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Author/Creator Schmuth Matthias guestEditor.

2. A novel de novo mutation p.Ala428Asp in KRT5 gene as a cause of localized epidermolysis bullosa simplex. Issue 10 (20th May 2019)

Authors:
Stawczyk‐Macieja, Marta; Wertheim‐Tysarowska, Katarzyna; Jakubowski, Rafał; Szczerkowska‐Dobosz, Aneta; Krygier, Magdalena; Wilkowska, Aleksandra; Sawicka, Justyna; Nowak, Wiesław; Bal, Jerzy; Nowicki, Roman
Other Names:
Bauer Johann W. guestEditor.; Bodemer Christine guestEditor.; Schmuth Matthias guestEditor.
Journal:
Experimental dermatology
Issue:
Volume 28:Issue 10(2019)
Page Start:
1131
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell death. Issue 10 (10th May 2018)

Authors:
Easton, Jennifer A.; Albuloushi, Ahmad K.; Kamps, Miriam A. F.; Brouns, Gladys H. M. R.; Broers, Jos L. V.; Coull, Barry J.; Oji, Vincent; van Geel, Michel; van Steensel, Maurice A. M.; Martin, Patricia E.
Other Names:
Bauer Johann W. guestEditor.; Bodemer Christine guestEditor.; Schmuth Matthias guestEditor.
Journal:
Experimental dermatology
Issue:
Volume 28:Issue 10(2019)
Page Start:
1106
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. ATP6V0A2‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype. Issue 10 (20th August 2018)

Authors:
Beyens, Aude; Moreno‐Artero, Ester; Bodemer, Christine; Cox, Helen; Gezdirici, Alper; Yilmaz Gulec, Elif; Kahloul, Najoua; Khau Van Kien, Philippe; Ogur, Gonul; Harroche, Annie; Vasse, Marc; Salhi, Aïcha; Symoens, Sofie; Hadj‐Rabia, Smail; Callewaert, Bert
Other Names:
Bauer Johann W. guestEditor.; Bodemer Christine guestEditor.; Schmuth Matthias guestEditor.
Journal:
Experimental dermatology
Issue:
Volume 28:Issue 10(2019)
Page Start:
1142
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. CCL3, IL‐7, IL‐13 and IFNγ transcripts are increased in skin's biopsy of systemic sclerosis. Issue 10 (3rd July 2019)

Authors:
Gonçalves, Rafaela Silva Guimarães; Pereira, Michelly Cristiny; Dantas, Andréa Tavares; Almeida, Anderson Rodrigues de; Rego, Moacyr J. B. M.; Lima, Emerson Andrade; Pitta, Ivan da Rocha; Duarte, Angela Luzia Branco Pinto; Pitta, Maira Galdino da Rocha
Other Names:
Bauer Johann W. guestEditor.; Bodemer Christine guestEditor.; Schmuth Matthias guestEditor.
Journal:
Experimental dermatology
Issue:
Volume 28:Issue 10(2019)
Page Start:
1172
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Issue 10 (19th February 2018)

Authors:
Vahidnezhad, Hassan; Youssefian, Leila; Saeidian, Amir Hossein; Zeinali, Sirous; Touati, Andrew; Abiri, Maryam; Sotoudeh, Soheila; Norouz‐zadeh, Sara; Amirinezhad, Niloufar; Mozafari, Nikoo; Daneshpazhooh, Maryam; Mahmoudi, Hamidreza; Hamid, Mohammad; Bradfield, Jonathan P.; Kim, Cecilia E.; Hako...
Other Names:
Bauer Johann W. guestEditor.; Bodemer Christine guestEditor.; Schmuth Matthias guestEditor.
Journal:
Experimental dermatology
Issue:
Volume 28:Issue 10(2019)
Page Start:
1118
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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