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PubPharm (425)
21
Pathophysiology and Management of Fatigue in Neuromuscular Diseases
enthalten in:
International journal of molecular sciences
| 2023
von
Torri, F.
|
Lopriore, P.
|
Montano, V.
| +3
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22
Age of onset of cerebral venous thrombosis : the BEAST study
enthalten in:
European stroke journal
| 2023
von
Ranjan, R.
|
Ken-Dror, G.
|
Martinelli, I.
| +41
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23
Factors associated with the severity of COVID-19 outcomes in people with neuromuscular diseases : Data from the International Neuromuscular COVID-19 Registry
enthalten in:
European journal of neurology
| 2023
von
Pizzamiglio, C.
|
Pitceathly, R.
|
Lunn, M.
| +91
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24
Complex neurological and multisystem presentations in mitochondrial disease
enthalten in:
Handbook of clinical neurology
| 2023
von
Mancuso, M.
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25
A Multisystem Mitochondrial Disease Caused by a Novel MT-TL1 mtDNA Variant : A Case Report
enthalten in:
Journal of neuromuscular diseases
| 2023
von
Giannese, D.
|
Montano, V.
|
Lopriore, P.
| +9
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26
Key priorities in rare neurological diseases : A statement from the Coordinating Panel on Rare Neurological Diseases of the European Academy of Neurology
enthalten in:
European Journal of Neurology
| 2023
von
Mancuso, M.
|
Graessner, H.
|
Visser, M.
| +2
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27
Iron-sensitive MR imaging of the primary motor cortex to differentiate hereditary spastic paraplegia from other motor neuron diseases
enthalten in:
European radiology
| 2022
von
Cosottini, M.
|
Donatelli, G.
|
Ricca, I.
| +11
CommentIn: Eur Radiol. 2022 Sep 8;:. - PMID 36074266
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28
Primary mitochondrial myopathy : 12-month follow-up results of an Italian cohort
enthalten in:
Journal of neurology
| 2022
von
Montano, V.
|
Lopriore, P.
|
Gruosso, F.
| +21
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29
Delayed Development of Aneurysmal Dilatations in Patients with Extracranial Carotid Artery Dissections
enthalten in:
European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery
| 2022
von
van Laarhoven, C.
|
Arnold, M.
|
Danilova, M.
| +13
CommentIn: Eur J Vasc Endovasc Surg. 2023 Feb;65(2):310-311. - PMID 36372207
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30
Defining the nuclear genetic architecture of a common maternally inherited mitochondrial disorder
enthalten in:
bioRxiv.org
| 2022
von
Boggan, R.
|
Ng, Y.
|
Franklin, I.
| +27
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