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Page 1
Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study.
Mov Disord. 2023 Dec;38(12):2241-2248. doi: 10.1002/mds.29617. Epub 2023 Sep 26.
Mov Disord. 2023.
PMID: 37750340
The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity.
Gambardella S, Ferese R, Biagioni F, Busceti CL, Campopiano R, Griguoli AMP, Limanaqi F, Novelli G, Storto M, Fornai F.
Gambardella S, et al. Among authors: griguoli amp.
Front Cell Neurosci. 2017 Apr 18;11:102. doi: 10.3389/fncel.2017.00102. eCollection 2017.
Front Cell Neurosci. 2017.
PMID: 28458632
Free PMC article.
Review.
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PCR-based approach for qualitative molecular analysis of six neurotropic pathogens.
Ferese R, Scorzolini L, Campopiano R, Albano V, Griguoli AM, Giardina E, Scala S, Ryskalin L, D'Alessio C, Zampatti S, Fantozzi R, Storto M, Fornai F, Gambardella S.
Ferese R, et al. Among authors: griguoli am.
Acta Virol. 2017;61(3):273-279. doi: 10.4149/av_2017_305.
Acta Virol. 2017.
PMID: 28854791
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A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS).
Ferese R, Zampatti S, Griguoli AM, Fornai F, Giardina E, Barrano G, Albano V, Campopiano R, Scala S, Novelli G, Gambardella S.
Ferese R, et al. Among authors: griguoli am.
J Mol Neurosci. 2016 Jul;59(3):376-81. doi: 10.1007/s12031-016-0754-3. Epub 2016 May 20.
J Mol Neurosci. 2016.
PMID: 27207492
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Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease).
Ferese R, Albano V, Falconi M, Iacovelli F, Campopiano R, Scala S, Griguoli AM, Gaglione A, Giardina E, Zampatti S, Storto M, Fornai F, D'Alessio C, Novelli G, Gambardella S.
Ferese R, et al. Among authors: griguoli am.
Arch Ital Biol. 2017 Dec 1;155(4):118-130. doi: 10.12871/000398292017410.
Arch Ital Biol. 2017.
PMID: 29405036
No abstract available.
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