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A Vahlquist

Showing results (131-140 of 146) with videos related to

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Acta Dermato-Venereologica|December 12, 1997
Topical application of a platelet-activating factor (PAF) antagonist in atopic dermatitisD Abeck, T Andersson, E Grosshans, et al.
Lakartidningen|February 19, 1986
[Isotretinoin is a help in severe acne--but the adverse effects are too many]H Mobacken, J Landegren, K Hersle, et al.
Acta Dermato-Venereologica|January 1, 1986
Changes in laboratory variables induced by isotretinoin treatment of acneG Michaëlsson, A Vahlquist, H Mobacken, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1980
The retinol-binding proteinL Rask, H Anundi, J Böhme, et al.
Journal of Medical Genetics|June 15, 2007
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermisJ Dahlqvist, J Klar, I Hausser, et al.
The British Journal of Dermatology|October 28, 2010
Immortalized keratinocytes derived from patients with epidermolytic ichthyosis reproduce the disease phenotype: a useful in vitro model for testing new treatmentsJ C Chamcheu, I Pihl-Lundin, C E Mouyobo, et al.
The British Journal of Dermatology|August 20, 2015
Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndromeN A Schlipf, A Vahlquist, N Teigen, et al.
Journal of Human Genetics|September 2, 2006
A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype associationM Melin, J Klar, T Jr Gedde-Dahl, et al.
Clinical and Experimental Dermatology|December 18, 2013
A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutationsA Vahlquist, M Virtanen, M Hellström-Pigg, et al.
The British Journal of Dermatology|September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosisA Hotz, C Fagerberg, A Vahlquist, et al.
Pageof 15

Showing results (131-140 of 146) with videos related to

Sort By:
Pageof 15
Acta Dermato-Venereologica|December 12, 1997
Topical application of a platelet-activating factor (PAF) antagonist in atopic dermatitisD Abeck, T Andersson, E Grosshans, et al.
Lakartidningen|February 19, 1986
[Isotretinoin is a help in severe acne--but the adverse effects are too many]H Mobacken, J Landegren, K Hersle, et al.
Acta Dermato-Venereologica|January 1, 1986
Changes in laboratory variables induced by isotretinoin treatment of acneG Michaëlsson, A Vahlquist, H Mobacken, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1980
The retinol-binding proteinL Rask, H Anundi, J Böhme, et al.
Journal of Medical Genetics|June 15, 2007
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermisJ Dahlqvist, J Klar, I Hausser, et al.
The British Journal of Dermatology|October 28, 2010
Immortalized keratinocytes derived from patients with epidermolytic ichthyosis reproduce the disease phenotype: a useful in vitro model for testing new treatmentsJ C Chamcheu, I Pihl-Lundin, C E Mouyobo, et al.
The British Journal of Dermatology|August 20, 2015
Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndromeN A Schlipf, A Vahlquist, N Teigen, et al.
Journal of Human Genetics|September 2, 2006
A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype associationM Melin, J Klar, T Jr Gedde-Dahl, et al.
Clinical and Experimental Dermatology|December 18, 2013
A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutationsA Vahlquist, M Virtanen, M Hellström-Pigg, et al.
The British Journal of Dermatology|September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosisA Hotz, C Fagerberg, A Vahlquist, et al.
Pageof 15