Detalhe da pesquisa
1.
FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees.
Neurogenetics
; 23(1): 59-65, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34518945
2.
De novo mutations in SOD1 are a cause of ALS.
J Neurol Neurosurg Psychiatry
; 93(2): 201-206, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34518333
3.
[Promotion of oral health in nursing-An interprofessional expert standard]. / Förderung der Mundgesundheit in der Pflege ein interprofessioneller Expertenstandard.
Z Gerontol Geriatr
; 55(3): 204-209, 2022 May.
Artigo
em Alemão
| MEDLINE | ID: mdl-35403859
4.
Biophysical and structural investigation of the regulation of human GTP cyclohydrolase I by its regulatory protein GFRP.
J Struct Biol
; 213(1): 107691, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33387654
5.
[Tracking systems in people with dementia in long-term care - Update of an integrative review]. / Tracking-Systeme bei Menschen mit Demenz in der stationären Langzeitpflege.
Pflege
; 34(4): 181-190, 2021 Aug.
Artigo
em Alemão
| MEDLINE | ID: mdl-34105985
6.
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency.
Hum Mol Genet
; 27(4): 706-715, 2018 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29315381
7.
Matrix effects in the analysis of polar organic water contaminants with HILIC-ESI-MS.
Anal Bioanal Chem
; 412(20): 4867-4879, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32130441
8.
Triphenylene-Derived Electron Acceptors and Donors on Ag(111): Formation of Intermolecular Charge-Transfer Complexes with Common Unoccupied Molecular States.
Small
; 15(33): e1901741, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31264784
9.
Different neuroinflammatory profile in amyotrophic lateral sclerosis and frontotemporal dementia is linked to the clinical phase.
J Neurol Neurosurg Psychiatry
; 90(1): 4-10, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30224549
10.
Morbus Fabry and Parkinson's Disease-More Evidence for a Possible Genetic Link.
Mov Disord
; 39(2): 449-451, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38226450
11.
Hot-spot KIF5A mutations cause familial ALS.
Brain
; 141(3): 688-697, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29342275
12.
[Tracking systems in people with dementia in long-term care - an integrative review]. / Tracking-Systeme bei Menschen mit Demenz in der stationären Langzeitpflege.
Pflege
; 32(6): 353-363, 2019.
Artigo
em Alemão
| MEDLINE | ID: mdl-31640470
13.
Comprehensive analysis of the mutation spectrum in 301 German ALS families.
J Neurol Neurosurg Psychiatry
; 89(8): 817-827, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29650794
14.
Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis.
Ann Neurol
; 79(1): 152-8, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26528863
15.
A systems-wide understanding of photosynthetic acclimation in algae and higher plants.
J Exp Bot
; 68(11): 2667-2681, 2017 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28830099
16.
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization.
Ann Neurol
; 77(1): 15-32, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363075
17.
Peripheral monocytes are functionally altered and invade the CNS in ALS patients.
Acta Neuropathol
; 132(3): 391-411, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26910103
18.
Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis.
Acta Neuropathol
; 131(3): 465-80, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26744351
19.
Cyano-Functionalized Triarylamines on Coinage Metal Surfaces: Interplay of Intermolecular and Molecule-Substrate Interactions.
Chemistry
; 22(2): 581-9, 2016 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26636437
20.
Comparing graphene growth on Cu(111) versus oxidized Cu(111).
Nano Lett
; 15(2): 917-22, 2015 Feb 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-25611528