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E Sprecher

Showing results (71-80 of 200) with videos related to

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European Journal of Endocrinology|February 1, 1997
Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final heightN Weintrob, Z Dickerman, E Sprecher, et al.
Leukemia Research|January 1, 1989
Cytofluorometric analysis of thymic interdigitating cells from C57BL/6 mice prior and after leukemogenic X-irradiationE Sprecher, H Giloh, E Rahamim, et al.
Clinical and Experimental Dermatology|January 25, 2005
Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1O Tal, R Bergman, J Alcalay, et al.
Clinical and Experimental Dermatology|March 23, 2013
Oesophageal involvement in bullous pemphigoidN Maharshak, M Sagi, E Santos, et al.
Clinical and Experimental Dermatology|February 13, 2013
Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9D Fuchs-Telem, G Padalon-Brauch, O Sarig, et al.
Clinical and Experimental Dermatology|November 21, 2008
Novel mutations in DSG1 causing striate palmoplantar keratodermaD Hershkovitz, J Lugassy, M Indelman, et al.
The British Journal of Dermatology|June 27, 2018
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey-Hailey disease are allelic disordersD Vodo, N Malchin, M Furman, et al.
Journal of Virological Methods|August 1, 1990
Mouse footpad Langerhans cells as an indicator for safety of foot and mouth disease virus vaccinesE Sprecher, D David, H Yadin, et al.
The British Journal of Dermatology|March 26, 2003
Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesionsM Indelman, R Bergman, G G Lestringant, et al.
Clinical and Experimental Dermatology|July 28, 2011
Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasiaM Pavlovsky, D Fuchs-Telem, J Nousbeck, et al.
Pageof 20

Showing results (71-80 of 200) with videos related to

Sort By:
Pageof 20
European Journal of Endocrinology|February 1, 1997
Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final heightN Weintrob, Z Dickerman, E Sprecher, et al.
Leukemia Research|January 1, 1989
Cytofluorometric analysis of thymic interdigitating cells from C57BL/6 mice prior and after leukemogenic X-irradiationE Sprecher, H Giloh, E Rahamim, et al.
Clinical and Experimental Dermatology|January 25, 2005
Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1O Tal, R Bergman, J Alcalay, et al.
Clinical and Experimental Dermatology|March 23, 2013
Oesophageal involvement in bullous pemphigoidN Maharshak, M Sagi, E Santos, et al.
Clinical and Experimental Dermatology|February 13, 2013
Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9D Fuchs-Telem, G Padalon-Brauch, O Sarig, et al.
Clinical and Experimental Dermatology|November 21, 2008
Novel mutations in DSG1 causing striate palmoplantar keratodermaD Hershkovitz, J Lugassy, M Indelman, et al.
The British Journal of Dermatology|June 27, 2018
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey-Hailey disease are allelic disordersD Vodo, N Malchin, M Furman, et al.
Journal of Virological Methods|August 1, 1990
Mouse footpad Langerhans cells as an indicator for safety of foot and mouth disease virus vaccinesE Sprecher, D David, H Yadin, et al.
The British Journal of Dermatology|March 26, 2003
Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesionsM Indelman, R Bergman, G G Lestringant, et al.
Clinical and Experimental Dermatology|July 28, 2011
Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasiaM Pavlovsky, D Fuchs-Telem, J Nousbeck, et al.
Pageof 20