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Lukasz M Milanowski

Explore the profile of Lukasz M Milanowski including associated specialties, affiliations and a list of published articles. Areas
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Articles 13
Citations 69
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Recent Articles
1.
Sosero Y, Bandres-Ciga S, Ferwerda B, Tocino M, Belloso D, Gomez-Garre P, et al.
Mov Disord . 2024 Aug; 39(10):1773-1783. PMID: 39132902
Background: Levodopa-induced dyskinesia (LID) is a common adverse effect of levodopa, one of the main therapeutics used to treat the motor symptoms of Parkinson's disease (PD). Previous evidence suggests a...
2.
Sosero Y, Bandres-Ciga S, Ferwerda B, Tocino M, Belloso D, Gomez-Garre P, et al.
medRxiv . 2023 Oct; PMID: 37790572
Background: Levodopa-induced dyskinesia (LID) is a common adverse effect of levodopa, one of the main therapeutics used to treat the motor symptoms of Parkinson's disease (PD). Previous evidence suggests a...
3.
Asthana P, Kumar G, Milanowski L, Au N, Chan S, Huang J, et al.
NPJ Regen Med . 2022 Sep; 7(1):45. PMID: 36064798
Peripheral nerve injury (PNI) often results in spontaneous motor recovery; however, how disrupted cerebellar circuitry affects PNI-associated motor recovery is unknown. Here, we demonstrated disrupted cerebellar circuitry and poor motor...
4.
Milanowski L, Hou X, Bredenberg J, Fiesel F, Cocker L, Soto-Beasley A, et al.
Int J Mol Sci . 2022 Jul; 23(13). PMID: 35806091
Parkinson's disease (PD) is generally considered a sporadic disorder, but a strong genetic background is often found. The aim of this study was to identify the underlying genetic cause of...
5.
Al-Shaikh R, Milanowski L, Holla V, Kurihara K, Yadav R, Kamble N, et al.
Parkinsonism Relat Disord . 2022 Jul; 101:66-74. PMID: 35803092
Background: PLA2G6-Associated Neurodegeneration, PLAN, is subdivided into: Infantile neuroaxonal dystrophy, atypical neuroaxonal dystrophy, and adult-onset dystonia parkinsonism [1]. It is elicited by a biallelic pathogenic variant in phospholipase A2 group...
6.
Milanowski L, Oshinaike O, Walton R, Soto-Beasley A, Al-Shaikh R, Strongosky A, et al.
Mov Disord . 2021 Sep; 36(12):2971-2973. PMID: 34586679
No abstract available.
7.
Figura M, Geremek M, Milanowski L, Meisner-Kramarz I, Duszynska-Was K, Szlufik S, et al.
Neurol Neurochir Pol . 2021 May; 55(3):300-305. PMID: 34037980
Introduction: Chromosomal aberrations are rare but important causes of various movement disorders. In cases of movement disorders associated with dysmorphic features, multiorgan involvement and/or intellectual disability, the identification of causative...
8.
Milanowski L, Lindemann J, Hoffman-Zacharska D, Soto-Beasley A, Barcikowska M, Boczarska-Jedynak M, et al.
Parkinsonism Relat Disord . 2021 Apr; 86:48-51. PMID: 33845304
Introduction: Approximately 10% of patients with Parkinson disease (PD) present with early-onset disease (EOPD), defined as diagnosis before 50 years of age. Genetic factors are known to contribute to EOPD,...
9.
Koziorowski D, Figura M, Milanowski L, Szlufik S, Alster P, Madetko N, et al.
Cells . 2021 Apr; 10(3). PMID: 33809527
Parkinson's disease (PD), dementia with Lewy body (DLB), progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and multiple system atrophy (MSA) belong to a group of neurodegenerative diseases called parkinsonian syndromes....
10.
Wernick A, Walton R, Soto-Beasley A, Koga S, Ren Y, Heckman M, et al.
Neurosci Lett . 2021 Feb; 749:135723. PMID: 33600908
Multiple system atrophy (MSA) is a rare sporadic, progressive parkinsonism characterised by autonomic dysfunction. A recent genome-wide association study reported an association at the Elongation of Very Long Fatty Acids...