Axel Neu
Priv.-Doz. Dr. med.
Axel Neu
  • Senior physician
  • Head of scientific working group
  • Medical Specialist in Pediatrics and Youth Medicine
Working area


O45 , 1st Floor
German (Mother tongue)

Areas of expertise




  • 2019
  • 2018
  • 2017
  • 2016
  • 2015
  • 2013
  • 2010
  • 2007
  • 2006
  • 2003
  • 2002
  • 2000
  • 1999
  • 1998

Guanidino compound ratios are associated with stroke etiology, internal carotid artery stenosis and CHADS-VASc score in three cross-sectional studies
Cordts K, Grzybowski R, Lezius S, Lüneburg N, Atzler D, Neu A, Hornig S, Böger R, Gerloff C, Magnus T, Thomalla G, Schwedhelm E, Grant P, Choe C
J NEUROL SCI. 2019;397:156-161.

de novo MEPCE nonsense variant associated with a neurodevelopmental disorder causes disintegration of 7SK snRNP and enhanced RNA polymerase II activation
Schneeberger P, Bierhals T, Neu A, Hempel M, Kutsche K
SCI REP-UK. 2019;9(1):12516.

Cognitive performance of 20 healthy humans supplemented with L-homoarginine for 4 weeks
Schönhoff M, Weineck G, Hoppe J, Hornig S, Cordts K, Atzler D, Gerloff C, Böger R, Neu A, Schwedhelm E, Choe C
J CLIN NEUROSCI. 2018;50:237-241.

A Mouse Model of Creatine Transporter Deficiency Reveals Impaired Motor Function and Muscle Energy Metabolism
Stockebrand M, Sasani A, Das D, Hornig S, Hermans-Borgmeyer I, Lake H, Isbrandt D, Lygate C, Heerschap A, Neu A, Choe C

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits
Glasgow R, Thompson K, Barbosa I, He L, Alston C, Deshpande C, Simpson M, Morris A, Neu A, Löbel U, Hall J, Prokisch H, Haack T, Hempel M, McFarland R, Taylor R
NEUROGENETICS. 2017;18(4):227-235.

Severe bone loss and multiple fractures in SCN8A-related epileptic encephalopathy
Rolvien T, Butscheidt S, Jeschke A, Neu A, Denecke J, Kubisch C, Meisler M, Püschel K, Barvencik F, Yorgan T, Oheim R, Schinke T, Amling M
BONE. 2017;103:136-143.

De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome
Kim J, Shinde D, Reijnders M, Hauser N, Belmonte R, Wilson G, Bosch D, Bubulya P, Shashi V, Petrovski S, Stone J, Park E, Veltman J, Sinnema M, Stumpel C, Draaisma J, Nicolai J, Yntema H, Lindstrom K, de Vries B, Jewett T, Santoro S, Vogt J, Bachman K, Seeley A, Krokosky A, Turner C, Rohena L, Hempel M, Kortüm F, Lessel D, Neu A, Strom T, Wieczorek D, Bramswig N, Laccone F, Behunova J, Rehder H, Gordon C, Rio M, Romana S, Tang S, El-Khechen D, Cho M, McWalter K, Douglas G, Baskin B, Begtrup A, Funari T, Schoch K, Stegmann A, Stevens S, Zhang D, Traver D, Yao X, MacArthur D, Brunner H, Mancini G, Myers R, Owen L, Lim S, Stachura D, Vissers L, Ahn E
AM J HUM GENET. 2016;99(3):711-9.

Transcriptomic and metabolic analyses reveal salvage pathways in creatine-deficient AGAT(-/-) mice
Stockebrand M, Nejad A, Neu A, Kharbanda K, Sauter K, Schillemeit S, Isbrandt D, Choe C
AMINO ACIDS. 2016;48(8):2025-39.

Treatment during a vulnerable developmental period rescues a genetic epilepsy
Marguet S, Le-Schulte V, Merseburg A, Neu A, Eichler R, Jakovcevski I, Ivanov A, Hanganu-Opatz I, Bernard C, Morellini F, Isbrandt D
NAT MED. 2015;21(12):1436-44.

