Network Profiles
LinkedIn: Pier Paolo Prontera | LinkedIn
Visualizza il profilo professionale di Pier Paolo Prontera (Italia) su LinkedIn. LinkedIn è la rete professionale più grande al mondo utilizzata dai professionisti ...
Interests
Bicknell, LS et al. 1 A molecular and clinical study of larsen ...jmg.bmj.com › jmedgenet › early › › jmg full.pdf
jmg.bmj.com
26 Jun · Paolo Prontera , Thomy de Ravel , Jean-Pierre. Fryns , Elizabeth Sweeney , Alan Fryer , Sheila Unger.
Books & Literature
Paolo Prontera | XanEdu Customization Platform
www.academicpub.com
Author: Paolo Prontera. Results. Heterozygous X-linked adrenoleukodystrophy-associated myelopathy mimicking primary progressive multiple sclerosis.
Prontera's Publications
publications.crs4.it
Eleonora Palagano, Dario Strina, Ciro Menale, Stefano Mantero, Paolo Prontera, Maria Leine Guion-Almeida, Paolo Uva, Andrea Angius, Anna Villa, Cristina ...
Comorbidities in Headache Disorders - Google Books
books.google.com.ua
This book provides up-to-date information on all aspects of the comorbidities that are associated with the headache disorders commonly seen in the primary care...
Related Documents
Paolo Prontera - Academia.edu
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Academia.edu is a place to share and follow research.
Aicardi Syndrome Associated with Autosomal Genomic Imbalance:...
www.karger.com
Paolo Prontera, PhD. Medical Genetics Unit, University of Perugia. Via E. dal Pozzo. IT Perugia (Italy) .it
Absence of deletion and duplication of MLL2 and KDM6A genes in a ...
mgmjournal.com
Affiliations. UOS Genetica Clinica Pediatrica, Clinica Pediatrica Università Milano Bicocca, Fondazione MBBM, AOS Gerardo Monza, Italy. ,. Paolo Prontera.
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsyn.neurology.org › content › e577.abstract
n.neurology.org
10 Aug · ... Barbara Carlini, Letizia Camerota, View ORCID ProfileVincenzo Belcastro, Paolo Prontera, View ORCID ProfileAlberto Fernández-Jaén, ...
Scientific Publications
Predictors of surgical outcomes of retroperitoneal laparoscopic...
pubmed.ncbi.nlm.nih.gov
Laparoscopic retroperitoneal partial nephrectomy represents an adequate and safe technique for the treatment of T1 renal cancer. Optimal MIC success rate can...
A multi-method approach to the molecular diagnosis of overt and...
clinicalepigeneticsjournal.biomedcentral.com
Paolo Prontera 7, Silvia Maitz 8, Giovanni Sorge 9, Annalisa Calcagno 10, ... Clinical Epigenetics The official journal of the Clinical Epigenetics Society :23.
Migraine and epilepsy: what value today? | The Journal of Headache...
thejournalofheadacheandpain.biomedcentral.com
28 Sept · Paolo Prontera,; Stefano Caproni,; Letizia M Cupini,; […] Paola Sarchielli &; Paolo Calabresi ...
Mutation spectrum of MLL2 in a cohort of kabuki syndrome patients |...
ojrd.biomedcentral.com
... Daniela Melis, Maria G Patricelli, Manuela Priolo, Paolo Prontera, Alessandra Renieri, Maria A Mencarelli, Gioacchino Scarano, Matteo della ...
Publications
Nablus mask-like facial syndrome: Deletion of chromosome 8q22.1 is...
core.ac.uk
Nablus mask-like facial syndrome: Deletion of chromosome 8q22.1 is necessary ... Bertrand Isidor, Katherine Lachlan, Cedric Le Caignec, Paolo Prontera, Annick Raas ...
IJMS | Free Full-Text | Expanding the Clinical Spectrum of Sotos...
www.mdpi.com
Annalisa Mencarelli 1, Paolo Prontera 2, Amedea Mencarelli 2, Daniela Rogaia 2, Gabriela Stangoni 2, Massimiliano Cecconi 3 and Susanna ...
Oalib search
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Search Results: of matches for " Paolo Prontera " ... Lapi, Teresa Mattina, Daniela Melis, Maria G Patricelli, Manuela Priolo, Paolo Prontera Orphanet ...
Orphanet Journal of Rare Diseases - oalib
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OA Library offers high quality and most updated free academic thesis,open access resource covering various fields.It also provides Comprehensive Research Tool.
Video & Audio
Le Malattie Rare ascoltando il punto di vista del Dr. Paolo Prontera ...www.youtube.com › watch
www.youtube.com
4 May · Il medico genetista del centro di riferimento regionale di Genetica Medica dell'Ospedale di Perugia, Paolo Prontera, ospite del giornalista ...
Reports & Statements
Schilbach–Rott syndrome associated with 9q22.32q duplication,...
www.nature.com
Paolo Prontera .it. 1. Medical Genetics Unit, University-Hospital “Santa Maria della. Misericordia”, Perugia ...
dicembre « Medicina in Biblioteca
blogpinali.wordpress.com
25 articoli pubblicati da giorgiobertin durante December 2014
DEFINE_ME
www.seizure-journal.com
Clinica Neurologica, University of Perugia, Ospedale S. Maria della Misericordia, S Andrea delle Fratte, Perugia, Italy. ,. Paolo Prontera. x. Paolo Prontera.
