The Addition of Platelet-Rich Plasma to Facial Lipofilling: A Double-Blind, Placebo-Controlled, Randomized Trial von Willemsen, Joep C. N., Van Dongen, Joris, Spiekman, Maroesjka, Vermeulen, Karin M., Harmsen, Martin C., van der Lei, Berend, Stevens, H. P. Jeroen

Volltext

Metastatic Crohn's disease: a review von Palamaras, I, El-Jabbour, J, Pietropaolo, N, Thomson, P, Mann, S, Robles, W, Stevens, HP

Volltext

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness von Kelsell, D. P, Dunlop, J, Stevens, H. P, Lench, N. J, Liang, J. N, Parry, G, Mueller, R. F, Leigh, I. M

Volltext

Lateral Hooding of the Brow Revisited: Reverse Brow Lifting Versus the ROOF Lift von Balado, A. Sanchez, Stevens, H. P.

Volltext

Platelet-Rich Plasma Influences Expansion and Paracrine Function of Adipose-Derived Stromal Cells in a Dose-Dependent Fashion von Willemsen, Joep C. N., Spiekman, Maroesjka, Stevens, H. P. Jeroen, van der Lei, Berend, Harmsen, Martin C.

Volltext

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix von Winter, Hermelita, Labrèze, Christine, Roul, Sylvie, Taieb, Alain, Krieg, Thomas, Schweizer, Jürgen, Stevens, Howard P, Langbein, Lutz, Rogers, Mike A, Leigh, Irene M

Volltext

Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi population von Sinclair, C., O'Toole, E.A., Paige, D., El Bashir, H., Robinson, J., Dobson, R., Lench, N., Stevens, H.P., Hitman, G.A., Booy, R., Mein, C.A., Kelsell, D.P.

Volltext

Efficacy and safety of autologous adipose-derived stromal vascular fraction enriched with platelet-rich plasma in flap repair of transsphincteric cryptoglandular fistulas von Schouten, W. R., Arkenbosch, J. H. C., van der Woude, C. J., de Vries, A. C., Stevens, H. P., Fuhler, G. M., Dwarkasing, R. S., van Ruler, O., de Graaf, E. J. R.

Volltext

Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress von SWENSSON, O, LANGBEIN, L, MCMILLAN, J. R, STEVENS, H. P, LEIGH, I. M, MCLEAN, W. H. I, LANE, E. B, EADY, R. A. J

Volltext

The rainbow scale for the assessment of dermatochalasis of the female upper eyelid: A validated scale von Mooij, J.J., van de Lande, L.S., Pool, S.M.W., Stevens, H.P.J.D., van der Lei, B., van Dongen, J.A.

Volltext

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma von 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

Volltext

Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families von Shamsher, M.K., Navsaria, H.A., Stevens, H.P., Ratnavel, R.C., Purkis, P.E., Keisell, D.P., McLean, W.H.I., Cook, L.J., Griffiths, W.A.D., Gschmeissner, S., Spurr, N., Leigh, I.M.

Volltext

Characterization of Paraneoplastic Pemphigus Autoantigens by Immunoblot Analysis von 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

Volltext

Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography von Rugg, E.L., Common, J.E.A., Wilgoss, A., Stevens, H.P., Buchan, J., Leigh, I.M., Kelsell, D.P.

Volltext

A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix von WINTER, H, ROGERS, M. A, GEBHARDT, M, WOLLINA, U, BOXALL, L, CHITAYAT, D, BABUL-HIRJI, R, STEVENS, H. P, ZLOTOGORSKI, A, SCHWEIZER, J

Volltext

Envoplakin, a Possible Candidate Gene for Focal NEPPK/Esophageal Cancer (TOC): The Integration of Genetic and Physical Maps of the TOC Region on 17q25 von Risk, J.M., Ruhrberg, C., Hennies, H.-C., Mills, H.S., Di Colandrea, T., Evans, K.E., Ellis, A., Watt, F.M., Bishop, D.T., Spurr, N.K., Stevens, H.P., Leigh, I.M., Reis, A., Kelsell, D.P., Field, J.K.

Volltext

Towards using a Monolithic Active Pixel Sensor for in vivo beam monitoring of Intensity Modulated Radiotherapy von Page, R.F., Abbott, N.L., Davies, J., Dyke, E.L., Randles, H.J., Velthuis, J.J., Fletcher, S., Gregory, S.D., Hall, C., John, A., Lawrence, H., Stevens, P.H., Hugtenburg, R.P., Tunbridge, V.

Volltext

The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing von 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

Volltext

Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping von LAASS, M. W, HENNIES, H. C, PREIS, S, STEVENS, H. P, JUNG, M, LEIGH, I. M, WIENKER, T. F, REIS, A

Volltext

Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family von Kelsell, DP, Wilgoss, AL, Richard, G, Stevens, HP, Munro, CS, Leigh, IM

Volltext