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Results: 1 to 20 of 264

1.

Phenotype of matrin-3-related distal myopathy in 16 German patients.

Müller TJ, Kraya T, Stoltenburg-Didinger G, Hanisch F, Kornhuber M, Stoevesandt D, Senderek J, Weis J, Baum P, Deschauer M, Zierz S.

Ann Neurol. 2014 Aug 26. doi: 10.1002/ana.24255. [Epub ahead of print]

PMID:
25154462
[PubMed - as supplied by publisher]
2.

SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions.

Hanisch F, Kornhuber M, Alston CL, Taylor RW, Deschauer M, Zierz S.

J Neurol Neurosurg Psychiatry. 2014 Aug 20. pii: jnnp-2013-306748. doi: 10.1136/jnnp-2013-306748. [Epub ahead of print]

PMID:
25143630
[PubMed - as supplied by publisher]
3.

Electrical human motor nerve stimulation by Johann Christian Reil in 1792.

Kornhuber ME, Zierz S.

Muscle Nerve. 2014 Jun;49(6):931-2. doi: 10.1002/mus.24200. Epub 2014 Apr 8. No abstract available.

PMID:
24715478
[PubMed - indexed for MEDLINE]
4.

Normal protein content but abnormally inhibited enzyme activity in muscle carnitine palmitoyltransferase II deficiency.

Lehmann D, Zierz S.

J Neurol Sci. 2014 Apr 15;339(1-2):183-8. doi: 10.1016/j.jns.2014.02.011. Epub 2014 Feb 20.

PMID:
24602495
[PubMed - in process]
5.

[Reply].

Pitz S, Jordan B, Zierz S.

Ophthalmologe. 2013 Dec;110(12):1202. German. No abstract available.

PMID:
24482815
[PubMed - in process]
6.

Carnitine palmitoyltransferase II (CPT II) deficiency: genotype-phenotype analysis of 50 patients.

Joshi PR, Deschauer M, Zierz S.

J Neurol Sci. 2014 Mar 15;338(1-2):107-11. doi: 10.1016/j.jns.2013.12.026. Epub 2013 Dec 23.

PMID:
24398345
[PubMed - in process]
7.

The significance of pathological spontaneous activity in various myopathies.

Hanisch F, Kronenberger C, Zierz S, Kornhuber M.

Clin Neurophysiol. 2014 Jul;125(7):1485-90. doi: 10.1016/j.clinph.2013.11.021. Epub 2013 Dec 2.

PMID:
24370491
[PubMed - in process]
8.

Sialylation and muscle performance: sialic acid is a marker of muscle ageing.

Hanisch F, Weidemann W, Großmann M, Joshi PR, Holzhausen HJ, Stoltenburg G, Weis J, Zierz S, Horstkorte R.

PLoS One. 2013 Dec 11;8(12):e80520. doi: 10.1371/journal.pone.0080520. eCollection 2013.

PMID:
24349002
[PubMed - in process]
Free PMC Article
9.

Distal myopathies: from clinical classification to molecular understanding.

Kraya T, Zierz S.

J Neural Transm. 2013 Sep;120 Suppl 1:S3-7. doi: 10.1007/s00702-013-1058-1. Epub 2013 Jul 11. Review.

PMID:
23842731
[PubMed - indexed for MEDLINE]
10.

[Treatability of sporadic late onset nemaline myopathy].

Hanisch F, Schneider I, Müller T, Romeike BF, Stoltenburg G, Holzhausen HJ, Zierz S.

Nervenarzt. 2013 Aug;84(8):955-61. doi: 10.1007/s00115-013-3825-5. Review. German.

PMID:
23836301
[PubMed - indexed for MEDLINE]
11.

[Ocular myasthenia gravis].

Pitz S, Jordan B, Zierz S.

Ophthalmologe. 2013 May;110(5):471-80; quiz 481-2. doi: 10.1007/s00347-013-2833-y. German.

