Ciccone, Roberto
236  results:
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2

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
 
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4

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
 
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5

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
 
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6

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
 
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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
 
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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
 
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10

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

, In: Sraffa and the Reconstruction of Economic Theory: Volume Two,
Ciccone, Roberto - p. 15-43 , 2013
 
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11

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
 
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12

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
 
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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
 
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15

19q13.11 cryptic deletion: description of two new cases and..:

Gana, Simone ; Veggiotti, Pierangelo ; Sciacca, Giusy...
European Journal of Human Genetics.  20 (2012)  8 - p. 852-856 , 2012
 
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