Schilbach–Rott syndrome associated with 9q22.32q Naturewww.nature.com › european journal of human genetics › articles
www.nature.com
1 Apr · 32q duplication, involving the PTCH1 gene. Paolo Prontera,; Daniela Rogaia, ...
Miscellaneous
Paolo Prontera | LinkedIn
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View Paolo Prontera’s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Paolo Prontera discover inside ...
paolo prontera | LinkedIn
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paolo prontera -- Località Italia Join LinkedIn and access paolo prontera’s full profile. It's free! As a LinkedIn member, you'll join 300 million other ...
Pier Paolo Prontera | LinkedIn
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View Pier Paolo Prontera's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Pier Paolo Prontera ...
Genetica Medica di Paolo Prontera - Medici spe…ti Perugia
www.webrica.it
Webrica: Trova tutte le aziende italiane suddivise per categoria e località: studi legali, ristoranti, studi professionali, scuole, hotel, concessionari auto,...
Dott. Paolo Prontera: genetista a Perugia - Top Doctorswww.topdoctors.it › ... › Genetisti a Perugia
www.topdoctors.it
Il Dott. Paolo Prontera è esperto in Genetica Medica. Laureato in Medicina e Chirurgia a Perugia nel 2002, si è specializzato prsso l'Università degli studi di ...
Prontera - Names Encyclopedia
namespedia.com
Paolo Prontera (1) Daniel Prontera (1) Anna Prontera (1) Massimo Prontera (1) Joseph Prontera (1) Karin Prontera (1) Rita Prontera (1) Stefania Prontera (1)
外文检索
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CNKI学术搜索是一个基于海量资源的跨学科、跨语种、跨文献类型的学术资源搜索平台，其资源库涵盖各类学术期刊、论文、报纸、专利、标准、年鉴、工具书等，旨在为国内外研究人员提供全面、权威、系统的知识网络。
Paolo Prontera, medico a Perugia
36medici.com
Indirizzo e telefono di Paolo Prontera, Perugia (06125). Elenco dei medici della provincia di Perugia.
Carriera di Prontera Paolo - PU Sport
www.pusport.com
Paolo Prontera. Ruolo preferito: Difensore. Anno di nascita: Clicca qui se vuoi aggiornare la tua carriera · Clicca qui se vuoi aggiornare i dati anagrafici.
Carriera di Prontera Paolo
www.romagnasport.com
Carriera di Prontera Paolo Risultati, classifiche e notizie dello sport in Romagna - Romagna Sport - Risultati, classifiche e notizie del calcio...
Sanità/ Premio della Società di Genetica umana al dott. Paolo...
www.umbrialeft.it
PERUGIA - ''Il riconoscimento ottenuto a livello nazionale ci incoraggia a proseguire nel nostro studio sulle cause genetiche dei disturbi neuropsichiatrici...
2p15-p16.1 microdeletions encompassing and proximal to BCL11A are...
ashpublications.org
Key Points. Elevation of HbF in 3 patients heterozygous for distinct 2p15-p16.1 syndrome microdeletions affecting BCL11A.Identification of novel, …tive regul
A molecular and clinical study of Larsen syndrome caused by ...research.rug.nl › publications › a-molecular-and-clinical-study-of-larsen-sy...
research.rug.nl
... Melissa Maisenbacher, Ellen Moran, John G. Pappas, Paolo Prontera, Thomy de Ravel, Jean-Pierre Fryns, Elizabeth Sweeney, Alan Fryer, Sheila Unger
DPP6 gene disruption in a family with Gilles de la Tourette syndrome.
schlr.cnki.net
Nicola Tambasco,Vincenzo Belcastro,Paolo Prontera,Pasquale Nigro,Emilio Donti,Aroldo Rossi,Paolo Calabresi. European Journal of Paediatric Neurology.
A molecular and clinical study of Larsen syndrome caused by mutations...
www.research.ed.ac.uk
... Melissa Maisenbacher, Ellen Moran, John G Pappas, Paolo Prontera, Thomy de Ravel, Jean-Pierre Fryns, Elizabeth Sweeney, Alan Fryer, Sheila Unger
JCI - RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome
www.jci.org
RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome. Nina ... Andrea Kranz, Martin Zenker, Dagmar Wieczorek, Nursel Elcioglu, Paolo Prontera, Stanislas ...
(PDF) Acrofrontofacionasal dysostosis 1 in two sisters of Indian...
www.academia.edu
Acrofrontofacionasal dysostosis 1 in two sisters of Indian origin
Understanding the genetic basis of Acrofrontofacionasal Dysostosis 1
publications.crs4.it
Eleonora Palagano, Dario Strina, Ciro Menale, Stefano Mantero, Paolo Prontera, Maria Leine Guion-Almeida, Paolo Uva, Andrea Angius, Gianmauro ...
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