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Items: 1 to 20 of 137

1.

Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.

Monasky MM, Micaglio E, Vicedomini G, Locati ET, Ciconte G, Giannelli L, Giordano F, Crisà S, Vecchi M, Borrelli V, Ghiroldi A, D'Imperio S, Resta CD, Benedetti S, Ferrari M, Santinelli V, Anastasia L, Pappone C.

Europace. 2019 Jul 10. pii: euz186. doi: 10.1093/europace/euz186. [Epub ahead of print]

PMID:
31292628
2.

Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype.

Micaglio E, Monasky MM, Ciconte G, Vicedomini G, Conti M, Mecarocci V, Giannelli L, Giordano F, Pollina A, Saviano M, Pozzi PR, Di Resta C, Benedetti S, Ferrari M, Santinelli V, Pappone C.

Front Genet. 2019 Jun 6;10:547. doi: 10.3389/fgene.2019.00547. eCollection 2019.

3.

Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene.

Monasky MM, Micaglio E, Ciconte G, Benedetti S, Di Resta C, Vicedomini G, Borrelli V, Ghiroldi A, Piccoli M, Anastasia L, Santinelli V, Ferrari M, Pappone C.

Front Physiol. 2019 May 28;10:666. doi: 10.3389/fphys.2019.00666. eCollection 2019.

4.

Expanding the spectrum of genes responsible for hereditary motor neuropathies.

Previtali SC, Zhao E, Lazarevic D, Pipitone GB, Fabrizi GM, Manganelli F, Mazzeo A, Pareyson D, Schenone A, Taroni F, Vita G, Bellone E, Ferrarini M, Garibaldi M, Magri S, Padua L, Pennisi E, Pisciotta C, Riva N, Scaioli V, Scarlato M, Tozza S, Geroldi A, Jordanova A, Ferrari M, Molineris I, Reilly MM, Comi G, Carrera P, Devoto M, Bolino A.

J Neurol Neurosurg Psychiatry. 2019 Jun 5. pii: jnnp-2019-320717. doi: 10.1136/jnnp-2019-320717. [Epub ahead of print]

PMID:
31167812
5.

Key questions about the future of laboratory medicine in the next decade of the 21st century: A report from the IFCC-Emerging Technologies Division.

Greaves RF, Bernardini S, Ferrari M, Fortina P, Gouget B, Gruson D, Lang T, Loh TP, Morris HA, Park JY, Roessler M, Yin P, Kricka LJ.

Clin Chim Acta. 2019 Aug;495:570-589. doi: 10.1016/j.cca.2019.05.021. Epub 2019 May 28.

PMID:
31145895
6.

ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria.

Akbari A, Pipitone GB, Anvar Z, Jaafarinia M, Ferrari M, Carrera P, Totonchi M.

Hum Reprod. 2019 Jun 4;34(6):1155-1164. doi: 10.1093/humrep/dez048.

PMID:
31119281
7.

New molecular approaches to Alzheimer's disease.

Di Resta C, Ferrari M.

Clin Biochem. 2019 Apr 21. pii: S0009-9120(19)30384-4. doi: 10.1016/j.clinbiochem.2019.04.010. [Epub ahead of print] Review.

PMID:
31018113
8.

Concurrence of NMOSD and ALS in a patient with hexanucleotide repeat expansions of C9orf72.

Falzone YM, Radaelli M, Agosta F, Domi T, Guerrieri S, Spinelli EG, Pozzi L, Carrera P, Ferrari M, Comi G, Filippi M, Quattrini A, Riva N.

Amyotroph Lateral Scler Frontotemporal Degener. 2019 Aug;20(5-6):449-452. doi: 10.1080/21678421.2019.1604761. Epub 2019 Apr 22.

PMID:
31007077
9.

Impaired testicular signaling of vitamin A and vitamin K contributes to the aberrant composition of the extracellular matrix in idiopathic germ cell aplasia.

Alfano M, Pederzoli F, Locatelli I, Ippolito S, Longhi E, Zerbi P, Ferrari M, Brendolan A, Montorsi F, Drago D, Andolfo A, Nebuloni M, Salonia A.

Fertil Steril. 2019 Apr;111(4):687-698. doi: 10.1016/j.fertnstert.2018.12.002.

10.

SCN5A Nonsense Mutation and NF1 Frameshift Mutation in a Family With Brugada Syndrome and Neurofibromatosis.

Micaglio E, Monasky MM, Ciconte G, Vicedomini G, Conti M, Mecarocci V, Giannelli L, Giordano F, Pollina A, Saviano M, Crisà S, Borrelli V, Ghiroldi A, D'Imperio S, Di Resta C, Benedetti S, Ferrari M, Santinelli V, Anastasia L, Pappone C.

