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jutta gärtner
jutta gärtner
University Medical Center Gottingen
Verified email at med.uni-goettingen.de
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Cited by
Cited by
Year
Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis
AK Pröbstel, K Dornmair, R Bittner, P Sperl, D Jenne, S Magalhaes, ...
Neurology 77 (6), 580-588, 2011
3402011
Inspiration is the major regulator of human CSF flow
S Dreha-Kulaczewski, AA Joseph, KD Merboldt, HC Ludwig, J Gärtner, ...
Journal of neuroscience 35 (6), 2485-2491, 2015
3262015
Choroid plexus transcytosis and exosome shuttling deliver folate into brain parenchyma
M Grapp, A Wrede, M Schweizer, S Hüwel, HJ Galla, N Snaidero, ...
Nature communications 4 (1), 2123, 2013
3252013
Trial of fingolimod versus interferon beta-1a in pediatric multiple sclerosis
T Chitnis, DL Arnold, B Banwell, W Brück, A Ghezzi, G Giovannoni, ...
New England Journal of Medicine 379 (11), 1017-1027, 2018
3222018
Cathepsin D deficiency is associated with a human neurodegenerative disorder
R Steinfeld, K Reinhardt, K Schreiber, M Hillebrand, R Kraetzner, W Brück, ...
The American Journal of Human Genetics 78 (6), 988-998, 2006
3182006
Mutations in the gene encoding gap junction protein α12 (connexin 46.6) cause Pelizaeus-Merzbacher–like disease
B Uhlenberg, M Schuelke, F Rüschendorf, N Ruf, AM Kaindl, M Henneke, ...
The American Journal of Human Genetics 75 (2), 251-260, 2004
3062004
High seroprevalence of Epstein–Barr virus in children with multiple sclerosis
D Pohl, B Krone, K Rostasy, E Kahler, E Brunner, M Lehnert, HJ Wagner, ...
Neurology 67 (11), 2063-2065, 2006
2942006
Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome
J Gärtner, H Moser, D Valle
Nature genetics 1 (1), 16-23, 1992
2881992
Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism
R Steinfeld, M Grapp, R Kraetzner, S Dreha-Kulaczewski, G Helms, ...
The American Journal of Human Genetics 85 (3), 354-363, 2009
2702009
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects
J Berger, J Gärtner
Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1763 (12), 1721-1732, 2006
2532006
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study
H Rosewich, H Thiele, A Ohlenbusch, U Maschke, J Altmüller, P Frommolt, ...
The Lancet Neurology 11 (9), 764-773, 2012
2512012
Genetic and clinical aspects of X‐linked hydrocephalus (L1 disease): Mutations in the L1CAM gene
S Weller, J Gärtner
Human mutation 18 (1), 1-12, 2001
2342001
Anti–myelin oligodendrocyte glycoprotein antibodies in pediatric patients with optic neuritis
K Rostasy, S Mader, K Schanda, P Huppke, J Gärtner, V Kraus, ...
Archives of neurology 69 (6), 752-756, 2012
2132012
Treatment of early onset multiple sclerosis with subcutaneous interferon beta-1a
D Pohl, K Rostasy, J Gärtner, F Hanefeld
Neurology 64 (5), 888-890, 2005
2022005
Clinical and biochemical spectrum of D‐bifunctional protein deficiency
S Ferdinandusse, S Denis, PAW Mooyer, C Dekker, M Duran, ...
Annals of neurology 59 (1), 92-104, 2006
1962006
Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals
F Schueren, T Lingner, R George, J Hofhuis, C Dickel, J Gärtner, S Thoms
Elife 3, e03640, 2014
1952014
Genetics of intellectual disability in consanguineous families
H Hu, K Kahrizi, L Musante, Z Fattahi, R Herwig, M Hosseini, C Oppitz, ...
Molecular psychiatry 24 (7), 1027-1039, 2019
1942019
Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2−/y knockout mice
GM Stettner, P Huppke, C Brendel, DW Richter, J Gärtner, M Dutschmann
The Journal of physiology 579 (3), 863-876, 2007
1752007
Identification of the upward movement of human CSF in vivo and its relation to the brain venous system
S Dreha-Kulaczewski, AA Joseph, KD Merboldt, HC Ludwig, J Gärtner, ...
Journal of Neuroscience 37 (9), 2395-2402, 2017
1692017
Leukodystrophy incidence in Germany
P Heim, M Claussen, B Hoffmann, E Conzelmann, J Gärtner, K Harzer, ...
American journal of medical genetics 71 (4), 475-478, 1997
1631997
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