Jutta Gärtner

University Children's Hospital Tübingen — Germany

Medicine · Health Sciences

60h-index11.6kcitations319works2.42yr avg
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Research Topics

Multiple Sclerosis Research Studies(52), Peroxisome Proliferator-Activated Receptors(50), RNA regulation and disease(45), Metabolism and Genetic Disorders(40), Lysosomal Storage Disorders Research(27)

Publications318 total

Diagnostic clues and pitfalls in pontocerebellar hypoplasia type 2A
Pediatric Neurology·2026
Aktualisierte Handlungsempfehlung nach der S1-Leitlinie Pädiatrische Multiple Sklerose
Monatsschrift Kinderheilkunde·2025Open Access
A Novel PEX13 Variant Causes Zellweger Spectrum Disorder with Mild/Intermediate Phenotype and Cystic Leukoencephalopathy
Neuropediatrics·2025Open Access
Microglia–neuron crosstalk through Hex–GM2–MGL2 maintains brain homeostasis
Nature·2025· 13 citedOpen Access
Super-resolution microscopy of mitochondrial mRNAs
Nature Communications·2025· 2 citedOpen Access
Biallelic <scp><i>ELOVL1</i></scp> Variants Are Linked to Hypomyelinating Leukodystrophy, Movement Disorder, and Ichthyosis
Movement Disorders·2025Open Access
The Inner Nuclear Layer in Pediatric Multiple Sclerosis
Neurology Neuroimmunology & Neuroinflammation·2025Open Access
The Inner Nuclear Layer in Pediatric Multiple Sclerosis
Neurology Neuroimmunology & Neuroinflammation·2025· 2 citedOpen Access
Das französisch-deutsche AFM-Téléthon Netzwerk zur Identifizierung von Biomarkern und Validierung von Ergebnismessungen an jungen CMT-Patienten (CMT-MODs)
Nervenheilkunde·2025Open Access
Super-resolution microscopy of mitochondrial mRNAs
2025Open Access
Mitochondrial Dysfunction and Impaired Oxidative Stress Defense as Potential Trigger of Cerebral X-linked Adrenoleukodystrophy
SSRN Electronic Journal·2025Open Access
UFM1-gene Mutation as a Cause of Hypomyelination with Atrophy of the Basal Ganglia and the Cerebellum: A Case Report
Neuropediatrics·2024Open Access
Longer-term (Up to 6 Years) Efficacy of Ofatumumab in People with Recently Diagnosed and Treatment-naive Relapsing Multiple Sclerosis (S31.003)
Neurology·2024· 3 citedOpen Access
Long term follow-up in GAMT deficiency – Correlation of therapy regimen, biochemical and in vivo brain proton MR spectroscopy data
Molecular Genetics and Metabolism Reports·2024· 7 citedOpen Access
CSF and venous blood flow from childhood to adulthood studied by real-time phase-contrast MRI
Child s Nervous System·2024· 9 citedOpen Access
Folate receptor α deficiency – Myelin‐sensitive <scp>MRI</scp> as a reliable biomarker to monitor the efficacy and long‐term outcome of a new therapeutic approach
Journal of Inherited Metabolic Disease·2024· 3 citedOpen Access
Multiple Sklerose im Kindes- und Jugendalter
Monatsschrift Kinderheilkunde·2023Open Access
Tazarotene and Bexarotene Show Efficacy as In Vitro Therapeutic Agents in Multiple Sulfatase Deficiency
Neuropediatrics·2023Open Access
Regional White Matter Hypertrophy Follows Cerebral ABCD1 Gene Expression Pattern in Asymptomatic X-Linked Adrenoleukodystrophy
Neuropediatrics·2023Open Access
Region-Specific Lipidomic Profiling in Brain and Spinal Cord Tissue of X-Linked Adrenoleukodystrophy Mice
Neuropediatrics·2023Open Access
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Frequent Co-authors

Steffi Dreha‐Kulaczewski(9), Wolfgang Brück(9), Peter Huppke(9), Jens Frahm(6), Robert Steinfeld(6), Brenda Huppke(6), H. Ludwig(5), Kevin Rostásy(5), Marco Henneke(5), Andreas Ohlenbusch(5), Knut Brockmann(5), Klaus‐Dietmar Merboldt(4), Peter Nürnberg(4), Sven Thoms(4), Peter Huppke(4), Arun Joseph(3), Marcel Grapp(3), Hölger Thiele(3), Hendrik Rosewich(3), Simone Diekmann(3)