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Georg M. Stettner
Georg M. Stettner
Neuromuscular Center and Department of Pediatric Neurology, University Children’s Hospital Zürich
Bestätigte E-Mail-Adresse bei kispi.uzh.ch - Startseite
Titel
Zitiert von
Zitiert von
Jahr
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
1742007
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population
M Oláhová, SA Hardy, J Hall, JW Yarham, TB Haack, WC Wilson, ...
Brain 138 (12), 3503-3519, 2015
1012015
Treatment of epilepsy in Rett syndrome
P Huppke, K Köhler, K Brockmann, GM Stettner, J Gärtner
European journal of paediatric neurology 11 (1), 10-16, 2007
852007
Upper airway dysfunction of Tau-P301L mice correlates with tauopathy in midbrain and ponto-medullary brainstem nuclei
M Dutschmann, C Menuet, GM Stettner, C Gestreau, P Borghgraef, ...
Journal of Neuroscience 30 (5), 1810-1821, 2010
752010
Treatment of Duchenne muscular dystrophy with ciclosporin A: a randomised, double-blind, placebo-controlled multicentre trial
J Kirschner, J Schessl, U Schara, B Reitter, GM Stettner, ...
The Lancet Neurology 9 (11), 1053-1059, 2010
742010
Delineating MT-ATP6-associated disease: From isolated neuropathy to early onset neurodegeneration
C Stendel, C Neuhofer, E Floride, S Yuqing, RD Ganetzky, J Park, ...
Neurology: Genetics 6 (1), e393, 2020
722020
Spontaneous central apneas occur in the C57BL/6J mouse strain
GM Stettner, S Zanella, P Huppke, J Gärtner, G Hilaire, M Dutschmann
Respiratory physiology & neurobiology 160 (1), 21-27, 2008
552008
Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I
A Rotthier, A Penno, B Rautenstrauss, M Auer‐Grumbach, GM Stettner, ...
Human mutation 32 (6), E2211-E2225, 2011
532011
Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis
K Huehne, C Zweier, K Raab, S Odent, M Bonnaure-Mallet, J Sixou, ...
Neuromuscular Disorders 18 (2), 159-166, 2008
452008
Disturbances of breathing in Rett syndrome: results from patients and animal models
GM Stettner, P Huppke, J Gärtner, DW Richter, M Dutschmann
Integration in respiratory control: from genes to systems, 503-507, 2008
422008
Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion
GM Stettner, M Shoukier, C Höger, K Brockmann, B Auber
American Journal of Medical Genetics Part A 155 (8), 2003-2007, 2011
372011
Postnatal emergence of synaptic plasticity associated with dynamic adaptation of the respiratory motor pattern
M Dutschmann, M Mörschel, J Reuter, W Zhang, C Gestreau, GM Stettner, ...
Respiratory physiology & neurobiology 164 (1-2), 72-79, 2008
352008
8-OH-DPAT suppresses spontaneous central apneas in the C57BL/6J mouse strain
GM Stettner, S Zanella, G Hilaire, M Dutschmann
Respiratory physiology & neurobiology 161 (1), 10-15, 2008
342008
CASPR2 autoimmunity in children expanding to mild encephalopathy with hypertension
S Syrbe, GM Stettner, J Bally, I Borggraefe, CI Bien, RI Ferfoglia, ...
Neurology 94 (22), e2290-e2301, 2020
282020
Somatropin treatment of spinal muscular atrophy: a placebo-controlled, double-blind crossover pilot study
J Kirschner, D Schorling, D Hauschke, C Rensing-Zimmermann, U Wein, ...
Neuromuscular Disorders 24 (2), 134-142, 2014
272014
Circadian dependence of receptors that mediate wake-related excitatory drive to hypoglossal motoneurons
DV Volgin, GM Stettner, L Kubin
Respiratory physiology & neurobiology 188 (3), 301-307, 2013
242013
Effect of chronic intermittent hypoxia on noradrenergic activation of hypoglossal motoneurons
GM Stettner, VB Fenik, L Kubin
Journal of Applied Physiology 112 (2), 305-312, 2012
222012
Survival among children with “Lethal” congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN)
JA Wambach, GM Stettner, TB Haack, K Writzl, A Škofljanec, A Maver, ...
Human mutation 38 (11), 1477-1484, 2017
192017
Antagonism of orexin receptors in the posterior hypothalamus reduces hypoglossal and cardiorespiratory excitation from the perifornical hypothalamus
GM Stettner, L Kubin
Journal of Applied Physiology 114 (1), 119-130, 2013
192013
Antagonism of orexin 1 receptors eliminates motor hyperactivity and improves homing response acquisition in juvenile rats exposed to alcohol during early postnatal period
GM Stettner, L Kubin, DV Volgin
Behavioural brain research 221 (1), 324-328, 2011
192011
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