Author

Patricia A. Lovell

Observed names: P A LOVELL, P Lovell, P. Lovell, P.A. Lovell, Patricia Lovell

Institution: St Thomas' Hospital

Observed institutions: St Thomas' Hospital, Institute of Cancer Research, St George's, University of London, Guy's and St Thomas' NHS Foundation Trust, St George’s University Hospitals NHS Foundation Trust, Institute of Cancer Research, Royal Marsden Hospital, McMaster University

OpenAlex ID: A5010655490

A Homozygous Nonsense Mutation within the Dystonin Gene Coding for the Coiled-Coil Domain of the Epithelial Isoform of BPAG1 Underlies a New Subtype of Autosomal Recessive Epidermolysis Bullosa Simplex

2010 · Richard W. Groves, Lu Liu, et al. · Journal of Investigative Dermatology · 143

Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa

2019 · Su M. Lwin, Farhatullah Syed, et al. · JCI Insight · 93

Autosomal Recessive Epidermolysis Bullosa Simplex Due to Loss of BPAG1-e Expression

2011 · Lu Liu, Patricia J. Dopping-Hepenstal, et al. · Journal of Investigative Dermatology · 61

Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1 ) in a patient with concomitant simplex and junctional epidermolysis bullosa

2018 · Hassan Vahidnezhad, Leila Youssefian, et al. · Human Mutation · 38

Autosomal dominant junctional epidermolysis bullosa

2008 · N. Almaani, L. Liu, et al. · British Journal of Dermatology · 38

Human Peritoneal Mesothelial Cells Display Phagocytic and Antigen-Presenting Functions to Contribute to Intraperitoneal Immunity

2016 · Tanya J. Shaw, Xiang Y. Zhang, et al. · International Journal of Gynecological Cancer · 27

Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica

2019 · Alexandros Onoufriadis, Chao-Kai Hsu, et al. · Journal of Investigative Dermatology · 16

Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica

2020 · Hassan Vahidnezhad, Leila Youssefian, et al. · Human Mutation · 15

Management and treatment of pruritus.

2007 · P Lovell, R B Vender · PubMed · 13

Normal and SV40 transfected human peritoneal mesothelial cells produce IL-6 and IL-8 : implication for gynaecological disease

2002 · X Y ZHANG, M GUCKIAN, et al. · Clinical & Experimental Immunology · 6

409 Next generation sequencing-directed treatment in a patient with two co-existing genodermatoses: Acrodermatitis enteropathica (AE) and recessive dystrophic epidermolysis bullosa (RDEB)

2019 · H. Vahidnezhad, L. Youssefian, et al. · Journal of Investigative Dermatology

796 Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) associated with different subtypes of epidermolysis bullosa

2018 · H. Vahidnezhad, L. Youssefian, et al. · Journal of Investigative Dermatology

Clinicopathologic and molecular significance of intra-epidermal type VII collagen in inherited skin blistering

2009 · Noor Almaani, Lei Liu, et al. · Research Portal (King's College London)

Works count: 13

Citation count: 450

H-index: 9

I10-index: 9