PMID:
23670841
[PubMed - indexed for MEDLINE]
12.

Diagnostic impact of myotonic discharges in myofibrillar myopathies.

Hanisch F, Kraya T, Kornhuber M, Zierz S.

Muscle Nerve. 2013 Jun;47(6):845-8. doi: 10.1002/mus.23716. Epub 2013 Apr 21.

PMID:
23605961
[PubMed - indexed for MEDLINE]
13.

Expanding mutation spectrum in CPT II gene: identification of four novel mutations.

Joshi PR, Young P, Deschauer M, Zierz S.

J Neurol. 2013 May;260(5):1412-4. doi: 10.1007/s00415-013-6887-1. Epub 2013 Mar 9. No abstract available.

PMID:
23475205
[PubMed - indexed for MEDLINE]
14.

[Myofibrillary myopathy due to the ZASP mutation Ala147Thr : two cases with exclusively distal leg involvement].

Kraya T, Kress W, Stoevesant D, Deschauer M, Zierz S.

Nervenarzt. 2013 Feb;84(2):209-13. doi: 10.1007/s00115-012-3689-0. German.

PMID:
23263837
[PubMed - indexed for MEDLINE]
15.

Clinically symptomatic heterozygous carnitine palmitoyltransferase II (CPT II) deficiency.

Joshi PR, Deschauer M, Zierz S.

Wien Klin Wochenschr. 2012 Dec;124(23-24):851-4. doi: 10.1007/s00508-012-0296-9. Epub 2012 Nov 27.

PMID:
23184072
[PubMed - indexed for MEDLINE]
16.

Respiratory function in late-onset Pompe disease patients receiving long-term enzyme replacement therapy for more than 48 months.

Schneider I, Hanisch F, Müller T, Schmidt B, Zierz S.

Wien Med Wochenschr. 2013 Jan;163(1-2):40-4. doi: 10.1007/s10354-012-0153-5. Epub 2012 Nov 19.

PMID:
23160972
[PubMed - indexed for MEDLINE]
17.

Hirayama disease is a pure spinal motor neuron disorder--a combined DTI and transcranial magnetic stimulation study.

Boelmans K, Kaufmann J, Schmelzer S, Vielhaber S, Kornhuber M, Münchau A, Zierz S, Gaul C.

J Neurol. 2013 Feb;260(2):540-8. doi: 10.1007/s00415-012-6674-4. Epub 2012 Sep 25.

PMID:
23007195
[PubMed - indexed for MEDLINE]
18.

A randomized, double blind, placebo-controlled trial of pioglitazone in combination with riluzole in amyotrophic lateral sclerosis.

Dupuis L, Dengler R, Heneka MT, Meyer T, Zierz S, Kassubek J, Fischer W, Steiner F, Lindauer E, Otto M, Dreyhaupt J, Grehl T, Hermann A, Winkler AS, Bogdahn U, Benecke R, Schrank B, Wessig C, Grosskreutz J, Ludolph AC; GERP ALS Study Group.

PLoS One. 2012;7(6):e37885. doi: 10.1371/journal.pone.0037885. Epub 2012 Jun 8.

PMID:
22715372
[PubMed - in process]
Free PMC Article
19.

C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis.

Deschauer M, Gaul C, Behrmann C, Prokisch H, Zierz S, Haack TB.

J Neurol. 2012 Nov;259(11):2434-9. doi: 10.1007/s00415-012-6521-7. Epub 2012 May 15.

PMID:
22584950
[PubMed - indexed for MEDLINE]
20.

Unusual manifestations in two cases of necrotizing myopathy associated with SRP-antibodies.

Hanisch F, Müller T, Stoltenburg G, Zierz S.

Clin Neurol Neurosurg. 2012 Sep;114(7):1104-6. doi: 10.1016/j.clineuro.2011.12.055. Epub 2012 Feb 3.

PMID:
22306424
[PubMed - indexed for MEDLINE]

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