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	The Medical Article of the Year 2008: Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007; 447:661-78. Free full-text

Neonatology

Free Subscription Articles published in Br J Dermatol Retrieve available abstracts of 25 articles: HTML format

Single Articles

August 2008
1. TSIANAKAS A , Kienast AK, Hoeger PH
   Infantile-onset cutaneous T-cell lymphoma.
   Br J Dermatol. 2008.
   PubMed     Related articles    Abstract available
   
   
   July 2008
2. KINSLER VA , Chong WK, Aylett SE, Atherton DJ, et al
   Complications of congenital melanocytic naevi in children: analysis of 16 years' experience and clinical practice.
   Br J Dermatol. 2008.
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3. KUBO T , Takagi T, Yamaguchi Y, Yano K, et al
   Congenital peristernal dermal sinuses: a new entity?
   Br J Dermatol. 2008;.
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   June 2008
4. GALLUS S , Naldi L
   Distribution of congenital melanocytic naevi and congenital naevus-like naevi in a survey of 3406 Italian schoolchildren.
   Br J Dermatol. 2008;.
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5. BADELOE S , van Geel M, Nagtzaam I, Rubio-Gozalbo ME, et al
   Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5.
   Br J Dermatol. 2008;158:1378-80.
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   April 2008
6. BASELGA E , Cordisco MR, Garzon M, Lee MT, et al
   Rapidly involuting congenital haemangioma associated with transient thrombocytopenia and coagulopathy: a case series.
   Br J Dermatol. 2008;.
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   March 2008
7. D'HAUW A , Seyger MM, Groenen PJ, Weemaes CM, et al
   Cutaneous graft-versus-host-like histology in childhood. Importance of clonality analysis in differential diagnosis. A case report.
   Br J Dermatol. 2008;.
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8. SETHURAMAN G , Khaitan BK, Dash SS, Chandramohan K, et al
   Ichthyosiform erythroderma with rickets: report of five cases.
   Br J Dermatol. 2008;158:603-6.
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   February 2008
9. LIANG MG , Maccario S, Rahbar R, Kozakewich HP, et al
   Glucose transporter-1 protein is immunohistochemically expressed in subglottic infantile haemangioma.
   Br J Dermatol. 2008;.
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10. AKIYAMA M , Sakai K, Hatamochi A, Yamazaki S, et al
    Novel compound heterozygous nonsense and missense ABCA12 mutations lead to nonbullous congenital ichthyosiform erythroderma.
    Br J Dermatol. 2008;.
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11. BROWN VL , Farrant PB, Turner RJ, Price ML, et al
    Multiple aggressive squamous skin cancers in association with nonbullous congenital ichthyosiform erythroderma.
    Br J Dermatol. 2008;.
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    January 2008
12. TORAL-LOPEZ J , Gonzalez-Huerta LM, Cuevas-Covarrubias SA
    Segregation analysis in X-linked ichthyosis: paternal transmission of the affected X-chromosome.
    Br J Dermatol. 2008;.
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    December 2007
13. CUEVAS-COVARRUBIAS SA , Gonzalez-Huerta LM
    Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis.
    Br J Dermatol. 2007;.
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14. MONARI P , Gualdi G, Fantini F, Giannetti A, et al
    Cutaneous neonatal lupus erythematosus in four siblings.
    Br J Dermatol. 2007;.
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15. CHISHTI MS , Kausar N, Rafiq MA, Amin M, et al
    A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani family.
    Br J Dermatol. 2007;.
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16. NERI I , Savoia F, Giacomini F, Patrizi A, et al
    Anonychia, hyponychia and spontaneous amputation of the distal phalanges as a consequence of ischaemic necrosis of the extremities after umbilical catheterization.
    Br J Dermatol. 2007;157:1299-301.
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    November 2007
17. THOMAS AC , Sinclair C, Mahmud N, Cullup T, et al
    Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis.
    Br J Dermatol. 2007;.
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    October 2007
18. TSUBOTA A , Akiyama M, Sakai K, Yanagi T, et al
    Congenital ichthyosiform erythroderma mimicking ichthyosis bullosa of Siemens.
    Br J Dermatol. 2007;.
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19. YU HJ , Shin H, Kang MS, Kim JS, et al
    A case of primary anetoderma in an infant.
    Br J Dermatol. 2007;.
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    September 2007
20. BERK DR , Bayliss SJ
    Sock-line bands in infancy.
    Br J Dermatol. 2007;.
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    July 2007
21. ESPOSITO G , Tadini G, Paparo F, Viola A, et al
    Transglutaminase 1 deficiency and corneocyte collapse: an indication for targeted molecular screening in autosomal recessive congenital ichthyosis.
    Br J Dermatol. 2007;.
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    May 2007
22. NISHIZAWA A , Toyomaki Y, Nakano A, Takeuchi S, et al
    A novel H1 domain mutation in the keratin 2 gene in a Japanese family with ichthyosis bullosa of Siemens.
    Br J Dermatol. 2007;156:1042-4.
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23. MAZEREEUW-HAUTIER J , Bitoun E, Chevrant-Breton J, Man SY, et al
    Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients.
    Br J Dermatol. 2007;156:1015-9.
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24. WANG WH , Li LF, Zhang Q, Yang SM, et al
    Ultrastructural features of ichthyosis hystrix strongly resembling Lambert type.
    Br J Dermatol. 2007;156:1027-31.
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    January 2007
25. VERFAILLE CJ , Vanhoutte FP, Blanchet-Bardon C, van Steensel MA, et al
    Oral liarozole vs. acitretin in the treatment of ichthyosis: a phase II/III multicentre, double-blind, randomized, active-controlled study.
    Br J Dermatol. 2007;.
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