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Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene

Acta neuropathologica communications, 2017-06, Vol.5 (1), p.43-43, Article 43

2017

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Confirmation of high frequency of C9orf72 mutations in patients with frontotemporal dementia from Sweden

Neurobiology of aging, 2019-12, Vol.84, p.241.e21-241.e25

2019

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Integrins Regulate Rac Targeting by Internalization of Membrane Domains

Science (American Association for the Advancement of Science), 2004-02, Vol.303 (5659), p.839-842

2004

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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Acta neuropathologica, 2014-09, Vol.128 (3), p.397-410

2014

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Top-emitting organic light-emitting devices using surface-modified Ag anode

Applied physics letters, 2003-12, Vol.83 (25), p.5127-5129

2003

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C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Neurology, 2020-12, Vol.95 (24), p.e3288

2020

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Ter(9,9-diarylfluorene)s: Highly Efficient Blue Emitter with Promising Electrochemical and Thermal Stability

Journal of the American Chemical Society, 2002-10, Vol.124 (39), p.11576-11577

2002

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Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

Human mutation, 2015-12, Vol.36 (12), p.1226-1235

2015

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Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

Neurobiology of aging, 2015-05, Vol.36 (5), p.2005.e15-2005.e22

2015

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No common founder for C9orf72 expansion mutation in Sweden

Journal of human genetics, 2017-02, Vol.62 (2), p.321-324

2017

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Methodology for optimizing viewing characteristics of top-emitting organic light-emitting devices

Applied physics letters, 2004-05, Vol.84 (20), p.3966-3968

2004

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Novel TARDBP mutations in Nordic ALS patients

Journal of human genetics, 2012-05, Vol.57 (5), p.316-319

2012

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The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of Aβ in different brain regions

European journal of human genetics : EJHG, 2010-11, Vol.18 (11), p.1202-1208

2010

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Clinical efficacy of 60-mg dexlansoprazole and 40-mg esomeprazole after 24 weeks for the on-demand treatment of gastroesophageal reflux disease grades A and B: a prospective randomized trial

Drug design, development and therapy, 2019-04, Vol.13, p.1347-1356

2019

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Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration

European journal of human genetics : EJHG, 2013-11, Vol.21 (11), p.1260-1265

2013

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Highly bright blue organic light-emitting devices using spirobifluorene-cored conjugated compounds

Applied physics letters, 2002-07, Vol.81 (4), p.577-579

2002

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Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

Archives of neurology (Chicago), 2011-05, Vol.68 (5), p.581

2011

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Bandgap engineering of well-aligned Zn1−xMgxO nanorods grown by metalorganic chemical vapor deposition

Chemical physics letters, 2005-03, Vol.404 (1-3), p.132-135

2005

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Synthesis and structure–activity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (23), p.5154-5159

2005

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Isolation of the Arabidopsis GA4 locus

The Plant cell, 1995-02, Vol.7 (2), p.195-201

1995

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New improvements in Boston Keratoprosthesis (KPro): titanium surface modifications

Acta ophthalmologica (Oxford, England), 2012-09, Vol.90 (s249), p.0-0

2012

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Informed choice of pregnant women in prenatal screening tests for Down’s syndrome

Journal of medical ethics, 2006-05, Vol.32 (5), p.273-277

2006

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Old-age hippocampal sclerosis associates with grn but not with ABCC9 gene variation in the population

JOURNAL OF NEUROCHEMISTRY, 2015, Vol.134, p.337

2015

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Neural-network-based optimal fuzzy controller design for nonlinear systems

Fuzzy sets and systems, 2005-09, Vol.154 (2), p.182-207

2005

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Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

Alzheimer's & dementia, 2008-11, Vol.4 (6), p.414-420

2008

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Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene

Confirmation of high frequency of C9orf72 mutations in patients with frontotemporal dementia from Sweden

Integrins Regulate Rac Targeting by Internalization of Membrane Domains

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Top-emitting organic light-emitting devices using surface-modified Ag anode

C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Ter(9,9-diarylfluorene)s: Highly Efficient Blue Emitter with Promising Electrochemical and Thermal Stability

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

No common founder for C9orf72 expansion mutation in Sweden

Methodology for optimizing viewing characteristics of top-emitting organic light-emitting devices

Novel TARDBP mutations in Nordic ALS patients

The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of Aβ in different brain regions

Clinical efficacy of 60-mg dexlansoprazole and 40-mg esomeprazole after 24 weeks for the on-demand treatment of gastroesophageal reflux disease grades A and B: a prospective randomized trial

Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration

Highly bright blue organic light-emitting devices using spirobifluorene-cored conjugated compounds

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

Bandgap engineering of well-aligned Zn1−xMgxO nanorods grown by metalorganic chemical vapor deposition

Synthesis and structure–activity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors

Isolation of the Arabidopsis GA4 locus

New improvements in Boston Keratoprosthesis (KPro): titanium surface modifications

Informed choice of pregnant women in prenatal screening tests for Down’s syndrome

Old-age hippocampal sclerosis associates with grn but not with ABCC9 gene variation in the population

Neural-network-based optimal fuzzy controller design for nonlinear systems

Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

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