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The Journal of Clinical Endocrinology and Metabolism|November 5, 2016
Loss of Functional Osteoprotegerin: More Than a Skeletal ProblemCorinna Grasemann, Nicole Unger, Matthias Hövel, et al.
The Journal of Pathology|October 2, 2021
Homozygous WASHC4 variant in two sisters causes a syndromic phenotype defined by dysmorphisms, intellectual disability, profound developmental disorder, and skeletal muscle involvementAndrea Gangfuß, Artur Czech, Andreas Hentschel, et al.
Pediatric Blood & Cancer|November 5, 2025
Melanoma of the Choroid and Ciliary Body in Children: Remission of Metastatic Melanoma of the Choroid After Treatment With Chemotherapy and Immune Checkpoint InhibitionPia Tüller, Tobias Kiefer, Leyla Jabbarli, et al.
American Journal of Medical Genetics. Part A|July 17, 2025
Growth Hormone Treatment in Patients With KBG Syndrome: Novel Insights, Challenges and Recommendations From Six New Patients and Literature ReviewSietse M Aukema, Kim Vandenput, Emanuela Scarano, et al.
Orphanet Journal of Rare Diseases|April 25, 2023
Transition for adolescents with a rare disease: results of a nationwide German projectCorinna Grasemann, Jakob Höppner, Peter Burgard, et al.
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