Schraen-Maschke S - Search Results

1

[Biological markers in Alzheimer disease: what are the chances for less slow diagnosis?].

Schraen-Maschke S, Dhaenens CM, Bombois S, Deramecourt V, Van Brussel E, Obriot H, Marzys C, Sergeant N, Maurage CA, Pasquier F, Sablonnière B, Buée L. Schraen-Maschke S, et al. Rev Neurol (Paris). 2009 Apr;165 Spec No 2:F97-103. Rev Neurol (Paris). 2009. PMID: 19593884 Review. French. No abstract available.

2

Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.

Schraen-Maschke S, Brique S, Chartier-Harlin MC, Brique E, Destée A, Sablonnière B. Schraen-Maschke S, et al. Am J Med Genet. 1999 Dec 15;88(6):738-41. Am J Med Genet. 1999. PMID: 10581499

3

Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype.

Vuillaume I, Meynieu P, Schraen-Maschke S, Destée A, Sablonnière B. Vuillaume I, et al. J Neurol Neurosurg Psychiatry. 2000 May;68(5):672-5. doi: 10.1136/jnnp.68.5.672. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766906 Free PMC article.

4

[Triplet expansion diseases].

Sablonnière B, Vuillaume I, Schraen-Maschke S. Sablonnière B, et al. Ann Biol Clin (Paris). 2000 May-Jun;58(3):356-60. Ann Biol Clin (Paris). 2000. PMID: 10846241 Free article. Review. French. No abstract available.

5

The first identified French family with dentatorubral-pallidoluysian atrophy.

Destée A, Delalande I, Vuillaume I, Schraen-Maschke S, Defebvre L, Sablonnière B. Destée A, et al. Mov Disord. 2000 Sep;15(5):996-9. doi: 10.1002/1531-8257(200009)15:5<996::aid-mds1036>3.0.co;2-9. Mov Disord. 2000. PMID: 11009212

6

Clinical features and genetic analysis of a new form of spinocerebellar ataxia.

Devos D, Schraen-Maschke S, Vuillaume I, Dujardin K, Nazé P, Willoteaux C, Destée A, Sablonnière B. Devos D, et al. Neurology. 2001 Jan 23;56(2):234-8. doi: 10.1212/wnl.56.2.234. Neurology. 2001. PMID: 11160961

7

Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1.

Sergeant N, Sablonnière B, Schraen-Maschke S, Ghestem A, Maurage CA, Wattez A, Vermersch P, Delacourte A. Sergeant N, et al. Hum Mol Genet. 2001 Sep 15;10(19):2143-55. doi: 10.1093/hmg/10.19.2143. Hum Mol Genet. 2001. PMID: 11590131

8

Real time RT-PCR shows correlation between retinoid-induced apoptosis and NGF-R mRNA levels.

Vuillaume I, Schraen-Maschke S, Formstecher P, Sablonnière B. Vuillaume I, et al. Biochem Biophys Res Commun. 2001 Dec 7;289(3):647-52. doi: 10.1006/bbrc.2001.6028. Biochem Biophys Res Commun. 2001. PMID: 11726196

9

ETR-3 represses Tau exons 2/3 inclusion, a splicing event abnormally enhanced in myotonic dystrophy type I.

Leroy O, Dhaenens CM, Schraen-Maschke S, Belarbi K, Delacourte A, Andreadis A, Sablonnière B, Buée L, Sergeant N, Caillet-Boudin ML. Leroy O, et al. J Neurosci Res. 2006 Sep;84(4):852-9. doi: 10.1002/jnr.20980. J Neurosci Res. 2006. PMID: 16862542

10

Overexpression of MBNL1 fetal isoforms and modified splicing of Tau in the DM1 brain: two individual consequences of CUG trinucleotide repeats.

Dhaenens CM, Schraen-Maschke S, Tran H, Vingtdeux V, Ghanem D, Leroy O, Delplanque J, Vanbrussel E, Delacourte A, Vermersch P, Maurage CA, Gruffat H, Sergeant A, Mahadevan MS, Ishiura S, Buée L, Cooper TA, Caillet-Boudin ML, Charlet-Berguerand N, Sablonnière B, Sergeant N. Dhaenens CM, et al. Exp Neurol. 2008 Apr;210(2):467-78. doi: 10.1016/j.expneurol.2007.11.020. Epub 2007 Dec 4. Exp Neurol. 2008. PMID: 18177861

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