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A Vahlquist

Explore the profile of A Vahlquist including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 146
Citations 945
Followers 0
Related Specialties
Dermatology
General Medicine
Biochemistry
Top 10 Co-Authors
H Torma
O Rollman
G Michaelsson
B Berne
P A Peterson
E Andersson
M Virtanen
C Vahlquist
A Ganemo
L Juhlin
Published In
Br J Dermatol
Acta Derm Venereol
J Invest Dermatol
Lakartidningen
Arch Dermatol Res
Affiliations
Soon will be listed here.
Recent Articles
1.
Pioneers in Dermatology and Venereology: an interview with Prof. Anders Vahlquist
Vahlquist A
J Eur Acad Dermatol Venereol . 2020 Dec; 34(12):2691-2692. PMID: 33351284
No abstract available.
2.
Management of congenital ichthyoses: European guidelines of care, part one
Mazereeuw-Hautier J, Vahlquist A, Traupe H, Bygum A, Amaro C, Aldwin M, et al.
Br J Dermatol . 2018 Sep; 180(2):272-281. PMID: 30216406
These guidelines for the management of congenital ichthyoses have been developed by a multidisciplinary group of European experts following a systematic review of the current literature, an expert conference held...
3.
Management of congenital ichthyoses: European guidelines of care, part two
Mazereeuw-Hautier J, Hernandez-Martin A, OToole E, Bygum A, Amaro C, Aldwin M, et al.
Br J Dermatol . 2018 Jun; 180(3):484-495. PMID: 29897631
These guidelines for the management of congenital ichthyoses have been developed by a multidisciplinary group of European experts following a systematic review of the current literature, an expert conference held...
4.
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis
Hotz A, Fagerberg C, Vahlquist A, Bygum A, Torma H, Rauschendorf M, et al.
Br J Dermatol . 2017 Sep; 178(3):e207-e209. PMID: 28906551
No abstract available.
5.
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, Kim G, Hotz A, Bourrat E, Hausser I, Has C, et al.
Br J Dermatol . 2017 Jan; 177(2):445-455. PMID: 28093717
Background: Autosomal recessive congenital ichthyosis (ARCI) is a genetically heterogeneous group of rare Mendelian skin disorders characterized by cornification and differentiation defects of keratinocytes. Mutations in nine genes including PNPLA1...
6.
Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome
Schlipf N, Vahlquist A, Teigen N, Virtanen M, Dragomir A, Fismen S, et al.
Br J Dermatol . 2015 Aug; 174(2):444-8. PMID: 26288349
No abstract available.
7.
A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations
Vahlquist A, Virtanen M, Hellstrom-Pigg M, Dragomir A, Ryberg K, Wilson N, et al.
Clin Exp Dermatol . 2013 Dec; 39(1):30-4. PMID: 24341478
Congenital skin fragility is a heterogeneous disorder with epidermolysis bullosa and various skin infections as the leading causes. However, even rare diseases must be considered in the differential diagnosis of...
8.
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 T, Winge M, Bradley M, Nordenskjold M, Vahlquist A, Torma H, et al.
J Eur Acad Dermatol Venereol . 2013 Dec; 29(1):174-7. PMID: 24330146
Background: Loss-of-function mutations in FLG (encoding filaggrin) are a predisposing factor for atopic dermatitis (AD) and cause ichthyosis vulgaris (IV). Patients with AD and IV display impaired skin barrier and...
9.
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 A, Blockhuys S, Steijlen P, van Rossem K, Didona B, Blanco D, et al.
Br J Dermatol . 2013 Oct; 170(1):173-81. PMID: 24102348
Background: Oral liarozole, a retinoic acid metabolism-blocking agent, may be an alternative to systemic retinoid therapy in patients with lamellar ichthyosis. Objective: To demonstrate the efficacy and safety of once-daily...
10.
X-linked recessive ichthyosis: an impaired barrier function evokes limited gene responses before and after moisturizing treatments
Hoppe T, Winge M, Bradley M, Nordenskjold M, Vahlquist A, Berne B, et al.
Br J Dermatol . 2012 Apr; 167(3):514-22. PMID: 22486194
Background: X-linked recessive ichthyosis (XLRI) is due to deletions or inactivating mutations in the steroid sulfatase (STS) gene. This results in an accumulation of cholesterol sulphate affecting the packing of...