Pestronk A - Search Results

1

Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.

Cady J, Allred P, Bali T, Pestronk A, Goate A, Miller TM, Mitra RD, Ravits J, Harms MB, Baloh RH. Cady J, et al. Among authors: pestronk a. Ann Neurol. 2015 Jan;77(1):100-13. doi: 10.1002/ana.24306. Epub 2014 Nov 27. Ann Neurol. 2015. PMID: 25382069 Free PMC article.

2

Peripheral neuropathy in an outpatient cohort of patients with Sjögren's syndrome.

Lopate G, Pestronk A, Al-Lozi M, Lynch T, Florence J, Miller T, Levine T, Rampy T, Beson B, Ramneantu I. Lopate G, et al. Among authors: pestronk a. Muscle Nerve. 2006 May;33(5):672-6. doi: 10.1002/mus.20514. Muscle Nerve. 2006. PMID: 16453296

3

Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations.

Baloh RH, Schmidt RE, Pestronk A, Milbrandt J. Baloh RH, et al. Among authors: pestronk a. J Neurosci. 2007 Jan 10;27(2):422-30. doi: 10.1523/JNEUROSCI.4798-06.2007. J Neurosci. 2007. PMID: 17215403 Free PMC article.

4

Frequent atrophic groups with mixed-type myofibers is distinctive to motor neuron syndromes.

Baloh RH, Rakowicz W, Gardner R, Pestronk A. Baloh RH, et al. Among authors: pestronk a. Muscle Nerve. 2007 Jul;36(1):107-10. doi: 10.1002/mus.20755. Muscle Nerve. 2007. PMID: 17299742

5

Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle.

Baloh RH, Salavaggione E, Milbrandt J, Pestronk A. Baloh RH, et al. Among authors: pestronk a. Arch Neurol. 2007 Jul;64(7):998-1000. doi: 10.1001/archneur.64.7.998. Arch Neurol. 2007. PMID: 17620490

6

TDP-43 A315T mutation in familial motor neuron disease.

Gitcho MA, Baloh RH, Chakraverty S, Mayo K, Norton JB, Levitch D, Hatanpaa KJ, White CL 3rd, Bigio EH, Caselli R, Baker M, Al-Lozi MT, Morris JC, Pestronk A, Rademakers R, Goate AM, Cairns NJ. Gitcho MA, et al. Among authors: pestronk a. Ann Neurol. 2008 Apr;63(4):535-8. doi: 10.1002/ana.21344. Epub 2008 Feb 20. Ann Neurol. 2008. PMID: 18288693 Free PMC article.

7

Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III.

Kaufmann P, Thompson JL, Levy G, Buchsbaum R, Shefner J, Krivickas LS, Katz J, Rollins Y, Barohn RJ, Jackson CE, Tiryaki E, Lomen-Hoerth C, Armon C, Tandan R, Rudnicki SA, Rezania K, Sufit R, Pestronk A, Novella SP, Heiman-Patterson T, Kasarskis EJ, Pioro EP, Montes J, Arbing R, Vecchio D, Barsdorf A, Mitsumoto H, Levin B; QALS Study Group. Kaufmann P, et al. Among authors: pestronk a. Ann Neurol. 2009 Aug;66(2):235-44. doi: 10.1002/ana.21743. Ann Neurol. 2009. PMID: 19743457 Free PMC article. Clinical Trial.

8

Novel GNE mutations in two phenotypically distinct HIBM2 patients.

Weihl CC, Miller SE, Zaidman CM, Pestronk A, Baloh RH, Al-Lozi M. Weihl CC, et al. Among authors: pestronk a. Neuromuscul Disord. 2011 Feb;21(2):102-5. doi: 10.1016/j.nmd.2010.11.002. Epub 2010 Dec 4. Neuromuscul Disord. 2011. PMID: 21131200 Free PMC article.

9

Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy.

Harms MB, Sommerville RB, Allred P, Bell S, Ma D, Cooper P, Lopate G, Pestronk A, Weihl CC, Baloh RH. Harms MB, et al. Among authors: pestronk a. Ann Neurol. 2012 Mar;71(3):407-16. doi: 10.1002/ana.22683. Epub 2012 Feb 14. Ann Neurol. 2012. PMID: 22334415 Free PMC article.

10

Multifocal radiculoneuropathy during ipilimumab treatment of melanoma.

Manousakis G, Koch J, Sommerville RB, El-Dokla A, Harms MB, Al-Lozi MT, Schmidt RE, Pestronk A. Manousakis G, et al. Among authors: pestronk a. Muscle Nerve. 2013 Sep;48(3):440-4. doi: 10.1002/mus.23830. Epub 2013 Jul 27. Muscle Nerve. 2013. PMID: 23447136

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