E-LIB Suche - Ergebnisse für: Ciccone, Roberto

1

Acceptance of COVID-19 and Influenza Vaccine Co-Administrat..:

Domnich, Alexander ; Grassi, Riccardo ; Fallani, Elettra...
Journal of Personalized Medicine. 12 (2022) 2 - p. 139 , 2022

Link: https://doi.org/10.3390/..

2

Mild encephalitis/encephalopathy with reversible splenial l..:

Gatto, Antonio ; Mariotti, Paolo ; De Rose, Domenico Umberto...
Neurological Sciences. 41 (2020) 8 - p. 2271-2274 , 2020

Link: https://doi.org/10.1007/..

3

Missense variants in the Arg206 residue of HNRNPH2: Further..:

Peron, Angela ; Novara, Francesca ; La Briola, Francesca...
American Journal of Medical Genetics Part A. 182 (2020) 4 - p. 823-828 , 2020

Link: https://doi.org/10.1002/..

4

Inherited human IRAK-1 deficiency selectively impairs TLR s..:

Della Mina, Erika ; Borghesi, Alessandro ; Zhou, Hao...
Proceedings of the National Academy of Sciences. 114 (2017) 4 - p. , 2017

Link: https://doi.org/10.1073/..

5

Inherited human IRAK-1 deficiency selectively impairs TLR s..:

Mina, Erika Della ; Borghesi, Alessandro ; Zhou, Hao...
Proceedings of the National Academy of Sciences of the United States of America. 114 (2017) 4 - p. E514-E523 , 2017

Link: https://www.jstor.org/st..

6

Loss-of-FunctionFANCLMutations Associate with Severe Fancon..:

Vetro, Annalisa ; Iascone, Maria ; Limongelli, Ivan...
Human Mutation. 36 (2015) 5 - p. 562-568 , 2015

Link: https://doi.org/10.1002/..

7

Next Generation Sequencing for Systematic Assessment of Gen..:

Bersano, Anna ; Zuffardi, Orsetta ; Pantoni, Leonardo...
Journal of Stroke and Cerebrovascular Diseases. 24 (2015) 4 - p. 759-765 , 2015

Link: https://doi.org/10.1016/..

8

A novel mutation in COL4A1 gene: A possible cause of early ..:

Decio, Alice ; Tonduti, Davide ; Pichiecchio, Anna...
American Journal of Medical Genetics Part A. 167 (2015) 4 - p. 810-815 , 2015

Link: https://doi.org/10.1002/..

9

Defining the phenotype associated with microduplication rec..:

Novara, Francesca ; Stanzial, Franco ; Rossi, Elena...
American Journal of Medical Genetics Part A. 164 (2014) 8 - p. 2084-2090 , 2014

Link: https://doi.org/10.1002/..

10

MECP2 duplication phenotype in symptomatic females: report ..:

Novara, Francesca ; Simonati, Alessandro ; Sicca, Federico...
Molecular Cytogenetics. 7 (2014) 1 - p. 10 , 2014

Link: https://doi.org/10.1186/..

11

Idiopathic Central Precocious Puberty Associated with 11 Mb..:

Cisternino, Mariangela ; Della Mina, Erika ; Losa, Laura...
Case Reports in Genetics. 2013 (2013) - p. 1-6 , 2013

Link: https://doi.org/10.1155/..

12

5p13 microduplication syndrome: A new case and better clini..:

Novara, Francesca ; Alfei, Enrico ; D'Arrigo, Stefano...
European Journal of Medical Genetics. 56 (2013) 1 - p. 54-58 , 2013

Link: https://doi.org/10.1016/..

13

Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23..:

Bayindir, Baran ; Piazza, Elena ; Della Mina, Erika...
European Journal of Medical Genetics. 56 (2013) 10 - p. 551-555 , 2013

Link: https://doi.org/10.1016/..

14

Public Debt and Aggregate Demand: Some Unconventional Analy..:

, In: Sraffa and the Reconstruction of Economic Theory: Volume Two,

Ciccone, Roberto - p. 15-43 , 2013

Link: https://doi.org/10.1057/..

15

MEF2C deletions and mutations versus duplications: A clinic..:

Novara, Francesca ; Rizzo, Ambra ; Bedini, Gloria...
European Journal of Medical Genetics. 56 (2013) 5 - p. 260-265 , 2013

Link: https://doi.org/10.1016/..