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Rare window on spinal muscular atrophy genetics
medicalxpress.com
Rare window on spinal muscular atrophy genetics Apr 07, Caused by a mutation of the SMN gene, ... Marina Fanin, Andrea Vettori, Paolo Laveder,
Network Profiles
LinkedIn: Marina Fanin | Profilo professionale - LinkedIn
Visualizza il profilo di Marina Fanin, Funzionario tecnico presso University of Padova (Padova, Italia), che ha frequentato Università degli Studi di Padova.
Interests
Rare Window On Spinal Muscular Atrophy Genetics - ScienceDailywww.sciencedaily.com › releases ›
www.sciencedaily.com
15 Apr · Caterina Millino, Marina Fanin, Andrea Vettori, Paolo Laveder, Maria Luisa Mostacciuolo, Corrado Angelini and Gerolamo Lanfranchi.
American Journal of Cardiology, The - Vol n° 3 - EM consulte
www.em-consulte.com
Daniela Miani, Matthew Taylor, Luisa Mestroni, Federica D'Aurizio, Nicoletta Finato, Marina Fanin, Silvana Brigido, Alessandro Proclemer. fleche fermer ...
diagnostica
www.webalice.it
di Marina Fanin Come e perché. La biopsia muscolare è il prelievo di una limitata porzione di muscolo (1 o 2 centimetri) dalla coscia o dal braccio, tramite una piccola incisione in anestesia locale (simile a quella utilizzata dal dentista). La ferita viene poi chiusa con qualche punto di sutura. L'intervento per biopsia richiede ...
Business Profiles
Researchgate: Marina Fanin
Padova, Veneto, Italy
Private Homepages
WikiGenes - Collaborative Publishing
www.wikigenes.org
Send message to Marina Fanin. To: Marina Fanin. Your name: Your email: Subject: Message: Dear Marina Fanin,. Security check: Enter both words below ...
Books & Literature
Genetic inheritance patterns (2008 edition) | Open Library
openlibrary.org
Genetic inheritance patterns by Ren Kimura, 2008, Nova Science Publishers edition, in English
authors:"Marina Fanin" - Search | Paperity
paperity.org
Paperity: the 1st multidisciplinary aggregator of Open Access journals & papers. Free fulltext PDF articles from hundreds of disciplines, all in one place
JIMD Reports - Google Books
books.google.de
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously...
Neurologia clinica - Google Books
books.google.com.ua
Alessandro Della Puppa Unità Operativa di Neurochirurgia, Azienda Ospedaliera di Padova Luca Denaro Dipartimento di Neuroscienze SNPSRR, Neurochirurgia, Università degli studi di Padova Mario Ermani Dipartimento di Neuroscienze SNPSRR, Università degli studi di Padova Marina Fanin Dipartimento di ...
Related Documents
CiteSeerX — The
citeseerx.ist.psu.edu
BibTeX @MISC{Cenacchi_the, author = {Giovanna Cenacchi and Lucia Tarantino and Arianna Corbu and Lucilla Badiali and De Giorgi and Marina Fanin and Elena …
Fanin, Marina [WorldCat Identities]
www.worldcat.org
View works by Marina Fanin Publications about Marina Fanin Publications by Marina Fanin off 0 Publications by Marina Fanin off ...
CURRICULUM VITAE INFORMAZIONI PERSONALI
www.ulss.belluno.it
Lodovica Vergani, Anna C. Nascimbeni, Luigi Fulizio and Marina Fanin Basic Appl Myol 14 (2): , Data _____ Con la ...
CiteSeerX — Gene expression profiling in dysferlinopathies using a...
citeseerx.ist.psu.edu
BibTeX @MISC{Campanaro02geneexpression, author = {Stefano Campanaro and Chiara Romualdi and Marina Fanin and Barbara Celegato and Beniamina Pacchioni and Silvia
Scientific Publications
Progress and challenges in diagnosis of dysferlinopathy - PubMed
pubmed.ncbi.nlm.nih.gov
Dysferlin-deficient limb girdle muscular dystrophy type 2B, distal Miyoshi myopathy, and other less frequent phenotypes are a group of recessive disorders...
Genetic inheritance patterns - NLM Catalog - NCBI
www.ncbi.nlm.nih.gov
Catalog of books, journals, and audiovisuals at the National Library of Medicine.
Analysis of malignant hyperthermia results in Padua and Siena | BMC...
bmcanesthesiol.biomedcentral.com
Vincenzo Tegazzin *, Alfredo Orrico, Lucia Galli, Marina Fanin and Daniela Rossi *
Calpainopathy - GeneReviews® - NCBI Bookshelf
www.ncbi.nlm.nih.gov
Calpainopathy is characterized by symmetric and progressive weakness of proximal limb-girdle muscles. The age at onset of muscle weakness ranges from two to
Publications
Create a SciFeed alert for new publications - MDPIwww.mdpi.com › scifeed_display
www.mdpi.com
Marina Fanin. Olimpia Musumeci. Jan De Bleecker. Lorenzo Peverelli. Maurizio Moggio. Eugenio Mercuri. Antonio Toscano. Marina Mora. Lucio Santoro.
Brain alterations in the classical form of congenital muscular...
link.springer.com
Child's Nerv Syst (1996) 12: Springer-Verlag Carlo P. Trevisan. Francesco Martinello. Emilia Ferruzza. Marina Fanin.
