Developing and Evaluating Rare Disease Educational Materials Co-Created by Expert Clinicians and Patients: the Paradigm of Congenital Hypogonadotropic Hypogonadism

AuthID
P-00M-KV1
29
Author(s)
Badiu, C
·
Bonomi, M
·
Borshchevsky, I
·
Cools, M
·
Craen, M
·
Ghervan, C
·
Hauschild, M
·
Hershkovitz, E
·
Hrabovszky, E
·
[+4]·
[+5]·
Pitteloud, N
·
Popovic, V
·
Quinton, R
·
Skordis, N
·
Smith, N
·
Stefanija, MA
·
Xu, C
·
Young, J
·
Dwyer, AA
1
Group Author(s)
COST Action BM1105
Document Type
Article
Year published
2017
Published
in ORPHANET JOURNAL OF RARE DISEASES, ISSN: 1750-1172
Volume: 12, Issue: 1
Indexing
Publication Identifiers
Scopus: 2-s2.0-85015737361
Wos: WOS:000397669000002
Source Identifiers
ISSN: 1750-1172
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Name Order Name   Name Order Name   Name Order Name
1 Badiu, C;   2 Bonomi, M;   3 Borshchevsky, I;
4 Cools, M;   5 Craen, M;   6 Ghervan, C;
7 Hauschild, M;   8 Hershkovitz, E;   9 Hrabovszky, E;
10 Juul, A;   11 Kim, SH;   12 Kumanov, P;
13 Lecumberri, B;   14 Lemos, MC;   15 Neocleous, V;
16 Niedziela, M;   17 Djurdjevic, SP;   18 Persani, L;
19 Phan Hug, F;   20 Pignatelli, D;   21 Pitteloud, N;
22 Popovic, V;   23 Quinton, R;   24 Skordis, N;
25 Smith, N;   26 Stefanija, MA;   27 Xu, C;
28 Young, J;   29 Dwyer, AA;