Ghent University Academic Bibliography

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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP)

Astrid Van den broecke, Alexander Decruyenaere (UGent) , Nika Schuermans (UGent) , Hannah Verdin (UGent) , Jody Ghijsels (UGent) , Anne Sieben, Bart Dermaut (UGent) and Dimitri Hemelsoet (UGent)

(2024) JOURNAL OF NEUROLOGY. 271. p.263-273
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Cognitive outcomes in Susac syndrome : a 2-year neuropsychological follow-up study

Tineke Van Vrekhem (UGent) , Marijke Miatton (UGent) , Dimitri Hemelsoet (UGent) , Liesbeth Van Hijfte (UGent) , Cathérine Dekeyser (UGent) , Julie De Zaeytijd (UGent) , Veroniek Van Driessche (UGent) , Helen Van Hoecke (UGent) , Leen Maes (UGent) and Guy Laureys (UGent)

(2024) EUROPEAN JOURNAL OF NEUROLOGY.
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SAMHD1 compound heterozygous rare variants associated with moyamoya and mitral valve disease in the absence of other features of Aicardi-Goutières syndrome

Aamuktha R. Karla, Amelie Pinard, Maura L. Boerio, Dimitri Hemelsoet (UGent) , Simon Tavernier (UGent) , Michel De Pauw (UGent) , Elke Vereecke (UGent) , Stuart Fraser, Michael J. Bamshad, Dongchuan Guo, et al.

(2024) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 194(4).
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- Conference Paper
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Causal evidence of anterior cingulate cortex function: an experimental study in patients with stroke in the frontal lobe

Joyce Oerlemans (UGent) , Ricardo Alejandro Benavides (UGent) , Dimitri Hemelsoet (UGent) , Paul Boon (UGent) , Clay Holroyd (UGent) and Veerle De Herdt (UGent)

(2023) EUROPEAN JOURNAL OF NEUROLOGY. 30. p.566-566
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Atypical clinical and novel radiological findings in Susac syndrome : experience from a large monocentric cohort

Cathérine Dekeyser (UGent) , Alexander Vanhoorne, Dimitri Hemelsoet (UGent) , Liesbeth Van Hijfte (UGent) , Julie De Zaeytijd (UGent) , Veroniek Van Driessche (UGent) , Helen Van Hoecke (UGent) , Marijke Miatton (UGent) , Tineke Van Vrekhem (UGent) , Leen Maes (UGent) , et al.

(2023) JOURNAL OF NEUROIMMUNOLOGY. 376.
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Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders

Nika Schuermans (UGent) , Hannah Verdin (UGent) , Jody Ghijsels (UGent) , Madeleine Hellemans (UGent) , Elke Debackere (UGent) , Elke Bogaert (UGent) , Sofie Symoens (UGent) , Leslie Naesens (UGent) , Elien Lecomte, David Crosiers, et al.

(2023) NEUROLOGY-GENETICS. 9(3).
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Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling

Nika Schuermans (UGent) , Salima El Chehadeh, Dimitri Hemelsoet (UGent) , Jérémie Gautheron, Marie-Christine Vantyghem, Sonia Nouioua, Meriem Tazir, Corinne Vigouroux, Martine Auclair, Elke Bogaert (UGent) , et al.

(2023) NATURE GENETICS. 55(11). p.1929-1940
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SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability

Elke Bogaert (UGent) , Aurore Garde, Thierry Gautier, Kathleen Rooney, Yannis Duffourd, Pontus LeBlanc (UGent) , Emma Van Reempts (UGent) , Frederic Tran Mau-Them, Ingrid M. Wentzensen, Kit Sing Au, et al.

(2023) AMERICAN JOURNAL OF HUMAN GENETICS. 110(5). p.790-808
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Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

Burcu Yaldiz, Erdi Kucuk, Juliet Hampstead, Tom Hofste, Rolph Pfundt, Jordi Corominas Galbany, Tuula Rinne, Helger G. Yntema, Alexander Hoischen, Marcel Nelen, et al.

(2023) HUMAN GENOMICS. 17(1).
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A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

Anne-Sophie Denommé-Pichon, Leslie Matalonga, Elke de Boer, Adam Jackson, Elisa Benetti, Siddharth Banka, Ange-Line Bruel, Andrea Ciolfi, Jill Clayton-Smith, Bruno Dallapiccola, et al.

