Schmidt C - Search Results

1

Morar B, Gresham D, Angelicheva D, Tournev I, Gooding R, Guergueltcheva V, Schmidt C, Abicht A, Lochmuller H, Tordai A, Kalmar L, Nagy M, Karcagi V, Jeanpierre M, Herczegfalvi A, Beeson D, Venkataraman V, Warwick Carter K, Reeve J, de Pablo R, Kucinskas V, Kalaydjieva L. Morar B, et al. Among authors: schmidt c. Am J Hum Genet. 2004 Oct;75(4):596-609. doi: 10.1086/424759. Epub 2004 Aug 20. Am J Hum Genet. 2004. PMID: 15322984 Free PMC article.

2

Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase.

Schmidt C, Abicht A, Krampfl K, Voss W, Stucka R, Mildner G, Petrova S, Schara U, Mortier W, Bufler J, Huebner A, Lochmüller H. Schmidt C, et al. Neuromuscul Disord. 2003 Mar;13(3):245-51. doi: 10.1016/s0960-8966(02)00273-0. Neuromuscul Disord. 2003. PMID: 12609506

3

Congenital myasthenic syndrome (CMS) in three European kinships due to a novel splice mutation (IVS7 - 2 A/G) in the epsilon acetylcholine receptor (AChR) subunit gene.

Barisic N, Schmidt C, Sidorova OP, Herczegfalvi A, Gekht BM, Song IH, Stucka R, Karcagi V, Abicht A, Lochmüller H. Barisic N, et al. Among authors: schmidt c. Neuropediatrics. 2002 Oct;33(5):249-54. doi: 10.1055/s-2002-36738. Neuropediatrics. 2002. PMID: 12536367

4

A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome.

Abicht A, Stucka R, Schmidt C, Briguet A, Höpfner S, Song IH, Pongratz D, Müller-Felber W, Ruegg MA, Lochmüller H. Abicht A, et al. Among authors: schmidt c. Brain. 2002 May;125(Pt 5):1005-13. doi: 10.1093/brain/awf095. Brain. 2002. PMID: 11960891

5

An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome.

Müller JS, Stucka R, Neudecker S, Zierz S, Schmidt C, Huebner A, Lochmüller H, Abicht A. Müller JS, et al. Among authors: schmidt c. Neurology. 2005 Aug 9;65(3):463-5. doi: 10.1212/01.wnl.0000172346.26219.fd. Neurology. 2005. PMID: 16087917

6

Variable reduction of caveolin-3 in patients with LGMD2B/MM.

Walter MC, Braun C, Vorgerd M, Poppe M, Thirion C, Schmidt C, Schreiber H, Knirsch UI, Brummer D, Müller-Felber W, Pongratz D, Müller-Höcker J, Huebner A, Lochmüller H. Walter MC, et al. Among authors: schmidt c. J Neurol. 2003 Dec;250(12):1431-8. doi: 10.1007/s00415-003-0234-x. J Neurol. 2003. PMID: 14673575

7

Long-term relaxation of orientational disorder and structural modifications in molecular nitrogen at high pressure.

Tschauner O, Navon O, Schmidt C, Wirth R, Weiss Y, Kempe Y, Remennik S, Liu W, Chariton S, Prakapenka VB. Tschauner O, et al. Among authors: schmidt c. J Chem Phys. 2024 Nov 28;161(20):204506. doi: 10.1063/5.0219186. J Chem Phys. 2024. PMID: 39601284

8

Praziquantel and factor H recruitment differentially affect the susceptibility of Schistosoma mansoni to complement-mediated damage.

van Beek AE, Jeanguenat H, Häberli C, Pouw RB, Lamers C, Pál G, Gál P, Schmidt CQ, Ricklin D, Keiser J. van Beek AE, et al. Among authors: schmidt cq. Front Immunol. 2024 Nov 12;15:1474358. doi: 10.3389/fimmu.2024.1474358. eCollection 2024. Front Immunol. 2024. PMID: 39600706 Free PMC article.

9

Ten Americas: a systematic analysis of life expectancy disparities in the USA.

Dwyer-Lindgren L, Baumann MM, Li Z, Kelly YO, Schmidt C, Searchinger C, La Motte-Kerr W, Bollyky TJ, Mokdad AH, Murray CJ. Dwyer-Lindgren L, et al. Among authors: schmidt c. Lancet. 2024 Nov 19:S0140-6736(24)01495-8. doi: 10.1016/S0140-6736(24)01495-8. Online ahead of print. Lancet. 2024. PMID: 39581204 Free article.

10

Granular Nanofiber-Hydrogel Composite-Programmed Regenerative Inflammation and Adipose Tissue Formation.

Kong J, Yao ZC, Stelzel JL, Yang YH, Chen J, Feng H, Schmidt C, Zhang C, Krishnan K, Chen L, Pan J, Ding K, Zhu Y, Li X, Doloff JC, Mao HQ, Reddy SK. Kong J, et al. Among authors: schmidt c. Adv Healthc Mater. 2024 Nov 24:e2403094. doi: 10.1002/adhm.202403094. Online ahead of print. Adv Healthc Mater. 2024. PMID: 39580666

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