Anders Vahlquist

In memoriam professor Annamari Ranki

Peltonen, Sirkku; Vahlquist, Anders; Lindberg, Magnus; Larkö, Olle

Ingår i Acta Dermato-Venereologica, 2024

• DOI för In memoriam professor Annamari Ranki
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The Syphilis Pandemic Prior to Penicillin: Origin, Health Issues, Cultural Representation and Ethical Challenges

Ekselius, Lisa; Gerdin, Bengt; Vahlquist, Anders

Ingår i Acta Dermato-Venereologica, 2024

• DOI för The Syphilis Pandemic Prior to Penicillin: Origin, Health Issues, Cultural Representation and Ethical Challenges
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Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

Hotz, Alrun; Kopp, Julia; Bourrat, Emmanuelle; Oji, Vinzenz et al.

Ingår i Genes, 2021

• DOI för Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients
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Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man

Zhang, Hanqing; Weström, Simone; Kappelin, Per; Virtanen, Marie et al.

Ingår i Differentiation, s. 19-27, 2021

• DOI för Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man

Pioneers in Dermatology and Venereology: an interview with Prof. Anders Vahlquist

Vahlquist, Anders

Ingår i Journal of the European Academy of Dermatology and Venereology, s. 2691-2692, 2020

• DOI för Pioneers in Dermatology and Venereology: an interview with Prof. Anders Vahlquist

In memoriam professor Annamari Ranki

Peltonen, Sirkku; Vahlquist, Anders; Lindberg, Magnus; Larkö, Olle

Ingår i Acta Dermato-Venereologica, 2024

• DOI för In memoriam professor Annamari Ranki
• Ladda ner fulltext (pdf) av In memoriam professor Annamari Ranki

Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

Hotz, Alrun; Kopp, Julia; Bourrat, Emmanuelle; Oji, Vinzenz et al.

Ingår i Genes, 2021

• DOI för Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients
• Ladda ner fulltext (pdf) av Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

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

Zhang, Hanqing; Weström, Simone; Kappelin, Per; Virtanen, Marie et al.

Ingår i Differentiation, s. 19-27, 2021

• DOI för Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man

Pioneers in Dermatology and Venereology: an interview with Prof. Anders Vahlquist

Vahlquist, Anders

Ingår i Journal of the European Academy of Dermatology and Venereology, s. 2691-2692, 2020

• DOI för Pioneers in Dermatology and Venereology: an interview with Prof. Anders Vahlquist

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

Zhang, Hanqian; Ericsson, Maja; Weström, Simone; Vahlquist, Anders et al.

Ingår i Experimental dermatology, s. 1164-1171, 2019

• DOI för Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?
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Management of congenital ichthyoses: European guidelines of care, part two

Mazereeuw-Hautier, J.; Hernandez-Martin, A.; O'Toole, E. A.; Bygum, A. et al.

Ingår i British Journal of Dermatology, s. 484-495, 2019

• DOI för Management of congenital ichthyoses: European guidelines of care, part two

Management of congenital ichthyoses: European guidelines of care, part one

Mazereeuw-Hautier, J.; Vahlquist, Anders; Traupe, H.; Bygum, A. et al.

Ingår i British Journal of Dermatology, s. 272-281, 2019

• DOI för Management of congenital ichthyoses: European guidelines of care, part one

Quantitative image analysis of protein expression and colocalisation in skin sections

Zhang, Hanqian; Ericsson, Maja; Virtanen, Marie; Weström, Simone et al.

Ingår i Experimental dermatology, s. 196-199, 2018

• DOI för Quantitative image analysis of protein expression and colocalisation in skin sections

Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis

Hotz, A.; Fagerberg, C.; Vahlquist, Anders; Bygum, A. et al.

Ingår i British Journal of Dermatology, 2018

• DOI för Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis

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

Gudmundsson, Sanna; Wilbe, Maria; Ekvall, Sara; Ameur, Adam et al.

Ingår i Human Molecular Genetics, s. 1070-1077, 2017

• DOI för Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26
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Proteins causing autosomal congenital recessive ichthyosis (ARCI) colocalize in differentiated primary keratinocytes and the interactions are altered in cells from patients with TGM1 mutations

Pettersson, M. H.; Zhang, Hanqian; Virtanen, Marie; Vahlquist, Anders et al.

