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J I Harper

Showing results (71-80 of 141) with videos related to

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Journal of the Royal Society of Medicine|March 1, 1988
Papuloerythroderma in a womanJ A Langtry, C M Payne, J I Harper, et al.
Journal of the Royal Society of Medicine|January 10, 2003
Phacomatosis pigmentokeratoticaVirginia A Hill, R H Felix, P S Mortimer, et al.
The British Journal of Dermatology|August 1, 1985
Lipoid proteinosis: an inherited disorder of collagen metabolism?J I Harper, V C Duance, T J Sims, et al.
British Medical Journal (Clinical Research Ed.)|March 14, 1987
Eczema herpeticum: a potentially fatal diseaseI R Sanderson, L A Brueton, M O Savage, et al.
The British Journal of Dermatology|May 15, 2009
A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteinsW-L Di, R C Hennekam, R E Callard, et al.
The British Journal of Dermatology|October 13, 2006
Absent/reduced glucose transporter-1 protein expression in infantile subglottic haemangiomasD J Purvis, J I Harper, B E Hartley, et al.
Clinical and Experimental Dermatology|November 1, 1993
Lichen planus pemphigoides in a child--immunopathological findingsD G Paige, B S Bhogal, M M Black, et al.
The British Journal of Dermatology|November 1, 1994
A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defectsD G Paige, G G Emilion, P M Bouloux, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 24, 2001
Omenn's syndrome: differential diagnosis in infants with erythroderma and immunodeficiencyI Scheimberg, P H Hoeger, J I Harper, et al.
Clinical and Experimental Dermatology|August 8, 2001
Juvenile xanthogranuloma as a sequel to Langerhans cell histiocytosis: a report of three casesP H Hoeger, C Diaz, M Malone, et al.
Pageof 15

Showing results (71-80 of 141) with videos related to

Sort By:
Pageof 15
Journal of the Royal Society of Medicine|March 1, 1988
Papuloerythroderma in a womanJ A Langtry, C M Payne, J I Harper, et al.
Journal of the Royal Society of Medicine|January 10, 2003
Phacomatosis pigmentokeratoticaVirginia A Hill, R H Felix, P S Mortimer, et al.
The British Journal of Dermatology|August 1, 1985
Lipoid proteinosis: an inherited disorder of collagen metabolism?J I Harper, V C Duance, T J Sims, et al.
British Medical Journal (Clinical Research Ed.)|March 14, 1987
Eczema herpeticum: a potentially fatal diseaseI R Sanderson, L A Brueton, M O Savage, et al.
The British Journal of Dermatology|May 15, 2009
A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteinsW-L Di, R C Hennekam, R E Callard, et al.
The British Journal of Dermatology|October 13, 2006
Absent/reduced glucose transporter-1 protein expression in infantile subglottic haemangiomasD J Purvis, J I Harper, B E Hartley, et al.
Clinical and Experimental Dermatology|November 1, 1993
Lichen planus pemphigoides in a child--immunopathological findingsD G Paige, B S Bhogal, M M Black, et al.
The British Journal of Dermatology|November 1, 1994
A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defectsD G Paige, G G Emilion, P M Bouloux, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 24, 2001
Omenn's syndrome: differential diagnosis in infants with erythroderma and immunodeficiencyI Scheimberg, P H Hoeger, J I Harper, et al.
Clinical and Experimental Dermatology|August 8, 2001
Juvenile xanthogranuloma as a sequel to Langerhans cell histiocytosis: a report of three casesP H Hoeger, C Diaz, M Malone, et al.
Pageof 15