Home The Word Brain My Amedeo FAQ Privacy About Flying Publisher   


OLIENA
Language recovery after stroke
App | Video | PDF (278 pp) | Web

  Neonatology

  Free Subscription


Articles published in Br J Dermatol

Retrieve available abstracts of 31 articles:
HTML format
Text format



Single Articles


    February 2019
  1. WELFRINGER-MORIN A, Fraitag S, Balguerie X, Laaengh-Massoni C, et al
    Late ulceration of residual abortive infantile hemangioma: a rare complication.
    Br J Dermatol. 2019 Feb 4. doi: 10.1111/bjd.17717.
    PubMed     Text format     Abstract available


    January 2019
  2. REHBINDER EM, Winger AJ, Landro L, Asarnoj A, et al
    Dry skin and skin barrier in early infancy.
    Br J Dermatol. 2019 Jan 13. doi: 10.1111/bjd.17626.
    PubMed     Text format     Abstract available


    December 2018
  3. ZHU PQ, Yan HM, Zhao HJ, Guo DY, et al
    A novel premature termination mutation in FDPS in a Chinese family with disseminated superficial actinic porokeratosis.
    Br J Dermatol. 2018 Dec 18. doi: 10.1111/bjd.17531.
    PubMed     Text format     Abstract available


    November 2018
  4. NOWROUZIAN FL, Ljung A, Nilsson S, Hesselmar B, et al
    Neonatal gut colonisation by Staphylococcus aureus strains with certain adhesins and superantigens is negatively associated with subsequent development of atopic eczema.
    Br J Dermatol. 2018 Nov 25. doi: 10.1111/bjd.17451.
    PubMed     Text format     Abstract available


  5. NOVOA M, Baselga E, Beltran S, Giraldo L, et al
    Interventions for infantile haemangiomas of the skin: abridged Cochrane systematic review including GRADE assessments.
    Br J Dermatol. 2018 Nov 10. doi: 10.1111/bjd.17407.
    PubMed     Text format     Abstract available


  6. XU CC, Chen H, Sun JF
    Image Gallery: Severe combined immunodeficiency presenting with disseminated bacille Calmette-Guerin.
    Br J Dermatol. 2018;179:e194.
    PubMed     Text format    


    October 2018
  7. NARANG T, Singh SM
    Letter in response: Mid-face Toddler Excoriation Syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.
    Br J Dermatol. 2018 Oct 19. doi: 10.1111/bjd.17338.
    PubMed     Text format     Abstract available


  8. ROMANO R, Grasso F, Gallo V, Cirillo E, et al
    A case of Incontinentia Pigmenti associated with congenital absence of portal vein system and nodular regenerative hyperplasia.
    Br J Dermatol. 2018 Oct 16. doi: 10.1111/bjd.17319.
    PubMed     Text format     Abstract available


  9. PLUMPTRE I, Stuart G, Cerullo A, Kinsler V, et al
    Use of sedation instead of general anaesthesia for screening MRI in congenital melanocytic naevi under the age of 1 year is a successful, safe, and economical first line approach.
    Br J Dermatol. 2018 Oct 3. doi: 10.1111/bjd.17263.
    PubMed     Text format     Abstract available


    September 2018
  10. MAZEREEUW-HAUTIER J, Vahlquist A, Traupe H, Bygum A, et al
    Management of congenital ichthyoses: European guidelines of care: Part One.
    Br J Dermatol. 2018 Sep 14. doi: 10.1111/bjd.17203.
    PubMed     Text format     Abstract available


  11. JANMOHAMED SR
    Minimizing differences in treatment: expert- and evidence-based guidelines for propranolol treatment of infantile haemangiomas in the U.K. and beyond.
    Br J Dermatol. 2018;179:553-554.
    PubMed     Text format    


    August 2018
  12. MCALEER MA, Jakasa I, Hurault G, Sarvari P, et al
    Systemic and stratum corneum biomarkers of severity in infant AD include markers of innate and Th-related immunity and angiogenesis.
    Br J Dermatol. 2018 Aug 22. doi: 10.1111/bjd.17088.
    PubMed     Text format     Abstract available


  13. GROOT J, Nybo Andersen AM, Adam A, Tind Nielsen TE, et al
    Associations between maternal socioeconomic position and psoriasis: A cohort study among the offspring of the Danish National Birth Cohort.
    Br J Dermatol. 2018 Aug 16. doi: 10.1111/bjd.17091.
    PubMed     Text format     Abstract available


    July 2018
  14. POLUBOTHU S, Glover M, Holder SE, Kinsler VA, et al
    Uniparental disomy as a mechanism for CERS3-mutated autosomal recessive congenital ichthyosis.
    Br J Dermatol. 2018 Jul 14. doi: 10.1111/bjd.16999.
    PubMed     Text format     Abstract available


    June 2018
  15. MOSS C, Srinivas SM, Sarveswaran N, Nahorski M, et al
    Mid-face Toddler Excoriation Syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.
    Br J Dermatol. 2018 Jun 27. doi: 10.1111/bjd.16893.
    PubMed     Text format     Abstract available