Ingår i Journal of Investigative Dermatology, 2017

Ichthyosis patients with TGM1 mutations show aberrant transcriptomic expression

Zhang, Hanqian; Vahlquist, Anders; Virtanen, Marie; Törmä, Hans

Ingår i Journal of Investigative Dermatology, 2017

Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

Zimmer, A. D.; Kim, G. J.; Hotz, A.; Bourrat, E. et al.

Ingår i British Journal of Dermatology, s. 445-455, 2017

• DOI för Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

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

Schlipf, N A; Vahlquist, Anders; Teigen, N; Virtanen, Marie et al.

Ingår i British Journal of Dermatology, s. 444-448, 2016

• DOI för Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome

Quantitative analysis of immunofluorescence and in situ PLA staining using CellProfiler reveals impaired epidermal lipid processing pathway in ARCI patients with CYP4F22 mutations

Zhang, Hanqian; Virtanen, Marie; Weström, Simone; Bygum, A. et al.

Ingår i Journal of Investigative Dermatology, 2016

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

Pigg, Maritta H.; Bygum, Anette; Ganemo, Agneta; Virtanen, Marie et al.

Ingår i Acta Dermato-Venereologica, s. 932-+, 2016

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

Moisturizing treatment of patients with atopic dermatitis and ichthyosis vulgaris improves dry skin, but has a modest effect on gene expression regardless of FLG genotype

Hoppe, Torborg; Winge, Mårten C G; Bradley, Maria; Nordenskjöld, Magnus et al.

Ingår i Journal of the European Academy of Dermatology and Venereology, s. 174-177, 2015

• DOI för Moisturizing treatment of patients with atopic dermatitis and ichthyosis vulgaris improves dry skin, but has a modest effect on gene expression regardless of FLG genotype

Recurrent Pyoderma Gangrenosum and Cystic Acne Associated with Leucocyte Adhesion Deficiency due to Novel Mutations in ITGB2: Successful Treatment with Infliximab and Adalimumab

Vahlquist, Anders; Håkansson, Lena Douhan; Rönnblom, Lars; Karawajczyk, Malgorzata et al.

Ingår i Acta Dermato-Venereologica, s. 349-351, 2015

• DOI för Recurrent Pyoderma Gangrenosum and Cystic Acne Associated with Leucocyte Adhesion Deficiency due to Novel Mutations in ITGB2: Successful Treatment with Infliximab and Adalimumab

Reply to Nellen et al's Comment on the Classification of Clinical/genetic Variants of Mal de Meleda

Zhao, Linshu; Vahlquist, Anders; Virtanen, Marie; Wennerstrand, Lena et al.

Ingår i Acta Dermato-Venereologica, s. 1034-1035, 2015

• DOI för Reply to Nellen et al's Comment on the Classification of Clinical/genetic Variants of Mal de Meleda

Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trial

Vahlquist, Anders; Blockhuys, S; Steijlen, P; van Rossem, K et al.

Ingår i British Journal of Dermatology, s. 173-181, 2014

• DOI för Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trial

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

Vahlquist, Anders; Virtanen, Marie; Hellström-Pigg, M.; Dragomir, Anca et al.

Ingår i Clincal and Experimental Dermatology, s. 30-34, 2014

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

Ultrastructure of desmosomes as a diagnostic clue in a case of congenital skin fragility syndrome

Vahlquist, Anders; Virtanen, Marie; Hellström-Pigg, Maritta; Dragomir, Anca et al.

Ingår i Journal of Investigative Dermatology, s. 1176-1176, 2014

Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda

Zhao, Linshu; Vahlquist, Anders; Virtanen, Marie; Wennerstrand, Lena et al.

Ingår i Acta Dermato-Venereologica, s. 707-710, 2014

• DOI för Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda
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Ultrastructure of desmosomes as a diagnostic clue in a case of congenital skin fragility syndrome

Vahlquist, Anders; Virtanen, Marie; Hellström-Pigg, Maritta; Dragomir, Anca et al.

