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E Sprecher

Showing results (81-90 of 200) with videos related to

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The British Journal of Dermatology|December 12, 2019
Revisiting pachyonychia congenita: a case-cohort study of 815 patientsL Samuelov, F J D Smith, C D Hansen, et al.
The British Journal of Dermatology|March 28, 2017
Report of the 13th Annual International Pachyonychia Congenita Consortium SymposiumL Rittié, R L Kaspar, E Sprecher, et al.
Journal of the Neurological Sciences|September 1, 1994
Variance of sensory threshold measurements: discrimination of feigners from trustworthy performersD Yarnitsky, E Sprecher, A Tamir, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 1, 2013
Best treatment practices for pachyonychia congenitaI Goldberg, D Fruchter, A Meilick, et al.
Chronobiology International|February 4, 2017
Seasonal variation in spontaneous intracerebral hemorrhage in northern IsraelG Telman, G E Sviri, E Sprecher, et al.
Archives of Dermatological Research|January 1, 1990
Effect of genetically determined immunodeficiency on epidermal dendritic cell populations in C57BL/6J miceE Sprecher, Y Becker, G Kraal, et al.
Bone Marrow Transplantation|March 30, 2010
Glutathione S-transferase T1-null seems to be associated with graft failure in hematopoietic SCTR Elhasid, N Krivoy, J M Rowe, et al.
The British Journal of Dermatology|December 24, 2017
Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authorsM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
American Journal of Human Genetics|April 17, 1999
Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichiasE Sprecher, R Bergman, R Szargel, et al.
Clinical and Experimental Dermatology|September 7, 2004
Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndromeE Sprecher, A Tesfaye-Kedjela, P Ratajczak, et al.
Pageof 20

Showing results (81-90 of 200) with videos related to

Sort By:
Pageof 20
The British Journal of Dermatology|December 12, 2019
Revisiting pachyonychia congenita: a case-cohort study of 815 patientsL Samuelov, F J D Smith, C D Hansen, et al.
The British Journal of Dermatology|March 28, 2017
Report of the 13th Annual International Pachyonychia Congenita Consortium SymposiumL Rittié, R L Kaspar, E Sprecher, et al.
Journal of the Neurological Sciences|September 1, 1994
Variance of sensory threshold measurements: discrimination of feigners from trustworthy performersD Yarnitsky, E Sprecher, A Tamir, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 1, 2013
Best treatment practices for pachyonychia congenitaI Goldberg, D Fruchter, A Meilick, et al.
Chronobiology International|February 4, 2017
Seasonal variation in spontaneous intracerebral hemorrhage in northern IsraelG Telman, G E Sviri, E Sprecher, et al.
Archives of Dermatological Research|January 1, 1990
Effect of genetically determined immunodeficiency on epidermal dendritic cell populations in C57BL/6J miceE Sprecher, Y Becker, G Kraal, et al.
Bone Marrow Transplantation|March 30, 2010
Glutathione S-transferase T1-null seems to be associated with graft failure in hematopoietic SCTR Elhasid, N Krivoy, J M Rowe, et al.
The British Journal of Dermatology|December 24, 2017
Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authorsM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
American Journal of Human Genetics|April 17, 1999
Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichiasE Sprecher, R Bergman, R Szargel, et al.
Clinical and Experimental Dermatology|September 7, 2004
Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndromeE Sprecher, A Tesfaye-Kedjela, P Ratajczak, et al.
Pageof 20