  16. MAZEREEUW-HAUTIER J, Hernandez-Martin A, O'Toole EA, Bygum A, et al
    Management of congenital ichthyoses: European guidelines of care: Part Two.
    Br J Dermatol. 2018 Jun 13. doi: 10.1111/bjd.16882.
    PubMed     Text format     Abstract available


    May 2018
  17. SOLMAN L, Glover M, Beattie PE, Buckley H, et al
    Oral propranolol in the treatment of proliferating infantile haemangiomas: The British Society for Paediatric Dermatology consensus guidelines.
    Br J Dermatol. 2018 May 17. doi: 10.1111/bjd.16779.
    PubMed     Text format     Abstract available


    February 2018
  18. LUNDIN S, Wahlgren CF, Bergstrom A, Johansson EK, et al
    Use of emollients and topical glucocorticoids among adolescents with eczema - datafrom the population-based birth cohort BAMSE.
    Br J Dermatol. 2018 Feb 25. doi: 10.1111/bjd.16484.
    PubMed     Text format     Abstract available


  19. CSOMA ZR, Kemeny L
    Image Gallery: Acquired zinc deficiency of prematurity.
    Br J Dermatol. 2018;178:e144.
    PubMed     Text format    


  20. ZHANG G, Chen J, Yan Liu X
    Image Gallery: Rapidly spontaneous onset of erythroderma in a neonate.
    Br J Dermatol. 2018;178:e142.
    PubMed     Text format    


    January 2018
  21. MAHON C, Heron G, Perkins D, Drage A, et al
    Oral propranolol for infantile haemangioma may be associated with transient gross motor delay.
    Br J Dermatol. 2018 Jan 12. doi: 10.1111/bjd.16334.
    PubMed     Text format     Abstract available


    December 2017
  22. LUO Y, Liu J
    Image Gallery: Primary cutaneous precursor B-lymphoblastic lymphoma in an infant.
    Br J Dermatol. 2017;177:e353.
    PubMed     Text format    


    November 2017
  23. MELLERIO JE
    Neonatal aggressive systemic mastocytosis.
    Br J Dermatol. 2017;177:1167-1168.
    PubMed     Text format    


    October 2017
  24. EGGEN CAM, Lommerts JE, van Zuuren EJ, Limpens J, et al
    Laser treatment of congenital melanocytic nevi: a systematic review.
    Br J Dermatol. 2017 Oct 27. doi: 10.1111/bjd.16094.
    PubMed     Text format     Abstract available


    September 2017
  25. HOTZ A, Fagerberg C, Vahlquist A, Bygum A, et al
    Identification of Mutations in SDR9C7 in 6 Families with Autosomal Recessive Congenital Ichthyosis.
    Br J Dermatol. 2017 Sep 14. doi: 10.1111/bjd.15994.
    PubMed     Text format     Abstract available


    April 2017
  26. HAUSSER I
    Ichthyoses: new insights unravel defects in skin barrier function resulting in diverse clinical and morphological phenotypes.
    Br J Dermatol. 2017;176:863-864.
    PubMed     Text format    


    February 2017
  27. DICK A, Tantcheva-Poor I, Oji V, Giehl KA, et al
    Diminished Protein-Bound omega-Hydroxylated Ceramides In The Skin Of Ichthyosis Patients With 12r-Lox Or Elox-3 Deficiency.
    Br J Dermatol. 2017 Feb 24. doi: 10.1111/bjd.15406.
    PubMed     Text format     Abstract available


  28. VERMA SB, Mittal A, Wollina U, Eckstein GH, et al
    Chanarin-Dorfman syndrome with rare renal involvement.
    Br J Dermatol. 2017;176:545-548.
    PubMed     Text format    


    January 2017
  29. TAKEICHI T, Nomura T, Takama H, Kono M, et al
    Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis by a homozygous deletion mutation in SDR9C7.
    Br J Dermatol. 2017 Jan 23. doi: 10.1111/bjd.15315.
    PubMed     Text format     Abstract available


    August 2016
  30. ORTEGA-RECALDE O, Silgado D, Fetiva C, Fonseca DJ, et al
    Transcriptome analysis of skin in a case of Ichthyosis Curth-Macklin caused by a KRT1 mutation.
    Br J Dermatol. 2016 Aug 12. doi: 10.1111/bjd.14969.
    PubMed     Text format     Abstract available


    June 2016
  31. SAITO R, Boyce A, Hsu CK, Rashidghamat E, et al
    Predictive phenotyping of inherited ichthyosis by next generation DNA sequencing.
    Br J Dermatol. 2016 Jun 13. doi: 10.1111/bjd.14807.
    PubMed     Text format     Abstract available


Thank you for your interest in scientific medicine.


AMEDEO Neonatology is free of charge.
This policy is made possible thanks to a media sponsorship by Boehringer Ingelheim.

Design: