R. Mineri

发表

The calcineurin inhibitor and the intensity of the conditioning regimen may affect the occurrence of polyomavirus-associated hemorrhagic cystitis after haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide

D. Blaise, R. Devillier, S. Harbi, 2017, Bone Marrow Transplantation.

Implementing Pre-Therapeutic UGT1A1 Genotyping in Clinical Practice: A Real-Life Study

A. Santoro, S. Bozzarelli, L. Rimassa, 2022, Journal of personalized medicine.

A case of esophageal squamous cell intraepithelial neoplasia with positivity for type 16 human papillomavirus successfully treated with radiofrequency ablation.

Prateek Sharma, A. Repici, V. Villanacci, 2014, Journal of gastrointestinal oncology.

Tandem autologous-haploidentical transplantation is a feasible and effective program for refractory Hodgkin lymphoma

A. Santoro, D. Blaise, C. Carlo-Stella, 2018, Bone Marrow Transplantation.

Depletion of mtDNA: syndromes and genes.

V. Tiranti, M. Zeviani, R. Mineri, 2007, Mitochondrion.

Building awareness on genetic counselling: the launch of Italian Association of Genetic Counsellors (AIGeCo)

M. Crimi, D. Coviello, B. Pivetta, 2020, Journal of Community Genetics.

Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy

V. Tiranti, M. Zeviani, Tatjana M. Hildebrandt, 2009, Nature Medicine.

The genetic variant of lactase persistence C/T (13910) and blood glucose control in type 1 diabetes mellitus patients

S. Brambilla, T. Sarno, A. Montanelli, 2009 .

Genomic Integration of HHV-6 Mimicking Viral Reactivation after Autologous Stem Cell Transplantation

A. Santoro, C. Carlo-Stella, L. Castagna, 2018, Mediterranean journal of hematology and infectious diseases.

Identification of new mutations in the ETHE1 gene in a cohort of 14 patients presenting with ethylmalonic encephalopathy

V. Tiranti, M. Zeviani, G. Uziel, 2008, Journal of Medical Genetics.

Dual prognostic significance of tumour-associated macrophages in human pancreatic adenocarcinoma treated or untreated with chemotherapy

P. Allavena, A. Mantovani, F. Grizzi, 2015, Gut.

Ethylmalonic encephalopathy: application of improved biochemical and molecular diagnostic approaches

V. Tiranti, A. Drousiotou, T. Georgiou, 2011, Clinical genetics.

How Do Human Cells React to the Absence of Mitochondrial DNA?

N. Pavelka, P. Ricciardi-Castagnoli, V. Tiranti, 2009, PloS one.

Spatial distribution of B cells predicts prognosis in human pancreatic adenocarcinoma

Fabio Grizzi, Francesco Novelli, Paola Allavena, 2016, Oncoimmunology.

Ethylmalonic encephalopathy is caused by mutations in ETHE1, a gene encoding a mitochondrial matrix protein.

Paolo Gasparini, Brigitte Vollmer, Massimo Zeviani, 2004, American journal of human genetics.

Single-cell profiling identifies impaired adaptive NK cells expanded after HCMV reactivation in haploidentical HSCT

C. Peano, A. Santoro, L. Castagna, 2021, JCI insight.

Infections after T‐replete haploidentical transplantation and high‐dose cyclophosphamide as graft‐versus‐host disease prophylaxis

C. Carlo-Stella, L. Castagna, B. Sarina, 2015, Transplant infectious disease : an official journal of the Transplantation Society.

Single-cell profiling reveals the dynamics of cytomegalovirus-specific T cells in haploidentical hematopoietic stem cell transplantation

A. Santoro, F. Ferrari, L. Castagna, 2021, Haematologica.

Risk Factors for early CMV reactivation and Impact of early CMV reactivation on Clinical Outcomes after T Cell-replete Haploidentical Transplantation with Post-transplant Cyclophosphamide.

A. Santoro, D. Blaise, L. Giordano, 2021, Transplantation and cellular therapy.

Human Herpesvirus 6 replication predicts Cytomegalovirus reactivation after allogeneic stem cell transplantation from haploidentical donor.

L. Giordano, L. Castagna, B. Sarina, 2016, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Erythema Toxicum

A. L. Wong, V. Tiranti, E. Sobie, 2011, Pediatric Dermatology.

ETHE1 mutations are specific to ethylmalonic encephalopathy

E. Papaleo, V. Tiranti, M. Zeviani, 2005, Journal of Medical Genetics.

Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy (Nature Medicine DOI: 10.1038/nm.1907)

V. Tiranti, M. Zeviani, Tatjana M. Hildebrandt, 2009 .

Frataxin gene point mutations in Italian Friedreich ataxia patients

B. Castellotti, C. Gellera, F. Taroni, 2007, Neurogenetics.

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

D. Gambi, B. Castellotti, C. Gellera, 2004, Neurological Sciences.

Independent expression of circulating and tissue levels of PD-L1: correlation of clusters with tumor metabolism and outcome in patients with non-small cell lung cancer

G. Veronesi, S. Rossi, D. Rahal, 2019, Cancer Immunology, Immunotherapy.

Selected memory T cells infused post–haploidentical hematopoietic stem cell transplantation persist and hyperexpand

C. Peano, L. Castagna, B. Sarina, 2022, Blood advances.

Erratum: Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy

V. Tiranti, Tatjana M. Hildebrandt, C. Viscomi, 2009, Nature Medicine.

Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study.

G. Comi, A. Albanese, E. Valente, 2023, Movement disorders : official journal of the Movement Disorder Society.