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Frances J.D. Smith

University of Dundee

104

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PSENEN mutation in coexistent hidradenitis suppurativa and dowling-degos disease

2021 Indian Dermatology Online Journal
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Identification of clinically useful predictive genetic variants in pachyonychia congenita.

2021 Clinical and Experimental Dermatology
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087 Revisiting pachyonychia congenita: a case cohort study in 815 patients

2019 Journal of Investigative Dermatology
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Pachyonychia congenita responding favorably to a combination of surgical and medical therapies

2019 Dermatologic Therapy
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Enamel Anomalies in a Pachyonychia Congenita Patient with a Mutation in KRT16

2019 Journal of Investigative Dermatology
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Skin fragility, woolly hair syndrome with a desmoplakin mutation – a case from India

2018 International Journal of Dermatology
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Management of Plantar Keratodermas

2017 Journal of the American Podiatric Medical Association
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Keratin 17 mutations in four families from India with pachyonychia congenita

2017 Indian Journal of Dermatology
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Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants

2017 The Journal of Allergy and Clinical Immunology
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A novel KRT6A mutation in a case of pachyonychia congenita from India

2017 Indian Journal of Dermatology, Venereology and Leprology
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