Ingår i Journal of Investigative Dermatology, s. 1172-1172, 2014

Interactions between FATP4 and ichthyin in epidermal lipid processing may provide clues to the pathogenesis of autosomal recessive congenital ichthyosis

Li, Hao; Vahlquist, Anders; Törmä, Hans

Ingår i Journal of dermatological science (Amsterdam), s. 195-201, 2013

• DOI för Interactions between FATP4 and ichthyin in epidermal lipid processing may provide clues to the pathogenesis of autosomal recessive congenital ichthyosis

Generalized and Naevoid Epidermolytic Ichthyosis in Denmark: Clinical and Mutational Findings

Bygum, Anette; Virtanen, Marie; Brandrup, Flemming; Ganemo, Agneta et al.

Ingår i Acta Dermato-Venereologica, s. 309-313, 2013

• DOI för Generalized and Naevoid Epidermolytic Ichthyosis in Denmark: Clinical and Mutational Findings
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Genotype-Phenotype Correlations Emerging from the Identification of Missense Mutations in MBTPS2

Bornholdt, Dorothea; Atkinson, T. Prescott; Bouadjar, Bakar; Catteau, Benoit et al.

Ingår i Human Mutation, s. 587-594, 2013

• DOI för Genotype-Phenotype Correlations Emerging from the Identification of Missense Mutations in MBTPS2

Epidermolysis bullosa simplex with PLEC mutations: new phenotypes and new mutations

Charlesworth, A.; Chiaverini, C.; Chevrant-Breton, J.; DelRio, M. et al.

Ingår i British Journal of Dermatology, s. 808-814, 2013

• DOI för Epidermolysis bullosa simplex with PLEC mutations: new phenotypes and new mutations

Detection of keratin filaments and aggregates in HeLa cells transfected with fluorescently tagged keratin 1 and 10 using a high content imaging assay

Törmä, Hans; Lindberg, Mikael; Li, Hao; Virtanen, Marie et al.

Ingår i Journal of Investigative Dermatology, 2013

Ichthyin/NIPAL4 localizes to keratins and desmosomes in epidermis and Ichthyin mutations affect epidermal lipid metabolism

Dahlqvist, Johanna; Westermark, Gunilla T.; Vahlquist, Anders; Dahl, Niklas

Ingår i Archives of Dermatological Research, s. 377-386, 2012

• DOI för Ichthyin/NIPAL4 localizes to keratins and desmosomes in epidermis and Ichthyin mutations affect epidermal lipid metabolism

The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis

Li, Hao; Pavez Lorie, Elizabeth; Fischer, Judith; Vahlquist, Anders et al.

Ingår i Journal of Investigative Dermatology, s. 2368-2375, 2012

• DOI för The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis

Oral Alitretinoin in Congenital Ichthyosis: A Pilot Study Shows Variable Effects and a Risk of Central Hypothyroidism

Ganemo, Agneta; Sommerlund, Mette; Vahlquist, Anders

Ingår i Acta Dermato-Venereologica, s. 256-257, 2012

• DOI för Oral Alitretinoin in Congenital Ichthyosis: A Pilot Study Shows Variable Effects and a Risk of Central Hypothyroidism

Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita

Wilson, Neil J.; Cardenas Perez, Monica L.; Vahlquist, Anders; Schwartz, Mary E. et al.

Ingår i Journal of Investigative Dermatology, s. 1921-1924, 2012

• DOI för Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita

X-linked recessive ichthyosis: an impaired barrier function evokes limited gene responses before and after moisturizing treatments

Hoppe, Torborg; Winge, Mårten C G; Bradley, Maria; Nordenskjöld, Magnus et al.

Ingår i British Journal of Dermatology, s. 514-522, 2012

• DOI för X-linked recessive ichthyosis: an impaired barrier function evokes limited gene responses before and after moisturizing treatments

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

Chamcheu, Jean Christopher; Pihl-Lundin, Inger; Eteti Mouyobo, Cedrique; Gester, Therese et al.

Ingår i British Journal of Dermatology, s. 263-272, 2011

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

Chemical Chaperones Protect Epidermolysis Bullosa Simplex Keratinocytes from Heat Stress-Induced Keratin Aggregation: Involvement of Heat Shock Proteins and MAP Kinases

Chamcheu, Jean Christopher; Navsaria, Harshad; Pihl-Lundin, Inger; Liovic, Mirjana et al.

