G. Dunnill

发表

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yang Liu, Sen Yang, Miao Sun, 2009, Nature Genetics.

Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02

Chrysanthi Ainali, Xavier Estivill, Alka Saxena, 2019, Nature Communications.

Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

S. Cichon, M. Nöthen, C. Bodemer, 2009, Nature Genetics.

Primary cutaneous acral CD8+ T‐cell lymphoma of the ear: A case report

G. Dunnill, J. Pawade, E. Ormerod, 2019, Journal of cutaneous pathology.

The PROCLIPI international registry of early‐stage mycosis fungoides identifies substantial diagnostic delay in most patients

M. Weichenthal, U. Wehkamp, C. Klemke, 2018, The British journal of dermatology.

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.

C. Rodeck, J. Uitto, J. McGrath, 1995, Genomics.

Diagnosis and treatment of pyoderma gangrenosum

G. Dunnill, C. Probert, T. Brooklyn, 2006, BMJ : British Medical Journal.

gangrenosum Diagnosis and treatment of pyoderma

G. Dunnill, T. Brooklyn, Chris Probert Pyoderma, 2006 .

Is tocilizumab a potential therapeutic option for refractory unicentric Castleman disease?

G. Dunnill, R. Peck, K. Staines, 2018, Hematological oncology.

Angiolymphoid hyperplasia with eosinophilia successfully treated with oral steroids.

G. Dunnill, A. Fasanmade, C. Hughes, 2010, Quintessence international.

Should we be imaging lymph nodes at initial diagnosis of early-stage mycosis fungoides? Results from the PROCLIPI international Study.

U. Wehkamp, R. Cowan, O. Akilov, 2020, The British journal of dermatology.

Should we be imaging lymph nodes at initial diagnosis of early‐stage mycosis fungoides? Results from the PROspective Cutaneous Lymphoma International Prognostic Index (PROCLIPI) international study *

U. Wehkamp, R. Cowan, O. Akilov, 2021 .

Erratum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis (Nature Genetics (2009) 41 (228-233))

S. Cichon, M. Nöthen, C. Bodemer, 2009 .

Capillary rarefaction in the forearm skin in essential hypertension

Peter S. Mortimer, G. Dunnill, G. MacGregor, 1995, Journal of hypertension.