(2023) GENETICS IN MEDICINE. 25(4).
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Ibrutinib-associated symptomatic intracerebral haemorrhage following IV thrombolysis for acute ischaemic stroke

Katrijn Madou, Sofie Carrette (UGent) , Marjan Acou (UGent) , Veerle De Herdt (UGent) and Dimitri Hemelsoet (UGent)

(2022) ACTA NEUROLOGICA BELGICA. 122(4). p.1111-1113
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Moyamoya disease emerging as an immune-related angiopathy

Caroline Asselman (UGent) , Dimitri Hemelsoet (UGent) , Denzel Eggermont (UGent) , Bart Dermaut (UGent) and Francis Impens (UGent)

(2022) TRENDS IN MOLECULAR MEDICINE. 28(11). p.939-950
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Clinical and subclinical findings in heterozygous ABCC6 carriers : results from a Belgian cohort and clinical practice guidelines

Lukas Nollet (UGent) , Laurence Campens (UGent) , Julie De Zaeytijd (UGent) , Bart Leroy (UGent) , Dimitri Hemelsoet (UGent) , Paul Coucke (UGent) and Olivier Vanakker (UGent)

(2022) JOURNAL OF MEDICAL GENETICS. 59(5). p.496-504
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- Conference Paper
- C3
Identifying the source of the reward positivity : two patient studies involving cortical lesions and intracranial recording

Joyce Oerlemans (UGent) , Ricardo Alejandro Benavides (UGent) , Dimitri Hemelsoet (UGent) , Alfred Meurs (UGent) , Paul Boon (UGent) , Veerle De Herdt (UGent) and Clay Holroyd (UGent)

(2022) PSYCHOPHYSIOLOGY. In Psychophysiology 59(Supplement 1). p.S153-S153
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- Conference Paper
- C3
Lipodystrophy due to genetic deficiency of picornavirus host factor and obesity regulator PLAAT3

Nika Schuermans (UGent) , Salima El Chehadeh, Dimitri Hemelsoet (UGent) , Elke Bogaert (UGent) , Elke Debackere (UGent) , Pascale Hilbert, Nike Van Doninck, Marie-Caroline Taquet, Toon Rosseel (UGent) , Griet De Clercq (UGent) , et al.

(2022) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 30(Supplement 1). p.80-80
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Mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF, and result in Aicardi-Goutières syndrome with severe end-organ involvement

Leslie Naesens (UGent) , Josephine Nemegeer (UGent) , Filip Roelens, Lore Vallaeys, Marije Meuwissen, Katrien Janssens, Patrick Verloo (UGent) , Benson Ogunjimi, Dimitri Hemelsoet (UGent) , Levi Hoste (UGent) , et al.

(2022) JOURNAL OF CLINICAL IMMUNOLOGY. 42(5). p.962-974
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Shortcutting the diagnostic odyssey : the multidisciplinary program for undiagnosed rare diseases in adults (UD-PrOZA)

Nika Schuermans (UGent) , Dimitri Hemelsoet (UGent) , Wim Terryn, Sanne Steyaert (UGent) , Rudy Van Coster (UGent) , Paul Coucke (UGent) , Wouter Steyaert, Bert Callewaert (UGent) , Elke Bogaert (UGent) , Patrick Verloo (UGent) , et al.

(2022) ORPHANET JOURNAL OF RARE DISEASES. 17(1).
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Is monitoring of antiplatelet therapy by light transmission aggregometry dependent on instrument and reagent used?

Tinne Monteyne, Laura Heireman, Dimitri Hemelsoet (UGent) , Ron H.N. Schaik and Katrien Devreese (UGent)

(2021) INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY. 43(4). p.786-794
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Microbleed patterns in critical illness and COVID-19

Jonas Toeback, Sofie DR Depoortere, Joris Vermassen (UGent) , Elke Vereecke (UGent) , Veroniek Van Driessche (UGent) and Dimitri Hemelsoet (UGent)

(2021) CLINICAL NEUROLOGY AND NEUROSURGERY. 203.
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The feasibility, usability and acceptability of a tablet-based aphasia therapy in the acute phase following stroke

