M. Virtanen

发表

Improved topical treatment of lamellar ichthyosis: a double‐blind study of four different cream formulations

A. Gånemo, M. Virtanen, A. Vahlquist, 1999, The British journal of dermatology.

Integrated pharmacokinetics and pharmacodynamics of the novel calcium sensitizer levosimendan as assessed by systolic time intervals.

H. Scheinin, M. Virtanen, L. Lehtonen, 1998, International journal of clinical pharmacology and therapeutics.

Epidermolysis bullosa simplex due to KRT5 mutations: mutation‐related differences in cellular fragility and the protective effects of trimethylamine N‐oxide in cultured primary keratinocytes

H. Törmä, M. Virtanen, A. Vahlquist, 2010, British Journal of Dermatology.

CARD14‐associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris

A. Bowcock, K. Holland, R. Lifton, 2018, Journal of the American Academy of Dermatology.

Genotype–Phenotype Correlations Emerging from the Identification of Missense Mutations in MBTPS2

K. Grzeschik, A. Mégarbané, R. Happle, 2013, Human mutation.

Generalized and naevoid epidermolytic ichthyosis in Denmark: clinical and mutational findings.

A. Gånemo, M. Virtanen, A. Vahlquist, 2013, Acta dermato-venereologica.

Immortalized keratinocytes derived from patients with epidermolytic ichthyosis reproduce the disease phenotype: a useful in vitro model for testing new treatments

A. Moustakas, H. Törmä, M. Virtanen, 2011, The British journal of dermatology.

The clinical spectrum of congenital ichthyosis in Sweden: a review of 127 cases.

P. Westermark, A. Gånemo, M. Virtanen, 2003, Acta dermato-venereologica. Supplementum.

Prognosis of acute otitis media: factors associated with poor outcome.

J. Eskola, M. Virtanen, M. Virtanen, 1997, Acta oto-laryngologica.

Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?

H. Törmä, M. Virtanen, A. Vahlquist, 2018, Experimental dermatology.

A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations

J. McGrath, M. Virtanen, A. Vahlquist, 2014, Clinical and experimental dermatology.

Keratin 4 upregulation by retinoic acid in vivo: a sensitive marker for retinoid bioactivity in human epidermis.

H. Törmä, M. Virtanen, A. Vahlquist, 2000, The Journal of investigative dermatology.

Safety, Efficacy, and Dosage of 1% Pimecrolimus Cream for the Treatment of Atopic Dermatitis in Daily Practice

K. Wolff, R. Houwing, R. Langley, 2006, American journal of clinical dermatology.

Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients.

J. Fischer, A. Gånemo, M. Virtanen, 2010, The Journal of investigative dermatology.

Topical retinoic acid alters the expression of cellular retinoic acid‐binding protein‐I and cellular retinoic acid‐binding protein‐II in non‐lesional but not lesional psoriatic skin

H. Törmä, A. Sirsjö, M. Virtanen, 2002, Experimental dermatology.

Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man.

H. Törmä, M. Virtanen, A. Vahlquist, 2021, Differentiation; research in biological diversity.

Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients.

J. Fischer, A. Gånemo, M. Virtanen, 2016, Acta dermato-venereologica.

Congenital ichthyosis: an overview of current and emerging therapies.

A. Gånemo, M. Virtanen, A. Vahlquist, 2008, Acta dermato-venereologica.

Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression.

I. Leigh, N. Mørk, M. Virtanen, 2001, Acta dermato-venereologica.

Reply to Nellen et al's comment on the classification of clinical/genetic variants of Mal de Meleda.

M. Virtanen, A. Vahlquist, Lin-shu Zhao, 2015, Acta dermato-venereologica.

Whole‐exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome

M. Barenboim, J. Fischer, T. Manke, 2016, The British journal of dermatology.

Keratins 2 and 4/13 in reconstituted human skin are reciprocally regulated by retinoids binding to nuclear receptor RARα

H. Törmä, A. Sirsjö, M. Virtanen, 2010, Experimental dermatology.

Autosomal recessive congenital ichthyosis in Sweden and Estonia: clinical, genetic and ultrastructural findings in eighty-three patients.

P. Westermark, N. Dahl, A. Gånemo, 2003, Acta dermato-venereologica.

Quantitative image analysis of protein expression and colocalisation in skin sections

Carolina Wählby, H. Törmä, M. Virtanen, 2018, Experimental dermatology.

Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients with epidermolytic hyperkeratosis.

M. Virtanen, A. Vahlquist, S. K. Smith, 2003, The Journal of investigative dermatology.

Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda.

M. Virtanen, A. Vahlquist, Lin-shu Zhao, 2014, Acta dermato-venereologica.

Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition.

A. Moustakas, H. Törmä, M. Virtanen, 2009, Journal of dermatological science.

Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26

A. Ameur, L. Alexandrov, S. Ekvall, 2017, Human Molecular Genetics.

Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy.

Å. Svensson, M. Lindberg, M. Bradley, 2023, Acta dermato-venereologica.