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Journal Article
Dobbertin-Welsch, Josefine 
ORCID: 0000-0003-4260-5879, Staudacher, Olga, Yuerek, Songuel, Trendelenburg, Valerie, Tschirner, Sebastian, Ziegert, Mandy, Ahrens, Frank, Millner-Uhlemann, Martina, Buesing, Susanne, Striegel, Anne, Ott, Hagen, Arens, Alisa, Gappa, Monica, Lange, Lars, Gernert, Sunhild, Niggemann, Bodo and Beyer, Kirsten
(2022).
Organ-specific symptom patterns during oral food challenge in children with peanut and tree nut allergy.
Pediatr. Allergy Immunol., 33 (5).
HOBOKEN:
WILEY.
ISSN 1399-3038
Fuchs, Susanne I., Schwerk, Nicolaus, Pittschieler, Klaus, Ahrens, Frank, Baden, Winfried, Bals, Robert, Faehndrich, Sebastian, Gleiber, Wolfgang, Griese, Matthias, Huelskamp, Georg, Koehnlein, Thomas, Reckling, Ludmilla, Rietschel, Ernst, Staab, Doris and Gappa, Monika (2016). Lung clearance index for monitoring early lung disease in alpha-1-antitrypsin deficiency. Respir. Med., 116. S. 93 - 100. LONDON: W B SAUNDERS CO LTD. ISSN 1532-3064
Prenzel, Freerk ORCID: 0000-0002-2838-593X, Harfst, Jacqueline, Schwerk, Nicolaus, Ahrens, Frank, Rietschel, Ernst, Schmitt-Groh, Sabina, Rubak, Sune M. L., Poplawska, Krystyna, Baden, Winfried, Vogel, Mandy, Hollizeck, Sebastian, Ley-Zaporozhan, Julia, Brasch, Frank, Reu, Simone and Griese, Matthias
(2020).
Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry-based case series.
Pediatr. Pulmonol., 55 (4).
S. 909 - 918.
HOBOKEN:
WILEY.
ISSN 1099-0496
Wallmeier, Julia, Frank, Diana, Shoemark, Amelia, Noethe-Menchen, Tabea, Cindric, Sandra, Olbrich, Heike, Loges, Niki T., Aprea, Isabella, Dougherty, Gerard W., Pennekamp, Petra, Kaiser, Thomas ORCID: 0000-0002-6699-0014, Mitchison, Hannah M., Hogg, Claire, Carr, Siobhan B., Zariwala, Maimoona A., Ferkol, Thomas, Leigh, Margaret W., Davis, Stephanie D., Atkinson, Jeffrey, Dutcher, Susan K., Knowles, Michael R., Thiele, Holger, Altmueller, Janine, Krenz, Henrike, Woeste, Marius, Brentrup, Angela, Ahrens, Frank, Vogelberg, Christian, Morris-Rosendahl, Deborah J. and Omran, Heymut
(2019).
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.
Am. J. Hum. Genet., 105 (5).
S. 1030 - 1040.
CAMBRIDGE:
CELL PRESS.
ISSN 1537-6605