Front Genet. 2019 Feb 15;10:50. doi: 10.3389/fgene.2019.00050. eCollection 2019.

11.

Analysis of KRAS, NRAS and BRAF mutational profile by combination of in-tube hybridization and universal tag-microarray in tumor tissue and plasma of colorectal cancer patients.

Damin F, Galbiati S, Soriani N, Burgio V, Ronzoni M, Ferrari M, Chiari M.

PLoS One. 2018 Dec 18;13(12):e0207876. doi: 10.1371/journal.pone.0207876. eCollection 2018.

12.

Evaluation of three advanced methodologies, COLD-PCR, microarray and ddPCR, for identifying the mutational status by liquid biopsies in metastatic colorectal cancer patients.

Galbiati S, Damin F, Burgio V, Brisci A, Soriani N, Belcastro B, Di Resta C, Gianni L, Chiari M, Ronzoni M, Ferrari M.

Clin Chim Acta. 2019 Feb;489:136-143. doi: 10.1016/j.cca.2018.12.004. Epub 2018 Dec 12.

PMID:
30550935
13.

Fluorescent Aptamer Immobilization on Inverse Colloidal Crystals.

Chiappini A, Pasquardini L, Nodehi S, Armellini C, Bazzanella N, Lunelli L, Pelli S, Ferrari M, Pietralunga SM.

Sensors (Basel). 2018 Dec 7;18(12). pii: E4326. doi: 10.3390/s18124326.

14.

Next Generation Sequencing: From Research Area to Clinical Practice.

Di Resta C, Ferrari M.

EJIFCC. 2018 Nov 7;29(3):215-220. eCollection 2018 Nov.

15.

About the Implementation of Frequency Conversion Processes in Solar Cell Device Simulations.

Quandt A, Aslan T, Mokgosi I, Warmbier R, Ferrari M, Righini G.

Micromachines (Basel). 2018 Aug 30;9(9). pii: E435. doi: 10.3390/mi9090435.

16.

Ag-Sensitized Yb3+ Emission in Glass-Ceramics.

Enrichi F, Cattaruzza E, Ferrari M, Gonella F, Ottini R, Riello P, Righini GC, Enrico T, Vomiero A, Zur L.

Micromachines (Basel). 2018 Jul 31;9(8). pii: E380. doi: 10.3390/mi9080380. Erratum in: Micromachines (Basel). 2019 Jan 29;10(2):.

17.

2D Optical Gratings Based on Hexagonal Voids on Transparent Elastomeric Substrate.

Piccolo V, Chiappini A, Armellini C, Barozzi M, Lukowiak A, Sazio PA, Vaccari A, Ferrari M, Zonta D.

Micromachines (Basel). 2018 Jul 10;9(7). pii: E345. doi: 10.3390/mi9070345.

18.

The role of clinical and neuroimaging features in the diagnosis of CADASIL.

Bersano A, Bedini G, Markus HS, Vitali P, Colli-Tibaldi E, Taroni F, Gellera C, Baratta S, Mosca L, Carrera P, Ferrari M, Cereda C, Grieco G, Lanfranconi S, Mazucchelli F, Zarcone D, De Lodovici ML, Bono G, Boncoraglio GB, Parati EA, Calloni MV, Perrone P, Bordo BM, Motto C, Agostoni E, Pezzini A, Padovani A, Micieli G, Cavallini A, Molini G, Sasanelli F, Sessa M, Comi G, Checcarelli N, Carmerlingo M, Corato M, Marcheselli S, Fusi L, Grampa G, Uccellini D, Beretta S, Ferrarese C, Incorvaia B, Tadeo CS, Adobbati L, Silani V, Faragò G, Trobia N, Grond-Ginsbach C, Candelise L; Lombardia GENS-group.

J Neurol. 2018 Dec;265(12):2934-2943. doi: 10.1007/s00415-018-9072-8. Epub 2018 Oct 11.

PMID:
30311053
19.

Laser surface structuring of diamond with ultrashort Bessel beams.

Kumar S, Eaton SM, Bollani M, Sotillo B, Chiappini A, Ferrari M, Ramponi R, Di Trapani P, Jedrkiewicz O.

Sci Rep. 2018 Sep 19;8(1):14021. doi: 10.1038/s41598-018-32415-0.

20.

Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches.

Di Resta C, Spiga I, Presi S, Merella S, Pipitone GB, Manitto MP, Querques G, Parodi MB, Ferrari M, Carrera P.

EJIFCC. 2018 Apr 30;29(1):15-25. eCollection 2018 Apr.

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