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Prof. Dr. Holm Schneider
List of publications:
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Professur für Kinderheilkunde/Experimentelle Perinatalmedizin
Award(s)
(11)
Project Leads
(7)
Publications
(90)
Types of publications
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Journal article
Journal article
Book chapter / Article in edited volumes
Book chapter / Article in edited volumes
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Authored book
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Translation
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Thesis
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Edited Volume
Conference contribution
Conference contribution
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Other publication type
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Unpublished / Preprint
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T Cell Impairment Is Predictive for a Severe Clinical Course in NEMO Deficiency (2020)
Heller S, Kölsch U, Magg T, Krüger R, Scheuern A, Schneider H, Eichinger A, et al.
Journal article
Homozygous Biallelic KRT5 Mutations in Epidermolysis Bullosa Simplex, Including a Complete Human Keratin 5 "Knock-Out", in Families with Extensive Consanguinity (2019)
Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, et al.
Conference contribution
Deficiency of Fhl2 leads to delayed neuronal cell migration and premature astrocyte differentiation (2019)
Kim SY, Ludwig S, Schneider H, Wixler V, Park J, Völkl S
Journal article
Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasia (2019)
Wohlfart S, Schneider H
Journal article
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway (2019)
Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, et al.
Journal article
Prenatal treatment of X-linked hypohidrotic ectodermal dysplasia using recombinant ectodysplasin in a canine model (2019)
Margolis CA, Schneider P, Huttner K, Kirby N, Houser TP, Wildman L, Grove GL, et al.
Journal article
Conditional Alox12b Knockout: Degradation of the Corneocyte Lipid Envelope in a Mouse Model of Autosomal Recessive Congenital Ichthyoses (2019)
Krieg P, Dick A, Latzko S, Rosenberger S, Meyer J, Crumrine D, Hielscher T, et al.
Journal article
Reliability of prenatal detection of X-linked hypohidrotic ectodermal dysplasia by tooth germ sonography (2019)
Hammersen J, Wohlfart S, Goecke TW, Köninger A, Stepan H, Gallinat R, Morris S, et al.
Journal article
Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 “knock-out” (2019)
Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, et al.
Journal article
Attenuation of Severe Generalized Junctional Epidermolysis Bullosa by Systemic Treatment with Gentamicin (2019)
Hammersen J, Neuner A, Wild F, Schneider H
Journal article
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