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Translating the WHA resolution in a member state: towards a German programme on ‘Destigmatization’ for individuals with visible chronic skin diseases
Translating the WHA resolution in a member state: towards a German programme on ‘Destigmatization’ for individuals with visible chronic skin diseases
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Translating the WHA resolution in a member state: towards a German programme on ‘Destigmatization’ for individuals with visible chronic skin diseases

Augustin, M. ; Mrowietz, U. ; Luck‐Sikorski, C. ; Kiedrowski, R. ; Schlette, S. ; Radtke, M.A. ; John, S.M. ; Zink, A. ; Suthakharan, N. ; Sommer, R.

Journal of the European Academy of Dermatology and Venereology, 2019-11, Vol.33 (11), p.2202-2208 [Periódico revisado por pares]

England

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2
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM‐1VWD study
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM‐1VWD study
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Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM‐1VWD study

EIKENBOOM, J. ; HILBERT, L ; RIBBA, A. S. ; HOMMAIS, A. ; HABART, D. ; MESSENGER, S. ; AL‐BUHAIRAN, A. ; GUILLIATT, A. ; LESTER, W. ; MAZURIER, C. ; MEYER, D. ; FRESSINAUD, E. ; BUDDE, U. ; WILL, K. ; SCHNEPPENHEIM, R. ; OBSER, T. ; MARGGRAF, O. ; ECKERT, E. ; CASTAMAN, G. ; RODEGHIERO, F. ; FEDERICI, A. B. ; BATLLE, J. ; GOUDEMAND, J. ; INGERSLEV, J. ; LETHAGEN, S. ; HILL, F. ; PEAKE, I. ; GOODEVE, A.

Journal of thrombosis and haemostasis, 2009-08, Vol.7 (8), p.1304-1312 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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3
First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene
First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene
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First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene

HILBERT, L. ; D'OIRON, R. ; FRESSINAUD, E. ; MEYER, D. ; MAZURIER, C.

Journal of thrombosis and haemostasis, 2004-12, Vol.2 (12), p.2271-2273 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Inc

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4
PMS76 PATIENT REPORTED QUALITY-OF-LIFE ISSUES IN MYOTONIC DYSTROPHY TYPE-1 (DMI): A FIRST STEP IN THE DEVELOPMENT OF A DISEASE-SPECIFIC INSTRUMENT
PMS76 PATIENT REPORTED QUALITY-OF-LIFE ISSUES IN MYOTONIC DYSTROPHY TYPE-1 (DMI): A FIRST STEP IN THE DEVELOPMENT OF A DISEASE-SPECIFIC INSTRUMENT
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PMS76 PATIENT REPORTED QUALITY-OF-LIFE ISSUES IN MYOTONIC DYSTROPHY TYPE-1 (DMI): A FIRST STEP IN THE DEVELOPMENT OF A DISEASE-SPECIFIC INSTRUMENT

Heatwole, C ; Chin, N ; Hilbert, J ; Holloway, R ; Johnson, N ; Pandya, S ; Moxley, R ; Quinn, C ; Thornton, C ; Vickrey, B ; Victorson, DE

Value in health, 2009, Vol.12 (7), p.A447-A447 [Periódico revisado por pares]

Elsevier Inc

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