Martina Rinelli

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Articles (15)

Collaborators (7)

Charlotte Brasch Andersen

Asso. professor

University of Southern Denmark

Angelo Minucci

University of Padova

concetta santonocito

Università Cattolica del Sacro Cuore

Francesco Fabozzi

Università degli Studi di Roma La Sapienza

Anne Marie Jelsig

Copenhagen University Hospital

Luciano Giaco'

Head of Bioinformatics

Policlinico Universitario Agostino Gemelli

Sebastiano Calandra

Emeritus Professor of General Pathology

University of Modena and Reggio Emilia

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Martina Rinelli

Research Interests

Explore related searches

Contact this professor

Articles (15)

Collaborators (7)

Charlotte Brasch Andersen

Angelo Minucci

concetta santonocito

Francesco Fabozzi

Anne Marie Jelsig

Luciano Giaco'

Sebastiano Calandra

Make your next move.

Martina Rinelli

Research Interests

Explore related searches

Contact this professor

Articles (15)

POLE mutations in endometrial carcinoma: Clinical and genomic landscape from a large prospective single‐center cohort

Potential pathogenetic role of a novel ABCC8 missense variant on both transient neonatal diabetes mellitus and fetal growth restriction: a case report

Identification of a False-positive Multiplex Ligationdependent Probe Amplification Result in BRCA1 Using a Copy Number Variation Algorithm Under Development for a Commercial Next-Generation Sequencing-based Homologous Recombination Deficiency Assay

G6PD Potenza: A Novel Pathogenic Variant Broadening the Mutational Landscape in the Italian Population

Identification and Molecular Characterization of a Novel Large-Scale Variant (Exons 4_18 Loss) in the LDLR Gene as a Cause of Familial Hypercholesterolaemia in an Italian Family

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology

Liquid Biopsy with Detection of NRASQ61K Mutation in Cerebrospinal Fluid: An Alternative Tool for the Diagnosis of Primary Pediatric Leptomeningeal Melanoma

Targeted therapy for pediatric diffuse intrinsic pontine glioma: a single-center experience

Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic Polr2a variant.

Establishment and Characterization of a Cell Line (S-RMS1) Derived from an Infantile Spindle Cell Rhabdomyosarcoma with <i>SRF-NCOA2</i> Fusion Transcript.

Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept.

Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review

Expansion of the clinical and molecular spectrum of an XPD-related disorder linked to biallelic mutations in ERCC2 gene.

Molecular Characterization of Medulloblastoma in a Patient with Neurofibromatosis Type 1: Case Report and Literature Review.

Rhabdoid Tumor Predisposition Syndrome: From Clinical Suspicion to General Management.

Collaborators (7)

Charlotte Brasch Andersen

Angelo Minucci

concetta santonocito

Francesco Fabozzi

Anne Marie Jelsig

Luciano Giaco'

Sebastiano Calandra

Make your next move.