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Author/Creator Opitz, L.

2. Phenotypical heterogeneity in RAG‐deficient patients from a highly consanguineous population. (4th November 2018)

Authors:
Meshaal, S. S.; El Hawary, R. E.; Abd Elaziz, D. S.; Eldash, A.; Alkady, R.; Lotfy, S.; Mauracher, A. A.; Opitz, L.; Pachlopnik Schmid, J.; van der Burg, M.; Chou, J.; Galal, N. M.; Boutros, J. A.; Geha, R.; Elmarsafy, A. M.
Journal:
Clinical and experimental immunology
Issue:
Volume 195:Number 2(2019)
Page Start:
202
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole‐exome sequencing and the potential benefit of newborn screening. (5th September 2016)

Authors:
Marquardt, L.; Lacour, M.; Hoernes, M.; Opitz, L.; Lecca, R.; Volkmer, B.; Reichenbach, J.; Hohl, D.; Ansari, M.; Ozsahin, H.; Güngör, T.; Pachlopnik Schmid, J.
Journal:
Journal of the European Academy of Dermatology and Venereology
Issue:
Volume 31:Number 3(2017)
Page Start:
e147
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Whole‐exome sequencing of T‐B+ severe combined immunodeficiency in Egyptian infants, JAK3 predominance and novel variants. (2nd November 2020)

Authors:
El Hawary, R.; Meshaal, S.; Mauracher, A.A.; Opitz, L.; Abd Elaziz, D.; Lotfy, S.; Eldash, A.; Boutros, J.; Galal, N.; Pachlopnik Schmid, J.; Elmarsafy, A.
Journal:
Clinical and experimental immunology
Issue:
Volume 203:Number 3(2021)
Page Start:
448
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