Lista publicaţiilor: Chelban Viorica Gheorghe - 34

2023 - 1

Multiple system atrophy

Goh Yee Yen , Saunders Emma , Pavey Samantha , Rushton Emma , Quinn Niall , Houlden Henry H., Chelban Viorica Gheorghe

1 UCL Queen Square Institute of Neurology, 2 Multiple System Atrophy Trust, London, 3 ”Nicolae Testemițanu” State University of Medicine and Pharmacy

Practical Neurology

Nr. / 2023 / ISSN 1474-7758 / ISSNe 1474-7766

Disponibil online 12 June, 2023

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2021 - 7

The utility of whole exome sequencing for genetic diagnosis in familial epilepsy

Gasnaș (Catereniuc) Daniela Ilia, Chelban Viorica Gheorghe, Groppa Stanislav Alexandru

1 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 2 Emergency Institute of Medicine, 3 UCL Queen Square Institute of Neurology

International Congress of Geneticists and Breeders from the Republic of Moldova

Ediția 11. 2021. Chișinău, Republica Moldova. Centrul Editorial-Poligrafic al Universităţii de Stat din Moldova. 52-52.

Disponibil online 15 June, 2021

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BDNF genotype influence on the efficacy of RTMS in after- stroke rehabilitation

Gasnaş Alexandru Vladimir, Chelban Viorica Gheorghe, Groppa Stanislav Alexandru

1 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 2 Emergency Institute of Medicine, 3 UCL Queen Square Institute of Neurology

International Congress of Geneticists and Breeders from the Republic of Moldova

Ediția 11. 2021. Chișinău, Republica Moldova. Centrul Editorial-Poligrafic al Universităţii de Stat din Moldova. 51-51.

Disponibil online 15 June, 2021

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Drug-resistant epilepsy: modern concepts, integrative mechanisms, and therapeutic advances

Chiosa Vitalie Andrei, Ciolac Dumitru Vasile, Chelban Viorica Gheorghe, Gasnaș (Catereniuc) Daniela Ilia, Vataman Anatolie Anatoli, Munteanu Cristina Victor, Groppa Stanislav Alexandru

1 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 2 Emergency Institute of Medicine, 3 University College London

Moldovan Medical Journal

Nr. 4(64) / 2021 / ISSN 2537-6373 / ISSNe 2537-6381

Disponibil online 21 October, 2021

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Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare Disease

Breza Marianthi , Hirst Jennifer , Chelban Viorica Gheorghe, Autor Nou

1 National and Kapodistrian University of Athens (N.K.U.A.), 2 Universitatea Cambridge, 3 UCL Queen Square Institute of Neurology, 4 Emergency Institute of Medicine

Movement Disorders

Nr. 4(36) / 2021 / ISSN 0885-3185 / ISSNe 1531-8257

Disponibil online 6 May, 2021

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Spastic paraplegia preceding psen1-related familial alzheimer’s disease

Chelban Viorica Gheorghe, Breza Marianthi , Szaruga Maria , Vandrovcova Jana , Bourinaris Thomas, Lee Chia Ju , Alikhwan S. , Noi Autori

1 University College London, 2 Emergency Institute of Medicine, 3 Hippokration Hospital, Medical School, National and Kapodistrian University of Athens, 4 KU Leuven-VIB Center for Brain and Disease Research, Leuven

Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring

Nr. 1(13) / 2021 / ISSN 2352-8729 / ISSNe 2352-8729

Disponibil online 29 June, 2021

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Familial epilepsy – clinical-epidemiological characteristics and next-generation sequencing in the Republic of Moldova’s population

Gasnaș (Catereniuc) Daniela Ilia, Chelban Viorica Gheorghe, Groppa Stanislav Alexandru

1 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 2 Emergency Institute of Medicine, 3 Diomid Gherman Institute of Neurology and Neurosurgery

7th Congress of the Society of Neurologists Issue of the Republic of Moldova

Vol.64. 2021. Chişinău. Revista Curier Medical. 26-26.

Disponibil online 27 September, 2021

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Understanding the genetic characteristics of moldovan multiplex epilepsy families using whole exome sequencing

Gasnaș (Catereniuc) Daniela Ilia, Chelban Viorica Gheorghe, Groppa Stanislav Alexandru

1 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 2 University College London

Cercetarea în biomedicină și sănătate: calitate, excelență și performanță

2021. Chișinău, Republica Moldova. 220-220.

Disponibil online 14 November, 2021

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2020 - 8

Automated brainstem segmentation detects differential involvement in atypical parkinsonian syndromes

Bocchetta Martina , Iglesias Juan Eugenio , Chelban Viorica Gheorghe

1 University College London, 2 Emergency Institute of Medicine

Journal of Movement Disorders

Nr. 1(13) / 2020 / ISSN 2005-940X

Disponibil online 21 October, 2020

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Applicability of next generation genetic testing in epilepsy through whole exome sequencing

Gasnaș (Catereniuc) Daniela Ilia, Chelban Viorica Gheorghe, Groppa Stanislav Alexandru

1 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 2 University College London

Moldovan Medical Journal

Nr. 5(63) / 2020 / ISSN 2537-6373 / ISSNe 2537-6381

Disponibil online 7 December, 2020

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An update on MSA: premotor and non-motor features open a window of opportunities for early diagnosis and intervention

Chelban Viorica Gheorghe, Gasnaș (Catereniuc) Daniela Ilia, Aftene Daniela Alexandr, Gasnaş Alexandru Vladimir, Vichayanrat Ekawat , Iodice Valeria , Groppa Stanislav Alexandru, Houlden Henry H.

