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F M Pope

Showing results (71-80 of 168) with videos related to

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Clinical and Experimental Dermatology|December 23, 1998
Giant bladder diverticulum in Ehlers-Danlos syndrome type I causing outflow obstructionN P Burrows, B E Monk, J B Harrison, et al.
Journal of Medical Genetics|December 1, 1985
Collagen genes and proteins in osteogenesis imperfectaF M Pope, A C Nicholls, J McPheat, et al.
The Journal of Biological Chemistry|November 15, 1989
Single base mutation in the type III procollagen gene that converts the codon for glycine 883 to aspartate in a mild variant of Ehlers-Danlos syndrome IVG Tromp, H Kuivaniemi, C Stolle, et al.
The British Journal of Dermatology|March 1, 1972
Out-patient treatment of ichthyosis: a double-blind trial of ointmentsF M Pope, J K Rees, R S Wells, et al.
Thorax|April 1, 1985
Abnormalities of the lungs and thoracic cage in the Ehlers-Danlos syndromeJ G Ayres, F M Pope, J F Reidy, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
A COL3A1 glycine 1006 to glutamic acid substitution in a patient with Ehlers-Danlos syndrome type IV detected by denaturing gradient gel electrophoresisP H Johnson, A J Richards, F M Pope, et al.
Clinical Genetics|February 1, 1997
Congenital cutis laxa and lysyl oxidase deficiencyA Khakoo, R Thomas, R Trompeter, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|May 1, 1997
Spontaneous rupture of the renal artery in a patient with Ehlers-Danlos syndrome type IVO Oyen, O P Clausen, I B Brekke, et al.
Journal of Medical Genetics|November 1, 1991
Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfectaA C Nicholls, J Oliver, D V Renouf, et al.
Archives of Disease in Childhood|September 1, 1988
Clinical presentations of Ehlers Danlos syndrome type IVF M Pope, P Narcisi, A C Nicholls, et al.
Pageof 17

Showing results (71-80 of 168) with videos related to

Sort By:
Pageof 17
Clinical and Experimental Dermatology|December 23, 1998
Giant bladder diverticulum in Ehlers-Danlos syndrome type I causing outflow obstructionN P Burrows, B E Monk, J B Harrison, et al.
Journal of Medical Genetics|December 1, 1985
Collagen genes and proteins in osteogenesis imperfectaF M Pope, A C Nicholls, J McPheat, et al.
The Journal of Biological Chemistry|November 15, 1989
Single base mutation in the type III procollagen gene that converts the codon for glycine 883 to aspartate in a mild variant of Ehlers-Danlos syndrome IVG Tromp, H Kuivaniemi, C Stolle, et al.
The British Journal of Dermatology|March 1, 1972
Out-patient treatment of ichthyosis: a double-blind trial of ointmentsF M Pope, J K Rees, R S Wells, et al.
Thorax|April 1, 1985
Abnormalities of the lungs and thoracic cage in the Ehlers-Danlos syndromeJ G Ayres, F M Pope, J F Reidy, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
A COL3A1 glycine 1006 to glutamic acid substitution in a patient with Ehlers-Danlos syndrome type IV detected by denaturing gradient gel electrophoresisP H Johnson, A J Richards, F M Pope, et al.
Clinical Genetics|February 1, 1997
Congenital cutis laxa and lysyl oxidase deficiencyA Khakoo, R Thomas, R Trompeter, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|May 1, 1997
Spontaneous rupture of the renal artery in a patient with Ehlers-Danlos syndrome type IVO Oyen, O P Clausen, I B Brekke, et al.
Journal of Medical Genetics|November 1, 1991
Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfectaA C Nicholls, J Oliver, D V Renouf, et al.
Archives of Disease in Childhood|September 1, 1988
Clinical presentations of Ehlers Danlos syndrome type IVF M Pope, P Narcisi, A C Nicholls, et al.
Pageof 17