Afiliat la University College London

2021 - 2

Spastic paraplegia preceding psen1-related familial alzheimer’s disease

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

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

Chiosa Vitalie , Ciolac Dumitru , Chelban Viorica , Gasnaș (Catereniuc) Daniela , Vataman Anatolie , Munteanu Cristina , Groppa Stanislav

Moldovan Medical Journal

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

Disponibil online 21 October, 2021

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2020 - 4

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

Chelban Viorica , Alsagob M. , Groppa Stanislav

European Journal of Neurology

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

Disponibil online 12 March, 2020

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Automated brainstem segmentation detects differential involvement in atypical parkinsonian syndromes

Bocchetta Martina , Iglesias Juan Eugenio , Chelban Viorica

Journal of Movement Disorders

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

Disponibil online 21 October, 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 , Gasnaș (Catereniuc) Daniela , Aftene Daniela , Gasnaş Alexandru , Vichayanrat Ekawat , Iodice Valeria , Groppa Stanislav , Houlden Henry H.

Journal of Neurology

Vol. 267, / 2020 / ISSN 0340-5354 / ISSNe 1432-1459

Disponibil online 13 October, 2020

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

Gasnaș (Catereniuc) Daniela , Chelban Viorica , Groppa Stanislav

Moldovan Medical Journal

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

Disponibil online 7 December, 2020

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2019 - 1

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

Chelban Viorica , Wilson Matthew P.

Annals of Neurology

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

Disponibil online 24 July, 2019

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2018 - 1

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

Chelban Viorica , Wiethoff Sarah

Movement Disorders

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

Disponibil online 8 December, 2018

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2017 - 3

Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia

Bettencourt C. , Salpietro Vincenzo , Efthymiou Stephanie , Chelban Viorica , Hughes Deborah , Houlden Henry H. , Federoff Monica , Bourinaris Thomas , Spilioti Martha G , Deretzi Georgia , Kalantzakou Triantafyllia , Singleton Andrew B. , Xiromerisiou Georgia

Orphanet Journal of Rare Diseases

Nr. 1(12) / 2017 / ISSN 1750-1172

Disponibil online 11 December, 2017

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Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination

Chelban Viorica , Patel Nisha

American Journal of Human Genetics

Nr. 6(100) / 2017 / ISSN 0002-9297

Disponibil online 21 February, 2018

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Analysis of the prion protein gene in multiple system atrophy

Chelban Viorica , Manole Andreea , Pihlstrom Lasse , Schottlaender Lucia V. , Efthymiou Stephanie , OConnor Emer , Meissner Wassilios G. , Holton Janice L. , Houlden Henry H.

Neurobiology of Aging

Nr. 49 / 2017 / ISSN 0197-4580

Disponibil online 3 July, 2018

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2016 - 1

Severe axonal neuropathy is a late manifestation of SPG11

Manole Andreea , Chelban Viorica , Haridy Nourelhoda , Hamed Sherifa Ahmed , Berardo Andres , Reilly Mary M. , Houlden Henry H.

Journal of Neurology

Vol. 263, / 2016 / ISSN 0340-5354 / ISSNe 1432-1459

Disponibil online 22 November, 2017

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