1 University College London, 2 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 3 Emergency Institute of Medicine, 4 National Hospital for Neurology and Neurosurgery, Queen Square

Journal of Neurology

Nr. / 2020 / ISSN 0340-5354 / ISSNe 1432-1459

Disponibil online 13 October, 2020

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MYORG-related disease is associated with central pontine calcifications and atypical parkinsonism

Chelban Viorica Gheorghe, Salsano Ettore , Groppa Stanislav Alexandru

1 UCL Queen Square Institute of Neurology, 2 Emergency Institute of Medicine, 3 University of Nottingham

Neurology: Genetics

Nr. 2(6) / 2020 / ISSN 2376-7839 / ISSNe 2376-7839

Disponibil online 2 October, 2020

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Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolism

Keller Natalie , Mendoza-Ferreira Natalia , Maroofian Reza , Chelban Viorica Gheorghe, Khalil Youssef , Mills Philippa B. , Boostani Reza , Torbati Paria Najarzadeh , Karimiani Ehsan Ghayoor , Thiele Holger , Houlden Henry H., Wirth Brunhilde , Karakaya Mert

1 University of Cologne, 2 St. George's University of London, 3 UCL Queen Square Institute of Neurology, 4 Emergency Institute of Medicine, 5 University College London, 6 Mashhad University of Medical Sciences, 7 Next Generation Genetic Polyclinic, Mashhad, 8 Necunoscută, Marea Britanie

Neuromuscular Disorders

Nr. 7(30) / 2020 / ISSN 0960-8966 / ISSNe 1874-2364

Disponibil online 9 October, 2020

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Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination

Chelban Viorica Gheorghe, Alsagob M. , Groppa Stanislav Alexandru

1 University College London, 2 Emergency Institute of Medicine, 3 Department of Genetics, KFSHRC, Riyadh

European Journal of Neurology

Nr. 2(27) / 2020 / ISSN 1351-5101 / ISSNe 1468-1331

Disponibil online 12 March, 2020

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Genetic and clinical heterogeneity in thirteen new cases with aceruloplasminemia. Atypical anemia as a clue for an early diagnosis

Cuenca Marc Vila , Chelban Viorica Gheorghe

1 Josep Carreras Leukaemia Research Institute (IJC), Barcelona, 2 Emergency Institute of Medicine

International Journal of Molecular Sciences

Nr. 7(21) / 2020 / ISSN 1661-6596 / ISSNe 1422-0067

Disponibil online 8 October, 2020

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Aplicabilitatea testării genetice de nouă generație în epilepsie prin prisma secvențierii întregului exom

Gasnaș (Catereniuc) Daniela Ilia, Chelban Viorica Gheorghe, Groppa Stanislav Alexandru

1 Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu“, 2 Institutul de Neurologie UCL Queen Square

Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”

2020. Chişinău. USMF. 332-332.

Disponibil online 29 March, 2021

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2019 - 2

An update on advances in magnetic resonance imaging of multiple system atrophy

Chelban Viorica Gheorghe, Bocchetta Martina , Hassanein Sara M. , Haridy Nourelhoda A., Houlden Henry H., Rohrer Jonathan Daniel

1 UCL Queen Square Institute of Neurology, 2 Emergency Institute of Medicine, 3 Assiut University Hospital, Assiut

Journal of Neurology

Nr. / 2019 / ISSN 0340-5354 / ISSNe 1432-1459

Disponibil online 28 April, 2021

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PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation

Chelban Viorica Gheorghe, Wilson Matthew P.

1 University College London, 2 Emergency Institute of Medicine

Annals of Neurology

Nr. 2(86) / 2019 / ISSN 0364-5134

Disponibil online 24 July, 2019

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2018 - 3

Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14

Chelban Viorica Gheorghe, Wiethoff Sarah

1 University College London, 2 National Hospital for Neurology and Neurosurgery, Queen Square, 3 Emergency Institute of Medicine, 4 Eberhard Karls University

Movement Disorders

Nr. 7(33) / 2018 / ISSN 0885-3185 / ISSNe 1531-8257

Disponibil online 8 December, 2018

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Lysosomal storage disorder gene variants in multiple system atrophy

Pihlstrøm Lasse, Schottlaender Lucia V., Chelban Viorica Gheorghe, Meissner Wassilios G., Federoff Monica, Singleton Andrew B., Houlden Henry H.

1 UCL Queen Square Institute of Neurology, 2 National Hospital for Neurology and Neurosurgery, Queen Square, 3 Oslo University Hospital, 4 UCL Great Ormond Street Institute of Child Health, London,, 5 Emergency Institute of Medicine, 6 University of Bordeaux, 7 National Institutes of Health, Department of Health and Human Services, Bethesda

Brain

Nr. 7(141) / 2018 / ISSN 0006-8950 / ISSNe 1460-2156

Disponibil online 20 July, 2021

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