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PubPharm (172)
21
Sjögren's syndrome and other rare and complex connective tissue diseases : an intriguing liaison
enthalten in:
Clinical and experimental rheumatology
| 2022
von
Baldini, C.
|
Arnaud, L.
|
Avčin, T.
| +31
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22
Systemic vasculitis : one year in review 2022
enthalten in:
Clinical and experimental rheumatology
| 2022
von
La Rocca, G.
|
Del Frate, G.
|
Delvino, P.
| +9
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23
An Opportunity to Harmonise the Approach to Patients' Care Pathways for Rare and Complex Diseases : RarERN Path™
enthalten in:
Frontiers in health services
| 2022
von
Talarico, R.
|
Marinello, D.
|
Cannizzo, S.
| +8
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24
An overlook on the current registries for rare and complex connective tissue diseases and the future scenario of TogethERN ReCONNET
enthalten in:
Frontiers in medicine
| 2022
von
Bandeira, M.
|
Di Cianni, F.
|
Marinello, D.
| +26
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25
Efficacy of anti-SARS-CoV-2 mRNA vaccine in systemic autoimmune disorders : induction of high avidity and neutralising anti-RBD antibodies
enthalten in:
RMD open
| 2021
von
Tani, C.
|
Pratesi, F.
|
Talarico, R.
| +9
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26
Being a caregiver of a Behçet's syndrome patient : challenges and perspectives during a complex journey
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Talarico, R.
|
Marinello, D.
|
Manzo, A.
| +12
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27
Being a caregiver of a Behçet’s syndrome patient: challenges and perspectives during a complex journey
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Talarico, R.
|
Marinello, D.
|
Manzo, A.
| +12
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28
One year in review 2021 : Behçet's syndrome
enthalten in:
Clinical and experimental rheumatology
| 2021
von
Hatemi, G.
|
Seyahi, E.
|
Fresko, I.
| +3
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29
Adherence to treatment in Behçet's syndrome : a multi-faceted issue
enthalten in:
Clinical and experimental rheumatology
| 2021
von
Pirri, S.
|
Marinello, D.
|
Lorenzoni, V.
| +6
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30
Correction to : RarERN Path: a methodology towards the optimisation of patients' care pathways in rare and complex diseases developed within the European Reference Networks
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Talarico, R.
|
Cannizzo, S.
|
Lorenzoni, V.
| +9
ErratumFor: Orphanet J Rare Dis. 2020 Dec 14;15(1):347. - PMID 33317578
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