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Cerebral venous sinus thrombosis and thrombocytopenia after COVID-19 vaccination – A report of two UK cases

Brain, behavior, and immunity, 2021-07, Vol.95, p.514-517

2021

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Neutrophil to lymphocyte ratio predicts intracranial hemorrhage after endovascular thrombectomy in acute ischemic stroke

Journal of neuroinflammation, 2018-11, Vol.15 (1), p.319-319, Article 319

2018

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Cerebrovascular manifestations of herpes simplex virus infection of the central nervous system: a systematic review

Journal of neuroinflammation, 2019-01, Vol.16 (1), p.19-19, Article 19

2019

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Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication

eLife, 2015-08, Vol.4

2015

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Fatal thrombolysis-related intracerebral haemorrhage associated with amyloid-β-related angiitis in a middle-aged patient - case report and literature review

BMC neurology, 2022-12, Vol.22 (1), p.500-500, Article 500

2022

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Idarucizumab in Dabigatran-Treated Patients with Acute Ischemic Stroke Receiving Alteplase: A Systematic Review of the Available Evidence

CNS drugs, 2017-09, Vol.31 (9), p.747-757

2017

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Contribution of Serum Lipid Profiles to Outcome After Endovascular Thrombectomy for Anterior Circulation Ischemic Stroke

Molecular neurobiology, 2019-06, Vol.56 (6), p.4582-4588

2019

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Carotid stenosis and the cognitive function

Journal of the neurological sciences, 2009-08, Vol.283 (1), p.36-40

2009

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Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III

Nature communications, 2015-07, Vol.6 (1), p.7623-7623, Article 7623

2015

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The effect of transcranial direct current stimulation on motor sequence learning and upper limb function after stroke

Clinical neurophysiology, 2017-07, Vol.128 (7), p.1389-1398

2017

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Safety and clinical outcome of thrombolysis in ischaemic stroke using a perfusion CT mismatch between 3 and 6 hours

PloS one, 2011-10, Vol.6 (10), p.e25796

2011

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Early prolonged ambulatory cardiac monitoring in stroke (EPACS): an open-label randomised controlled trial

European journal of medical research, 2019-07, Vol.24 (1), p.25-25, Article 25

2019

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Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability

Journal of human genetics, 2018-11, Vol.63 (11), p.1189-1193

2018

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Determinants of mismatch in acute ischaemic stroke

Journal of the neurological sciences, 2013-11, Vol.334 (1), p.10-13

2013

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Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

Brain (London, England : 1878), 2011-01, Vol.134 (Pt 1), p.143-156

2011

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Blood pressure characteristics in patients with acute basilar artery occlusion undergoing endovascular thrombectomy

Scientific reports, 2019-09, Vol.9 (1), p.13224-10, Article 13224

2019

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A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature

Journal of applied genetics, 2019-05, Vol.60 (2), p.151-162

2019

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Endovascular Therapy for Tandem Occlusion in Acute Ischemic Stroke: Intravenous Thrombolysis Improves Outcomes

Journal of clinical medicine, 2019-02, Vol.8 (2), p.228

2019

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Kynurenic acid and kynurenine aminotransferase are potential biomarkers of early neurological improvement after thrombolytic therapy: A pilot study

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2021-12, Vol.30 (12), p.1225-1232

2021

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High Prevalence of New Clinically Significant Findings in Patients With Embolic Stroke of Unknown Source Evaluated by Cardiac Magnetic Resonance Imaging

Journal of the American Heart Association, 2024-02, Vol.13 (3), p.e031489-e031489

2024

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Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

Orphanet journal of rare diseases, 2014-05, Vol.9 (1), p.72-72, Article 72

2014

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Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria

American journal of human genetics, 2004-12, Vol.75 (6), p.979-987

2004

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A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia

Journal of pediatric genetics (Birmingham, Ala.), 2021-06, Vol.10 (2), p.159-163

2021

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Intracerebral haemorrhage and COVID-19: Clinical characteristics from a case series

Brain, behavior, and immunity, 2020-08, Vol.88, p.940-944

2020

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Cerebral venous sinus thrombosis and thrombocytopenia after COVID-19 vaccination – A report of two UK cases

Neutrophil to lymphocyte ratio predicts intracranial hemorrhage after endovascular thrombectomy in acute ischemic stroke

Cerebrovascular manifestations of herpes simplex virus infection of the central nervous system: a systematic review

Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication

Fatal thrombolysis-related intracerebral haemorrhage associated with amyloid-β-related angiitis in a middle-aged patient - case report and literature review

Idarucizumab in Dabigatran-Treated Patients with Acute Ischemic Stroke Receiving Alteplase: A Systematic Review of the Available Evidence

Contribution of Serum Lipid Profiles to Outcome After Endovascular Thrombectomy for Anterior Circulation Ischemic Stroke

Carotid stenosis and the cognitive function

Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III

The effect of transcranial direct current stimulation on motor sequence learning and upper limb function after stroke

Safety and clinical outcome of thrombolysis in ischaemic stroke using a perfusion CT mismatch between 3 and 6 hours

Mutations in INPP5E , encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies

Early prolonged ambulatory cardiac monitoring in stroke (EPACS): an open-label randomised controlled trial

Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability

Determinants of mismatch in acute ischaemic stroke

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

Blood pressure characteristics in patients with acute basilar artery occlusion undergoing endovascular thrombectomy

A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature

Endovascular Therapy for Tandem Occlusion in Acute Ischemic Stroke: Intravenous Thrombolysis Improves Outcomes

Kynurenic acid and kynurenine aminotransferase are potential biomarkers of early neurological improvement after thrombolytic therapy: A pilot study

High Prevalence of New Clinically Significant Findings in Patients With Embolic Stroke of Unknown Source Evaluated by Cardiac Magnetic Resonance Imaging

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria

A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia

Intracerebral haemorrhage and COVID-19: Clinical characteristics from a case series

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