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Neurogenetics|March 30, 2006
Identification of Alu elements mediating a partial PMP22 deletionVerena Matejas, Kathrin Huehne, Christian Thiel, et al.Applied and Environmental Microbiology|July 8, 2005
Characterization of a new bacteriocin operon in sakacin P-producing Lactobacillus sakei, showing strong translational coupling between the bacteriocin and immunity genesGeir Mathiesen, Kathrin Huehne, Lothar Kroeckel, et al.Journal of Neurology|January 7, 2012
A novel mutation of myelin protein zero associated with late-onset predominantly axonal Charcot-Marie-Tooth diseaseMaria Marttila, Bernd Rautenstrauss, Kathrin Huehne, et al.European Journal of Medical Genetics|July 4, 2008
Clinical, pathological and molecular findings in two siblings with giant axonal neuropathy (GAN): report from IndiaA Nalini, N Gayathri, T C Yasha, et al.Gene|August 12, 2003
A novel myosin heavy chain gene in human chromosome 19q13.3Alejandro Leal, Sabine Endele, Corinna Stengel, et al.Journal of Human Genetics|May 9, 2009
Mutations in the LMNA gene do not cause axonal CMT in Czech patientsPetra Lassuthová, Lucia Baránková, Jana Haberlová, et al.Neuromuscular Disorders : NMD|February 24, 2009
Phenotypic variability in giant axonal neuropathyMeriem Tazir, Sonia Nouioua, Laurent Magy, et al.European Journal of Pain (London, England)|January 27, 2009
High post surgical opioid requirements in Crohn's disease are not due to a general change in pain sensitivityKathrin Huehne, Stefan Leis, Tino Muenster, et al.Journal of Neurology|April 22, 2008
Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutationsKnut Brockmann, Steffi Dreha-Kulaczewski, Peter Dechent, et al.Human Mutation|December 24, 2002
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1Kathrin Huehne, Vladimir Benes, Christian Thiel, et al.Pageof 2