72 results filtered with: Muscular Dystrophies
- Books
10 years of Life : a partnership between Life, a centre for world-class science, Newcastle University, the Newcastle upon Tyne Hospitals NHS Foundation Trust / Centre for Life.
Centre for LifeDate: [2010]- Archives and manuscripts
Myopathies
Date: 1904-1951Reference: PP/FPW/B.220Part of: Parkes Weber, Frederick (1863-1962)- Books
Research in muscular dystrophy : the proceedings of the Third Symposium on Current Research in Muscular Dystrophy held at The National Hospital, Queen Square, London W.C.1 8th-9th January 1965 / edited by the members of the research committee of the Muscular Dystrophy Group.
Symposium on Current Research in Muscular Dystrophy 1965 : London)Date: 1965- Books
The plain guide to making or amending your will / Muscular Dystrophy Group of Great Britain and Northern Ireland.
Date: [1992]
- Books
- Online
On some disorders of nutrition related with affections of the nervous system : neurotic dystrophies / by William M. Ord.
William Miller OrdDate: 1885- Videos
Muscle fatigue.
Date: 1974- Books
Muscular dystrophy in children : a guide for families / Irwin M. Siegel.
Irwin M. SiegelDate: 1999
- Digital Images
- Online
Nerve in skeletal muscle, showing dystrophin location
Prof. Peter Brophy- Books
Experimental muscular dystrophies in animals : a comparative study / by Ira Rockwood Telford, in collaboration with Lárus Einarson.
Ira Rockwood TelfordDate: [1971]- Archives and manuscripts
Amyoplasia congenita, myodystrophia foetalis deformans dysmyoplasia, hypomyoplasia
Date: 1929-1948Reference: PP/FPW/B.15Part of: Parkes Weber, Frederick (1863-1962)- Books
Die Dystrophie / von Heinrich Berning.
Berning, Heinrich.Date: 1949
- Digital Images
- Online
Duchenne muscular dystrophy control, FISH
Wessex Reg. Genetics Centre
- Digital Images
- Online
Cow with muscular dystrophy causing prominence of
ROYAL VETERINARY COLLEGE
- Digital Images
- Online
Duchenne muscular dystrophy - normal female, chromosomes have been highlighted by a fluorescent probe for exon 45/47 (note the double yellow band). This disorder is caused by a recessive gene on the X chromosome, so is normally shown only by males, who lack a second X chromosome. The condition starts with difficulty in walking and climbing stairs in early childhood, usually resulting in confinement to a wheelchair by the age of 10, with death from respiratory infection or cardiac failure by about the age of 20.
Wessex Reg. Genetics Centre- Archives and manuscripts
[Myopathies and muscle wasting]
Date: 1904-1951Reference: PP/FPW/B.220/2Part of: Parkes Weber, Frederick (1863-1962)
- Digital Images
- Online
Lamb with muscular dystrophy
ROYAL VETERINARY COLLEGE
- Digital Images
- Online
Duchenne muscular dystrophy carrier female
Wessex Reg. Genetics Centre- Books
Research for results / Heather Russell.
Russell, HeatherDate: 1977- Archives and manuscripts
Pembrey, Marcus Edred (b.1943)
Pembrey, Marcus Edred (b.1943)Date: 1960s-2011Reference: PP/MEP- Archives and manuscripts
Gwen Prout stamp collection vol.68 Genetics
Date: 1939-2015Reference: EPH751:68Part of: Gwen Prout Stamp Collection- Archives and manuscripts
Peroneal type of muscular atrophy. This is also my collection on 'Myopathies, 1st series'.
Date: 1905-1941Reference: PP/FPW/B.220/1Part of: Parkes Weber, Frederick (1863-1962)
- Digital Images
- Online
Lamb with muscular dystrophy - terminal
ROYAL VETERINARY COLLEGE
- Ephemera
- Online
Organon presenta el anabólico oral idóneo para niños, mujeres y ancianos, Orgabolin : ...y para la terapéutica parenteral, Deca-Durabolin / Organon.
Date: [1962]- Books
The therapeutic implications of muscular dystrophy genomics : the transcript of a Witness Seminar held by the History of Modern Biomedicine Research Group, Queen Mary University of London, on 27 October 2015 / edited by A Zarros, C Overy, K Mikami, S Sturdy, and E M Tansey.
Date: 2017- Ephemera
Muscular diseases ephemera. Box 1.