Successful treatment with oral alitretinoin in women of childbearing potential with Darier's disease von Zamiri, M., Munro, C.S.

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Diagnosis of and Screening for Cytomegalovirus Infection in Pregnant Women von Munro, S. C, Hall, B, Whybin, L. R, Leader, L, Robertson, P, Maine, G. T, Rawlinson, W. D

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The neuropsychiatric phenotype in Darier disease von Gordon-Smith, K., Jones, L.A., Burge, S.M., Munro, C.S., Tavadia, S., Craddock, N.

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Development of Multiplex PCRs for Detection of Common Viral Pathogens and Agents of Congenital Infections von McIver, C. J, Jacques, C. F. H, Chow, S. S. W, Munro, S. C, Scott, G. M, Roberts, J. A, Craig, M. E, Rawlinson, W. D

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Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene von Nellen, R.G.L., Steijlen, P.M., Hennies, H.C., Fischer, J., Munro, C.S., Jonkman, M.F., van Steensel, M.A.M., van Geel, M.

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Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease von SAKUNTABHAI, A, RUIZ-PEREZ, V, KUCHERLAPATI, R, REES, J. L, OWEN, M, LATHROP, G. M, MONACO, A. P, STRACHAN, T, HOVNANIAN, A, CARTER, S, JACOBSEN, N, BURGE, S, MONK, S, SMITH, M, MUNRO, C. S, O'DONOVAN, M, CRADDOCK, N

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Peripheral nerve blockade for biopsy of plantar skin von Zamiri, M., Wylie, D., Munro, C.S.

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A Missense Mutation in Connexin26, D66H, Causes Mutilating Keratoderma with Sensorineural Deafness (Vohwinkel's Syndrome) in Three Unrelated Families von Maestrini, Elena, Korge, Bernhard P., Ocaña-Sierra, Juan, Calzolari, Elisa, Cambiaghi, Stefano, Scudder, Pat M., Hovnanian, Alain, Monaco, Anthony P., Munro, Colin S.

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Correlates of placental infection with cytomegalovirus, parvovirus B19 or human herpes virus 7 von Chow, S.S.W., Craig, M.E., Jacques, C.F.H., Hall, B., Catteau, J., Munro, S.C., Scott, G.M., Camaris, C., McIver, C.J., Rawlinson, W.D.

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Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2 von COVELLO, S. P, SMITH, F. J. D, SMITT, J. H. S, PALLER, A. S, MUNRO, C. S, JONKMAN, M. F, UITTO, J, MCLEAN, W. H. I

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Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma von Zamiri, M., Smith, F.J.D., Campbell, L.E., Tetley, L., Eady, R.A.J., Hodgins, M.B., McLean, W.H.I., Munro, C.S.

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Genetic epidemiology of Darier's disease: a population study in the west of Scotland von Tavadia, S., Mortimer, E., Munro, C.S.

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ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class von RUIZ-PEREZ, V. L, CARTER, S. A, VAHLQUIST, A, GOBELLO, T, MAZZANTI, C, REGGAZINI, R, NAGY, G, MUNRO, C. S, STRACHAN, T, HEALY, E, TODD, C, REES, J. L, STEIJLEN, P. M, CARMICHAEL, A. J, LEWIS, H. M, HOHL, D, ITIN, P

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Expression of the sarco/endoplasmic reticulum calcium ATPase type 2 and 3 isoforms in normal skin and Darier's disease von Tavadia, S., Authi, K.S., Hodgins, M.B., Munro, C.S.

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Post-menopausal frontal fibrosing alopecia von Dawn, G., Holmes, S. C., Moffat, D., Munro, C. S.

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Pachyonychia congenita type 2: abnormal dentition extending into adulthood von Zamiri, M., McLean, W.H.I., Hodgins, M.B., Munro, C.S.

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Loricrin Mutation in Vohwinkel’s Keratoderma Is Unique to the Variant with Ichthyosis von Korge, Bernhard P., Ishida-Yamamoto, Akemi, Pünter, Claudia, Dopping-Hepenstal, Patricia J.C., Iizuka, Hajime, Stephenson, Anthea, Eady, Robin A.J., Munro, Colin S.

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The phenotype of Darier's disease: penetrance and expressivity in adults and children von MUNRO, C.S.

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Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis von Pohler, E., Cunningham, F., Sandilands, A., Cole, C., Digby, S., McMillan, J.R., Aristodemou, S., McGrath, J.A., Smith, F.J.D., McLean, W.H.I., Munro, C.S., Zamiri, M.

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Cross-linked envelopes in nail plate in lamellar ichthyosis von Rice, R.H., Crumrine, D., Hohl, D., Munro, C.S., Elias, P.M.

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