RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome
Blaydon, Diana C., Etheridge, Sarah L., Risk, Janet M., Hennies, Hans-Christian, Gay, Laura J., Carroll, Rebecca, Plagnol, Vincent, McRonald, Fiona E., Stevens, Howard P., Spurr, Nigel K., Bishop, D. Timothy, Ellis, Anthony, Jankowski, Janusz, Field, John K., Leigh, Irene M., South, Andrew P., Kelsell, David P.
Published in American journal of human genetics (10.02.2012)
Published in American journal of human genetics (10.02.2012)
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Journal Article
Reflectance confocal microscopy to diagnose malignant melanoma and lentigo maligna in the UK: a single-centre prospective observational trial
Stevens, Howard P, Pellacani, Giovanni, Angus, Colin, El-Jabbour, Joseph N
Published in British journal of dermatology (1951) (29.10.2024)
Published in British journal of dermatology (1951) (29.10.2024)
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Journal Article
Reflectance confocal microscopy in diagnosing basal cell carcinoma in the UK: a prospective observational single-centre trial
Stevens, Howard P, Pampena, Riccardo, Farnetani, Francesca, Pellacani, Giovanni, Angus, Colin, El-Jabbour, Joseph N
Published in British journal of dermatology (1951) (23.10.2024)
Published in British journal of dermatology (1951) (23.10.2024)
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Journal Article
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
Winter, Hermelita, Labrèze, Christine, Roul, Sylvie, Taieb, Alain, Krieg, Thomas, Schweizer, Jürgen, Stevens, Howard P, Langbein, Lutz, Rogers, Mike A, Leigh, Irene M
Published in Nature genetics (01.08.1997)
Published in Nature genetics (01.08.1997)
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Journal Article
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma
NORGETT, Elizabeth E, HATSELL, Sarah J, CARVAJAL-HUERTA, Luis, CABEZAS, Juan-Carlos Ruiz, COMMON, John, PURKIS, Patricia E, WHITTOCK, Neil, LEIGH, Irene M, STEVENS, Howard P, KELSELL, David P
Published in Human molecular genetics (01.11.2000)
Published in Human molecular genetics (01.11.2000)
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Journal Article
Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates
ECKL, Katja Martina, STEVENS, Howard P, REIS, André, HENNIES, Hans Christian, LESTRINGANT, Gilles G, WESTENBERGER-TREUMANN, Margaretha, TRAUPE, Heiko, HINZ, Britta, FROSSARD, Philippe M, STADLER, Rudolf, LEIGH, Irene M, NÜRNBERG, Peter
Published in Human genetics (2003)
Published in Human genetics (2003)
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Journal Article
The use of Reflectance Confocal Microscopy to diagnose Basal Cell Carcinoma in the United Kingdom: A Prospective Observational Trial at a Single Centre
Stevens, Howard P, Pampena, Riccardo, Farnetani, Francesca, Pellicani, Giovanni, Angus, Colin, El-Jabbour, Joseph N
Published in British journal of dermatology (1951) (11.09.2024)
Published in British journal of dermatology (1951) (11.09.2024)
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Journal Article
The use of Reflectance Confocal Microscopy to diagnose Malignant Melanoma and Lentigo Maligna in the United Kingdom: A Prospective Observational Trial at a Single Centre
Stevens, Howard P, Pellacani, Giovanni, Angus, Colin, El-Jabbour, Joseph N
Published in British journal of dermatology (1951) (10.09.2024)
Published in British journal of dermatology (1951) (10.09.2024)
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Journal Article
Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma
Hunt, D M, Rickman, L, Whittock, N V, Eady, R A, Simrak, D, Dopping-Hepenstal, P J, Stevens, H P, Armstrong, D K, Hennies, H C, Küster, W, Hughes, A E, Arnemann, J, Leigh, I M, McGrath, J A, Kelsell, D P, Buxton, R S
Published in European journal of human genetics : EJHG (01.03.2001)
Published in European journal of human genetics : EJHG (01.03.2001)
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Journal Article
An unusual presentation of a common disease
Palamaras, Ioulios, Kench, Peter, Thomson, Penelope, Al-Dulaimi, Abdal Hameed, Stevens, Howard P, Robles, Wanda
Published in Dermatology online journal (15.03.2008)
Published in Dermatology online journal (15.03.2008)
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Journal Article
Characterization of Paraneoplastic Pemphigus Autoantigens by Immunoblot Analysis
Hashimoto, Takashi, Amagai, Masayuki, Watanabe, Kyoko, Chorzelski, Tadeusz P, Bhogal, Balbir S, Black, Martin M, Stevens, Howard P, Boorsma, Dick M, Korman, Neil J, Gamou, Shinobu, Shimizu, Nobuyoshi, Nishikawa, Takeji
Published in Journal of investigative dermatology (01.05.1995)
Published in Journal of investigative dermatology (01.05.1995)
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Journal Article
A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
WINTER, H, ROGERS, M. A, GEBHARDT, M, WOLLINA, U, BOXALL, L, CHITAYAT, D, BABUL-HIRJI, R, STEVENS, H. P, ZLOTOGORSKI, A, SCHWEIZER, J
Published in Human genetics (01.12.1997)
Published in Human genetics (01.12.1997)
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Journal Article
The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing
van Steensel, Maurice, Smith, Frances J.D., Steijlen, Peter M., Kluijt, Irma, Stevens, Howard P., Messenger, Andrew, Kremer, Hannie, Dunnill, M. Giles S., Kennedy, Cameron, Munro, Colin S., Doherty, Valerie R., McGrath, John A., Covello, Seana P., Coleman, Carrie M., Uitto, Jouni, McLean, W. H. Irwin
Published in American journal of human genetics (01.08.1999)
Published in American journal of human genetics (01.08.1999)
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Journal Article
The palmoplantar keratodermas: much more than palms and soles
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Book Review
Journal Article
N-Terminal Deletion in a Desmosomal Cadherin Causes the Autosomal Dominant Skin Disease Striate Palmoplantar Keratoderma
Rickman, Lisa, Šimrak, Danijela, Stevens, Howard P., Hunt, Debbie M., King, Ian A., Bryant, Stephen P., Eady, Robin A.J., Leigh, Irene M., Arnemann, Joachim, Magee, Anthony I., Kelsell, David P., Buxton, Roger S.
Published in Human molecular genetics (01.06.1999)
Published in Human molecular genetics (01.06.1999)
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Journal Article