Sana, Maria Elena: search on Z-Library

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1

Unconventional experimental technologies available for phase change materials (PCM) characterization. Part 1. Thermophysical properties

Cabeza, Luisa F., Barreneche, Camila, Martorell, Ingrid, Miró, Laia, Sari-Bey, Sana, Fois, Magali, Paksoy, Halime O., Sahan, Nurten, Weber, Robert, Constantinescu, Mariaella, Anghel, Elena Maria, Mali

Journal:

Renewable and Sustainable Energy Reviews

Year:

2015

Language:

english

File:

PDF, 5.64 MB

english, 2015

2

First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutation

Acquaviva, Fabio, Sana, Maria Elena, Della Monica, Matteo, Pinelli, Michele, Postorivo, Diana, Fontana, Paolo, Falco, Maria Teresa, Nardone, Anna Maria, Lonardo, Fortunato, Iascone, Maria, Scarano, Gi

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 5.96 MB

english, 2016

3

Author Correction: Children’s first handwriting productions show a rhythmic structure

Pagliarini, Elena, Scocchia, Lisa, Vernice, Mirta, Zoppello, Marina, Balottin, Umberto, Bouamama, Sana, Guasti, Maria Teresa, Stucchi, Natale

Journal:

Scientific Reports

Year:

2018

Language:

english

File:

PDF, 664 KB

english, 2018

4

Children’s first handwriting productions show a rhythmic structure

Pagliarini, Elena, Scocchia, Lisa, Vernice, Mirta, Zoppello, Marina, Balottin, Umberto, Bouamama, Sana, Guasti, Maria Teresa, Stucchi, Natale

Journal:

Scientific Reports

Year:

2017

Language:

english

File:

PDF, 1.50 MB

english, 2017

5

Identification of a novel de novo deletion in RAF1 associated with biventricular hypertrophy in Noonan syndrome

Sana, Maria Elena, Spitaleri, Andrea, Spiliotopoulos, Dimitrios, Pezzoli, Laura, Preda, Laura, Musco, Giovanna, Ferrazzi, Paolo, Iascone, Maria

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 414 KB

english, 2014

6

Microcephaly, ectodermal dysplasia, multiple skeletal anomalies and distinctive facial appearance: Delineation of cerebro-dermato-osseous-dysplasia

Castori, Marco, Pascolini, Giulia, Parisi, Valentina, Sana, Maria Elena, Novelli, Antonio, Nürnberg, Peter, Iascone, Maria, Grammatico, Paola

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 1.74 MB

english, 2015

7

A Novel HRAS Mutation Independently Contributes to Left Ventricular Hypertrophy in a Family with a Known MYH7 Mutation

Sana, Maria Elena, Quilliam, Lawrence A., Spitaleri, Andrea, Pezzoli, Laura, Marchetti, Daniela, Lodrini, Chiara, Candiago, Elisabetta, Lincesso, Anna Rita, Ferrazzi, Paolo, Iascone, Maria, González,

Journal:

Year:

2016

Language:

english

File:

PDF, 1.51 MB

english, 2016

8

A new mutational mechanism for hypertrophic cardiomyopathy

Laura Pezzoli, Maria Elena Sana, Paolo Ferrazzi, Maria Iascone

Journal:

Year:

2012

Language:

english

File:

PDF, 1.03 MB

english, 2012

9

Interleukinâ1 receptorâassociated kinase 4 inhibitor interrupts tollâlike receptor signalling and sensitizes chronic lymphocytic leukaemia cells to apoptosis

Delvecchio, Vincenza Simona, Sana, Ilenia, Mantione, Maria Elena, Vilia, Maria Giovanna, Ranghetti, Pamela, Rovida, Alessandra, Angelillo, Piera, ScarfÃ², Lydia, Ghia, Paolo, Muzio, Marta

Journal:

British Journal of Haematology

Year:

2020

File:

PDF, 1.13 MB

2020

10

Non-coding RNAs: a key to future personalized molecular therapy?

Marco Galasso,Maria Elena Sana,Stefano Volinia

Journal:

Genome Medicine

Year:

2010

Language:

english

File:

PDF, 472 KB

english, 2010

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