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	31	An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee Enthalten in Orphanet journal of rare diseases Bd. 16, 12.11.2021, Nr. 1, date:12.2021: 1-13
	32	Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Enthalten in Nature genetics Bd. 57, 24.6.2025, Nr. 7, date:7.2025: 1790-1791
	33	Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency Enthalten in Nature Bd. 623, 8.11.2023, Nr. 7988, date:11.2023: 803-813
	34	Correction to: A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature Enthalten in Journal of clinical immunology Bd. 44, 16.1.2024, Nr. 1, date:1.2024: 1
	35	Correction to: The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity Enthalten in Journal of clinical immunology Bd. 42, 9.2.2022, Nr. 3, date:4.2022: 499
	36	Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE Enthalten in Monatsschrift Kinderheilkunde Bd. 170, 3.12.2021, Nr. 1, date:1.2022: 52-60
	37	Gentherapien bei monogenen Erkrankungen Enthalten in Pädiatrie Bd. 36, 19.2.2024, Nr. 1, date:2.2024: 40-46
	38	Incidence of SCID in Germany from 2014 to 2015 an ESPED* Survey on Behalf of the API* Erhebungseinheit für Seltene Pädiatrische Erkrankungen in Deutschland (German Paediatric Surveillance Unit) Arbeitsgemeinschaft Pädiatrische Immunologie Enthalten in Journal of clinical immunology Bd. 40, 26.5.2020, Nr. 5, date:7.2020: 708-717
	39	Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency Enthalten in Journal of clinical immunology Bd. 41, 2.6.2021, Nr. 7, date:10.2021: 1536-1548
	40	Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Enthalten in Nature genetics Bd. 56, 22.7.2024, Nr. 8, date:8.2024: 1644-1653