Ingår i Journal of Investigative Dermatology, s. 1684-1691, 2011

• DOI för Chemical Chaperones Protect Epidermolysis Bullosa Simplex Keratinocytes from Heat Stress-Induced Keratin Aggregation: Involvement of Heat Shock Proteins and MAP Kinases

Homozygosity of dominant missense mutations in keratin 17 leads to alopecia in addition to severe pachyonychia congenita

Wilson, N. J.; Hansen, C. D.; Cardenas Perez, M. L.; Vahlquist, Anders et al.

Ingår i Journal of Investigative Dermatology, 2011

Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris

Winge, Mårten C G; Hoppe, Torborg; Berne, Berit; Vahlquist, Anders et al.

Ingår i PLOS ONE, 2011

• DOI för Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris
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Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis

Winge, Mårten C G; Hoppe, Torborg; Liedén, Agne; Nordenskjöld, Magnus et al.

Ingår i Journal of dermatological science (Amsterdam), s. 62-64, 2011

• DOI för Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis

Keratinocyte differentiation induced by calcium, phorbol ester or interferon-γ elicits distinct changes in the retinoid signalling pathways

Karlsson, Teresa; Vahlquist, Anders; Törmä, Hans

Ingår i Journal of dermatological science (Amsterdam), s. 207-213, 2010

• DOI för Keratinocyte differentiation induced by calcium, phorbol ester or interferon-γ elicits distinct changes in the retinoid signalling pathways
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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

Chamcheu, Jean Christopher; Virtanen, Marie; Navsaria, Harshad; Bowden, Paul E. et al.

Ingår i British Journal of Dermatology, s. 980-989, 2010

• DOI för 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

Effect of synthetic retinoids on keratin aggregate formation in immortalized cells from Epidermolytic lchthyosis patients

Li, Hao; Chamcheu, Jean Christopher; Vahlquist, Anders; Törmä, Hans

Ingår i Journal of Investigative Dermatology, 2010

Immortalized keratinocytes from Epidermolytic Ichthyosis-patients reproduce the disease phenotype in vitro

Chamcheu, Jean Christopher; Virtanen, Marie; Moustakas, Aristidis; Navsaria, Harshad et al.

Ingår i Journal of Investigative Dermatology, 2010

Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009

Oji, Vinzenz; Tadini, Gianluca; Akiyama, Masashi; Blanchet Bardon, Claudine et al.

Ingår i The Journal of American Academy of Dermatology, s. 607-641, 2010

• DOI för Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009

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

Virtanen, Marie; Sirsjö, Allan; Vahlquist, Anders; Törmä, Hans

Ingår i Experimental dermatology, s. 674-681, 2010

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

Epidermolysis bullosa care in Scandinavia

Vahlquist, Anders; Tasanen, Kaisa

Ingår i Dermatologic clinics, s. 425-427, 2010

• DOI för Epidermolysis bullosa care in Scandinavia

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

Vahlquist, Anders; Bygum, Anette; Gånemo, Agneta; Virtanen, Marie et al.

Ingår i Journal of Investigative Dermatology, s. 438-443, 2010

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

Botulinum toxin in the treatment of sweat-worsened foot problems in patients with epidermolysis bullosa simplex and pachyonychia congenita

Swartling, Carl; Karlqvist, Mattias; Hymnelius, K.; Weis, Jan et al.

Ingår i British Journal of Dermatology, s. 1072-1076, 2010

• DOI för Botulinum toxin in the treatment of sweat-worsened foot problems in patients with epidermolysis bullosa simplex and pachyonychia congenita

A single-nucleotide deletion in the POMP 5' UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis

Dahlqvist, Johanna; Klar, Joakim; Tiwari, Neha; Schuster, Jens et al.

Ingår i American Journal of Human Genetics, s. 596-603, 2010

• DOI för A single-nucleotide deletion in the POMP 5' UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis

Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome

Klar, Joakim; Schweiger, Martina; Zimmerman, Robert; Zechner, Rudolf et al.

