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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2003 3
2004 1
2005 1
2006 1
2007 18
2008 3
2009 5
2010 2
2011 1
2012 1
2024 0

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37 results

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Page 1
Phenotypic variability in giant axonal neuropathy.
Tazir M, Nouioua S, Magy L, Huehne K, Assami S, Urtizberea A, Grid D, Hamadouche T, Rautenstrauss B, Vallat JM. Tazir M, et al. Among authors: huehne k. Neuromuscul Disord. 2009 Apr;19(4):270-4. doi: 10.1016/j.nmd.2009.01.011. Epub 2009 Feb 23. Neuromuscul Disord. 2009. PMID: 19231187
A novel myosin heavy chain gene in human chromosome 19q13.3.
Leal A, Endele S, Stengel C, Huehne K, Loetterle J, Barrantes R, Winterpacht A, Rautenstrauss B. Leal A, et al. Among authors: huehne k. Gene. 2003 Jul 17;312:165-71. doi: 10.1016/s0378-1119(03)00613-9. Gene. 2003. PMID: 12909352
Mutations in the LMNA gene do not cause axonal CMT in Czech patients.
Lassuthová P, Baránková L, Haberlová J, Mazanec R, Wallace A, Huehne K, Rautenstrauss B, Seeman P. Lassuthová P, et al. Among authors: huehne k. J Hum Genet. 2009 Jun;54(6):365-8. doi: 10.1038/jhg.2009.43. Epub 2009 May 8. J Hum Genet. 2009. PMID: 19424285
Identification of Alu elements mediating a partial PMP22 deletion.
Matejas V, Huehne K, Thiel C, Sommer C, Jakubiczka S, Rautenstrauss B. Matejas V, et al. Among authors: huehne k. Neurogenetics. 2006 May;7(2):119-26. doi: 10.1007/s10048-006-0030-8. Epub 2006 Mar 29. Neurogenetics. 2006. PMID: 16570190
Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis.
Huehne K, Zweier C, Raab K, Odent S, Bonnaure-Mallet M, Sixou JL, Landrieu P, Goizet C, Sarlangue J, Baumann M, Eggermann T, Rauch A, Ruppert S, Stettner GM, Rautenstrauss B. Huehne K, et al. Neuromuscul Disord. 2008 Feb;18(2):159-66. doi: 10.1016/j.nmd.2007.10.005. Epub 2008 Feb 20. Neuromuscul Disord. 2008. PMID: 18077166
37 results