E-LIB Suche - Ergebnisse für: Donti, Emilio

1

Comparative proteomic analysis of two distinct stem-cell po..:

Romani, Rita ; Fallarino, Francesca ; Pirisinu, Irene...
Molecular BioSystems. 11 (2015) 6 - p. 1622-1632 , 2015

2

Stem cells from human amniotic fluid exert immunoregulatory..:

Romani, Rita ; Pirisinu, Irene ; Calvitti, Mario...
Journal of Cellular and Molecular Medicine. 19 (2015) 7 - p. 1593-1605 , 2015

Link: https://doi.org/10.1111/..

3

Recurrent ∼100 Kb microdeletion in the chromosomal region 1..:

Prontera, Paolo ; Ottaviani, Valentina ; Toccaceli, Daniela...
American Journal of Medical Genetics Part A. 164 (2014) 12 - p. 3137-3141 , 2014

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

4

Hypothesis: gonadal temperature influences sex-specific imp..:

Prontera, Paolo ; Donti, Emilio
Frontiers in Genetics. 5 (2014) - p. , 2014

Link: https://doi.org/10.3389/..

5

Shapiro's syndrome: Defining the clinical spectrum of the s..:

Tambasco, Nicola ; Belcastro, Vincenzo ; Prontera, Paolo...
European Journal of Paediatric Neurology. 18 (2014) 4 - p. 453-457 , 2014

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

6

7q11.23 dosage-dependent dysregulation in human pluripotent..:

Adamo, Antonio ; Atashpaz, Sina ; Germain, Pierre-Luc...
Nature Genetics. 47 (2014) 2 - p. 132-141 , 2014

Link: https://doi.org/10.1038/..

7

Brief Report: Functional MRI of a Patient with 7q11.23 Dupl..:

Prontera, Paolo ; Serino, Domenico ; Caldini, Bernardo...
Journal of Autism and Developmental Disorders. 44 (2014) 10 - p. 2608-2613 , 2014

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

8

DPP6 gene disruption in a family with Gilles de la Tourette..:

Prontera, Paolo ; Napolioni, Valerio ; Ottaviani, Valentina...
neurogenetics. 15 (2014) 4 - p. 237-242 , 2014

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

9

A novel ATP1A2 gene mutation in familial hemiplegic migrain..:

Costa, Cinzia ; Prontera, Paolo ; Sarchielli, Paola...
Cephalalgia. 34 (2013) 1 - p. 68-72 , 2013

Link: https://doi.org/10.1177/..

10

Nablus mask‐like facial syndrome: Deletion of chromosome 8q..:

Allanson, Judith ; Smith, Amanda ; Hare, Heather...
American Journal of Medical Genetics Part A. 158A (2012) 9 - p. 2091-2099 , 2012

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

11

Xq12‐q13.3 duplication: Evidence of a recurrent syndrome:

Prontera, Paolo ; Ottaviani, Valentina ; Isidori, Ilenia..
Annals of Neurology. 72 (2012) 5 - p. 821-822 , 2012

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

12

Deletion 2p15–16.1 syndrome: Case report and review:

Prontera, Paolo ; Bernardini, Laura ; Stangoni, Gabriela...
American Journal of Medical Genetics Part A. 155 (2011) 10 - p. 2473-2478 , 2011

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

13

Craniometaphyseal dysplasia with severe craniofacial involv..:

Prontera, Paolo ; Rogaia, Daniela ; Sobacchi, Cristina...
American Journal of Medical Genetics Part A. 155 (2011) 5 - p. 1106-1108 , 2011

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

14

Germline PTPN11 mutation affecting exon 8 in a case of synd..:

Prontera, Paolo ; Pantaleoni, Francesca ; Martinelli, Simone...
Leukemia Research. 35 (2011) 3 - p. e13-e14 , 2011

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

15

Acrofrontofacionasal dysostosis 1 in two sisters of Indian ..:

Prontera, Paolo ; Urciuoli, Riccardo ; Siliquini, Sabrina...
American Journal of Medical Genetics Part A. 155 (2011) 12 - p. 3125-3127 , 2011

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