Udd B - Search Results

1

Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy.

Pareyson D, Fratta P, Pradat PF, Sorarù G, Finsterer J, Vissing J, Jokela ME, Udd B, Ludolph AC, Sagnelli A, Weydt P. Pareyson D, et al. Among authors: udd b. J Mol Neurosci. 2016 Mar;58(3):394-400. doi: 10.1007/s12031-015-0704-5. Epub 2016 Jan 7. J Mol Neurosci. 2016. PMID: 26744358

2

Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia.

Lund A, Udd B, Juvonen V, Andersen PM, Cederquist K, Ronnevi LO, Sistonen P, Sörensen SA, Tranebjaerg L, Wallgren-Pettersson C, Savontaus ML. Lund A, et al. Among authors: udd b. Eur J Hum Genet. 2000 Aug;8(8):631-6. doi: 10.1038/sj.ejhg.5200517. Eur J Hum Genet. 2000. PMID: 10951525

3

Late-onset lower motor neuronopathy: a new autosomal dominant disorder.

Jokela M, Penttilä S, Huovinen S, Hackman P, Saukkonen AM, Toivanen J, Udd B. Jokela M, et al. Among authors: udd b. Neurology. 2011 Jul 26;77(4):334-40. doi: 10.1212/WNL.0b013e3182267b71. Epub 2011 Jun 29. Neurology. 2011. PMID: 21715705

4

Double trouble: spinal muscular atrophy type II and seropositive myasthenia gravis in the same patient.

Jokela M, Udd B, Päivärinta M. Jokela M, et al. Among authors: udd b. Neuromuscul Disord. 2012 Feb;22(2):129-30. doi: 10.1016/j.nmd.2011.07.011. Epub 2011 Aug 20. Neuromuscul Disord. 2012. PMID: 21862330

5

Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2.

Penttilä S, Jokela M, Hackman P, Maija Saukkonen A, Toivanen J, Udd B. Penttilä S, et al. Among authors: udd b. Eur J Hum Genet. 2012 Nov;20(11):1193-6. doi: 10.1038/ejhg.2012.76. Epub 2012 Apr 25. Eur J Hum Genet. 2012. PMID: 22535186 Free PMC article.

6

[The expanding spectrum of LGMD--recently discovered disease genes are important also in Finnish patients].

Jokela M, Palmio J, Sandell S, Penttilä S, Suominen T, Udd B. Jokela M, et al. Among authors: udd b. Duodecim. 2013;129(19):2011-20. Duodecim. 2013. PMID: 24218732 Finnish.

7

Late-onset spinal motor neuronopathy - a common form of dominant SMA.

Penttilä S, Jokela M, Huovinen S, Saukkonen AM, Toivanen J, Lindberg C, Baumann P, Udd B. Penttilä S, et al. Among authors: udd b. Neuromuscul Disord. 2014 Mar;24(3):259-68. doi: 10.1016/j.nmd.2013.11.010. Epub 2013 Nov 26. Neuromuscul Disord. 2014. PMID: 24360573

8

Late onset spinal motor neuronopathy is caused by mutation in CHCHD10.

Penttilä S, Jokela M, Bouquin H, Saukkonen AM, Toivanen J, Udd B. Penttilä S, et al. Among authors: udd b. Ann Neurol. 2015 Jan;77(1):163-72. doi: 10.1002/ana.24319. Epub 2014 Dec 12. Ann Neurol. 2015. PMID: 25428574

9

Spontaneous activity in electromyography may differentiate certain benign lower motor neuron disease forms from amyotrophic lateral sclerosis.

Jokela ME, Jääskeläinen SK, Sandell S, Palmio J, Penttilä S, Saukkonen A, Soikkeli R, Udd B. Jokela ME, et al. Among authors: udd b. J Neurol Sci. 2015 Aug 15;355(1-2):143-6. doi: 10.1016/j.jns.2015.06.002. Epub 2015 Jun 3. J Neurol Sci. 2015. PMID: 26059445

10

Reply: To PMID 25428574.

Jokela M, Penttilä S, Udd B. Jokela M, et al. Among authors: udd b. Ann Neurol. 2015 Nov;78(5):831-2. doi: 10.1002/ana.24465. Epub 2015 Aug 31. Ann Neurol. 2015. PMID: 26095158 No abstract available.

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