Noor Almaani

New Glycine Substitution Mutations in Type VII Collagen Underlying Epidermolysis Bullosa Pruriginosa but the Phenotype is not Explained by a Common Polymorphism in the Matrix Metalloproteinase-1 Gene Promoter

Noor Almaani, Lu Liu, Naomi Harrison et al. · Acta Dermato Venereologica · 2009 · 47 citations · Full text

Medicine, Dermatology, Genetics +15

Loss-of-Function FERMT1 Mutations in Kindler Syndrome Implicate a Role for Fermitin Family Homolog-1 in Integrin Activation

Joey E. Lai‐Cheong, Maddy Parsons, Akio Tanaka et al. · American Journal Of Pathology · 2009 · 43 citations · Full text

Life Sciences, Genetics, Molecular Biology +12

The molecular skin pathology of familial primary localized cutaneous amyloidosis

Akio Tanaka, Joey E. Lai‐Cheong, Peter C. van den Akker et al. · Experimental Dermatology · 2010 · 43 citations · Full text

Medicine, Dermatology, Pathology +13

Autosomal dominant junctional epidermolysis bullosa

Noor Almaani, L. Liu, Patricia J.C. Dopping-Hepenstal et al. · British Journal of Dermatology · 2008 · 36 citations

Dentistry, Dermatology, Genetics +17

Raltegravir-induced Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) syndrome – Implications for clinical practice and patient safety

Melissa Perry, Noor Almaani, Nemesha Desai et al. · International Journal of STD & AIDS · 2013 · 26 citations

Medicine, Infectious Diseases, Pharmacotherapy +17