K. Becker

发表

Report of a Novel ALOX12B Mutation in Self-Improving Collodion Ichthyosis with an Overview of the Genetic Background of the Collodion Baby Phenotype

I. Kocsis, B. Mayer, N. Ács, 2021, Life.

Novel keratin 14 gene mutations in patients from Hungary with epidermolysis bullosa simplex

Z. Szalai, M. Csikós, S. Kárpáti, 2004, Experimental dermatology.

Contact urticaria from watermelon in a patient with pollen allergy

K. Becker, Erzséber Temesvári, 1993, Contact dermatitis.

[Skin diseases associated with chronic hepatitis C].

A. Horváth, J. Hársing, G. Lengyel, 1998, Orvosi hetilap.

Epidemiological and molecular genetic examination in epidermolysis bullosa

B. Mayer, Mária Katona, S. Kárpáti, 2015 .

Identification of a novel mutation in 3β‐hydroxysteroid‐Δ8‐Δ7‐isomerase in a case of Conradi–Hünermann–Happle syndrome

M. Csikós, S. Kárpáti, K. Becker, 2001, Experimental dermatology.

Identification of two novel nonsense mutations in the transglutaminase 1 gene in a Hungarian patient with congenital ichthyosiform erythroderma

Z. Szalai, M. Csikós, S. Kárpáti, 2003, Experimental dermatology.

Novel N160I mutation of keratin 9 in a large pedigree from Hungary with epidermolytic palmoplantar keratoderma.

P. Holló, M. Csikós, S. Kárpáti, 2003, Acta dermato-venereologica.

Visualization of Keratin with Diffuse Reflectance and Autofluorescence Imaging and Nonlinear Optical Microscopy in a Rare Keratinopathic Ichthyosis

Alexey Lihachev, Ilze Lihacova, Marta Lange, 2021, Sensors.

Ultrastructural features of the epidermis in a light form of Conradi-Hünermann-Happle syndrome

S. Kárpáti, A. Horváth, H. Traupe, 1998 .

Simultaneous infection by human herpesvirus 7 and human parvovirus B19 in papular-purpuric gloves-and-socks syndrome.

A. Horváth, J. Ongrádi, K. Becker, 2000, Archives of dermatology.