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Author/Creator Faleschini, Michela

1. ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia. (23rd October 2018)

Authors:
Faleschini, Michela; Melazzini, Federica; Marconi, Caterina; Giangregorio, Tania; Pippucci, Tommaso; Cigalini, Elena; Pecci, Alessandro; Bottega, Roberta; Ramenghi, Ugo; Siitonen, Timo; Seri, Marco; Pastore, Annalisa; Savoia, Anna; Noris, Patrizia
Journal:
British journal of haematology
Issue:
Volume 183:Number 2(2018)
Page Start:
276
Record Type:
Journal Article
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2. Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing. Issue 12 (2nd June 2015)

Authors:
Nicchia, Elena; Benedicenti, Francesco; Rocco, Daniela De; Greco, Chiara; Bottega, Roberta; Inzana, Francesca; Faleschini, Michela; Bonin, Serena; Cappelli, Enrico; Mogni, Massimo; Stanzial, Franco; Svahn, Johanna; Dufour, Carlo; Savoia, Anna
Journal:
Birth defects research
Issue:
Volume 103:Issue 12(2015)
Page Start:
1003
Record Type:
Journal Article
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3. Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism‐array analysis. Issue 3 (9th January 2019)

Authors:
Bottega, Roberta; Cappellani, Stefania; Fabretto, Antonella; Spinelli, Alessandro Mauro; Severini, Giovanni Maria; Aloisio, Michelangelo; Faleschini, Michela; Athanasakis, Emmanouil; Bruno, Irene; Faletra, Flavio; Pecile, Vanna
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 3(2019)
Page Start:
n/a
Record Type:
Journal Article
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4. Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia. Issue 8 (11th January 2021)

Authors:
Bottega, Roberta; Ravera, Silvia; Napolitano, Luisa M. R.; Chiappetta, Viviana; Zini, Nicoletta; Crescenzi, Barbara; Arniani, Silvia; Faleschini, Michela; Cortone, Giuseppe; Faletra, Flavio; Medagli, Barbara; Sirchia, Fabio; Moretti, Martina; de Lange, Job; Cappelli, Enrico; Mecucci, Cristina; On...
Journal:
Journal of cellular physiology
Issue:
Volume 236:Issue 8(2021)
Page Start:
5664
Record Type:
Journal Article
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5. Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis. Issue 6 (29th March 2022)

Authors:
Persico, Ilaria; Feresin, Agnese; Faleschini, Michela; Fontana, Giorgia; Sirchia, Fabio; Faletra, Flavio; La Bianca, Martina; Suergiu, Sarah; Morgutti, Marcello; Maschio, Massimo; D'Adamo, Adamo Pio; Raraigh, Karen S.; Savoia, Anna; Bottega, Roberta
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 10:Issue 6(2022)
Page Start:
n/a
Record Type:
Journal Article
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