Lista publicaţiilor: Chelban Viorica Gheorghe - 7

2020 - 2

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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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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2019 - 1

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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2017 - 2

Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination

Chelban Viorica Gheorghe, Patel Nisha

1 University College London, 2 Emergency Institute of Medicine, 3 Developmental Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center

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

1 University College London, 2 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 3 National Hospital for Neurology and Neurosurgery, Queen Square, 4 University of Oslo, 5 Universite de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, 6 Centre de référence atrophie multisystématisée, CHU de Bordeaux, Bordeaux, 7 Reta Lila Weston Institute of Neurological Studies and Queen Square Brain Bank for Neurological Disorders, London

Neurobiology of Aging

Nr. 49 / 2017 / ISSN 0197-4580

Disponibil online 3 July, 2018

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2016 - 2

Severe axonal neuropathy is a late manifestation of SPG11

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

1 University College London (UCL), London, 2 University College London, 3 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 4 Assiut University Hospital, Assiut, 5 Instituto de Investigaciónes Medicas “Mercedes y Martín Ferreyra”

Journal of Neurology

Nr. / 2016 / ISSN 0340-5354 / ISSNe 1432-1459

Disponibil online 22 November, 2017

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Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia

Chelban Viorica Gheorghe, Lynch David S. , Houlden Henry H., Wood Nick

1 National Hospital for Neurology and Neurosurgery, Queen Square, 2 ”Nicolae Testemițanu” State University of Medicine and Pharmacy

Journal of Neurology

Nr. / 2016 / ISSN 0340-5354 / ISSNe 1432-1459

Disponibil online 31 July, 2022

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