Ingår i American Journal of Human Genetics, s. 248-253, 2009

• DOI för Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome

Sjögren-Larsson syndrome: a study of clinical symptoms and dermatological treatment in 34 Swedish patients

Gånemo, Agneta; Jagell, Sten; Vahlquist, Anders

Ingår i Acta Dermato-Venereologica, s. 68-73, 2009

• DOI för Sjögren-Larsson syndrome: a study of clinical symptoms and dermatological treatment in 34 Swedish patients

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

Chamcheu, Jean Christopher; Lorié, Elizabeth Pavez; Akgul, Baki; Bannbers, Elin et al.

Ingår i Journal of dermatological science (Amsterdam), s. 198-206, 2009

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

Both all-trans retinoic acid and cytochrome P450 (CYP26)  inhibitors affect the expression of vitamin A metabolizing enzymes and Retinoic biomarkers in organotypic epidermis

Pavez Loriè, Elizabeth; Chamcheu, Jean-Christopher; Vahlquist, Anders; Törmä, Hans

Ingår i Archives of Dermatological Research, s. 475-485, 2009

• DOI för Both all-trans retinoic acid and cytochrome P450 (CYP26)  inhibitors affect the expression of vitamin A metabolizing enzymes and Retinoic biomarkers in organotypic epidermis

Topical treatment with CYP26 inhibitor talarozole (R115866) dose dependently alters the expression of retinoid-regulated genes in normal human epidermis

Pavez Loriè, Elizabeth; Cools, Marina; Borgers, Marcel; Wouters, Luc et al.

Ingår i British Journal of Dermatology, s. 26-36, 2009

• DOI för Topical treatment with CYP26 inhibitor talarozole (R115866) dose dependently alters the expression of retinoid-regulated genes in normal human epidermis

The involvement of cytochrome p450 (CYP) 26 in the retinoic acid metabolism of human epidermal keratinocytes

Pavez Loriè, Elizabeth; Li, Hao; Vahlquist, Anders; Törmä, Hans

Ingår i Biochimica et Biophysica Acta, s. 220-228, 2009

• DOI för The involvement of cytochrome p450 (CYP) 26 in the retinoic acid metabolism of human epidermal keratinocytes

Expression of retinoid-regulated genes in lamellar ichthyosis vs. healthy control epidermis: changes after oral treatment with liarozole

Pavez Loriè, Elizabeth; Gånemo, Agneta; Borgers, Marcel; Wouters, Luc et al.

Ingår i Acta Dermato-Venereologica, s. 12-20, 2009

• DOI för Expression of retinoid-regulated genes in lamellar ichthyosis vs. healthy control epidermis: changes after oral treatment with liarozole

Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis

Thomas, A C; Sinclair, C; Mahmud, N; Cullup, T et al.

Ingår i British Journal of Dermatology, s. 611-613, 2008

• DOI för Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB

Fine, Jo-David; Eady, Robin A J; Bauer, Eugene A; Bauer, Johann W et al.

Ingår i The Journal of American Academy of Dermatology, s. 931-950, 2008

• DOI för The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB

Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis

Dahlqvist, Johanna; Klar, Joakim; Hausser, I; Anton-Lamprecht, I et al.

Ingår i Journal of Medical Genetics, s. 615-620, 2007

• DOI för Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis

Five new homozygous mutations in the KIND1 Gene in Kindler Syndrome

Lai-Cheong, JE; Liu, L; Sethuraman, G; Kumar, R et al.

Ingår i Journal of Investigative Dermatology, s. 2268-2270, 2007

• DOI för Five new homozygous mutations in the KIND1 Gene in Kindler Syndrome

Connexin 26 (GJB2) mutations in two Swedish patients with atypical Vohwinkel (mutilating keratoderma plus deafness) and KID syndrome both extensively treated with acitretin

Bondeson, Marie-Louise; Nyström, Anna-Maja; Gunnarsson, Ulrika; Vahlquist, Anders

Ingår i Acta Dermato-Venereologica, s. 503-508, 2006

• DOI för Connexin 26 (GJB2) mutations in two Swedish patients with atypical Vohwinkel (mutilating keratoderma plus deafness) and KID syndrome both extensively treated with acitretin

Conflicts of interest in dermatology

Williams, H.C.; Naldi, L.; Paul, C.; Vahlquist, Anders et al.

