Results 291 to 300 of about 31,665 (304)

Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

British Journal of Dermatology, 2017
A. Zimmer, Gwang-Jin Kim, A. Hotz, E. Bourrat, I. Hausser, C. Has, V. Oji, K. Stieler, A. Vahlquist, V. Kunde, Benedikt Weber, F. Radner, S. Leclerc‐Mercier, N. Schlipf, P. Demmer, J. Küsel, J. Fischer   +16 more
semanticscholar   +1 more source

Ichthyosis

1985
L. Fry, M. N. P. Cornell
openaire   +2 more sources

Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: A tight junction disease

Gastroenterology, 2004
Pierre Vabres, Stanislas Lyonnet
exaly  

Ichthyosis vulgaris: the filaggrin mutation disease

British Journal of Dermatology, 2013
exaly  

Ichthyosis

2017
openaire   +1 more source

Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

British Journal of Dermatology, 2016
exaly  

Ichthyosis

2018
openaire   +1 more source

[Ichthyosis].

Ryoikibetsu shokogun shirizu, 2001
openaire   +1 more source

Ichthyosis

1914
openaire   +1 more source

Ichthyosis.

Nursing times, 2006
openaire   +1 more source