-
1دورية أكاديمية
المؤلفون: R. Cardani, G. Rossi, E. Bugiardini, G. Meola, M. Giagnacovo, L.V. Renna, C. Pizzamiglio, A. Botta
المساهمون: R. Cardani, M. Giagnacovo, G. Rossi, L.V. Renna, E. Bugiardini, C. Pizzamiglio, A. Botta, G. Meola
مصطلحات موضوعية: Alternative splicing, Disease progression, Muscle histology, Myotonic dystrophy type 2, Ribonuclear inclusions, Settore MED/26 - Neurologia, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25139674; info:eu-repo/semantics/altIdentifier/wos/WOS:000347770100003; volume:24; issue:12; firstpage:1042; lastpage:1053; numberofpages:12; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/2434/257762Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84919461424
-
2
المؤلفون: Enrico Bugiardini, Giovanni Meola, C. Chiara Pizzamiglio, Rosanna Cardani, Laura Valentina Renna, Giulia Rossi, Annalisa Botta, M. Giagnacovo
المصدر: Neuromuscular disorders : NMD. 24(12)
مصطلحات موضوعية: Male, Pathology, Messenger, Muscle histology, chemistry.chemical_compound, Myosin, MBNL1, Myotonic Dystrophy, In Situ Hybridization, Genetics (clinical), In Situ Hybridization, Fluorescence, biology, medicine.diagnostic_test, Blotting, Myotonic dystrophy type 2, Settore BIO/13, Cardiac muscle, RNA-Binding Proteins, Alternative splicing, Disease progression, Ribonuclear inclusions, Adult, Alternative Splicing, Biological Markers, Blotting, Western, Chloride Channels, Disease Progression, Female, Follow-Up Studies, Humans, Immunohistochemistry, Middle Aged, Muscle, Skeletal, RNA, Messenger, Skeletal, medicine.anatomical_structure, Neurology, Muscle, Western, musculoskeletal diseases, medicine.medical_specialty, Fluorescence, Internal medicine, medicine, CLCN1, Muscle biopsy, Skeletal muscle, Myotonia, medicine.disease, Endocrinology, Settore MED/03 - Genetica Medica, chemistry, Pediatrics, Perinatology and Child Health, biology.protein, RNA, Histopathology, Neurology (clinical), Biomarkers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eb7a8c8470faee0c53ceab311762565Test
https://pubmed.ncbi.nlm.nih.gov/25139674Test -
3مؤتمر
المؤلفون: G. Meola, R. Cardani, E. Mancinelli, G. Rotondo
المساهمون: J. Puymirat, C. Pearson, G. Meola, R. Cardani, E. Mancinelli, G. Rotondo
مصطلحات موضوعية: ribonuclear inclusions, MBNL1 foci, muscle differentiation, DM2, myotonic dystrophy type 2, Settore MED/26 - Neurologia, Settore BIO/09 - Fisiologia
العلاقة: ispartofbook:5th International myotonic dystrophy consortium meeting : (IDMC-5); International Myotonic Dystrophy Consortium Meeting; firstpage:44; http://hdl.handle.net/2434/17887Test
الإتاحة: http://hdl.handle.net/2434/17887Test
-
4دورية أكاديمية
المؤلفون: G. Meola, L.V. Renna, E. Bugiardini, R. Cardani
المساهمون: G. Meola, E. Bugiardini, L.V. Renna, R. Cardani
مصطلحات موضوعية: Muscle histopathology, italian DM2 patient, diagnostic role, ribonuclear inclusions, Settore MED/26 - Neurologia
العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000289992800531; European Neurological Society; volume:258; issue:suppl. 1; firstpage:S15; lastpage:S15; numberofpages:1; journal:JOURNAL OF NEUROLOGY; http://hdl.handle.net/2434/160190Test
-
5دورية أكاديمية
المؤلفون: E. Bugliardini, R. Cardani, L.V. Renna, E. Mancinelli, V. Sansone, G. Meola
المساهمون: E. Bugliardini, R. Cardani, L.V. Renna, E. Mancinelli, V. Sansone, G. Meola
مصطلحات موضوعية: central nucleation, type 2 atrophy, ribonuclear inclusions, histopathological markers, myotonic dystrophy type 2, DM2, Settore MED/26 - Neurologia
العلاقة: International Congress on Neuromuscular Diseases; volume:29; issue:suppl.; firstpage:SM57-120; lastpage:SM57-121; journal:ACTA MYOLOGICA; http://hdl.handle.net/2434/149548Test
-
6دورية أكاديمية
