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Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 12, 2025
Immunoprofiling to guide treatment decision in SAM syndrome
Olivia Bochnig, Thomas Giese, Judith Fischer, et al.
Archives of Dermatology
|
June 22, 2005
Two new mutations of the ABHD5 gene in a new adult case of Chanarin Dorfman syndrome: an uncommon lipid storage disease
Nicolas Schleinitz, Judith Fischer, Angélique Sanchez, et al.
Plos One
|
September 20, 2007
ADAM33, a new candidate for psoriasis susceptibility
Fabienne Lesueur, Tiphaine Oudot, Simon Heath, et al.
Clinical and Experimental Dermatology
|
February 6, 2025
A striking hand phenotype and guselkumab efficacy in NIPAL4-linked autosomal recessive congenital ichthyosis
Henning Klapproth, Jonas Rauterberg, Philipp Koll, et al.
Orphanet Journal of Rare Diseases
|
April 6, 2018
Alitretinoin reduces erythema in inherited ichthyosis
Giuliana Onnis, Christine Chiaverini, Geoffroy Hickman, et al.
Acta Dermato-Venereologica
|
July 30, 2020
Gene Mutation Mapping in a Fatal Case of Phacomatosis Pigmentokeratotica Happle
Kinan Hayani, Kathrin Giehl, Jörg Kumbrink, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
May 1, 2019
Neue Therapieansätze für entzündliche und bullöse Formen kongenitaler Ichthyosen: erste klinische Erfahrungen
Kira Süßmuth, Dieter Metze, Nora Ullrich, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
June 27, 2019
Ein neues Forum für seltene Hauterkrankungen
Steffen Emmert, Sebastian Iben, Judith Fischer, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2010
A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis
Fanny Morice-Picard, Christine Léauté-Labrèze, Aude Décor, et al.
Clinical Dysmorphology
|
January 8, 2015
A novel mutation in the ABCA12 gene in a Turkish case of Harlequin ichthyosis
Hakan Gürkan, Judith Fischer, Selma Ulusal, et al.
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Search research articles
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Showing results (51-60 of 174) with videos related to
Sort By:
Page
of 18
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 12, 2025
Immunoprofiling to guide treatment decision in SAM syndrome
Olivia Bochnig, Thomas Giese, Judith Fischer, et al.
Archives of Dermatology
|
June 22, 2005
Two new mutations of the ABHD5 gene in a new adult case of Chanarin Dorfman syndrome: an uncommon lipid storage disease
Nicolas Schleinitz, Judith Fischer, Angélique Sanchez, et al.
Plos One
|
September 20, 2007
ADAM33, a new candidate for psoriasis susceptibility
Fabienne Lesueur, Tiphaine Oudot, Simon Heath, et al.
Clinical and Experimental Dermatology
|
February 6, 2025
A striking hand phenotype and guselkumab efficacy in NIPAL4-linked autosomal recessive congenital ichthyosis
Henning Klapproth, Jonas Rauterberg, Philipp Koll, et al.
Orphanet Journal of Rare Diseases
|
April 6, 2018
Alitretinoin reduces erythema in inherited ichthyosis
Giuliana Onnis, Christine Chiaverini, Geoffroy Hickman, et al.
Acta Dermato-Venereologica
|
July 30, 2020
Gene Mutation Mapping in a Fatal Case of Phacomatosis Pigmentokeratotica Happle
Kinan Hayani, Kathrin Giehl, Jörg Kumbrink, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
May 1, 2019
Neue Therapieansätze für entzündliche und bullöse Formen kongenitaler Ichthyosen: erste klinische Erfahrungen
Kira Süßmuth, Dieter Metze, Nora Ullrich, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
June 27, 2019
Ein neues Forum für seltene Hauterkrankungen
Steffen Emmert, Sebastian Iben, Judith Fischer, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2010
A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis
Fanny Morice-Picard, Christine Léauté-Labrèze, Aude Décor, et al.
Clinical Dysmorphology
|
January 8, 2015
A novel mutation in the ABCA12 gene in a Turkish case of Harlequin ichthyosis
Hakan Gürkan, Judith Fischer, Selma Ulusal, et al.
Page
of 18