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Hanns Lochmüller

Senior Scientist

Canada

Research Interests

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Professors in Canada Professors in Biochemistry Biochemistry professors in Canada

Articles (16)

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2026

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2026

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2026

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2026

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2023

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2022

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2021

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2020

Collaborators (7)

Kathryn Selby

Clinical Assistant Professor

BC Children's Hospital

CANADA

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Andreas Roos

GERMANY

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Lola E. R Lessard

Adult neurologist (Assistant Chef de Clinique)

Hospices Civils de Lyon

FRANCE

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Eric Hoffman

Associate Dean Research, Professor

Binghamton University School of Pharmacy and Pharmaceutical Sciences

UNITED STATES

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Maryam Oskoui

CANADA

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Cynthia Gagnon

CANADA

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Danielle Bourque

Assistant Professor

University of Ottawa

CANADA

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Hanns Lochmüller

Research Interests

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Articles (16)

MT-ATP6 variant as a cause of adult-onset hereditary spastic paraparesis: A case report and literature review

Muscle Strength, Balance, and Indoor Mobility in Oculopharyngeal Muscular Dystrophy: An Exploratory Canadian Multicenter Study

Vamorolone Safety, Pharmacokinetics, and Exploratory Efficacy in Duchenne Muscular Dystrophy

Hexosamine Pathway Disruption by GFPT1 Loss Drives Coordinated Defects in Glycosylation, Autophagy, and Trafficking

Results of a phase II open-label, multiple-dose study of vamorolone (VBP15-006) in 7- to < 18-year-old boys with duchenne muscular dystrophy

Financial Toxicity and Its Determinants in Individuals Living With Inherited and Acquired Neuromuscular Disorders

Assessing the socio-economic burden of inherited and inflammatory neuromuscular diseases (BIND study): a study protocol

Counting the Cost: The Hidden Financial Realities of Neuromuscular Disease Through Patient and Family Perspectives

Galactose treatment rescues neuromuscular junction transmission in glutamine-fructose-6-phosphate transaminase 1 (Gfpt1) deficient mice

Variant-specific deep phenotyping as a tool to develop precision therapies

Thinking outside the box: A re-evaluation of Canadian recommended outcome measures in adult spinal muscular atrophy – report of a national consensus workshop

Pontocerebellar Hypoplasia and Periventricular Leukomalacia Associated With p.Phe262Val Homozygous Variant in TTC1 Gene: A Report of 4 Cases

Sustained clinical benefit following systemic gene replacement therapy in <scp>Duchenne</scp> muscular dystrophy

Congenital myasthenic syndrome in a cohort of patients with ‘double’ seronegative myasthenia gravis

Disease monitoring programs of rare genetic diseases: transparent data sharing between academic and commercial stakeholders

Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker for Duchenne muscular dystrophy

Collaborators (7)

Kathryn Selby

Andreas Roos

Lola E. R Lessard

Eric Hoffman

Maryam Oskoui

Cynthia Gagnon

Danielle Bourque

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