المؤلفون: Cardani, R, Baldassa, S, Rinaldi, F, Mancinelli, E, Meola G., BOTTA, ANNALISA, NOVELLI, GIUSEPPE
المساهمون: Cardani, R, Baldassa, S, Botta, A, Rinaldi, F, Novelli, G, Mancinelli, E, Meola, G
مصطلحات موضوعية: Alternative splicing, In vitro myoblasts differentiation, MBNL1, Myotonic dystrophy type 2, Ribonuclear inclusions, Settore MED/03 - GENETICA MEDICA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/19345584; info:eu-repo/semantics/altIdentifier/wos/WOS:000266794600006; volume:19; issue:5; firstpage:335; lastpage:343; numberofpages:9; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/2108/38881Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-67349117382
-
7دورية أكاديمية
المؤلفون: R. Cardani, S. Baldassa, E. Mancinelli, G. Meola, A. Botta, F. Rinaldi, G. Novelli
المساهمون: R. Cardani, S. Baldassa, A. Botta, F. Rinaldi, G. Novelli, E. Mancinelli, G. Meola
مصطلحات موضوعية: Myotonic dystrophy type 2, MBNL1, Ribonuclear inclusions, In vitro myoblasts differentiation, Alternative splicing, Settore MED/26 - Neurologia, Settore BIO/09 - Fisiologia
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/19345584; info:eu-repo/semantics/altIdentifier/wos/WOS:000266794600006; volume:19; issue:5; firstpage:335; lastpage:343; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/2434/73275Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-67349117382
-
8دورية أكاديمية
المؤلفون: V. Caldiera, R. Cardani, R. Perbellini, P. Tremolada, E. Mancinelli, G. Meola
المساهمون: V. Caldiera, R. Cardani, R. Perbellini, P. Tremolada, E. Mancinelli, G. Meola
مصطلحات موضوعية: Ribonuclear inclusions, myotonic dystrophy type 2, DM2, Settore MED/26 - Neurologia, Settore BIO/09 - Fisiologia
العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000255747000566; European Neurological Society : ENS; volume:255; issue:Suppl. 2; firstpage:150; lastpage:150; numberofpages:1; journal:JOURNAL OF NEUROLOGY; http://hdl.handle.net/2434/60456Test
الإتاحة: http://hdl.handle.net/2434/60456Test
-
9دورية أكاديمية
المؤلفون: R. Cardani, E. Mancinelli, G. Meola, G. Saino, L. Bonavina
المساهمون: R. Cardani, E. Mancinelli, G. Saino, L. Bonavina, G. Meola
مصطلحات موضوعية: Myotonic dystrophy type 1, Gallbladder, Ribonuclear inclusions, MBNL1, Smooth muscle, Settore MED/26 - Neurologia, Settore BIO/09 - Fisiologia
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/18653337; info:eu-repo/semantics/altIdentifier/wos/WOS:000259594000007; volume:18; issue:8; firstpage:641; lastpage:645; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/2434/73276Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-48749105274
-
10
المصدر: European Journal of Histochemistry, Vol 53, Iss 2, Pp e13-e13 (2009)
Europe PubMed Central
European Journal of Histochemistry : EJH
European Journal of Histochemistry, Vol 53, Iss 2, Pp 107-112 (2009)مصطلحات موضوعية: Pathology, medicine.medical_specialty, Histology, Somatic cell, Biopsy, Biophysics, ribonuclear inclusions, In situ hybridization, Biology, Specimen Handling, Technical Report, Freezing, medicine, Humans, Myotonic Dystrophy, RNA, Messenger, Muscle, Skeletal, myotonic dystrophy type 2, lcsh:QH301-705.5, In Situ Hybridization, Fluorescence, Cell Nucleus, Cryopreservation, DNA Repeat Expansion, Muscle biopsy, medicine.diagnostic_test, RNA-Binding Proteins, Skeletal muscle, Cell Biology, Muscle Fibers, Slow-Twitch, medicine.anatomical_structure, lcsh:Biology (General), Muscle Fibers, Fast-Twitch, Biomarker (medicine), fluorescence, in situ hybridization, Trinucleotide repeat expansion, Biomarkers, defrozen muscle biopsy, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2471700de967b09ef31c91e8a907f412Test
http://www.ejh.it/index.php/ejh/article/view/1239Test