Elien De Cock, Katja Batens (UGent) , Judith Feiken, Dimitri Hemelsoet (UGent) , Kristine Oostra (UGent) and Veerle De Herdt (UGent)

(2021) JOURNAL OF COMMUNICATION DISORDERS. 89.
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- Journal Article
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Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation

Antoon Meylemans, Pieter Depuydt (UGent) , Elfride De Baere (UGent) , Katrien Hertegonne (UGent) , Eric Derom (UGent) , Bart Dermaut (UGent) and Dimitri Hemelsoet (UGent)

(2021) ACTA NEUROLOGICA BELGICA. 121. p.23-35
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Dysarthria following acute ischemic stroke : prospective evaluation of characteristics, type and severity

Elien De Cock, Kristine Oostra (UGent) , Lisa Bliki, Anne-Sophie Volkaerts, Dimitri Hemelsoet (UGent) , Veerle De Herdt (UGent) and Katja Batens (UGent)

(2021) INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS. 56(3). p.549-557
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Alemtuzumab in multiple sclerosis : a retrospective analysis of occult hemorrhagic magnetic resonance imaging lesions and risk factors

Helen Bachmann (UGent) , Melissa Cambron, JW Casselman, Veroniek Van Driessche (UGent) , Eline Van Haute (UGent) , Liesbeth Van Hijfte (UGent) , Tim Kelderman, Dimitri Hemelsoet (UGent) and Guy Laureys (UGent)

(2021) EUROPEAN JOURNAL OF NEUROLOGY. 28(12). p.4209-4213
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- Conference Paper
- C3
Novel mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF and result in Aicardi-Goutières syndrome with severe end-organ involvement

Leslie Naesens (UGent) , Josephine Nemegeer (UGent) , Filip Roelens, Lore Vallaeys, Marije Meuwissen, Katrien Janssens, Patrick Verloo (UGent) , Benson Ogunjimi (UGent) , Dimitri Hemelsoet (UGent) , Program for Undiagnosed Rare Diseases (UD-PrOZA), et al.

(2021) 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts.
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Search for a practical approach for detection of clopidogrel resistance : comparison of light transmission aggregometry and INNOVANCE® PFA P2Y cartridge and correlation with CYP2C19 variants

Laura Heireman, Tinne Monteyne, Dimitri Hemelsoet (UGent) , Ron H. N. Schaik and Katrien Devreese (UGent)

(2020) INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY. 42(4). p.E189-E191
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Evolution of surgical treatment of carotid artery stenosis : a single center observational study

Gilles Soenens (UGent) , Nathalie Moreels (UGent) , Frank Vermassen (UGent) , Veerle De Herdt (UGent) , Dimitri Hemelsoet (UGent) and Isabelle Van Herzeele (UGent)

(2020) ACTA CHIRURGICA BELGICA. 120(5). p.301-309
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Dysphagia, dysarthria and aphasia following a first acute ischemic stroke : incidence and associated factors

Elien De Cock, Katja Batens (UGent) , Dimitri Hemelsoet (UGent) , Paul Boon (UGent) , Kristine Oostra (UGent) and Veerle De Herdt (UGent)

(2020) EUROPEAN JOURNAL OF NEUROLOGY. 27(10). p.2014-2021
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- Conference Paper
- C3
The feasibility, usability and acceptability of a tablet-based aphasia therapy in the acute phase following stroke

Elien De Cock, Katja Batens (UGent) , Judith Feiken, Dimitri Hemelsoet (UGent) , Kristine Oostra (UGent) and Veerle De Herdt (UGent)

(2020) 11th World Congress for Neurorehabilitation, Abstracts.
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Dysphagia, dysarthria and aphasia following a first acute ischemic stroke : incidence and associated factors

Elien De Cock, Katja Batens (UGent) , Dimitri Hemelsoet (UGent) , Paul Boon (UGent) , Kristine Oostra (UGent) and Veerle De Herdt (UGent)

(2020) The joint European Stroke Organisation and World Stroke Organization Conference (ESO-WSO 2020), Abstracts.
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Long-term EEG monitoring for the detection of epileptic activity in the acute phase of stroke

