K. Jeltsch
发表
M. Verbeek,
N. Blau,
R. Artuch,
2017,
Orphanet Journal of Rare Diseases.
D. Zafeiriou,
G. Horvath,
G. Hoffmann,
2022,
Annals of neurology.
J. Friedman,
M. Kurian,
G. Horvath,
2016,
Molecular genetics and metabolism reports.
E. Tocha,
Y. Hu,
S. Vervoort,
2018
.
G. Kochs,
R. Bartenschlager,
T. Iftner,
2020,
JAMA pediatrics.
T. Iftner,
T. Ganzenmueller,
B. Tönshoff,
2021,
Emerging infectious diseases.
D. Zafeiriou,
M. Verbeek,
H. Goez,
2021,
Nature Communications.
M. Verbeek,
H. Goez,
J. Friedman,
2020,
Orphanet Journal of Rare Diseases.
M. Verbeek,
H. Goez,
J. Friedman,
2020,
Orphanet Journal of Rare Diseases.
R. Kaiser,
B. Hero,
S. Lohse,
2021,
EClinicalMedicine.
I. Harting,
D. Zafeiriou,
J. Friedman,
2021,
Journal of inherited metabolic disease.
C. Stephan-Otto,
Jordi Muchart López,
T. Opladen,
2022,
Neuroradiology.
Mitsuhiro Kato,
M. Kurian,
Á. García-Cazorla,
2020,
Journal of inherited metabolic disease.
R. Bartenschlager,
B. Tönshoff,
H. Kräusslich,
2023,
Journal of medical virology.
R. Bartenschlager,
B. Tönshoff,
H. Kräusslich,
2022,
Pediatrics.
M. Verbeek,
E. Sabidó,
J. Friedman,
2020,
Movement disorders : official journal of the Movement Disorder Society.
C. Thiel,
K. Tsiakas,
S. Kölker,
2021,
Journal of inherited metabolic disease.
D. Zafeiriou,
H. Goez,
J. Friedman,
2021,
Journal of inherited metabolic disease.
F. Schaefer,
S. Kölker,
D. Martinelli,
2020,
Orphanet Journal of Rare Diseases.
A. Rotenberg,
M. Bertoldi,
P. Pearl,
2023,
Epilepsia.
A. Rotenberg,
M. Bertoldi,
E. Arning,
2023,
Research square.
Y. Chien,
W. Hwu,
N. Blau,
2023,
Molecular genetics and metabolism.
M. Bertoldi,
E. Arning,
J. Roullet,
2023,
Human Genetics.
G. Kochs,
R. Bartenschlager,
T. Iftner,
2021,
JAMA pediatrics.