Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trial

Por Vahlquist, A, Blockhuys, S, Steijlen, P, van Rossem, K, Didona, B, Blanco, D, Traupe, H
Publicado no Br J Dermatol (2014)

Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3–34.13

Por Klar, J, Gedde-Dahl, T, Larsson, M, Pigg, M, Carlsson, B, Tentler, D, Vahlquist, A, Dahl, N
Publicado em 2004

Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis

Por Dahlqvist, J, Klar, J, Hausser, I, Anton‐Lamprecht, I, Pigg, M Hellström, Gedde‐Dahl, T, Gånemo, A, Vahlquist, A, Dahl, N
Publicado em 2007

Mutational spectrum of NSDHL in CHILD syndrome

Por Bornholdt, D, Konig, A, Happle, R, Leveleki, L, Bittar, M, Danarti, R, Vahlquist, A, Tilgen, W, Reinhold, U, Poiares, B, Grosshans, E, Vabres, P, Niiyama, S, Sasaoka, K, Tanaka, T, Meiss, A, Treadwell, P, Lambert, D, Camacho, F, Grzeschik, K
Publicado em 2005