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Phase 2 study of sodium phenylbutyrate in ALS

Amyotrophic lateral sclerosis, 2009-01, Vol.10 (2), p.99-106

2009

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Sixteen novel mutations in the Cu Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes

Amyotrophic lateral sclerosis, 2003-06, Vol.4 (2), p.62-73

2003

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Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS

Amyotrophic lateral sclerosis, 2008-01, Vol.9 (3), p.141-148

2008

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A common haplotype within the PON1 promoter region is associated with sporadic ALS

Amyotrophic lateral sclerosis, 2008-01, Vol.9 (5), p.306-314

2008

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50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis, 2008-01, Vol.9 (4), p.229-237

2008

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Medications and laboratory parameters as prognostic factors in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis, 2008-01, Vol.9 (6), p.369-374

2008

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Thrombopoietin is ineffective in a mouse model of motor neuron disease

Amyotrophic lateral sclerosis, 2008-01, Vol.9 (6), p.354-358

2008

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No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: A tagging SNP approach

Amyotrophic lateral sclerosis, 2006-03, Vol.7 (1), p.46-56

2006

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Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis, 2011-11, Vol.12 (6), p.430-438

2011

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Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients

Amyotrophic lateral sclerosis, 2012-05, Vol.13 (3), p.265-269

2012

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Vanadium, aluminum, magnesium and manganese are not elevated in hair samples in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis, 2010-10, Vol.11 (5), p.492-493

2010

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The characterization and functional significance of surface negative charges in cardiac muscle

Brown, Robert H. Jr

1973

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Mutations in the Sphingolipid Pathway Gene SPTLC1 are a Cause of Amyotrophic Lateral Sclerosis

SSRN Electronic Journal

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Thermochemical Processing of Biomass: Conversion into Fuels, Chemicals and Power

Brown, Robert C

2nd Edition edition., 2019

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LBJ’s Neglected Legacy: How Lyndon Johnson Reshaped Domestic Policy and Government

First edition, 2015

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The New Negro: Readings on Race, Representation, and African American Culture, 1892-1938

Henry Louis Gates, Gene Andrew Jarrett / Henry Louis Gates, Gene Andrew Jarrett

1, 2021

Volltextzugriff (PDF)

African American fraternities and sororities: The legacy and the vision

2005

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Handbook of Population

2nd ed. 2019, 2019

Volltextzugriff (PDF)

The New Negro: Readings on Race, Representation, and African American Culture, 1892-1938

2021

Volltextzugriff (PDF)

Ecological communities: conceptual issues and the Evidence.

1, 2014

Volltextzugriff (PDF)

Gene targets for engineering osmotolerance in Caldicellulosiruptor bescii

Biotechnology for biofuels, 2020-03, Vol.13 (1), Article 50

2020

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Consolidated bioprocessing of Populus using Clostridium (Ruminiclostridium) thermocellum: a case study on the impact of lignin composition and structure

Biotechnology for biofuels, 2016-02, Vol.9 (1), Article 31

2016

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Visualizing the Sacred: Cosmic Visions, Regionalism, and the Art of the Mississippian World

1, 2011

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Dynamic Reconstruction of the Spine

2, 2015

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Phase 2 study of sodium phenylbutyrate in ALS

Sixteen novel mutations in the Cu Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes

Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS

A common haplotype within the PON1 promoter region is associated with sporadic ALS

50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis

Medications and laboratory parameters as prognostic factors in amyotrophic lateral sclerosis

Thrombopoietin is ineffective in a mouse model of motor neuron disease

No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: A tagging SNP approach

Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosis

Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients

Vanadium, aluminum, magnesium and manganese are not elevated in hair samples in amyotrophic lateral sclerosis

The characterization and functional significance of surface negative charges in cardiac muscle

Mutations in the Sphingolipid Pathway Gene SPTLC1 are a Cause of Amyotrophic Lateral Sclerosis

Thermochemical Processing of Biomass: Conversion into Fuels, Chemicals and Power

LBJ’s Neglected Legacy: How Lyndon Johnson Reshaped Domestic Policy and Government

Status and prospects for renewable energy using wood pellets from the southeastern United States

The New Negro: Readings on Race, Representation, and African American Culture, 1892-1938

African American fraternities and sororities: The legacy and the vision

Handbook of Population

The New Negro: Readings on Race, Representation, and African American Culture, 1892-1938

Ecological communities: conceptual issues and the Evidence.

Gene targets for engineering osmotolerance in Caldicellulosiruptor bescii

Consolidated bioprocessing of Populus using Clostridium (Ruminiclostridium) thermocellum: a case study on the impact of lignin composition and structure

Visualizing the Sacred: Cosmic Visions, Regionalism, and the Art of the Mississippian World

Dynamic Reconstruction of the Spine

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