Silke Proesmans (UGent) , Stephanie Hödl (UGent) , Helena Janssen, Dimitri Hemelsoet (UGent) , Paul Boon (UGent) and Veerle De Herdt (UGent)

(2020) EUROPEAN JOURNAL OF NEUROLOGY. In European Journal of Neurology 27(Supplement 1). p.120-120
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CT perfusion as a selection tool for mechanical thrombectomy, a single-centre study

Emilie De Muynck (UGent) , Vincent Huybrechts (UGent) , Dimitri Hemelsoet (UGent) , Elisabeth Dhondt (UGent) , Peter Vanlangenhove (UGent) and Luc Defreyne (UGent)

(2020) JOURNAL OF THE BELGIAN SOCIETY OF RADIOLOGY. 104(1).
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A new dimension in patent foramen ovale size estimation

Laurent Demulier (UGent) , Bernard Pierre Paelinck, Ilse Coomans (UGent) , Dimitri Hemelsoet (UGent) , Julie De Backer (UGent) , Laurence Campens (UGent) and Daniël De Wolf (UGent)

(2020) ECHOCARDIOGRAPHY - A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES. 37(7). p.1049-1055
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Neurological manifestations and neuro-invasive mechanisms of the severe acute respiratory syndrome coronavirus type 2

Kristl Vonck (UGent) , Ieme Garrez (UGent) , Veerle De Herdt (UGent) , Dimitri Hemelsoet (UGent) , Guy Laureys (UGent) , Robrecht Raedt (UGent) and Paul Boon (UGent)

(2020) EUROPEAN JOURNAL OF NEUROLOGY. 27(8). p.1578-1587
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Impact of a code stroke protocol on the door-to-needle time for IV thrombolysis : a feasibility study

JOKE VANHOUCKE (UGent) , Dimitri Hemelsoet (UGent) , Eric Achten (UGent) , Veerle De Herdt (UGent) , Marjan Acou (UGent) , Elke Vereecke (UGent) and Saïd Hachimi Idrissi (UGent)

(2020) ACTA CLINICA BELGICA. 75(4). p.267-274
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Prior stroke in PFO patients is associated with both PFO-related and -unrelated factors

Timo Kahles, Patrik Michel, Alexander Hapfelmeier, Franz R. Eberli, Marialuisa Zedde, Vincent Thijs, Markus Kraemer, Stefan T. Engelter, Joaquin Serena, Christian Weimar, et al.

(2020) FRONTIERS IN NEUROLOGY. 11.
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Charting extracellular transcriptomes in the human biofluid RNA atlas

Eva Hulstaert, Annelien Morlion (UGent) , Francisco Avila Cobos (UGent) , Kimberly Verniers (UGent) , Justine Nuytens (UGent) , Eveline Vanden Eynde (UGent) , Nurten Yigit (UGent) , Jasper Anckaert (UGent) , Anja Geerts (UGent) , Pieter Hindryckx (UGent) , et al.

(2020) CELL REPORTS. 33(13).
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Enrichment of rare variants in Loeys-Dietz syndrome genes in spontaneous coronary artery dissection but not in severe fibromuscular dysplasia

Aline Verstraeten, Melanie H.A.M. Perik, Anna A. Baranowska, Josephina A.N. Meester, Lotte Van Den Heuvel, Jarl Bastianen, Marlies Kempers, Ingrid P.C. Krapels, Angela Maas, Andrea Rideout, et al.

(2020) CIRCULATION. 142(10). p.1021-1024
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A likely pathogenic variant in the SLC20A2 gene presenting with progressive myoclonus

Simon Lamquet (UGent) , Eliana M Ramos, Andrea Legati, Giovanni Coppola, Dimitri Hemelsoet (UGent) and Olivier Vanakker (UGent)

(2019) ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY. 6(3). p.605-609
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- Conference Paper
- C3
Atypical clinical and novel radiological findings in Susac syndrome

Zoë Delaruelle, Alexander Vanhoorne, Julie De Zaeytijd (UGent) , Els De Leenheer (UGent) , Veroniek Van Driessche (UGent) , Guy Laureys (UGent) and Dimitri Hemelsoet (UGent)

(2019) EUROPEAN JOURNAL OF NEUROLOGY. In European Journal of Neurology 26(Supplement 1). p.375-375
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Evolution of surgical treatment of carotid artery stenosis

