Bulst S - Search Results

Year	Number of Results
2007	1
2009	3
2010	3
2011	1
2012	1
2013	1
2014	2
2017	2
2018	1
2025	0

1

A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature.

Brusa R, Magri F, Papadimitriou D, Govoni A, Del Bo R, Ciscato P, Savarese M, Cinnante C, Walter MC, Abicht A, Bulst S, Corti S, Moggio M, Bresolin N, Nigro V, Comi GP. Brusa R, et al. Among authors: bulst s. Neuromuscul Disord. 2018 Jun;28(6):532-537. doi: 10.1016/j.nmd.2018.04.006. Epub 2018 Apr 13. Neuromuscul Disord. 2018. PMID: 29759638 Review.

2

Novel TPM3 mutation in a family with cap myopathy and review of the literature.

Schreckenbach T, Schröder JM, Voit T, Abicht A, Neuen-Jacob E, Roos A, Bulst S, Kuhl C, Schulz JB, Weis J, Claeys KG. Schreckenbach T, et al. Among authors: bulst s. Neuromuscul Disord. 2014 Feb;24(2):117-24. doi: 10.1016/j.nmd.2013.10.002. Epub 2013 Oct 23. Neuromuscul Disord. 2014. PMID: 24239060 Review.

3

Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient.

Ikenberg E, Karin I, Ertl-Wagner B, Abicht A, Bulst S, Krause S, Schoser B, Reilich P, Walter MC. Ikenberg E, et al. Among authors: bulst s. Neuromuscul Disord. 2017 Sep;27(9):856-860. doi: 10.1016/j.nmd.2017.05.017. Epub 2017 Jun 1. Neuromuscul Disord. 2017. PMID: 28666572

4

In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletion.

Bulst S, Holinski-Feder E, Payne B, Abicht A, Krause S, Lochmüller H, Chinnery PF, Walter MC, Horvath R. Bulst S, et al. Mol Genet Metab. 2012 Sep;107(1-2):95-103. doi: 10.1016/j.ymgme.2012.04.022. Epub 2012 May 3. Mol Genet Metab. 2012. PMID: 22608879 Free PMC article.

5

Divergent molecular effects of desmin mutations on protein assembly in myofibrillar myopathy.

Levin J, Bulst S, Thirion C, Schmidt F, Bötzel K, Krause S, Pertl C, Kretzschmar H, Walter MC, Giese A, Lochmüller H. Levin J, et al. Among authors: bulst s. J Neuropathol Exp Neurol. 2010 Apr;69(4):415-24. doi: 10.1097/NEN.0b013e3181d71305. J Neuropathol Exp Neurol. 2010. PMID: 20448486

6

Polymerase γ gene POLG determines the risk of sodium valproate-induced liver toxicity.

Stewart JD, Horvath R, Baruffini E, Ferrero I, Bulst S, Watkins PB, Fontana RJ, Day CP, Chinnery PF. Stewart JD, et al. Among authors: bulst s. Hepatology. 2010 Nov;52(5):1791-6. doi: 10.1002/hep.23891. Hepatology. 2010. PMID: 21038416 Free PMC article.

7

Novel ETFDH mutation and imaging findings in an adult with glutaric aciduria type II.

Rosenbohm A, Süssmuth SD, Kassubek J, Müller HP, Pontes C, Abicht A, Bulst S, Ludolph AC, Pinkhardt E. Rosenbohm A, et al. Among authors: bulst s. Muscle Nerve. 2014 Mar;49(3):446-50. doi: 10.1002/mus.23979. Epub 2014 Jan 31. Muscle Nerve. 2014. PMID: 23893693

8

Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2.

Walter MC, Czermin B, Muller-Ziermann S, Bulst S, Stewart JD, Hudson G, Schneiderat P, Abicht A, Holinski-Feder E, Lochmüller H, Chinnery PF, Klopstock T, Horvath R. Walter MC, et al. Among authors: bulst s. J Neurol. 2010 Sep;257(9):1517-23. doi: 10.1007/s00415-010-5565-9. Epub 2010 Apr 20. J Neurol. 2010. PMID: 20405137

9

In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes.

Bulst S, Abicht A, Holinski-Feder E, Müller-Ziermann S, Koehler U, Thirion C, Walter MC, Stewart JD, Chinnery PF, Lochmüller H, Horvath R. Bulst S, et al. Hum Mol Genet. 2009 May 1;18(9):1590-9. doi: 10.1093/hmg/ddp074. Epub 2009 Feb 16. Hum Mol Genet. 2009. PMID: 19221117

10

Add-on salmeterol compared to double dose fluticasone in pediatric asthma: a double-blind, randomized trial (VIAPAED).

Gappa M, Zachgo W, von Berg A, Kamin W, Stern-Sträter C, Steinkamp G; VIAPAED Study Group. Gappa M, et al. Pediatr Pulmonol. 2009 Nov;44(11):1132-42. doi: 10.1002/ppul.21120. Pediatr Pulmonol. 2009. PMID: 19824054 Clinical Trial.

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