Mortier W - Search Results

1

Relating pore structure to activity at the subcrystal level for ZSM-5: an electron backscattering diffraction and fluorescence microscopy study.

Roeffaers MB, Ameloot R, Bons AJ, Mortier W, De Cremer G, de Kloe R, Hofkens J, De Vos DE, Sels BF. Roeffaers MB, et al. Among authors: mortier w. J Am Chem Soc. 2008 Oct 15;130(41):13516-7. doi: 10.1021/ja8048767. Epub 2008 Sep 19. J Am Chem Soc. 2008. PMID: 18800795

2

H.R.E.M. on intergrowths of cubic and hexagonal faujasite.

Bons AJ, Lievens JL, Verduijn JP, Mortier WJ. Bons AJ, et al. Among authors: mortier wj. Microsc Res Tech. 1993 Jun 1;25(2):175-6. doi: 10.1002/jemt.1070250211. Microsc Res Tech. 1993. PMID: 8390875 No abstract available.

3

The use of global and local molecular parameters for the analysis of the gas-phase basicity of amines.

Yang W, Mortier WJ. Yang W, et al. Among authors: mortier wj. J Am Chem Soc. 1986 Sep 1;108(19):5708-11. doi: 10.1021/ja00279a008. J Am Chem Soc. 1986. PMID: 22175316 No abstract available.

4

Quick scheme for evaluation of atomic charges in arbitrary aluminophosphate sieves on the basis of electron densities calculated with DFT methods.

Larin AV, Mortier WJ, Vercauteren DP. Larin AV, et al. Among authors: mortier wj. J Comput Chem. 2007 Jul 30;28(10):1695-703. doi: 10.1002/jcc.20660. J Comput Chem. 2007. PMID: 17342708

5

[Neuromuscular diseases 2: muscular dystrophies (MD)].

Schara U, Mortier W. Schara U, et al. Among authors: mortier w. Nervenarzt. 2005 Feb;76(2):219-37; quiz 238-9. doi: 10.1007/s00115-004-1847-8. Nervenarzt. 2005. PMID: 16092148 Review. German.

6

[Neuromuscular diseases (NME). I. Spinal muscular atrophy, peripheral nerve diseases, congenital myasthenia gravis].

Schara U, Mortier W. Schara U, et al. Among authors: mortier w. Nervenarzt. 2004 Dec;75(12):1231-45; quiz 1246-7. doi: 10.1007/s00115-004-1846-9. Nervenarzt. 2004. PMID: 15756726 Review. German.

7

A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome.

Müller JS, Abicht A, Christen HJ, Stucka R, Schara U, Mortier W, Huebner A, Lochmüller H. Müller JS, et al. Among authors: mortier w. Neuromuscul Disord. 2004 Nov;14(11):744-9. doi: 10.1016/j.nmd.2004.06.010. Neuromuscul Disord. 2004. PMID: 15482960

8

Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.

Arning L, Jagiello P, Schara U, Vorgerd M, Dahmen N, Gencikova A, Mortier W, Epplen JT, Gencik M. Arning L, et al. Among authors: mortier w. J Neurol. 2004 Jan;251(1):72-8. doi: 10.1007/s00415-004-0274-x. J Neurol. 2004. PMID: 14999492

9

Severe mucous membrane involvement in epidermolysis bullosa simplex with muscular dystrophy due to a novel plectin gene mutation.

Schara U, Tücke J, Mortier W, Nüsslein T, Rouan F, Pfendner E, Zillikens D, Bruckner-Tuderman L, Uitto J, Wiche G, Schröder R. Schara U, et al. Among authors: mortier w. Eur J Pediatr. 2004 Apr;163(4-5):218-22. doi: 10.1007/s00431-004-1410-4. Epub 2004 Feb 13. Eur J Pediatr. 2004. PMID: 14963703

10

Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patients.

Müller JS, Mildner G, Müller-Felber W, Schara U, Krampfl K, Petersen B, Petrova S, Stucka R, Mortier W, Bufler J, Kurlemann G, Huebner A, Merlini L, Lochmüller H, Abicht A. Müller JS, et al. Among authors: mortier w. Neurology. 2003 Jun 10;60(11):1805-10. doi: 10.1212/01.wnl.0000072262.14931.80. Neurology. 2003. PMID: 12796535

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