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Gruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2022
Danandeh, Khashayar; Jabbari, Parnian; Rayzan, Elham; Zoghi, Samaneh; Shahkarami, Sepideh; Heredia, Raul Jimenez; Krolo, Ana; Shamsian, Bibi Shahin; Boztug, Kaan und Rezaei, Nima
(2022):
Case Report of a Novel NFkB Mutation in a Lymphoproliferative Disorder Patient.
In: Endocrine Metabolic & Immune Disorders - Drug Targets, Bd. 22, Nr. 10: S. 1040-1046
2021
Shafeghat, Melika; Esmaeilzadeh, Hossein; Sadeghalvad, Mona; Rayzan, Elham; Zoghi, Samaneh; Shahkarami, Sepideh; Heredia, Raul Jimenez; Krolo, Ana; Boztug, Kaan und Rezaei, Nima
(2021):
A novel homozygous RAG1 mutation is associated with severe combined immunodeficiency and neurological presentations.
In: Allergologia et Immunopathologia, Bd. 49, Nr. 4: S. 91-97
2017
Hauck, Fabian; Magg, Thomas; Krolo, Ana; Bilic, Ivan; Hirschmugl, Tatjana; Laass, Martin; Rösen-Wolff, Angela; Luksch, Hella; Boztug, Kaan und Rösler, Joachim
(2017):
Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma.
In: Klinische Pädiatrie, Bd. 229, Nr. 3: S. 113-117