Enza Maria Valente - Search Results

Year	Number of Results
2002	5
2003	3
2004	6
2005	6
2006	8
2007	10
2008	9
2009	9
2010	6
2011	12
2012	13
2013	22
2014	14
2015	12
2016	17
2017	15
2018	16
2019	17
2020	20
2021	28
2022	32
2023	33
2024	22

1

Feasibility and Efficacy of a Virtual Reality Social Prediction Training in Children and Young Adults with Congenital Cerebellar Malformations.

Butti N, Biffi E, Romaniello R, Finisguerra A, Valente EM, Strazzer S, Borgatti R, Urgesi C. Butti N, et al. Among authors: valente em. J Autism Dev Disord. 2024 May 3. doi: 10.1007/s10803-024-06349-8. Online ahead of print. J Autism Dev Disord. 2024. PMID: 38700776

2

Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report.

Imarisio A, Pilotto A, Lupini A, Biasiotto G, Zanella I, Currò R, Vegezzi E, Cortese A, Palmieri I, Valente EM, Padovani A. Imarisio A, et al. Among authors: valente em. Parkinsonism Relat Disord. 2024 Mar 20;123:106943. doi: 10.1016/j.parkreldis.2024.106943. Online ahead of print. Parkinsonism Relat Disord. 2024. PMID: 38555792

3

Understanding monogenic Parkinson's disease at a global scale.

Junker J, Lange LM, Vollstedt EJ, Roopnarain K, Doquenia MLM, Annuar AA, Avenali M, Bardien S, Bahr N, Ellis M, Galandra C, Gasser T, Heutink P, Illarionova A, Kanana Y, Keller Sarmiento IJ, Kumar KR, Lim SY, Madoev H, Mata IF, Mencacci NE, Nalls MA, Padmanabhan S, Shambetova C, Solle J, Tan AH, Trinh J, Valente EM, Singleton A, Blauwendraat C, Lohmann K, Fang ZH, Klein C; Global Parkinson’s Genetics Program (GP2). Junker J, et al. Among authors: valente em. medRxiv [Preprint]. 2024 Apr 9:2024.03.12.24304154. doi: 10.1101/2024.03.12.24304154. medRxiv. 2024. PMID: 38529492 Free PMC article. Preprint.

4

Glycogen storage disease type V: a still under-recognized condition lacking definitive genotype-phenotype correlates.

Ravaglia S, Gana S, Valente EM. Ravaglia S, et al. Among authors: valente em. Pediatr Res. 2024 Mar 21. doi: 10.1038/s41390-024-03149-9. Online ahead of print. Pediatr Res. 2024. PMID: 38514859 No abstract available.

5

Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro.

De Mori R, Tardivo S, Pollara L, Giliani SC, Ali E, Giordano L, Leuzzi V, Fischetto R, Gener B, Diprima S, Morelli MJ, Monti MC, Sottile V, Valente EM. De Mori R, et al. Among authors: valente em. Cell Tissue Res. 2024 May;396(2):255-267. doi: 10.1007/s00441-024-03876-9. Epub 2024 Mar 19. Cell Tissue Res. 2024. PMID: 38502237 Free PMC article.

6

Functional Study of SNCA p.V15A Variant: Further Linking α-Synuclein and Glucocerebrosidase.

Avenali M, Cerri S, Palmieri I, Ongari G, Stiuso R, Buongarzone G, Tassorelli C, Biagini T, Valente M, Cereda C, Mazza T, Gana S, Pacchetti C, Valente EM. Avenali M, et al. Among authors: valente em. Mov Disord. 2024 Mar 4. doi: 10.1002/mds.29736. Online ahead of print. Mov Disord. 2024. PMID: 38436488

7

Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements.

Prato A, Cirnigliaro L, Maugeri F, Luca A, Giuliano L, Vitiello G, Errichiello E, Valente EM, Del Giudice E, Mostile G, Rizzo R, Barone R. Prato A, et al. Among authors: valente em. J Clin Med. 2024 Feb 16;13(4):1109. doi: 10.3390/jcm13041109. J Clin Med. 2024. PMID: 38398422 Free PMC article.

8

GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians.

Ojo OO, Bandres-Ciga S, Makarious MB, Crea PW, Hernandez DG, Houlden H, Rizig M, Singleton AB, Noyce AJ, Nalls MA, Blauwendraat C, Okubadejo NU; Nigeria Parkinson's Disease Research Network and the Global Parkinson's Genetics Program (GP2). Ojo OO, et al. Mov Disord. 2024 Apr;39(4):728-733. doi: 10.1002/mds.29753. Epub 2024 Feb 23. Mov Disord. 2024. PMID: 38390630

9

Joubert syndrome and hydrocephalus: Further expanding the phenotypic spectrum of a pleiotropic ciliopathy.

Gana S, Valente EM. Gana S, et al. Among authors: valente em. Dev Med Child Neurol. 2024 Feb 22. doi: 10.1111/dmcn.15887. Online ahead of print. Dev Med Child Neurol. 2024. PMID: 38385764 No abstract available.

10

Parkin mRNA Expression Levels in Peripheral Blood Mononuclear Cells in Parkin-Related Parkinson's Disease.

Papagiannakis N, Liu H, Koros C, Simitsi AM, Stamelou M, Maniati M, Buena-Atienza E, Kartanou C, Karadima G, Makrythanasis P, Vatsellas G, Valente EM, Gasser T, Stefanis L. Papagiannakis N, et al. Among authors: valente em. Mov Disord. 2024 Apr;39(4):715-722. doi: 10.1002/mds.29739. Epub 2024 Feb 15. Mov Disord. 2024. PMID: 38357851

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