Sorina Gorcenco

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2024
Mark Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4 : A poly-glycine disease
Wallenius, Joel ^LU ; Kafantari, Efthymia ^LU ; Jhaveri, Emma ; Gorcenco, Sorina ^LU ; Ameur, Adam ; Karremo, Christin ^LU ; Dobloug, Sigurd ^LU ; Karrman, Kristina ^LU ; de Koning, Tom ^LU and Ilinca, Andreea ^LU , et al. (2024) In American Journal of Human Genetics 111(1). p.82-95
- Contribution to journal › Article
Mark Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
Gorcenco, Sorina ^LU ; Kafantari, Efthymia ^LU ; Wallenius, Joel ^LU ; Karremo, Christin ^LU ; Alinder, Erik ; Dobloug, Sigurd ^LU ; Landqvist Waldö, Maria ^LU ; Englund, Elisabet ^LU ; Ehrencrona, Hans ^LU and Wictorin, Klas ^LU , et al. (2024) In Journal of Neurology 271(1). p.526-542
- Contribution to journal › Article
2023
Mark Clinical and genetic studies of patients and families with ataxia
Gorcenco, Sorina ^LU (2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
Mark Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxia
Cundari, Maurizio ^LU ; Vestberg, Susanna ^LU ; Gustafsson, Peik ^LU ; Gorcenco, Sorina ^LU and Rasmussen, Anders ^LU (2023) In Frontiers in Systems Neuroscience 17. p.1-20
- Contribution to journal › Scientific review
Mark A Swedish SCA34 family with late onset ataxia, cerebellar atrophy and ocular movement abnormalities with a novel mutation in ELOVL4
Dobloug, S. ^LU ; Gorcenco, S. ^LU ; Ehrencrona, H. ^LU and Puschmann, A. ^LU (2023) In Parkinsonism & Related Disorders 113(Suppl). p.72-72
- Contribution to journal › Published meeting abstract
Mark Patient perspective in hereditary ataxia
Gorcenco, S. ^LU ; Karremo, C. ^LU and Puschmann, A. ^LU (2023) In Parkinsonism & Related Disorders 113(Supp). p.9-9
- Contribution to journal › Published meeting abstract
2022
Mark Tau and neurofilament light-chain as fluid biomarkers in spinocerebellar ataxia type 3
Garcia-Moreno, Hector ; Prudencio, Mercedes ; Thomas-Black, Gilbert ; Solanky, Nita ; Jansen-West, Karen R ; Hanna Al-Shaikh, Rana ; Heslegrave, Amanda ; Zetterberg, Henrik ^LU ; Santana, Magda M and Pereira de Almeida, Luis , et al. (2022) In European Journal of Neurology 29(8). p.2439-2452
- Contribution to journal › Article
Mark Patients’ Perspective in Hereditary Ataxia
Gorcenco, Sorina ^LU ; Karremo, Christin ^LU and Puschmann, Andreas ^LU (2022) In Cerebellum
- Contribution to journal › Article
2020
Mark Ataxia project in Scania, Sweden: Study outline and current status
Gorcenco, Sorina ^LU ; Karremo, Christin ^LU ; Kafantari, Efthymia ^LU and Puschmann, Andreas ^LU (2020) In Parkinsonism & Related Disorders 79(Suppl 1). p.112-112
- Contribution to journal › Published meeting abstract
Mark Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3
Prudencio, Mercedes ; Garcia-Moreno, Hector ; Jansen-West, Karen R ; Al-Shaikh, Rana Hanna ; Gendron, Tania F ; Heckman, Michael G ; Spiegel, Matthew R ; Carlomagno, Yari ; Daughrity, Lillian M and Song, Yuping , et al. (2020) In Science Translational Medicine 12(566).
- Contribution to journal › Article

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