Andreas Puschmann

31 – 40 of 123

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/person/c794039b-9611-4930-b773-a545aa9783b9?embed=1&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
…
3
4
5
6
…
13
next »

2022
Mark Serum Neurofilament Light Chain as a Marker of Progression in Parkinson's Disease : Long-Term Observation and Implications of Clinical Subtypes
Ygland Rödström, Emil ^LU ; Mattsson-Carlgren, Niklas ^LU ; Janelidze, Shorena ^LU ; Hansson, Oskar ^LU and Puschmann, Andreas ^LU (2022) In Journal of Parkinson's Disease 12(2). p.571-584
- Contribution to journal › Article
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
2021
Mark Clinical classification systems and long-term outcome in mid- and late-stage Parkinson’s disease
Ygland Rödström, Emil ^LU and Puschmann, Andreas ^LU (2021) In npj Parkinson's Disease 7(1).
- Contribution to journal › Article
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
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
2020
Mark New generation genetic testing entering the clinic
Gorcenco, Sorina ^LU ; Ilinca, Andreea ^LU ; Almasoudi, Wejdan ^LU ; Kafantari, Efthymia ^LU ; Lindgren, Arne G. ^LU and Puschmann, Andreas ^LU (2020) In Parkinsonism and Related Disorders 73. p.72-84
- Contribution to journal › Article
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
Mark Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?
Kafantari, Efthymia ^LU ; Andréasson, Sten ^LU ; Säll, Torbjörn ^LU and Puschmann, Andreas ^LU (2020) In Parkinsonism and Related Disorders 79. p.138-140
- Contribution to journal › Debate/Note/Editorial
Mark Abstracts of the IAPRD XXV World Congress on Parkinson's Disease and Related Disorders, 2020. Congress theme : Diagnosing and treating movement disorders in the era of personalized medicine
Fujioka, Shinsuke and Puschmann, Andreas ^LU (2020) In Parkinsonism and Related Disorders 79(S1). p.1-2
- Contribution to journal › Debate/Note/Editorial
Mark Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
Ilinca, Andreea ^LU ; Martinez-Majander, Nicolas ; Samuelsson, Sofie ^LU ; Piccinelli, Paul ^LU ; Truvé, Katarina ; Cole, John ; Kittner, Steven ; Soller, Maria ^LU ; Kristoffersson, Ulf ^LU and Tatlisumak, Turgut , et al. (2020) In Stroke 51(4). p.1056-1063
- Contribution to journal › Article

« previous
1
…
3
4
5
6
…
13
next »