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Lange, Lara
693
results:
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1
Die digitale Transformation der sozialen Dienste:
Hager, Jolina
;
Krauskopf, Karsten
;
Lange, Lara
...
https://opus4.kobv.de/opus4-fhpotsdam/frontdoor/index/index/docId/2911. , 2022
Link:
https://opus4.kobv.de/op..
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2
Genetics of Paroxysmal Dyskinesia: Novel Variants Corrobora..:
Kegele, Josua
;
Krüger, Johanna
;
Koko, Mahmoud
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297685/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
3
Author Correction: Elucidating causative gene variants in h..:
Lange, Lara M
;
Avenali, Micol
;
Ellis, Melina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499986/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
4
Elucidating causative gene variants in hereditary Parkinson..:
Lange, Lara M
;
Avenali, Micol
;
Ellis, Melina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300084/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
5
Author Correction: Elucidating causative gene variants in h..:
Lange, Lara Mariah
;
Avenali, Micol
;
Solle, Justin
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41531-023-00560-7. , 2023
Link:
https://pub.dzne.de/reco..
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6
Author Correction: Elucidating causative gene variants in h..:
Lange, Lara M
;
Avenali, Micol
;
Ellis, Melina
...
https://boris.unibe.ch/189661/. , 2023
Link:
https://boris.unibe.ch/1..
?
7
Elucidating causative gene variants in hereditary Parkinson..:
Lange, Lara M
;
Avenali, Micol
;
Ellis, Melina
...
10.1038/s41531-023-00526-9. , 2023
Link:
https://hdl.handle.net/1..
?
8
Elucidating causative gene variants in hereditary Parkinson..:
Lange, Lara M
;
Avenali, Micol
;
Solle, Justin
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41531-023-00526-9. , 2023
Link:
https://pub.dzne.de/reco..
?
9
Nomenclature of Genetic Movement Disorders: Recommendations..:
Lange, Lara M
;
Gonzalez-Latapi, Paulina
;
Rajalingam, Rajasumi
...
https://discovery.ucl.ac.uk/id/eprint/10153352/1/Movement%20Disorders%20-%202022%20-%20Lange%20-%20Nomenclature%20of%20Genetic%20Movement%20Disorders%20%20Recommendations%20of%20the%20International.pdf. , 2022
Link:
https://discovery.ucl.ac..
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10
Nomenclature of Genetic Movement Disorders:Recommendations ..:
Lange, Lara M
;
Gonzalez-Latapi, Paulina
;
Rajalingam, Rajasumi
...
https://research.rug.nl/en/publications/fda9aea2-a46d-4fd3-bb70-05b0aca492ff. , 2022
Link:
https://hdl.handle.net/1..
?
11
Genetics of Paroxysmal Dyskinesia: Novel Variants Corrobora..:
Josua Kegele
;
Johanna Krüger
;
Mahmoud Koko
...
https://www.frontiersin.org/articles/10.3389/fneur.2021.701351/full. , 2021
Link:
https://doi.org/10.3389/..
?
12
Author Correction: Elucidating causative gene variants in h..:
Lara M. Lange
;
Micol Avenali
;
Melina Ellis
...
https://doi.org/10.1038/s41531-023-00560-7. , 2023
Link:
https://doi.org/10.1038/..
?
13
Elucidating causative gene variants in hereditary Parkinson..:
Lara M. Lange
;
Micol Avenali
;
Melina Ellis
...
https://doi.org/10.1038/s41531-023-00526-9. , 2023
Link:
https://doi.org/10.1038/..
?
14
Data Augmentation Scheme for Raman Spectra with Highly Corr..:
Lange, Christoph
;
Thiele, Isabel
;
Santolin, Lara
...
http://arxiv.org/abs/2402.00851. , 2024
Link:
http://arxiv.org/abs/240..
?
15
Stereotactical normalization with multiple templates repres..:
Apostolova, Ivayla
;
Schiebler, Tassilo
;
Lange, Catharina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060476/. , 2023
Link:
http://www.ncbi.nlm.nih...
1-15