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Corticosteroids for the treatment of Duchenne muscular dystrophy.
Matthews E, Brassington R, Kuntzer T, Jichi F, Manzur AY. Matthews E, et al. Among authors: kuntzer t. Cochrane Database Syst Rev. 2016 May 5;2016(5):CD003725. doi: 10.1002/14651858.CD003725.pub4. Cochrane Database Syst Rev. 2016. PMID: 27149418 Free PMC article. Review.
Glucocorticoid corticosteroids for Duchenne muscular dystrophy.
Manzur AY, Kuntzer T, Pike M, Swan A. Manzur AY, et al. Among authors: kuntzer t. Cochrane Database Syst Rev. 2004;(2):CD003725. doi: 10.1002/14651858.CD003725.pub2. Cochrane Database Syst Rev. 2004. PMID: 15106215 Updated. Review.
Glucocorticoid corticosteroids for Duchenne muscular dystrophy.
Manzur AY, Kuntzer T, Pike M, Swan A. Manzur AY, et al. Among authors: kuntzer t. Cochrane Database Syst Rev. 2008 Jan 23;(1):CD003725. doi: 10.1002/14651858.CD003725.pub3. Cochrane Database Syst Rev. 2008. PMID: 18254031 Updated. Review.
Marked hemiatrophy in carriers of Duchenne muscular dystrophy.
Rajakulendran S, Kuntzer T, Dunand M, Yau SC, Ashton EJ, Storey H, McCauley J, Abbs S, Thonney F, Leturcq F, Lobrinus JA, Yousry T, Farmer S, Holton JL, Hanna MG. Rajakulendran S, et al. Among authors: kuntzer t. Arch Neurol. 2010 Apr;67(4):497-500. doi: 10.1001/archneurol.2010.58. Arch Neurol. 2010. PMID: 20385919 Free article.
Acetylcholinesterase inhibitor treatment for myasthenia gravis.
Mehndiratta MM, Pandey S, Kuntzer T. Mehndiratta MM, et al. Among authors: kuntzer t. Cochrane Database Syst Rev. 2011 Feb 16;(2):CD006986. doi: 10.1002/14651858.CD006986.pub2. Cochrane Database Syst Rev. 2011. PMID: 21328290 Updated. Review.
Acetylcholinesterase inhibitor treatment for myasthenia gravis.
Mehndiratta MM, Pandey S, Kuntzer T. Mehndiratta MM, et al. Among authors: kuntzer t. Cochrane Database Syst Rev. 2014 Oct 13;2014(10):CD006986. doi: 10.1002/14651858.CD006986.pub3. Cochrane Database Syst Rev. 2014. PMID: 25310725 Free PMC article. Review.
Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study.
Salort-Campana E, Nguyen K, Bernard R, Jouve E, Solé G, Nadaj-Pakleza A, Niederhauser J, Charles E, Ollagnon E, Bouhour F, Sacconi S, Echaniz-Laguna A, Desnuelle C, Tranchant C, Vial C, Magdinier F, Bartoli M, Arne-Bes MC, Ferrer X, Kuntzer T, Levy N, Pouget J, Attarian S. Salort-Campana E, et al. Among authors: kuntzer t. Orphanet J Rare Dis. 2015 Jan 21;10:2. doi: 10.1186/s13023-014-0218-1. Orphanet J Rare Dis. 2015. PMID: 25603992 Free PMC article.
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients.
Molenaar JP, Verhoeven JI, Rodenburg RJ, Kamsteeg EJ, Erasmus CE, Vicart S, Behin A, Bassez G, Magot A, Péréon Y, Brandom BW, Guglielmi V, Vattemi G, Chevessier F, Mathieu J, Franques J, Suetterlin K, Hanna MG, Guyant-Marechal L, Snoeck MM, Roberts ME, Kuntzer T, Fernandez-Torron R, Martínez-Arroyo A, Seeger J, Kusters B, Treves S, van Engelen BG, Eymard B, Voermans NC, Sternberg D. Molenaar JP, et al. Among authors: kuntzer t. Brain. 2020 Feb 1;143(2):452-466. doi: 10.1093/brain/awz410. Brain. 2020. PMID: 32040565 Free PMC article.
[Statins and muscular side-effects].
Brosteaux C, Ruiz J, Buclin T, Kuntzer T, Rodondi N. Brosteaux C, et al. Among authors: kuntzer t. Rev Med Suisse. 2010 Mar 10;6(239):510, 512-4, 516-7. Rev Med Suisse. 2010. PMID: 20373698 Review. French.
Sporadic late-onset nemaline myopathy with MGUS: long-term follow-up after melphalan and SCT.
Voermans NC, Benveniste O, Minnema MC, Lokhorst H, Lammens M, Meersseman W, Delforge M, Kuntzer T, Novy J, Pabst T, Bouhour F, Romero N, Leblond V, Bergh Pv, Vekemans MC, van Engelen BG, Eymard B. Voermans NC, et al. Among authors: kuntzer t. Neurology. 2014 Dec 2;83(23):2133-9. doi: 10.1212/WNL.0000000000001047. Epub 2014 Nov 5. Neurology. 2014. PMID: 25378674 Free article.
250 results