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Author/Creator Ott, H.

4. Congenital ichthyoses: European guidelines of care, part two. (1st March 2019)

Authors:
Mazereeuw‐Hautier, J.; Hernández‐Martín, A.; O'Toole, E.A.; Bygum, A.; Amaro, C.; Aldwin, M.; Audouze, A.; Bodemer, C.; Bourrat, E.; Diociaiuti, A.; Dolenc‐Voljč, M.; Dreyfus, I.; El Hachem, M.; Fischer, J.; Ganemo, A.; Gouveia, C.; Gruber, R.; Hadj‐Rabia, S.; Hohl, D.; Jonca, N.
Journal:
British journal of dermatology
Issue:
Volume 180:Number 3(2019)
Page Start:
e80
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Congenital ichthyoses: European guidelines of care, part two. (1st March 2019)

Authors:
Mazereeuw‐Hautier, J.; Hernández‐Martín, A.; O'Toole, E.A.; Bygum, A.; Amaro, C.; Aldwin, M.; Audouze, A.; Bodemer, C.; Bourrat, E.; Diociaiuti, A.; Dolenc‐Voljč, M.; Dreyfus, I.; El Hachem, M.; Fischer, J.; Ganemo, A.; Gouveia, C.; Gruber, R.; Hadj‐Rabia, S.; Hohl, D.; Jonca, N.
Journal:
British journal of dermatology
Issue:
Volume 180:Number 3(2019)
Page Start:
e80
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Drug hypersensitivity in children: report from the pediatric task force of the EAACI Drug Allergy Interest Group. Issue 2 (17th November 2015)

Authors:
Gomes, E. R.; Brockow, K.; Kuyucu, S.; Saretta, F.; Mori, F.; Blanca‐Lopez, N.; Ott, H.; Atanaskovic‐Markovic, M.; Kidon, M.; Caubet, J.‐C.; Terreehorst, I.
Journal:
Allergy
Issue:
Volume 71:Issue 2(2016:Feb.)
Page Start:
149
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

9. Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome. (1st June 2021)

Authors:
Vornweg, J.; Gläser, S.; Ahmad‐Anwar, M.; Zimmer, A.D.; Kuhn, M.; Hörer, S.; Korenke, G.C.; Grothaus, J.; Ott, H.; Fischer, J.
Journal:
British journal of dermatology
Issue:
Volume 184:Number 6(2021)
Page Start:
1190
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

10. Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome. (3rd March 2021)

Authors:
Vornweg, J.; Gläser, S.; Ahmad‐Anwar, M.; Zimmer, A.D.; Kuhn, M.; Hörer, S.; Korenke, G.C.; Grothaus, J.; Ott, H.; Fischer, J.
Journal:
British journal of dermatology
Issue:
Volume 184:Number 6(2021)
Page Start:
1190
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