Andreea Ilinca

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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 Small vessel disease in primary familial brain calcification with novel truncating PDGFB variants
Yektay Farahmand, Maha ^LU ; Wasselius, Johan ^LU ; Englund, Elisabet ^LU ; Braverman, Irwin ; Puschmann, Andreas ^LU and Ilinca, Andreea ^LU (2024) In Neurologia i neurochirurgia polska 58(1). p.94-105
- Contribution to journal › Article
Mark Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiency
Hedberg-Oldfors, Carola ^LU ; Lindgren, Ulrika ; Visuttijai, Kittichate ; Shen, Yan ; Ilinca, Andreea ^LU ; Nordström, Sara ; Lindberg, Christopher and Oldfors, Anders (2024) In Acta Neuropathologica 148(1).
- Contribution to journal › Article
Mark Diagnosing Monogenic Stroke at Younger Age
Ilinca, Andreea ^LU ; Kafantari, Efthymia ^LU ; Wallenius, Joel ^LU ; Kristoffersson, Ulf ^LU ; Englund, Elisabet ^LU ; Puschmann, Andreas ^LU and Lindgren, Arne G. ^LU (2024) In Stroke 55(12). p.2846-2855
- Contribution to journal › Article
2023
Mark Updated Stroke Gene Panels : Rapid evolution of knowledge on monogenic causes of stroke
Ilinca, Andreea ^LU ; Puschmann, Andreas ^LU ; Putaala, Jukka ; de Leeuw, Frank Erik ; Cole, John ; Kittner, Stephen ; Kristoffersson, Ulf ^LU and Lindgren, Arne G ^LU (2023) In European Journal of Human Genetics 31(2). p.239-242
- Contribution to journal › Article
Mark Varicella-zoster virus vasculopathy in a patient with multiple sclerosis receiving natalizumab
Elmståhl, Anna ; Buchwald, Fredrik ^LU and Ilinca, Andreea ^LU (2023) In BMJ Case Reports 16(12).
- Contribution to journal › Article
2022
Mark A relatively common hypomorphic variant in WARS2 causes monogenic disease
Ilinca, Andreea ^LU ; Kafantari, Efthymia ^LU and Puschmann, Andreas ^LU (2022) In Parkinsonism and Related Disorders 94. p.129-131
- Contribution to journal › Debate/Note/Editorial
Mark Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke
Jaworek, T. ; Durda, J.P. ; Engstrom, G. ^LU ; Ilinca, A. ^LU ; Smith, Jennifer A. ; Söderholm, M. ^LU ; Weir, D.R. ; Lindgren, Arne G. ^LU and Kittner, S.J. (2022) In Neurology 99(16). p.1738-1754
- Contribution to journal › Article
2021
Mark Throat-Clearing Vocalizations in Primary Brain Calcification Syndromes
Mulroy, Eoin ; Ilinca, Andreea ^LU ; Gonzalez-Robles, Cristina ; Magrinelli, Francesca ; Puschmann, Andreas ^LU and Bhatia, Kailash P. (2021) In Movement Disorders Clinical Practice 8(4). p.627-630
- Contribution to journal › Letter
Mark MAP3K6 Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor
Ilinca, Andreea ^LU ; Englund, Elisabet ^LU ; Samuelsson, Sofie ^LU ; Truvé, Katarina ; Kafantari, Efthymia ^LU ; Martinez-Majander, Nicolas ; Putaala, Jukka ; Håkansson, Claes ^LU ; Lindgren, Arne G ^LU and Puschmann, Andreas ^LU (2021) In Neurology: Genetics 7(1).
- Contribution to journal › Article

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