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A H Child

Showing results (21-30 of 45) with videos related to

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Lancet (London, England)|April 23, 1983
Aortic compliance in patients with ruptured intracranial aneurysmsG Neil-Dwyer, A H Child, D E Dorrance, et al.
Journal of the Royal Society of Medicine|June 1, 1983
Type III collagen deficiency with normal phenotypeF M Pope, A H Child, A C Nicholls, et al.
British Journal of Rheumatology|March 1, 1992
Segregation analysis of collagen genes in two families with joint hypermobility syndromeA M Henney, D H Brotherton, A H Child, et al.
Human Genetics|February 11, 2003
Gene symbol: FBN1. Disease: Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.
Eye (London, England)|December 3, 2011
Alternative diagnoses with ectopia lentisA Chandra, J A Aragon Martin, A H Child, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 1994
Fibrillin secretion and microfibril assembly by Marfan dermal fibroblastsC M Kielty, J E Phillips, A H Child, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|September 21, 2005
Infantile scoliosis in Beals syndrome: the use of a non-fusion technique for surgical correctionAnthony Gwynne Martin, Pedro R Foguet, David S Marks, et al.
The Biochemical Journal|June 15, 1987
Biochemical characterization of individual normal, floppy and rheumatic human mitral valvesY Lis, M C Burleigh, D J Parker, et al.
British Heart Journal|March 1, 1989
Genetic evidence that mutations in the COL1A1, COL1A2, COL3A1, or COL5A2 collagen genes are not responsible for mitral valve prolapseA M Henney, P Tsipouras, R C Schwartz, et al.
Heart (British Cardiac Society)|February 20, 2009
The unravelling of primary myocardial impairment in Marfan syndrome by modern echocardiographyA Kiotsekoglou, G R Sutherland, J C Moggridge, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Lancet (London, England)|April 23, 1983
Aortic compliance in patients with ruptured intracranial aneurysmsG Neil-Dwyer, A H Child, D E Dorrance, et al.
Journal of the Royal Society of Medicine|June 1, 1983
Type III collagen deficiency with normal phenotypeF M Pope, A H Child, A C Nicholls, et al.
British Journal of Rheumatology|March 1, 1992
Segregation analysis of collagen genes in two families with joint hypermobility syndromeA M Henney, D H Brotherton, A H Child, et al.
Human Genetics|February 11, 2003
Gene symbol: FBN1. Disease: Marfan syndromeP Comeglio, A L Evans, G W Brice, et al.
Eye (London, England)|December 3, 2011
Alternative diagnoses with ectopia lentisA Chandra, J A Aragon Martin, A H Child, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 1994
Fibrillin secretion and microfibril assembly by Marfan dermal fibroblastsC M Kielty, J E Phillips, A H Child, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|September 21, 2005
Infantile scoliosis in Beals syndrome: the use of a non-fusion technique for surgical correctionAnthony Gwynne Martin, Pedro R Foguet, David S Marks, et al.
The Biochemical Journal|June 15, 1987
Biochemical characterization of individual normal, floppy and rheumatic human mitral valvesY Lis, M C Burleigh, D J Parker, et al.
British Heart Journal|March 1, 1989
Genetic evidence that mutations in the COL1A1, COL1A2, COL3A1, or COL5A2 collagen genes are not responsible for mitral valve prolapseA M Henney, P Tsipouras, R C Schwartz, et al.
Heart (British Cardiac Society)|February 20, 2009
The unravelling of primary myocardial impairment in Marfan syndrome by modern echocardiographyA Kiotsekoglou, G R Sutherland, J C Moggridge, et al.
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