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Publications by authors named "Verena Leppmeier"
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A de novo BCL11B variant case manifesting with dystonic movement disorder regarding the article "BCL11B-related disorder in two canadian children: Expanding the clinical phenotype (Prasad et al., 2020).".
Philip Harrer
Verena Leppmeier
Andrea Berger
Simone Demund
Juliane Winkelmann
Eur J Med Genet
November 2022
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"Weak with Laughter"-Cataplexy as a Hint for Early Diagnosis of Niemann-Pick Type C?
Verena Leppmeier
Sybille Veit
Simone Demund
Christine Makowski
Gerhard Kluger
Neuropediatrics
April 2022
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