D. Gardner‐Medwin

Biochemistry, Genetics and Molecular Biology · Life Sciences

37h-index4.6kcitations151works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(47), Neurogenetic and Muscular Disorders Research(17), Genetic Neurodegenerative Diseases(15), Metabolism and Genetic Disorders(11), Mitochondrial Function and Pathology(10)

Publications151 total

List of Contributors
Child Neurology·2021
John Walton
Child Neurology·2021
Objectives in the Management of Duchenne Muscular Dystrophy
2015· 6 cited
Clinical Examination as a Tool for Diagnosis: Historical Perspective
Humana Press eBooks·2003
A short life rich in images: New records of the life of John Kirkpatrick (1892-1915) "Simpson" of the Australian Army Medical Corps
Queensland's institutional digital repository (The University of Queensland)·2003
Tethering of the vertebral artery in the congenital arcuate foramen of the atlas vertebra: a possible cause of vertebral artery dissection in children
Developmental Medicine & Child Neurology·2001· 76 cited
Tethering of the vertebral artery in the congenital arcuate foramen of the atlas vertebra: a possible cause of vertebral artery dissection in children
Developmental Medicine & Child Neurology·2001· 18 citedOpen Access
SAUER, Gordon C. <i>John Gould the bird man: associates and subscribers</i>. Maurizio Martino, Mansfield, Connecticut: 1995. Pp 190. No price or ISBN given. Edition of 300 signed and numbered copies.
Archives of Natural History·1998Open Access
FARBER, Paul Lawrence. <i>Discovering birds: The emergence of ornithology as a scientific discipline: 1760–1850</i>. The Johns Hopkins University Press, Baltimore and London: 1997. Paperback. Pp xxiii, 191. No price given. ISBN 0-8018-5537-3.
Archives of Natural History·1998· 1 cited
CSF antigliadin antibodies and the Ramsay Hunt syndrome
Neurology·1997· 53 cited
Absent nails, kinesogenic choreoathetosis, epilepsy and developmental delay - a new autosomal dominant disorder?
Clinical Dysmorphology·1997· 9 cited
PYRIDOXINE‐DEPENDENT SEIZURES: DEMOGRAPHIC, CLINICAL, MRI AND PSYCHOMETRIC FEATURES, AND EFFECT OF DOSE ON INTELLIGENCE QUOTIENT
Developmental Medicine & Child Neurology·1996· 115 cited
Respiratory Chain Dysfunction in Progressive Neuronal Degeneration of Childhood With Liver Disease
Journal of Child Neurology·1996· 10 cited
Co‐dominant Inheritance of Hyperekplexia and Spastic Paraparesis
Developmental Medicine & Child Neurology·1996· 11 cited
The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon's Disease
Journal of Medical Genetics·1996· 6 cited
Arthrogryposis Multiplex Congenita and Bilateral Parietal Polymicrogyria in Association with the Intrauterine Death of a Twin
Neuropediatrics·1996· 45 cited
Winging of the Scapula: The Underlying Biomechanics and an Orthotic Solution
Proceedings of the Institution of Mechanical Engineers Part H Journal of Engineering in Medicine·1995· 12 cited
New questions about the muscular dystrophies.
Annals of the Rheumatic Diseases·1995· 1 citedOpen Access
Congenital myotonic dystrophy
Pediatric Neurology·1995· 3 cited
Book review
Neuromuscular Disorders·1995
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Frequent Co-authors

L. V. B. Nicholson(8), Kate Bushby(7), P. Hudgson(6), R. J. Pennington(6), J. N. Walton(5), Mark A. Johnson(4), John L. Welch(4), Mark Johnson(3), Douglass M. Turnbull(3), J. N. Walton(3), Ann Curtis(3), Johan T. den Dunnen(3), Thomas Bütler(3), Egbert Bakker(3), A. Gholkar(3), John Burn(2), J.B. Harris(2), Irene D. Haggerty(2), Laurence A. Bindoff(2), John N. Walton(2)