F. Browne

发表

Ichthyosis with confetti presenting as collodion baby: a novel mutation in KRT10

D. Baty, A. Terron-Kwiatkowski, S. H. Foo, 2017, Clinical and experimental dermatology.

Predicting complications with pretreatment testing in infantile haemangioma treated with oral propranolol

Lilian Y. T. Tang, H. Shahidullah, M. Parulekar, 2015, British Journal of Ophthalmology.

Segmental pigmentation disorder – response

C. Moss, S. Taibjee, F. Browne, 2011, The British journal of dermatology.

Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines

K. Martin, A. Downe, K. Mayre‐Chilton, 2019, Orphanet Journal of Rare Diseases.

Under‐recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations

J. McGrath, C. Has, J. Mellerio, 2014, The British journal of dermatology.

Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12

M. Nahorski, Vykuntaraju K Gowda, C. Moss, 2018, The British journal of dermatology.

Use of a Novel Laparoscopic Gastrostomy Technique in Children With Severe Epidermolysis Bullosa

Rosie Jones, D. Parikh, K. Patel, 2014, Journal of pediatric gastroenterology and nutrition.

Dermatitis in an irritable infant

C. Ryan, M. McDermott, L. Roche, 2022, Clinical and experimental dermatology.

The p.Glu477Lys Mutation in Keratin 5 Is Strongly Associated with Mortality in Generalized Severe Epidermolysis Bullosa Simplex.

J. McGrath, J. Mellerio, S. Hoey, 2016, The Journal of investigative dermatology.

Multiple cerebral abscesses in Papillon–Lefèvre syndrome

I. Chapple, H. Kanthimathinathan, A. Kay, 2013, Child's Nervous System.

A randomized controlled trial protocol assessing the effectiveness, safety and cost‐effectiveness of methotrexate vs. ciclosporin in the treatment of severe atopic eczema in children: the TREatment of severe Atopic eczema Trial (TREAT)

C. Flohr, P. Williamson, P. Beattie, 2018, The British journal of dermatology.

Cutaneous Eruption Associated with Sirolimus in a Child with FAS-Associated Autoimmune Lymphoproliferative Syndrome.

J. Trayer, T. Leahy, F. Browne, 2023, Journal of clinical immunology.

A congenital smooth muscle hamartoma masquerading as a reticulate vascular naevus

M. Brundler, C. Moss, J. Hughes, 2013, Clincal and Experimental Dermatology.