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1 Ergebnisse
1
Congenital myopathies: Clinical phenotypes and new diagnost..:
Cassandrini D
;
Trovato R
;
Rubegni A
...
info:eu-repo/semantics/altIdentifier/pmid/29141652. , 2017
Link:
http://hdl.handle.net/2108/256280
RT Journal T1
Congenital myopathies: Clinical phenotypes and new diagnostic tools
UL https://suche.suub.uni-bremen.de/peid=base-ftunivromatorver:oai:art.torvergata.it:2108_256280&Exemplar=1&LAN=DE A1 Cassandrini D A1 Trovato R A1 Rubegni A A1 Lenzi S A1 Fiorillo C A1 Baldacci J A1 Minetti C A1 Astrea G A1 Bruno C A1 Santorelli F. M A1 Berardinelli A A1 Bertini E. S A1 Comi G A1 D'Amico A A1 Donati M. A A1 Dotti M. T A1 Fattori F A1 Grandis M A1 Maggi L A1 Magri F A1 Maioli M. A A1 Malandrini A A1 Mari F A1 Massa R A1 Mercuri E A1 Merlini L A1 Moggio M A1 Mora M A1 Morandi L. O A1 Musumeci O A1 Nigro V A1 Pane M A1 Pegoraro E A1 Pennisi E. M A1 Peverelli L A1 Ricci G A1 Rodolico C A1 Ruggiero L A1 Sacchini M A1 Santoro L A1 Savarese M A1 Siciliano G A1 Simonati A A1 Tonin P A1 Toscano A PB BIOMED CENTRAL LTD YR 2017 K1 Congenital myopathy K1 Muscle MRI K1 Muscle biopsy K1 Next generation sequencing K1 Biopsy K1 Needle K1 Disease Progression K1 Female K1 Genetic Predisposition to Disease K1 Genotype K1 Humans K1 Immunohistochemistry K1 Incidence K1 Magnetic Resonance Imaging K1 Male K1 Muscular Dystrophies K1 Myopathies K1 Nemaline K1 Prognosis K1 Risk Assessment K1 Severity of Illness Index K1 Settore MED/26 - NEUROLOGIA JF info:eu-repo/semantics/altIdentifier/pmid/29141652 LK http://hdl.handle.net/2108/256280 DO http://hdl.handle.net/2108/256280 SF ELIB - SuUB Bremen
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