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S P MacDonald-Hull

Showing results (1-10 of 5) with videos related to

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The British Journal of Dermatology|June 26, 2001
Chronic urticaria associated with intra-articular methylprednisoloneB Pollock, S M Wilkinson, S P MacDonald Hull
The British Journal of Dermatology|August 1, 1996
Ultrastructural abnormalities in the dermal papillae of both lesional and clinically normal follicles from alopecia areata scalpsM Nutbrown, S P MacDonald Hull, T G Baker, et al.
The British Journal of Dermatology|December 1, 1993
Isotretinoin therapy for acne vulgaris: a re-evaluation of the need for measurements of plasma lipids and liver function testsJ H Barth, S P Macdonald-Hull, J Mark, et al.
Tissue Antigens|January 16, 2008
Genetic analysis of autoimmune regulator haplotypes in alopecia areataD A Wengraf, A J G McDonagh, T R J Lovewell, et al.
Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
The British Journal of Dermatology|June 26, 2001
Chronic urticaria associated with intra-articular methylprednisoloneB Pollock, S M Wilkinson, S P MacDonald Hull
The British Journal of Dermatology|August 1, 1996
Ultrastructural abnormalities in the dermal papillae of both lesional and clinically normal follicles from alopecia areata scalpsM Nutbrown, S P MacDonald Hull, T G Baker, et al.
The British Journal of Dermatology|December 1, 1993
Isotretinoin therapy for acne vulgaris: a re-evaluation of the need for measurements of plasma lipids and liver function testsJ H Barth, S P Macdonald-Hull, J Mark, et al.
Tissue Antigens|January 16, 2008
Genetic analysis of autoimmune regulator haplotypes in alopecia areataD A Wengraf, A J G McDonagh, T R J Lovewell, et al.
Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.
Pageof 1