jutta gärtner
机构: University Medical Center Gottingen
每年引用次数
引用次数
引用: 14,165
H-指数: 65
I10-指数 : 200
出版物: 508
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes.
A A Roscher , H Ambach , A Braun , J Gärtner
American Journal of Human Genetics 56 ( 4) 854 -861
74
1995
Hugo Wolfgang Moser--an excellent "science dealer".
J Gärtner
Neuropediatrics 31 ( 5) 225 -226
2000
Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders
K Brockmann , H Rosewich , H Thiele , U Maschke
Neuropediatrics 44 ( 02)
2013
Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency
R Steinfeld , S Dreha-Kulaczewski , K Weigt-Usinger , T Lücke
Neuropediatrics 44 ( 02)
2013
Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders
H Rosewich , H Thiele , A Ohlenbusch , M Hillebrand
Neuropediatrics 44 ( 02)
2013
Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder
P Huppke , J Mühlhausen , T Friede , D Ellenberger
Neuropediatrics 44 ( 02)
2013
Autosomal-recessive Kearns-Sayre syndrome is caused by mutations in the RRM2B gene with altered mitochondrial transcription
E Wilichowski , R Horvath , J Mayr , J Gärtner
Neuropediatrics 44 ( 02)
2013
Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations
L Schlotawa , A Hotz , C Zeschnigk , B Hartmann
Neuropediatrics 44 ( 02)
2013
Mitochondrial encephalomyopathy presenting with deafness, mutism, ataxia and late onset external ophthalmoplegia caused by a mutation in the X-linked gene AIFM1
M Kettwig , S Biskup , L Klinge , J Gärtner
Neuropediatrics 44 ( 02)
2013
Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis
E Würfel , HM Hummel , J Würfel , J Gärtner
Neuropediatrics 44 ( 02)
2013
Mitochondrial Myopathies in childhood and adolescence – Presentation, diagnosis und treatment
E Wilichowski , E Hobbiebrunken , W Schulz-Schaeffer , K Gempel
Neuropediatrics 37 ( 03)
2006
Identification of a novel inborn neurodegenerative disease of childhood: cathepsin D deficiency
R Steinfeld , K Reinhardt , K Schreiber , M Hillebrand
Neuropediatrics 37 ( 03)
2006
Comparative studies on the respiratory dysfunction in Rett syndrome patients and the corresponding mouse model
GM Stettner , M Dutschmann , J Gärtner , P Huppke
Neuropediatrics 37 ( 03)
2006
Proinflammatory molecules such as IFN-gamma and iNOS are not expressed in 25F9 positive macrophages in dermatomyositis
E Bahn , T Pfander , W Schulz-Schaeffer , J Schmidt
Neuropediatrics 37 ( 03)
2006
Motor neuropathy and alacrima: oligosymptomatic triple A syndrome
K Brockmann , K Koehler , M Krumbholz , J Gärtner
Neuropediatrics 37 ( 03)
2006
RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder
M Henneke , S Diekmann , N Haud , A Hurlstone
Neuropediatrics 41 ( 02)
2010
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
P Huppke , M Blüthner , O Bauer , W Stark
Neuropediatrics 41 ( 02)
2010
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
M Henneke , S Gegner , A Hahn , B Plecko-Startinig
Neuropediatrics 41 ( 02)
2010
Clinical signs and treatment of cerebral folate transport deficiency, a novel inherited disorder of folate metabolism
R Steinfeld , M Grapp , S Dreha-Kulaczewski , J Gärtner
Neuropediatrics 41 ( 02)
2010
Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene
L Klinge , NF Clarke , HH Goebel , J Schmidt
Neuropediatrics 41 ( 02)
2010