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Eine Ebene nach oben |
Gruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2021
Ordenewitz, Lisa K.; Weinmann, Tobias 
ORCID: https://orcid.org/0000-0002-4582-5191; Schlueter, Julia A.; Moder, Judith E.; Jung, Jessica; Kerber, Katharina; Greif-Kohistani, Naschla; Heinen, Florian und Landgraf, Mirjam N.
(2021):
Evidence-based interventions for children and adolescents with fetal alcohol spectrum disorders-A systematic review.
In: European Journal of Paediatric Neurology, Bd. 33: S. 50-60
ORCID: https://orcid.org/0000-0002-4582-5191; Schlueter, Julia A.; Moder, Judith E.; Jung, Jessica; Kerber, Katharina; Greif-Kohistani, Naschla; Heinen, Florian und Landgraf, Mirjam N.
(2021):
Evidence-based interventions for children and adolescents with fetal alcohol spectrum disorders-A systematic review.
In: European Journal of Paediatric Neurology, Bd. 33: S. 50-60
2017
Bahrami, Ehsan; Witzel, Maximilian; Racek, Tomas; Puchaka, Jacek; Hollizeck, Sebastian; Greif-Kohistani, Naschla; Kotlarz, Daniel; Horny, Hans-Peter; Feederle, Regina; Schmidt, Heinrich; Sherkat, Roya; Steinemann, Doris; Göhring, Gudrun; Schlegelbeger, Brigitte; Albert, Michael H.; Al-Herz, Waleed und Klein, Christoph
(2017):
Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations.
In: Journal of Allergy and Clinical Immunology, Bd. 140, Nr. 4: S. 1112-1119
Aghamohammadi, Asghar; Abolhassani, Hassan; Puchalka, Jacek; Greif-Kohistani, Naschla; Zoghi, Samaneh; Klein, Christoph und Rezaei, Nima
(2017):
Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.
In: Journal of Clinical Immunology, Bd. 37, Nr. 3: S. 282-286