Marina Fanin Eva Masiero Corrado Angelini Marco Europe PMC ...
www.biomedsearch.com
THE ROLE OF AUTOPHAGY IN THE PATHOGENESIS OF GLYCOGEN STORAGE DISEASE TYPE II (GSDII) Anna Chiara Nascimbeni1, Marina Fanin1, Eva Masiero2, Corrado Angelini1,4, and Marco
Reports & Statements
Wikipedia: Malaltia de Danon - Viquipèdia, l'enciclopèdia lliure
Anar ↑ Marina Fanin, Anna C. Nascimbeni, Luigi Fulizio, Marco Spinazzi, Paola Melacini, Corrado Angelini «Generalized Lysosome-Associated Membrane Protein-2 Defect Explains Multisystem Clinical Involvement and Allows Leukocyte Diagnostic Screening in Danon Disease». Am J Pathol, 168, 4, pàg
Autophagy dysregulation in Danon disease - Naturewww.nature.com › cell death & disease › original article
www.nature.com
19 Jan · Autophagy dysregulation in Danon disease. Anna Chiara Nascimbeni,; Marina Fanin,; […] Corrado Angelini &; Marco Sandri; -Show fewer authors.
Miscellaneous
Marina Fanin | LinkedIn
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View Marina Fanin's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Marina Fanin discover inside ...
NEUROMUSCULAR BANK OF TISSUES AND DNA SAMPLES - ppt scaricare
slideplayer.it
Neuropathologie, Brussels, Belgium Leonardo SalviatiUniversity of Padova, Italy Marina Fanin University of Padova, Italy Roberto Massa Tor Vergata University ...
Dr Marina FANIN - Orphanetwww.orpha.net › cgi-bin › Directory_Professionals
www.orpha.net
Dr Marina FANIN. Activities registered with Orphanet : Responsible for diagnostic tests; E-mail : email; Phone : -; Mobile : -. Neuromuscular Laboratory ...
Dr Marina FANIN - Orphanetwww.orpha.net › consor › cgi-bin
www.orpha.net
Dr Marina FANIN. Attività registrata in Orphanet : Responsabile del/i test diagnostico/i; E-mail : email; Telefono : -; telefonino/fax : -. Neuromuscular Laboratory ...
SCHOLAR - CNKI学术搜索
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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。
Aortic Valve Stenosis: Fanin, Marina - Expertscape.com
www.expertscape.com
Marina Fanin has special expertise in Aortic Valve Stenosis
Marina Fanin
www.infona.pl
Loss of Calpain-3 Autocatalytic Activity in LGMD2A Patients with Normal Protein Expression · Marina Fanin, Anna Chiara Nascimbeni, Luigi ...
Marina Fanin - Telethonwww.telethon.it › ... › Ricercatori › Marina Fanin
www.telethon.it
Progetti. Un migliorato approccio genetico-biochimico alla diagnosi precoce di LGMD2A: nuovo test della funzione proteica e rapida analisi di mutazioni ...
Scheda Personale MARINA FANIN - Ordine degli Psicologi...
www.ordinepsicologier.it
Ordine degli Psicologi dell'Emilia-Romagna
All variants in the CAPN3 gene - Global Variome shared LOVDdatabases.lovd.nl › shared › variants › CAPN3
databases.lovd.nl
(Pro20Glnfs*37), -, pathogenic, g del, g del, 59delC, -, CAPN3_ , -, -, -, -, Germline, yes, -, -, 0, -, Marina Fanin. +/.
Annals of Indian Academy of Neurology: Reviewers Team
www.annalsofian.org
The journal has a clinical foundation and has been utilized most by clinical neurologists for improving the practice of neurology
Borghi, Ascari, Balletta: in tre per San Prospero - SulPanaro | News
www.sulpanaro-archivio.net
Ylenia Albano, Rita Artioli, Marina Fanin, Antonio Morselli, Massimo Giacchini, Andrea Sala, Sergio Rossi, Aurelio Iarrera, Eugenio Ligabue.
Clinical phenotype, muscle MRI and muscle pathology of LGMD1Fwww.proquest.com › scholarly-journals › docview
www.proquest.com
Enrico Peterle Marina Fanin Claudio Semplicini. Juan Jesus Vilchez Padilla Vincenzo Nigro. Corrado Angelini. Received: 15 March Revised: 11 April ...
Cristiano De Pittà - Publications List
publicationslist.org
Stefano Campanaro, Chiara Romualdi, Marina Fanin, Barbara Celegato, Beniamina Pacchioni, Silvia Trevisan, Paolo Laveder, Cristiano De Pittà, Elena ...
Dustri Online Services
www.dustri.com
Original Gender difference in limb-girdle muscular dystrophy: a muscle fiber morphometric study in 101 patients Marina Fanin, Anna C. Nascimbeni, and Corrado Angelini.
GYG1 gene mutations in a family with polyglucosan body myopathyng.neurology.org › content
ng.neurology.org
Marina Fanin, Annalaura Torella, Marco Savarese, Vincenzo Nigro, Corrado Angelini. First published September 24, 2015, DOI: https://doi.org NXG.
GYG1 gene mutations in a family with polyglucosan body myopathy |...
ng.neurology.org
Marina Fanin, PhD *, Annalaura Torella, PhD *, Marco Savarese, PhD, Vincenzo Nigro, MD, PhD and
Limb girdle muscular dystrophies — Italian Ministry of Health
moh-it.pure.elsevier.com
Corrado Angelini, Marina Fanin. Istituto di Neuroriabilitazione Motoria San Camillo; Research output: Chapter in Book/Report/Conference proceeding › Chapter. Abstract.
McArdle's Disease - The American Journal of Pathologyajp.amjpathol.org › article › fulltext
ajp.amjpathol.org
Marina Fanin. Marina Fanin. Affiliations. Conegliano Research Centre, Conegliano, and the Neuromuscular Center, Department of Neurology, University of ...
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