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Variants in Miro1 Cause Alterations of ER-Mitochondria Contact Sites in Fibroblasts from Parkinson's Disease Patients.
Published in:
Journal of Clinical Medicine, 2019, v. 8, n. 12, p. 2226, doi. 10.3390/jcm8122226
By:
- Berenguer-Escuder, Clara;
- Grossmann, Dajana;
- Massart, Franҫois;
- Antony, Paul;
- Burbulla, Lena F.;
- Glaab, Enrico;
- Imhoff, Sophie;
- Trinh, Joanne;
- Seibler, Philip;
- Grünewald, Anne;
- Krüger, Rejko
Publication type:
Article
Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment.
Published in:
Journal of Neurology, 2020, v. 267, n. 3, p. 770, doi. 10.1007/s00415-019-09640-2
By:
- Trinh, Joanne;
- Imhoff, Sophie;
- Dulovic-Mahlow, Marija;
- Kandaswamy, Krishna Kumar;
- Tadic, Vera;
- Schäfer, Jochen;
- Dobricic, Valerija;
- Nolte, Achim;
- Werber, Martin;
- Rolfs, Arndt;
- Münchau, Alexander;
- Klein, Christine;
- Lohmann, Katja;
- Brüggemann, Norbert
Publication type:
Article
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci.
Published in:
Frontiers in Neurology, 2019, v. 10, p. 1, doi. 10.3389/fneur.2019.01284
By:
- Germer, Elisabeth Luisa;
- Imhoff, Sophie;
- Vilariño-Güell, Carles;
- Kasten, Meike;
- Seibler, Philip;
- Brüggemann, Norbert;
- Klein, Christine;
- Trinh, Joanne
Publication type:
Article
Utility and implications of exome sequencing in early-onset Parkinson's disease.
Published in:
2019
By:
- Trinh, Joanne;
- Lohmann, Katja;
- Baumann, Hauke;
- Balck, Alexander;
- Borsche, Max;
- Brüggemann, Norbert;
- Dure, Leon;
- Dean, Marissa;
- Volkmann, Jens;
- Tunc, Sinem;
- Prasuhn, Jannik;
- Pawlack, Heike;
- Imhoff, Sophie;
- Lill, Christina M.;
- Kasten, Meike;
- Bauer, Peter;
- Rolfs, Arndt;
- Klein, Christine;
- International Parkinson's Disease Genomics Consortium (IPDGC)
Publication type:
journal article

Found: 4

Variants in Miro1 Cause Alterations of ER-Mitochondria Contact Sites in Fibroblasts from Parkinson's Disease Patients.

Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment.

The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci.

Utility and implications of exome sequencing in early-onset Parkinson's disease.