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Publications by A M Lund

Molecular Characterisation of Six Patients With Prolidase Deficiency: Identification of the First Small Duplication in the Prolidase Gene and of a Mutation Generating Symptomatic and Asymptomatic Outcomes Within the Same Family

Journal of Medical Genetics

Genetics

2006

English

A Musculoskeletal Full-Body Simulation of Cross-Country Skiing

Proceedings of the Institution of Mechanical Engineers, Part P: Journal of Sports Engineering and Technology

Engineering

Sports Science

2008

English

Related publications

A Novel Nonsense Mutation of the PEPD Gene in a Japanese Patient With Prolidase Deficiency

Journal of Human Genetics

Genetics

2000

English

A Study on the Role of Oxidative Stress and Prolidase Enzyme in the Clinical Evaluation of Irritable Bowel Syndrome (IBS)

International Journal of Contemporary Medical Research [IJCMR]

2020

English

Identification and Characterisation of a Hyper-Variable Apoplastic Effector Gene Family of the Potato Cyst Nematodes

English

Identification of a Novel TTC19 Mutation in a Portuguese Family With Complex III Deficiency

English

Gene Mutation and Pedigree Analysis of Tetrahydrobiopterin Deficiency in a Uygur Family of China

Journal of Clinical Laboratory Analysis

Medical Laboratory Technology

Clinical Biochemistry

English

Molecular Epidemiology of C9 Deficiency Heterozygotes With an Arg95Stop Mutation of the C9 Gene in Japan

Journal of Human Genetics

Genetics

1999

English

Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) Gene

English

Identification of a Mutation in the Beta Cardiac Myosin Heavy Chain Gene in a Family With Hypertrophic Cardiomyopathy.

Heart

Cardiovascular Medicine

Cardiology

1993

English

Musculoskeletal Loading in the Symptomatic and Asymptomatic Knees of Middle-Aged Osteoarthritis Patients

Journal of Orthopaedic Research

Orthopedics

Sports Medicine

2016

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by A M Lund

Molecular Characterisation of Six Patients With Prolidase Deficiency: Identification of the First Small Duplication in the Prolidase Gene and of a Mutation Generating Symptomatic and Asymptomatic Outcomes Within the Same Family

A Musculoskeletal Full-Body Simulation of Cross-Country Skiing

Related publications

A Novel Nonsense Mutation of the PEPD Gene in a Japanese Patient With Prolidase Deficiency

A Study on the Role of Oxidative Stress and Prolidase Enzyme in the Clinical Evaluation of Irritable Bowel Syndrome (IBS)

Identification and Characterisation of a Hyper-Variable Apoplastic Effector Gene Family of the Potato Cyst Nematodes

Identification of a Novel TTC19 Mutation in a Portuguese Family With Complex III Deficiency

Gene Mutation and Pedigree Analysis of Tetrahydrobiopterin Deficiency in a Uygur Family of China

Molecular Epidemiology of C9 Deficiency Heterozygotes With an Arg95Stop Mutation of the C9 Gene in Japan

Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) Gene

Identification of a Mutation in the Beta Cardiac Myosin Heavy Chain Gene in a Family With Hypertrophic Cardiomyopathy.

Musculoskeletal Loading in the Symptomatic and Asymptomatic Knees of Middle-Aged Osteoarthritis Patients