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

eLife, 2015-08, Vol.4

2015

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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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Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1

Brain & development (Tokyo. 1979), 2021-01, Vol.43 (1), p.144-151

2021

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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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Craniofacial features of POLR3-related leukodystrophy caused by biallelic variants in POLR3A, POLR3B and POLR1C

Journal of medical genetics, 2023-10, Vol.60 (10), p.1026-1034

2023

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A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder

BMC pediatrics, 2024-01, Vol.24 (1), p.47-47, Article 47

2024

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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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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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Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly

Brain (London, England : 1878), 2017-10, Vol.140 (10), p.2610-2622

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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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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DWI-FLAIR mismatch guided thrombolysis in patients without large-vessel occlusion: real-world data from a comprehensive stroke centre

Heliyon, 2022-12, Vol.8 (12), p.e12069-e12069, Article e12069

2022

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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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Clinical presentation and outcome in a series of 88 patients with the cblC defect

Journal of inherited metabolic disease, 2014-09, Vol.37 (5), p.831-840

2014

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

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

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

Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1

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

Craniofacial features of POLR3-related leukodystrophy caused by biallelic variants in POLR3A, POLR3B and POLR1C

A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder

Carotid stenosis and the cognitive function

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

Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly

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

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

DWI-FLAIR mismatch guided thrombolysis in patients without large-vessel occlusion: real-world data from a comprehensive stroke centre

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

Clinical presentation and outcome in a series of 88 patients with the cblC defect

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

Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome

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

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

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

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