Pubblicazioni per linea Myriapod NGS

28 02, 2022

Filippo Nozzoli et al., NTRK Fusions Detection in Paediatric Sarcomas to Expand the Morphological Spectrum and Clinical Relevance of Selected Entities

adlitterio663392022-10-14T11:57:02+02:00

15 02, 2022

Luigi Spagnoli et al., A look towards the clonal origin of metastatic pulmonary carcinosarcoma: Report of a patient with an unexpected long-term survival

adlitterio663392022-10-13T16:26:54+02:00

1 02, 2022

Laura Antolino et al., Is TP53 Arg72Pro a risk factor for pancreatic cancer in diabetic patients?

adlitterio663392022-10-13T16:23:34+02:00

24 08, 2021

Umberto Malapelle et al., Reference standards for gene fusion molecular assays on cytological samples: an international validation study.

adlitterio663392022-10-14T12:09:36+02:00

5 08, 2021

Antonio Marchetti et al., Real-World Data on NGS Diagnostics: a survey from the Italian Society of Pathology (SIAPeC) NGS Network

adlitterio663392022-10-13T16:30:06+02:00

17 03, 2021

Umberto Malapelle et al., Dealing with NSCLC EGFR mutation testing and treatment: A comprehensive review with an Italian real-world perspective.

adlitterio663392022-10-14T14:08:31+02:00

10 01, 2021

Alberto Pavan et al., Role of next generation sequencing-based liquid biopsy in advanced non-small cell lung cancer patients treated with immune checkpoint inhibitors: impact of STK11, KRAS and TP53 mutations and co-mutations on outcome

adlitterio663392022-10-13T16:35:11+02:00

9 09, 2020

Magda Zanelli et. al., Acute Radiation Colitis after Preoperative Short-Course Radiotherapy for Rectal Cancer: A Morphological, Immunohistochemical and Genetic Study

Diatech Pharmacogenetics2020-11-03T12:02:43+01:00

18 07, 2020

Moira Ragazzi et. al., Coexisting well-differentiated and anaplastic thyroid carcinoma in the same primary resection specimen: immunophenotypic and genetic comparison of the two components in a consecutive series of 13 cases and a review of the literature

Diatech Pharmacogenetics2020-11-03T14:25:31+01:00

10 07, 2020

Francesca Consoli et. al., A Rare Complex BRAF Mutation Involving Codon V600 and K601 in Primary Cutaneous Melanoma: Case Report

Diatech Pharmacogenetics2020-11-03T14:10:41+01:00

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