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	Amedeo Prize 2008 The 21 Finalists

Neonatology

Free Subscription Articles published in Br J Dermatol Retrieve available abstracts of 27 articles: HTML format

Single Articles

April 2008
1. 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
2. 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
3. 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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4. 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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5. 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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   December 2007
6. 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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7. 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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8. 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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9. 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
10. 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
11. 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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12. 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
13. BERK DR , Bayliss SJ
    Sock-line bands in infancy.
    Br J Dermatol. 2007;.
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    July 2007
14. 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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15. HOSHINA D , Akiyama M, Hamasaka K, Shimizu H, et al
    An infantile case of pityriasis lichenoides et varioliformis acuta.
    Br J Dermatol. 2007;157:194-6.
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16. UGAJIN T , Yahara H, Moriyama Y, Sato T, et al
    Two siblings with neonatal pemphigus vulgaris associated with mild maternal disease.
    Br J Dermatol. 2007;157:192-4.
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17. REGNIER S , Dupin N, Le Danff C, Wassef M, et al
    Endothelial cells in infantile haemangiomas originate from the child and not from the mother (a fluorescence in situ hybridization-based study).
    Br J Dermatol. 2007;157:158-60.
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    June 2007
18. SHETH N , Greenblatt D, McGrath JA
    New KRT10 gene mutation underlying the annular variant of bullous congenital ichthyosiform erythroderma with clinical worsening during pregnancy.
    Br J Dermatol. 2007;.
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19. SEITZ CS , van Steensel M, Frank J, Senderek J, et al
    The Wnt signalling ligand RSPO4, causing inherited anonychia, is not mutated in a patient with congenital nail hypoplasia/aplasia with underlying skeletal defects.
    Br J Dermatol. 2007;.
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20. KISHI K , Matsuda N, Kubota Y, Katsube KI, et al
    Rapid, severe repigmentation of congenital melanocytic naevi after curettage and dermabrasion: histological features.
    Br J Dermatol. 2007;156:1251-7.
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    May 2007
21. NAKANO H , Toyomaki Y, Ohashi S, Nakano A, et al
    Novel COL7A1 mutations in a Japanese family with transient bullous dermolysis of the newborn associated with pseudosyndactyly.
    Br J Dermatol. 2007;.
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22. DALLE S , Marrou K, Balme B, Thomas L, et al
    Neonatal follicular mucinosis.
    Br J Dermatol. 2007;.
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23. 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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24. 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.
    PubMed     Related articles    Abstract available
    
    
    
25. 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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    March 2007
26. MARQUE MM , Guillot B, Le Gallic G, Bessis D, et al
    Raised limb bands in infancy: a post-traumatic aetiology?
    Br J Dermatol. 2007;156:578-9.
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    January 2007
27. 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;.
    PubMed     Related articles    Abstract available
    
    

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