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pro vyhledávání: '"Scalco, Renata Siciliani"'
Autor:
Scalco, Renata Siciliani, Morrow, Jasper M, Manole, Andreea, Skorupinska, Iwona, Ricciardi, Federico, Matthews, Emma, Hanna, Michael G, Fialho, Doreen
Publikováno v:
In Neuromuscular Disorders February 2024 35:33-38
Autor:
Scalco, Renata Siciliani *, Morrow, Jasper M., Booth, Suzanne, Chatfield, Sherryl, Godfrey, Richard, Quinlivan, Ros
Publikováno v:
In Neuromuscular Disorders September 2017 27(9):852-855
Autor:
Scalco, Renata Siciliani *, Gardiner, Alice R., Pitceathly, Robert D.S., Hilton-Jones, David, Schapira, Anthony H., Turner, Chris, Parton, Matt, Desikan, Mahalekshmi, Barresi, Rita, Marsh, Julie, Manzur, Adnan Y., Childs, Anne-Marie, Feng, Lucy, Murphy, Elaine, Lamont, Phillipa J., Ravenscroft, Gianina, Wallefeld, William, Davis, Mark R., Laing, Nigel G., Holton, Janice L., Fialho, Doreen, Bushby, Kate, Hanna, Michael G., Phadke, Rahul, Jungbluth, Heinz, Houlden, Henry, Quinlivan, Ros
Publikováno v:
In Neuromuscular Disorders August 2016 26(8):504-510
Autor:
Porcello Marrone, Luiz Carlos ∗, Diogo, Luciano Passamani †, de Oliveira, Faberson Mocelin ‡, Trentin, Sheila §, Scalco, Renata Siciliani §, de Almeida, Andréa Garcia ∗, Gutierres, Luis del Carmo Vega ∗, Marrone, Antônio Carlos Huf ¶, da Costa, Jaderson Costa ‖
Publikováno v:
In Journal of Stroke and Cerebrovascular Diseases January 2013 22(1):32-35
Autor:
Scalco, Renata Siciliani1,2,3, Lorenzoni, Paulo José4, Lynch, David S.1, Martins, William Alves2, Jungbluth, Heinz5,6,7, Quinlivan, Ros1, Becker, Jefferson2, Houlden, Henry1 h.houlden@ucl.ac.uk
Publikováno v:
American Journal of Case Reports. 2017, Vol. 18, p17-21. 5p.
Autor:
Scalco, Renata Siciliani, Chatfield, Sherryl, Junejo, Muhammad Hyder, Booth, Suzanne, Pattni, Jatin, Godfrey, Richard, Quinlivan, Ros
Publikováno v:
The American Journal of Case Reports
Patient: Female, 44 Final Diagnosis: McArdle disease Symptoms: Exercise intolerance • muscle contracture • myalgia • myoglobinuria • recurrent rhabdomyolysis Medication: — Clinical Procedure: — Specialty: Neurology Objective: Rare disease
Autor:
Scalco, Renata Siciliani1,2,3 renata_scalco@hotmail.com, Gardiner, Alice R.1, Pitceathly, Robert D. S.1,4, Zanoteli, Edmar5, Becker, Jefferson2, Holton, Janice L.1, Houlden, Henry1, Jungbluth, Heinz4,6,7, Quinlivan, Ros1,8
Publikováno v:
Orphanet Journal of Rare Diseases. Aug2015, Vol. 10 Issue 1, p1-15. 15p.
Autor:
Scalco, Renata Siciliani, Lorenzoni, Paulo José, Lynch, David S, Martins, William Alves, Jungbluth, Heinz, Quinlivan, Ros, Becker, Jefferson, Houlden, Henry
Publikováno v:
Scalco, R S, Lorenzoni, P J, Lynch, D S, Martins, W A, Jungbluth, H, Quinlivan, R, Becker, J & Houlden, H 2017, ' Polymyositis without Beneficial Response to Steroid Therapy : Should Miyoshi Myopathy be a Differential Diagnosis? ', American Journal of Case Reports, vol. 18, pp. 17-21 . https://doi.org/10.12659/AJCR.900970
BACKGROUND Miyoshi myopathy (MM) is an autosomal-recessive muscle disorder caused by mutations in the DYSF gene. Clinical features and histopathological changes in dysferlinopathies may mimic inflammatory myopathies and a high degree of clinical susp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2761::b0bcc4c02f50f74b494f507ad99ea603
https://kclpure.kcl.ac.uk/ws/files/63087752/Polymyositis_without_Beneficial_Response_SCALCO_Published5January2017_GOLD_VoR_CC_BY_NC_ND_.pdf
https://kclpure.kcl.ac.uk/ws/files/63087752/Polymyositis_without_Beneficial_Response_SCALCO_Published5January2017_GOLD_VoR_CC_BY_NC_ND_.pdf
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