional neuroanatomy of social behaviour : Changes in cerebral blood flow when people with autistic disorder process facial expressions

Brain (London, England : 1878), 2000-11, Vol.123 (11), p.2203-2212

2000

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Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia

Thrombosis and haemostasis, 1997-12, Vol.78 (6), p.1426

1997

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