Hannele P. Heikkila
Helsinki, Finland
Last Updated: 09/26/2026
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Found 9 publications
Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: February 08, 2021
Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma.
Journal: Acta dermato-venereologica
Published: January 16, 2020
Novel TMEM173 Mutation and the Role of Disease Modifying Alleles.
Journal: Frontiers in immunology
Published: August 07, 2019
Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutation.
Journal: Journal of the American Academy of Dermatology
Published: May 02, 2019
Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility.
Journal: American journal of human genetics
Published: October 14, 2016
Intrafamily and Interfamilial Phenotype Variation and Immature Immunity in Patients With Netherton Syndrome and Finnish SPINK5 Founder Mutation.
Journal: JAMA dermatology
Published: February 12, 2016
IgE allergen component-based profiling and atopic manifestations in patients with Netherton syndrome.
Journal: The Journal of allergy and clinical immunology
Published: February 27, 2014
Skin problems in a swollen lower limb
Journal: Duodecim; laaketieteellinen aikakauskirja
Published: October 29, 2013
The histopathology of idiopathic pulmonary fibrosis in West Highland white terriers shares features of both non-specific interstitial pneumonia and usual interstitial pneumonia in man.
Journal: Journal of comparative pathology
Published: November 19, 2012
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Last Updated: 09/26/2026