Ingår i Acta Dermato-Venereologica, s. 485-497, 2006

• DOI för Conflicts of interest in dermatology

Treatment of pachyonychia congenita with plantar injections of botulinum toxin.

Swartling, Carl; Vahlquist, Anders

Ingår i Br J Dermatol, s. 763-765, 2006

Betungande regler för klinisk forskning står inte i proportion till patientnyttan

Vahlquist, Anders; Westermark, Per; Ståhle, Elisabeth; Venge, Per et al.

Ingår i Läkartidningen, s. 1832-1834, 2005

Betungande regler för klinisk prövning står inte i proportion till patientnyttan

Vahlquist, Anders; Westermark, Per; Ståhle, Elisabeth; Venge, Per et al.

Ingår i Läkartidningen, s. 1832-1834, 2005

Mutational spectrum of NSDHL in CHILD syndrome.

Bornholdt, D; König, A; Happle, R; Leveleki, L et al.

Ingår i J Med Genet, s. 1-6, 2005

• DOI för Mutational spectrum of NSDHL in CHILD syndrome.

Sweat gland morphology and periglandular innervation in essential palmar hyperhidrosis before and after treatment with intradermal botulinum toxin

Swartling, Carl; Naver, Hans; Pihl-Lundin, Inger; Hagforsen, Eva et al.

Ingår i The Journal of American Academy of Dermatology, s. 739-745, 2004

• DOI för Sweat gland morphology and periglandular innervation in essential palmar hyperhidrosis before and after treatment with intradermal botulinum toxin

Inefficacy of topical thyroid hormone analogue TriAc in plaque psoriasis: results of a double-blind placebo-controlled trial

Vahlquist, Anders; Törmä, Hans; Carlsson, B.

Ingår i British Journal of Dermatology, s. 489-491, 2004

• DOI för Inefficacy of topical thyroid hormone analogue TriAc in plaque psoriasis: results of a double-blind placebo-controlled trial

The Syphilis Pandemic Prior to Penicillin: Origin, Health Issues, Cultural Representation and Ethical Challenges

Ekselius, Lisa; Gerdin, Bengt; Vahlquist, Anders

Ingår i Acta Dermato-Venereologica, 2024

• DOI för The Syphilis Pandemic Prior to Penicillin: Origin, Health Issues, Cultural Representation and Ethical Challenges
• Ladda ner fulltext (pdf) av The Syphilis Pandemic Prior to Penicillin: Origin, Health Issues, Cultural Representation and Ethical Challenges

Ichthyosis: A Road Model for Skin Research

Vahlquist, Anders; Törmä, Hans

Ingår i Acta Dermato-Venereologica, s. 197-206, 2020

• DOI för Ichthyosis: A Road Model for Skin Research
• Ladda ner fulltext (pdf) av Ichthyosis: A Road Model for Skin Research

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment

Vahlquist, Anders; Fischer, Judith; Törmä, Hans

Ingår i American Journal of Clinical Dermatology, s. 51-66, 2018

• DOI för Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment
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Harlequin Ichthyosis A Review of Clinical and Molecular Findings in 45 Cases

Rajpopat, Shefali; Moss, Celia; Mellerio, Jemima; Vahlquist, Anders et al.

Ingår i Archives of Dermatology, s. 681-686, 2011

• DOI för Harlequin Ichthyosis A Review of Clinical and Molecular Findings in 45 Cases

Pleomorphic ichthyosis: proposed name for a heterogeneous group of congenital ichthyoses with phenotypic shifting and mild residual scaling

Vahlquist, Anders

Ingår i Acta Dermato-Venereologica, s. 454-460, 2010

• DOI för Pleomorphic ichthyosis: proposed name for a heterogeneous group of congenital ichthyoses with phenotypic shifting and mild residual scaling

Congenital ichthyosis: an overview of current and emerging therapies

Vahlquist, Anders; Gånemo, Agneta; Virtanen, Marie

Ingår i Acta Dermato-Venereologica, s. 4-14, 2008

• DOI för Congenital ichthyosis: an overview of current and emerging therapies

Mutational spectrum of NSDHL in CHILD syndrome.

Bornholdt, D; König, A; Happle, R; Leveleki, L et al.

2004