Dropout or Drop-In Experiences in an Internet-Delivered Intervention to Prevent Depression and Enhance Subjective Well-Being During the Perinatal Period: Qualitative Study

Valla, L., Haga, S. M., Garthus-Niegel, S. & Drozd, F., Jan 2023, In: JMIR Pediatrics and Parenting. 6, 1, e46982.

Research output: Contribution to journal › Research article › Contributed › peer-review

Vernetzte Versorgung - heute und in 10 Jahren

Vogel, T., Albertowski, A. S., Bienenstein, E., Christ, S., Brennenstuhl, H., Ferger, M. D., Karara, N., & 10 othersKerth, J-L., Krey, I., Meyer, R., Michaelis, A., Obitz, J., Töpfner, N., Tuncel, A. T., Winter, J., Yoosefi, M. & Kohlfürst, D. S., Sept 2023, In: Monatsschrift Kinderheilkunde. 171, 9, p. 804-812 9 p.

Research output: Contribution to journal › Case report › Contributed › peer-review

Diagnostik seltener Erkrankungen in der Pädiatrie

Krude, H., Berner, R. & Hoffmann, G. F., Jan 2022, In: Monatsschrift fur Kinderheilkunde. 170, 1, p. 13-20 8 p.

Research output: Contribution to journal › Review article › Contributed › peer-review

Metamizole-induced agranulocytosis (MIA): a mini review

Tomidis Chatzimanouil, M. K., Goppelt, I., Zeissig, Y., Sachs, U. J. & Laass, M. W., Dec 2023, In: Molecular and Cellular Pediatrics. 10, 1, p. 6 7 p., 6.

Research output: Contribution to journal › Short survey/Review › Contributed › peer-review

Chorioretinitis in a 7-year-old African Girl, probably related to JSSc resolving to methotrexate therapy

Hedrich, C. M., Leszczynska, A., Hammermann, J., Bau, V. & Gahr, M., 2011, In: Klinische Padiatrie. 223, 2, p. 92-94 3 p.

Research output: Contribution to journal › Case report › Contributed › peer-review

The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotin

Friebel, D., Von Der Hagen, M., Baumgartner, E. R., Fowler, B., Hahn, G., Feyh, P., Heubner, G., & 2 othersBaumgartner, M. R. & Hoffmann, G. F., Apr 2006, In: Neuropediatrics. 37, 2, p. 72-78 7 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Unusual radiological presentation of tuberous sclerosis complex with leptomeningeal angiomatosis associated with a hypomorphic mutation in the TSC2 gene

Ramantani, G., Niggemann, P., Hahn, G., Näke, A., Fahsold, R. & Lee-Kirsch, A. M., 2009, In: Journal of child neurology. 24, 3, p. 333-337 5 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Psycho-organic symptoms as early manifestation of adult onset POMT1-related limb girdle muscular dystrophy

Haberlova, J., Mitrović, Z., Žarković, K., Lovrić, D., Barić, V., Berlengi, L., Bilić, K., & 9 othersFumić, K., Kranz, K., Huebner, A., von der Hagen, M., Barresi, R., Bushby, K., Straub, V., Barić, I. & Lochmüller, H., 2014, In: Neuromuscular disorders. 24, 11, p. 990-992 3 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

The role of ret genomic variants in infantile hypertrophic pyloric stenosis

Serra, A., Schuchardt, K., Genuneit, J., Leriche, C., Grgens, H. S., Schackert, H. K. & Fitze, G., 2011, In: European journal of pediatric surgery. 21, 6, p. 389-394 6 p.

Research output: Contribution to journal › Research article › Contributed › peer-review