Gilles Soenens (UGent) , Bart Doyen, Nathalie Moreels (UGent) , Dimitri Hemelsoet (UGent) , Veerle De Herdt (UGent) , Frank Vermassen (UGent) and Isabelle Van Herzeele (UGent)

(2019) Controversies and Updates in Vascular Surgery (CACVS), Abstracts.
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- C3
The incidence, severity and recovery of aphasia following acute stroke in a tertiary hospital

Elien De Cock, Elien De Schamphelaere, Tim Kelderman, Antoon Meylemans, Dimitri Hemelsoet (UGent) , Kristine Oostra (UGent) and Veerle De Herdt (UGent)

(2019) 5th European Stroke Organisation Conference (ESOC 2019), Abstracts.
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Category specific recall in acute stroke : a case with letter speech

Miet De Letter (UGent) , John Van Borsel (UGent) , Ellen Lanckmans (UGent) , Katja Batens (UGent) , Dimitri Hemelsoet (UGent) , Wouter Duyck (UGent) , Wim Fias (UGent) and Patrick Santens (UGent)

(2019) NEUROCASE. 25(6). p.251-258
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- Miscellaneous
Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults

Vincent Van Iseghem, Mathieu Sprengers (UGent) , Julie De Zaeytijd (UGent) , Sindic CJM, B Willekens, Bart Dermaut (UGent) , Dimitri Hemelsoet (UGent) and Guy Laureys (UGent)

(2019) Multiple Sclerosis and Related Disorders. 32. p.64-65
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HIV rebound is predominantly fueled by genetically identical viral expansions from diverse reservoirs

Marie-Angélique De Scheerder (UGent) , Bram Vrancken, Simon Dellicour, Timothy Schlub, Eunok Lee, Wei Shao, Sofie Rutsaert (UGent) , Chris Verhofstede (UGent) , Tessa Kerre (UGent) , Thomas Malfait (UGent) , et al.

(2019) CELL HOST & MICROBE. 26(3). p.347-358
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- C3
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The human biofluid RNA atlas : expanding the liquid biopsy field beyond the blood stream

Eva Hulstaert, Kimberly Verniers (UGent) , Justine Nuytens (UGent) , Eveline Vanden Eynde (UGent) , Nurten Yigit (UGent) , Jasper Anckaert (UGent) , Anja Geerts (UGent) , Peggy Jacques (UGent) , Guy Brusselle (UGent) , Thierry Derveaux (UGent) , et al.

(2019) OncoPoint, 7th Research seminar, Abstracts.
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An easily overlooked cause of toxic encephalopathy : methylene blue in a patient on an SSRI

PIETER-JAN HONORE (UGent) , Nancy Deianova (UGent) , Griet Loret and Dimitri Hemelsoet (UGent)

(2018) ACTA NEUROLOGICA BELGICA. 118(1). p.121-122
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Rehabilitation of visuospatial neglect by prism adaptation : effects of a mild treatment regime : a randomised controlled trial

Nathalie Vaes (UGent) , Gudrun Nys, Christophe Lafosse, Lutgart Dereymaeker, Kristine Oostra (UGent) , Dimitri Hemelsoet (UGent) and Guy Vingerhoets (UGent)

(2018) NEUROPSYCHOLOGICAL REHABILITATION. 28(6). p.899-918
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Future perspectives of genome-scale sequencing

Wouter Steyaert (UGent) , Steven Callens (UGent) , Paul Coucke (UGent) , Bart Dermaut (UGent) , Dimitri Hemelsoet (UGent) , Wim Terryn and Bruce Poppe (UGent)

(2018) ACTA CLINICA BELGICA. 73(1). p.7-10
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Cognate effects and cognitive control in patients with parallel and differential bilingual aphasia

Lize Van der Linden, Nele Verreyt (UGent) , Miet De Letter (UGent) , Dimitri Hemelsoet (UGent) , Peter Mariën, Patrick Santens (UGent) , Michaël Stevens (UGent) , Arnaud Szmalec (UGent) and Wouter Duyck (UGent)

(2018) INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS. 53(3). p.515-525
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Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C > T mutation in MTFMT

Dimitri Hemelsoet (UGent) , Arnaud Vanlander (UGent) , Joél Smet (UGent) , Elise Vantroys, Marjan Acou (UGent) , Ingeborg Goethals (UGent) , Tom Sante (UGent) , Sara Seneca, Björn Menten (UGent) and Rudy Van Coster (UGent)

(2018) NEUROLOGY-GENETICS. 4(6).

Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP)

Cognitive outcomes in Susac syndrome : a 2-year neuropsychological follow-up study

SAMHD1 compound heterozygous rare variants associated with moyamoya and mitral valve disease in the absence of other features of Aicardi-Goutières syndrome

Causal evidence of anterior cingulate cortex function: an experimental study in patients with stroke in the frontal lobe

Atypical clinical and novel radiological findings in Susac syndrome : experience from a large monocentric cohort

Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders

Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling

SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability

Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

Ibrutinib-associated symptomatic intracerebral haemorrhage following IV thrombolysis for acute ischaemic stroke

Moyamoya disease emerging as an immune-related angiopathy

Clinical and subclinical findings in heterozygous ABCC6 carriers : results from a Belgian cohort and clinical practice guidelines

Identifying the source of the reward positivity : two patient studies involving cortical lesions and intracranial recording

Lipodystrophy due to genetic deficiency of picornavirus host factor and obesity regulator PLAAT3

Mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF, and result in Aicardi-Goutières syndrome with severe end-organ involvement

Shortcutting the diagnostic odyssey : the multidisciplinary program for undiagnosed rare diseases in adults (UD-PrOZA)

Is monitoring of antiplatelet therapy by light transmission aggregometry dependent on instrument and reagent used?

Microbleed patterns in critical illness and COVID-19

The feasibility, usability and acceptability of a tablet-based aphasia therapy in the acute phase following stroke

Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation

Dysarthria following acute ischemic stroke : prospective evaluation of characteristics, type and severity

Alemtuzumab in multiple sclerosis : a retrospective analysis of occult hemorrhagic magnetic resonance imaging lesions and risk factors

Novel mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF and result in Aicardi-Goutières syndrome with severe end-organ involvement

Search for a practical approach for detection of clopidogrel resistance : comparison of light transmission aggregometry and INNOVANCE® PFA P2Y cartridge and correlation with CYP2C19 variants

Evolution of surgical treatment of carotid artery stenosis : a single center observational study

Dysphagia, dysarthria and aphasia following a first acute ischemic stroke : incidence and associated factors

The feasibility, usability and acceptability of a tablet-based aphasia therapy in the acute phase following stroke

Dysphagia, dysarthria and aphasia following a first acute ischemic stroke : incidence and associated factors

Long-term EEG monitoring for the detection of epileptic activity in the acute phase of stroke

CT perfusion as a selection tool for mechanical thrombectomy, a single-centre study

A new dimension in patent foramen ovale size estimation

Neurological manifestations and neuro-invasive mechanisms of the severe acute respiratory syndrome coronavirus type 2

Impact of a code stroke protocol on the door-to-needle time for IV thrombolysis : a feasibility study

Prior stroke in PFO patients is associated with both PFO-related and -unrelated factors

Charting extracellular transcriptomes in the human biofluid RNA atlas

Enrichment of rare variants in Loeys-Dietz syndrome genes in spontaneous coronary artery dissection but not in severe fibromuscular dysplasia

A likely pathogenic variant in the SLC20A2 gene presenting with progressive myoclonus

Atypical clinical and novel radiological findings in Susac syndrome

Evolution of surgical treatment of carotid artery stenosis

The incidence, severity and recovery of aphasia following acute stroke in a tertiary hospital

Category specific recall in acute stroke : a case with letter speech

Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults

HIV rebound is predominantly fueled by genetically identical viral expansions from diverse reservoirs

The human biofluid RNA atlas : expanding the liquid biopsy field beyond the blood stream

An easily overlooked cause of toxic encephalopathy : methylene blue in a patient on an SSRI

Rehabilitation of visuospatial neglect by prism adaptation : effects of a mild treatment regime : a randomised controlled trial

Future perspectives of genome-scale sequencing

Cognate effects and cognitive control in patients with parallel and differential bilingual aphasia

Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C > T mutation in MTFMT