PuSH - Publication Server of Helmholtz Zentrum München

5 Records found.
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1.
Khan, K.* et al.: Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia. Genet. Med., accepted (2019)
2.
Salminen, A.V. ; Lam, D. & Winkelmann, J.: Role of MEIS1 in RLS: From GWAS to functional studies in mice. In: Advances in Pharmacology. 2019. accepted
3.
Jochim, A.* et al.: Microstructural white matter abnormalities in patients with COL6A3 mutations (DYT27 dystonia). Parkinsonism Relat. Disord. 46, 74-78 (2018)
4.
Zech, M. et al.: A unique de novo gain-of-function variant in CAMK4 associated with intellectual disability and hyperkinetic movement disorder. Cold Spring Harb. Mol. Case Stud. 4, accepted (2018)
5.
Heisler, L.K.* & Lam, D.: An appetite for life: Brain regulation of hunger and satiety. Curr. Opin. Pharmacol. 37, 100-106 (2017)