Homoarginine supplementation improves blood glucose in diet-induced obese mice
Stockebrand M, Hornig S, Neu A, Atzler D, Cordts K, Böger R, Isbrandt D, Schwedhelm E, Choe C
AMINO ACIDS. 2015;47(9):1921-9.

L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome.
Choe C, Nabuurs C, Stockebrand M, Neu A, Nunes P, Morellini F, Sauter K, Schillemeit S, Hermans-Borgmeyer I, Marescau B, Heerschap A, Isbrandt D
HUM MOL GENET. 2013;22(1):110-123.

Differential regulation of AMPK activation in leptin- and creatine-deficient mice
Stockebrand M, Sauter K, Neu A, Isbrandt D, Choe C
FASEB J. 2013;27(10):4147-56.

A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.
Neu A, Eiselt M, Paul M, Sauter K, Stallmeyer B, Isbrandt D, Schulze-Bahr E
HUM MUTAT. 2010;31(8):1609-1621.

Prevention of plasticity of endocannabinoid signaling inhibits persistent limbic hyperexcitability caused by developmental seizures
Chen K, Neu A, Howard A, Földy C, Echegoyen J, Hilgenberg L, Smith M, Mackie K, Soltesz I
J NEUROSCI. 2007;27(1):46-58.

Homeostatic plasticity studied using in vivo hippocampal activity-blockade: synaptic scaling, intrinsic plasticity and age-dependence
Echegoyen J, Neu A, Graber K, Soltesz I
PLOS ONE. 2007;2(8):e700.

Cell type-specific gating of perisomatic inhibition by cholecystokinin
Földy C, Lee S, Szabadics J, Neu A, Soltesz I
NAT NEUROSCI. 2007;10(9):1128-30.

Opposing modifications in intrinsic currents and synaptic inputs in post-traumatic mossy cells: evidence for single-cell homeostasis in a hyperexcitable network
Howard A, Neu A, Morgan R, Echegoyen J, Soltesz I
J NEUROPHYSIOL. 2007;97(3):2394-409.

Postsynaptic origin of CB1-dependent tonic inhibition of GABA release at cholecystokinin-positive basket cell to pyramidal cell synapses in the CA1 region of the rat hippocampus
Neu A, Földy C, Soltesz I
J PHYSIOL-LONDON. 2007;578(Pt 1):233-47.

Presynaptic, activity-dependent modulation of cannabinoid type 1 receptor-mediated inhibition of GABA release
Földy C, Neu A, Jones M, Soltesz I
J NEUROSCI. 2006;26(5):1465-9.

Pacemaker channel dysfunction in a patient with sinus node disease
Schulze-Bahr E, Neu A, Friederich P, Kaupp U, Breithardt G, Pongs O, Isbrandt D
J CLIN INVEST. 2003;111(10):1537-45.

Activation of GABA(A) receptors by guanidinoacetate: a novel pathophysiological mechanism
Neu A, Neuhoff H, Trube G, Fehr S, Ullrich K, Roeper J, Isbrandt D
NEUROBIOL DIS. 2002;11(2):298-307.

I(h) channels contribute to the different functional properties of identified dopaminergic subpopulations in the midbrain
Neuhoff H, Neu A, Liss B, Roeper J
J NEUROSCI. 2002;22(4):1290-302.

Single-cell mRNA expression of HCN1 correlates with a fast gating phenotype of hyperpolarization-activated cyclic nucleotide-gated ion channels (Ih) in central neurons
Franz O, Liss B, Neu A, Roeper J
EUR J NEUROSCI. 2000;12(8):2685-93.

The weaver mouse gain-of-function phenotype of dopaminergic midbrain neurons is determined by coactivation of wvGirk2 and K-ATP channels
Liss B, Neu A, Roeper J
J NEUROSCI. 1999;19(20):8839-48.

Cloning and functional expression of rat ether-à-go-go-like K+ channel genes
Engeland B, Neu A, Ludwig J, Roeper J, Pongs O
J PHYSIOL-LONDON. 1998;513 ( Pt 3):647-54.

Letzte Aktualisierung aus dem FIS: 11.12.2019 - 06:18 Uhr