Detalhe da pesquisa
1.
Combinatorial ASO-mediated therapy with low dose SMN and the protective modifier Chp1 is not sufficient to ameliorate SMA pathology hallmarks.
Neurobiol Dis
; 171: 105795, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35724821
2.
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies.
Rev Neurol (Paris)
; 176(10): 846-855, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32709422
3.
Nanoscope based on nanowaveguides.
Opt Express
; 22(5): 5228-33, 2014 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24663862
4.
SMN oligomerization defect correlates with spinal muscular atrophy severity.
Nat Genet
; 19(1): 63-6, 1998 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-9590291
5.
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics.
Nat Genet
; 20(1): 83-6, 1998 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-9731538
6.
Objective measurement of oral function in adults with spinal muscular atrophy.
Orphanet J Rare Dis
; 18(1): 103, 2023 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37138365
7.
Is a positive clinical outcome after exercise therapy for chronic non-specific low back pain contingent upon a corresponding improvement in the targeted aspect(s) of performance? A systematic review.
Eur Spine J
; 21(4): 575-98, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22072093
8.
Whole body vibration added to endurance training in obese women - a pilot study.
Int J Sports Med
; 33(9): 740-3, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22562734
9.
Wakefulness impairs selective consolidation of relevant trauma-associated memories resulting in more frequent intrusions.
Behav Res Ther
; 136: 103776, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33276275
10.
Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counselling.
Clin Genet
; 76(2): 168-78, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19780763
11.
Congenital heart disease is a feature of severe infantile spinal muscular atrophy.
J Med Genet
; 45(10): 635-8, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18662980
12.
Hydrogen interactions with low-index surface orientations of tungsten.
J Phys Condens Matter
; 31(25): 255002, 2019 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30865943
13.
Differential evolution of the Saccharomyces cerevisiae DUP240 paralogs and implication of recombination in phylogeny.
Nucleic Acids Res
; 32(7): 2069-78, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15087486
14.
Respiratory muscle endurance training reduces chronic neck pain: A pilot study.
J Back Musculoskelet Rehabil
; 29(4): 825-834, 2016 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-27002668
15.
Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.
Hum Mutat
; 25(1): 64-71, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15580564
16.
[Prostate biopsy: Procedure in the clinical routine]. / Prostatabiopsie : Durchführung im klinischen Alltag.
Urologe A
; 54(12): 1811-20; quiz 1821-2, 2015 Dec.
Artigo
em Alemão
| MEDLINE | ID: mdl-26704284
17.
Best practice guidelines for molecular analysis in spinal muscular atrophy.
Eur J Hum Genet
; 9(7): 484-91, 2001 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-11464239
18.
An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA).
Eur J Hum Genet
; 8(7): 493-9, 2000 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-10909848
19.
Efficiency of various strategies and materials to generate new markers: saturating the region 5q11.2-q13.3 with 30 new randomly distributed clones.
Eur J Hum Genet
; 1(4): 314-21, 1993.
Artigo
em Inglês
| MEDLINE | ID: mdl-8081945
20.
Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellites.
Eur J Hum Genet
; 3(1): 56-60, 1995.
Artigo
em Inglês
| MEDLINE | ID: mdl-7767657