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Clinical Endocrinology|May 14, 1998
Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acneL S Ostlere, G Rumsby, P Holownia, et al.International Journal of Dermatology|April 1, 1996
Skin surface lipids in HIV-positive patients with and without seborrheic dermatitisL S Ostlere, C R Taylor, D W Harris, et al.The British Journal of Dermatology|October 10, 1998
E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosaJ E Mellerio, R A Eady, D J Atherton, et al.Archives of Disease in Childhood|November 1, 1989
Growth in atopic eczema: a controlled study by questionnaireM G Pike, C L Chang, D J Atherton, et al.Archives of Disease in Childhood|January 29, 2000
Gastrointestinal symptoms in patients with asthmaC Caffarelli, F M Deriu, V Terzi, et al.Archives of Disease in Childhood|February 13, 2001
Central nervous system imaging and congenital melanocytic naeviV A Kinsler, S E Aylett, S C Coley, et al.The British Journal of Dermatology|June 26, 1998
Prognostic implications of determining 180 kDa bullous pemphigoid antigen (BPAG2) gene/protein pathology in neonatal junctional epidermolysis bullosaJ E Mellerio, J E Denyer, D J Atherton, et al.Experimental Dermatology|October 28, 1999
Fine genetic mapping of diffuse non-epidermolytic palmoplantar keratoderma to chromosome 12q11-q13: exclusion of the mapped type II keratinsD P Kelsell, H P Stevens, P E Purkis, et al.Journal of Immunology (Baltimore, Md. : 1950)|August 26, 1998
The role of apoptosis in the resolution of T cell-mediated cutaneous inflammationC H Orteu, L W Poulter, M H Rustin, et al.Helvetica Paediatrica Acta|February 1, 1989
Lactulose in trimethylaminuria, the fish-odour syndromeM G Pike, G S King, B R Pettit, et al.Pageof 17