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Results: 1-17 |
Results: 17

Authors: Choudry, K Charles-Holmes, R Vella, EJ Burge, S
Citation: K. Choudry et al., Scarring alopecia due to folliculitis decalvans in a patient with Darier'sDisease, CLIN EXP D, 26(3), 2001, pp. 307-308

Authors: Burge, S
Citation: S. Burge, Should inhaled corticosteroids be used in the long term treatment of chronic obstructive pulmonary disease?, DRUGS, 61(11), 2001, pp. 1535-1544

Authors: Khumalo, NP Joss, DV Huson, SM Burge, S
Citation: Np. Khumalo et al., Pigmentary anomalies in ataxia-telangiectasia: a clue to diagnosis and an example of twin spotting, BR J DERM, 144(2), 2001, pp. 369-371

Authors: Khumalo, NP Huson, S Burge, S
Citation: Np. Khumalo et al., Development of lentigines within naevoid hypopigmentation, BR J DERM, 144(1), 2001, pp. 188-189

Authors: Sudbrak, R Brown, J Dobson-Stone, C Carter, S Ramser, J White, J Healy, E Dissanayake, M Larregue, M Perrussel, M Lehrach, H Munro, CS Strachan, T Burge, S Hovnanian, A Monaco, AP
Citation: R. Sudbrak et al., Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump, HUM MOL GEN, 9(7), 2000, pp. 1131-1140

Authors: Kellogg, ND Burge, S Taylor, ER
Citation: Nd. Kellogg et al., Wanted and unwanted sexual experiences and family dysfunction during adolescence, J FAM VIOL, 15(1), 2000, pp. 55-68

Authors: Burge, S
Citation: S. Burge, Occupation and lung disease, SC J WORK E, 26(5), 2000, pp. 369-371

Authors: Sakuntabhai, A Dhitavat, J Burge, S Hovnanian, A
Citation: A. Sakuntabhai et al., Mosaicism for ATP2A2 mutations causes segmental Darier's disease, J INVES DER, 115(6), 2000, pp. 1144-1147

Authors: Powell, J Sakuntabhai, A James, M Burge, S Hovnanian, A
Citation: J. Powell et al., Grover's disease, despite histological similarity to Darier's disease, does not share an abnormality in the ATP2A2 gene, BR J DERM, 143(3), 2000, pp. 658-658

Authors: Sakuntabhai, A Ruiz-Perez, V Carter, S Jacobsen, N Burge, S Monk, S Smith, M Munro, CS O'Donovan, M Craddock, N Kucherlapati, R Rees, JL Owen, M Lathrop, GM Monaco, AP Strachan, T Hovnanian, A
Citation: A. Sakuntabhai et al., Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease, NAT GENET, 21(3), 1999, pp. 271-277

Authors: Sakuntabhai, A Burge, S Monk, S Hovnanian, A
Citation: A. Sakuntabhai et al., Spectrum of novel ATP2A2 mutations in patients with Darier's disease, HUM MOL GEN, 8(9), 1999, pp. 1611-1619

Authors: Jacobsen, NJO Lyons, I Hoogendoorn, B Burge, S Kwok, PY O'Donovan, MC Craddock, N Owen, MJ
Citation: Njo. Jacobsen et al., ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes, HUM MOL GEN, 8(9), 1999, pp. 1631-1636

Authors: Stone, N Sheerin, S Burge, S
Citation: N. Stone et al., Toxic epidermal necrolysis and graft vs. host disease: a clinical spectrumbut a diagnostic dilemma, CLIN EXP D, 24(4), 1999, pp. 260-262

Authors: Burge, S
Citation: S. Burge, Management of Darier's disease, CLIN EXP D, 24(2), 1999, pp. 53-56

Authors: Stone, N Burge, S
Citation: N. Stone et S. Burge, Bowen's disease of the leg treated with weekly pulses of 5% fluorouracil cream, BR J DERM, 140(5), 1999, pp. 987-988

Authors: Harris, A O'Hea, AM Burge, S
Citation: A. Harris et al., Ulceration associated with stable myelodysplastic syndrome: atypical pyoderma gangrenosum?, CLIN EXP D, 23(6), 1998, pp. 293-295

Authors: Stone, N Burge, S
Citation: N. Stone et S. Burge, Focal facial dermal dysplasia with a hair collar, BR J DERM, 139(6), 1998, pp. 1136-1137
Risultati: 1-17 |