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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 4 |
2020 | 1 |
2021 | 2 |
2024 | 0 |
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7 results
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Page 1
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era.
Neurogenetics. 2019 May;20(2):57-64. doi: 10.1007/s10048-019-00575-4. Epub 2019 Mar 25.
Neurogenetics. 2019.
PMID: 30911870
Review.
Genetic Counseling and NGS Screening for Recessive LGMD2A Families.
Strafella C, Caputo V, Campoli G, Galota RM, Mela J, Zampatti S, Minozzi G, Sancricca C, Servidei S, Giardina E, Cascella R.
Strafella C, et al. Among authors: campoli g.
High Throughput. 2020 May 10;9(2):13. doi: 10.3390/ht9020013.
High Throughput. 2020.
PMID: 32397577
Free PMC article.
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The variability of SMCHD1 gene in FSHD patients: evidence of new mutations.
Strafella C, Caputo V, Galota RM, Campoli G, Bax C, Colantoni L, Minozzi G, Orsini C, Politano L, Tasca G, Novelli G, Ricci E, Giardina E, Cascella R.
Strafella C, et al. Among authors: campoli g.
Hum Mol Genet. 2019 Dec 1;28(23):3912-3920. doi: 10.1093/hmg/ddz239.
Hum Mol Genet. 2019.
PMID: 31600781
Free PMC article.
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Genetic Variants Allegedly Linked to Antisocial Behaviour Are Equally Distributed Across Different Populations.
Zampatti S, Ragazzo M, Fabrizio C, Termine A, Campoli G, Caputo V, Strafella C, Cascella R, Caltagirone C, Giardina E.
Zampatti S, et al. Among authors: campoli g.
J Pers Med. 2021 Mar 16;11(3):213. doi: 10.3390/jpm11030213.
J Pers Med. 2021.
PMID: 33809805
Free PMC article.
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Precision Medicine into Clinical Practice: A Web-Based Tool Enables Real-Time Pharmacogenetic Assessment of Tailored Treatments in Psychiatric Disorders.
Zampatti S, Fabrizio C, Ragazzo M, Campoli G, Caputo V, Strafella C, Pellicano C, Cascella R, Spalletta G, Petrosini L, Caltagirone C, Termine A, Giardina E.
Zampatti S, et al. Among authors: campoli g.
J Pers Med. 2021 Aug 27;11(9):851. doi: 10.3390/jpm11090851.
J Pers Med. 2021.
PMID: 34575628
Free PMC article.
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Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report.
Strafella C, Campoli G, Galota RM, Caputo V, Pagliaroli G, Carboni S, Zampatti S, Peconi C, Mela J, Sancricca C, Primiano G, Minozzi G, Servidei S, Cascella R, Giardina E.
Strafella C, et al. Among authors: campoli g.
Front Neurol. 2019 Jun 13;10:619. doi: 10.3389/fneur.2019.00619. eCollection 2019.
Front Neurol. 2019.
PMID: 31263448
Free PMC article.
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NGS Analysis for Molecular Diagnosis of Retinitis Pigmentosa (RP): Detection of a Novel Variant in PRPH2 Gene.
Strafella C, Caputo V, Pagliaroli G, Iozzo N, Campoli G, Carboni S, Peconi C, Galota RM, Zampatti S, Minozzi G, Novelli G, Giardina E, Cascella R.
Strafella C, et al. Among authors: campoli g.
Genes (Basel). 2019 Oct 12;10(10):792. doi: 10.3390/genes10100792.
Genes (Basel). 2019.
PMID: 31614793
Free PMC article.
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