Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

…, G Calabrese, F Bernardi, E Meneghelli… - Journal of medical …, 2007 - jmg.bmj.com
Using array comparative genome hybridisation (CGH) 41 de novo reciprocal translocations
and 18 de novo complex chromosome rearrangements (CCRs) were screened. All cases …

[HTML][HTML] t (6; 11) renal cell carcinoma: a study of seven cases including two with aggressive behavior, and utility of CD68 (PG-M1) in the differential diagnosis with pure …

…, R Tardanico, A Remo, S Gobbo, E Meneghelli… - Modern Pathology, 2018 - Elsevier
Renal cell carcinomas with t (6; 11) chromosome translocation involving the TFEB gene are
indolent neoplasms which often occur in young patients. In this study, we report seven cases …

[HTML][HTML] Unexpected results in the constitution of small supernumerary marker chromosomes

…, G Croci, F Franchi, M Marinelli, E Meneghelli… - European journal of …, 2012 - Elsevier
Traditional approaches for the classification of Small Supernumerary Marker Chromosomes
(sSMC), mostly based on FISH techniques, are time-consuming and not always sufficient to …

Rapid reconstitution of functionally active 6-sulfoLacNAc+ dendritic cells (slanDCs) of donor origin following allogeneic haematopoietic stem cell transplant

…, S Lonardi, C Costantini, E Meneghelli… - Clinical & …, 2014 - academic.oup.com
The role of dendritic cells (DCs) and macrophages in allogeneic haematopoietic stem cell
transplant (HSCT) is critical in determining the extent of graft-versus-host response. The goal …

[HTML][HTML] A novel de novo partial xq duplication in a girl with short stature, nonverbal learning disability and diminished ovarian reserve-effect of growth hormone …

F Parissone, M Pucci, E Meneghelli, O Zuffardi… - International Journal of …, 2020 - Springer
Background Xq duplication is a rare condition with a very variable phenotype, which could
mimic other genetic syndromes involving the long arm of chromosome X. Sometimes short …

[PDF][PDF] CASE REPORT Open Access

F Parissone, M Pucci, E Meneghelli, O Zuffardi… - 2020 - ijpeonline.biomedcentral.com
Background: Xq duplication is a rare condition with a very variable phenotype, which could
mimic other genetic syndromes involving the long arm of chromosome X. Sometimes short …

[CITATION][C] ``Balanced''complex rearrangements: how many are really balanced?

…, G Calabrese, F Bernardi, E Meneghelli… - CHROMOSOME …, 2007 - iris.unibs.it

Nuovi approcci diagnostici al ritardo mentale.

E Danese, E Meneghelli, F Aprili, M Montagnana… - BIOCHIMICA …, 2012 - iris.univr.it
Genomic imbalances are considered the most frequent causes of mental retardation (MR).
Although widespread screening with novel molecular karyotyping methods, such as …

UTILIZAÇÃO DE ARTES MARCIAIS PARA TREINO E PREVENÇÃO DE QUEDAS EM IDOSOS-REVISÃO DE LITERATURA.

B Cadorin de Castilho… - … Inspirar Movimento & …, 2021 - search.ebscohost.com
Com a chegada do envelhecimento, ocorrem alterações fisiológicas em nossos sistemas,
podendo ocorrer comprometimento de alguns destes que são essenciais para o equilíbrio …

Applicazione della tecnica MLPA (Multiplex Ligation-Dependent Probe Amplification) per lo screening dei riarrangiamenti subtelomerici in pazienti pediatrici con …

E Danese, F Bernardi, E Meneghelli, F Darra… - LA RIVISTA ITALIANA …, 2010 - iris.univr.it
Subtelomeric rearrangements have been reported to be an important cause of mental
retardation. These aberrations may remain undetected by routine conventional cytogenetic …