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Neonatology

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

Single Articles

January 2012
1. LI Q , Schumacher W, Siegel D, Jablonski D, et al
   Cutaneous features of pseudoxanthoma elasticum in a patient with generalized arterial calcification of infancy due to a homozygous missense mutation in the ENPP1 gene.
   Br J Dermatol. 2012 Jan 9. doi: 10.1111/j.1365-2133.2012.10811.
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   November 2011
2. DUFOUR C , Souillet AL, Chaneliere C, Jouen F, et al
   Successful management of severe infant bullous pemphigoid with omalizumab.
   Br J Dermatol. 2011 Nov 19. doi: 10.1111/j.1365-2133.2011.10748.
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   October 2011
3. ASSFALG M , Bortoletti E, D'Onofrio M, Pigozzi R, et al
   An Exploratory (1) H-NMR Metabolomics Study Reveals Altered Urine Spectral Profiles in Infants with Atopic Dermatitis.
   Br J Dermatol. 2011 Oct 27. doi: 10.1111/j.1365-2133.2011.10711.
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4. TANAKA T , Satoh T, Tanaka A, Yokozeki H, et al
   Congenital insensitivity to pain with anhidrosis: a case with preserved itch sensation to histamine and partial pain sensation.
   Br J Dermatol. 2011 Oct 27. doi: 10.1111/j.1365-2133.2011.10706.
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5. FLUHR JW , Darlenski R, Lachmann N, Baudouin C, et al
   Infant epidermal skin-physiology: Adaptation after birth.
   Br J Dermatol. 2011 Oct 3. doi: 10.1111/j.1365-2133.2011.10659.
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   September 2011
6. YUN SJ , Kwon OS, Han JH, Kweon SS, et al
   Clinical Characteristics and Risk of Melanoma Development from Giant Congenital Melanocytic Naevi in Korea: A Nationwide Retrospective Study.
   Br J Dermatol. 2011 Sep 16. doi: 10.1111/j.1365-2133.2011.10636.
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   July 2011
7. STINCO G , Argenziano G, Favot F, Valent F, et al
   Absence of Clinical and Dermoscopic Differences Between Congenital and Non-Congenital Melanocytic Nevi in a Cohort of Two-Year-Old Children.
   Br J Dermatol. 2011 Jul 25. doi: 10.1111/j.1365-2133.2011.10538.
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8. FUKUDA S , Hamada T, Ishii N, Sakaguchi S, et al
   Novel ATP-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma.
   Br J Dermatol. 2011 Jul 5. doi: 10.1111/j.1365-2133.2011.10516.
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9. BODEMER C , Bourrat E, Mazereew-Hautier J, Boralevi F, et al
   Short and medium-term efficacy of specific hydrotherapy in inherited ichthyosis.
   Br J Dermatol. 2011 Jul 5. doi: 10.1111/j.1365-2133.2011.10510.
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   June 2011
10. FEITO-RODRIGUEZ M , de Lucas-Laguna R, Bastian BC, Leboit P, et al
    Nodular lesions arising in a large congenital melanocytic nevus in a newborn with eruptive disseminated spitz nevi (nodular lesions arising in a congenital melanocytic nevus and eruptive spitz nevi).
    Br J Dermatol. 2011 Jun 28. doi: 10.1111/j.1365-2133.2011.10502.
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11. RODRIGUEZ-PAZOS L , Ginarte M, Fachal L, Toribio J, et al
    Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in Autosomal Recessive Congenital Ichthyosis from Galicia (NW Spain): evidence of founder effects.
    Br J Dermatol. 2011 Jun 11. doi: 10.1111/j.1365-2133.2011.10454.
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12. SAMUELOV L , Fuchs-Telem D, Sarig O, Sprecher E, et al
    An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous family.
    Br J Dermatol. 2011;164:1390-2.
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    May 2011
13. ITINTEANG T , Tan ST, Brasch HD, Vishvanath A, et al
    Primitive erythropoiesis in infantile haemangioma.
    Br J Dermatol. 2011;164:1097-100.
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    April 2011
14. NATSUGA K , Akiyama M, Shimizu H
    Malignant Skin Tumours in Inherited Ichthyosis Patients.
    Br J Dermatol. 2011 Apr 25. doi: 10.1111/j.1365-2133.2011.10381.
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    February 2011
15. HOEGER PH
    Infantile haemangioma: New aspects on the pathogenesis of the most common skin tumour in children.
    Br J Dermatol. 2011;164:234-5.
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16. ARIN MJ , Oji V, Emmert S, Hausser I, et al
    Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis.
    Br J Dermatol. 2011;164:442-7.
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    January 2011
17. AUGUST PJ , Ferguson JE, Madan V
    A study of the efficacy of carbon dioxide and pigment specific lasers in the treatment of medium sized congenital melanocytic naevi.
    Br J Dermatol. 2011 Jan 28. doi: 10.1111/j.1365-2133.2011.10236.
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18. HOREV L , Babay S, Ramot Y, Saad-Edin B, et al
    Mutations in two genes on chromosome 13, resulting in a complex hair and skin phenotype due to two rare genodermatoses, KLICK and ARWH/HS.
    Br J Dermatol. 2011 Jan 28. doi: 10.1111/j.1365-2133.2011.10229.
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19. PHILLIPS R
    Aquagenic palmoplantar keratoderma: a new sign of cystic fibrosis?
    Br J Dermatol. 2011;164:224-5.
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20. OBARZANEK-FOJT M , Favre B, Huber M, Ryser S, et al
    Induction of p38, tumour necrosis factor-alpha and RANTES by mechanical stretching of keratinocytes expressing mutant keratin 10R156H.
    Br J Dermatol. 2011;164:125-34.
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    November 2010
21. GILD R , Clay CD, Morey S
    Aquagenic wrinkling of the palms in cystic fibrosis and the cystic fibrosis carrier state: a case-control study.
    Br J Dermatol. 2010;163:1082-4.
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    October 2010
22. CHAMCHEU JC , Pihl-Lundin I, Mouyobo CE, Gester T, et al
    Immortalized keratinocytes derived from epidermolytic ichthyosis patients reproduce the disease phenotype: a useful in vitro model for testing new treatments.
    Br J Dermatol. 2010 Oct 26. doi: 10.1111/j.1365-2133.2010.10092.
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23. DING YG , Wang JY, Qiao JJ, Mao XH, et al
    A novel mutation in MBTPS2 causes ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome in a Chinese family.
    Br J Dermatol. 2010;163:886-9.
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24. ARNOLD AW , Itin PH, Pigors M, Kohlhase J, et al
    Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria.
    Br J Dermatol. 2010;163:866-9.
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    September 2010
25. NAKAI K , Yoneda K, Moriue T, Munehiro A, et al
    Seborrhoeic keratoses and acanthosis nigricans in a long-term survivor of thanatophoric dysplasia.
    Br J Dermatol. 2010;163:656-8.
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    May 2010
26. SHINGAKI K , Matsuzaki S, Taniguchi M, Kubo T, et al
    Molecular mechanism of kallikrein-related peptidase 8/neuropsin-induced hyperkeratosis in inflamed skin.
    Br J Dermatol. 2010.
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    March 2010
27. COVACIU C , Castori M, De Luca N, Ghirri P, et al
    Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10.
    Br J Dermatol. 2010.
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