Gambardella S - Search Results

1

A novel POLR3A genotype leads to leukodystrophy type-7 in two siblings with unusually late age of onset.

Campopiano R, Ferese R, Zampatti S, Giardina E, Biagioni F, Colonnese C, Centonze D, Storto M, Buttari F, Fraviga E, Broccoli V, Fanelli M, Fornai F, Gambardella S. Campopiano R, et al. Among authors: gambardella s. BMC Neurol. 2020 Jun 29;20(1):258. doi: 10.1186/s12883-020-01835-9. BMC Neurol. 2020. PMID: 32600288 Free PMC article.

2

A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01.

Giardina E, Stocchi L, Foti Cuzzola V, Zampatti S, Gambardella S, Patrizi MP, Bramanti P, Pirazzoli A, Novelli G. Giardina E, et al. Among authors: gambardella s. Electrophoresis. 2010 Oct;31(21):3525-30. doi: 10.1002/elps.201000283. Electrophoresis. 2010. PMID: 20925049

3

Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01.

Cascella R, Strafella C, Ragazzo M, Zampatti S, Borgiani P, Gambardella S, Pirazzoli A, Novelli G, Giardina E. Cascella R, et al. Among authors: gambardella s. Pharmacogenomics J. 2015 Apr;15(2):196-200. doi: 10.1038/tpj.2014.48. Epub 2014 Sep 9. Pharmacogenomics J. 2015. PMID: 25201286 Free PMC article.

4

Four Copies of SNCA Responsible for Autosomal Dominant Parkinson's Disease in Two Italian Siblings.

Ferese R, Modugno N, Campopiano R, Santilli M, Zampatti S, Giardina E, Nardone A, Postorivo D, Fornai F, Novelli G, Romoli E, Ruggieri S, Gambardella S. Ferese R, et al. Among authors: gambardella s. Parkinsons Dis. 2015;2015:546462. doi: 10.1155/2015/546462. Epub 2015 Nov 9. Parkinsons Dis. 2015. PMID: 26635992 Free PMC article.

5

Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations.

Cascella R, Strafella C, Gambardella S, Longo G, Borgiani P, Sangiuolo F, Novelli G, Giardina E. Cascella R, et al. Among authors: gambardella s. Electrophoresis. 2016 Mar;37(5-6):860-4. doi: 10.1002/elps.201500346. Epub 2016 Jan 15. Electrophoresis. 2016. PMID: 26681637

6

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: gambardella s. 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

7

The Autophagoproteasome a Novel Cell Clearing Organelle in Baseline and Stimulated Conditions.

Lenzi P, Lazzeri G, Biagioni F, Busceti CL, Gambardella S, Salvetti A, Fornai F. Lenzi P, et al. Among authors: gambardella s. Front Neuroanat. 2016 Jul 21;10:78. doi: 10.3389/fnana.2016.00078. eCollection 2016. Front Neuroanat. 2016. PMID: 27493626 Free PMC article.

8

Vacuolar Protein Sorting Genes in Parkinson's Disease: A Re-appraisal of Mutations Detection Rate and Neurobiology of Disease.

Gambardella S, Biagioni F, Ferese R, Busceti CL, Frati A, Novelli G, Ruggieri S, Fornai F. Gambardella S, et al. Front Neurosci. 2016 Nov 24;10:532. doi: 10.3389/fnins.2016.00532. eCollection 2016. Front Neurosci. 2016. PMID: 27932943 Free PMC article. Review.

9

Neurons other than motor neurons in motor neuron disease.

Ruffoli R, Biagioni F, Busceti CL, Gaglione A, Ryskalin L, Gambardella S, Frati A, Fornai F. Ruffoli R, et al. Among authors: gambardella s. Histol Histopathol. 2017 Nov;32(11):1115-1123. doi: 10.14670/HH-11-895. Epub 2017 Apr 11. Histol Histopathol. 2017. PMID: 28397197 Review.

10

Rapamycin promotes differentiation increasing βIII-tubulin, NeuN, and NeuroD while suppressing nestin expression in glioblastoma cells.

Ferrucci M, Biagioni F, Lenzi P, Gambardella S, Ferese R, Calierno MT, Falleni A, Grimaldi A, Frati A, Esposito V, Limatola C, Fornai F. Ferrucci M, et al. Among authors: gambardella s. Oncotarget. 2017 May 2;8(18):29574-29599. doi: 10.18632/oncotarget.15906. Oncotarget. 2017. PMID: 28418837 Free PMC article.

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