Rosemarie M Watson

Rosemarie M Watson

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Rosemarie M Watson

Rosemarie M Watson

Publications by authors named "Rosemarie M Watson"

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Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

Orphanet J Rare Dis 2015 Oct 15;10:135. Epub 2015 Oct 15.

CHU Nantes, Service de Génétique Médicale, Unité de Génétique Moléculaire, 9 quai Moncousu, 44093, Nantes CEDEX 1, France.

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http://link.springer.com/content/pdf/10.1186%2Fs13023-015-03
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http://www.ojrd.com/content/10/1/135
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http://dx.doi.org/10.1186/s13023-015-0352-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608180PMC
October 2015

Use of systemic corticosteroids in management of a large congenital haemangioma of the scalp.

Pediatr Dermatol 2013 Nov-Dec;30(6):e121-4. Epub 2012 Sep 25.

Department of Paediatric Dermatology, Our Lady's Children's Hospital, Dublin, IrelandPaediatric Radiology, Our Lady's Children's Hospital, Dublin, IrelandDepartment of Paediatrics and Child Health, University College Cork, Cork, IrelandDepartment of Obstetrics, University College Cork, Cork, IrelandDepartment of Dermatology, South Infirmary Victoria Hospital, Cork, Ireland.

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http://dx.doi.org/10.1111/j.1525-1470.2012.01795.xDOI Listing
August 2014

Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.

J Allergy Clin Immunol 2014 Jul 28;134(1):82-91. Epub 2014 May 28.

Centre for Dermatology and Genetic Medicine, Division of Molecular Medicine, Colleges of Life Sciences and Medicine, Dentistry & Nursing, University of Dundee, Dundee, United Kingdom; National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2014.04.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090750PMC
July 2014

Response to IL-1-receptor antagonist in a child with familial cold autoinflammatory syndrome.

Pediatr Dermatol 2007 Jan-Feb;24(1):85-9

Department of Dermatology, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.

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http://dx.doi.org/10.1111/j.1525-1470.2007.00343.xDOI Listing
May 2007

ABCA12 is the major harlequin ichthyosis gene.

J Invest Dermatol 2006 Nov 10;126(11):2408-13. Epub 2006 Aug 10.

Centre for Cutaneous Research, Institute of Cell and Molecular Science, Queen Mary's School of Medicine and Dentistry, Queen Mary, University of London, London, UK.

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http://dx.doi.org/10.1038/sj.jid.5700455DOI Listing
November 2006

Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis.

J Invest Dermatol 2006 Aug 29;126(8):1770-5. Epub 2006 Jun 29.

Epithelial Genetics Group, Human Genetics Unit, Division of Pathology and Neuroscience, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK.

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http://dx.doi.org/10.1038/sj.jid.5700459DOI Listing
August 2006