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E Sprecher

Showing results (171-180 of 200) with videos related to

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The British Journal of Dermatology|April 14, 2020
Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndromeD J Ralser, S Kumar, O Borisov, et al.
Clinical and Experimental Dermatology|November 15, 2020
Molecular epidemiology of pachyonychia congenita in the Israeli populationM Pavlovsky, A Peled, L Samuelov, et al.
Diabetes Care|April 24, 2001
Type 1 diabetes environmental factors and correspondence analysis of HLA class II genes in the Yemenite Jewish community in IsraelN Weintrob, E Sprecher, S Israel, et al.
Nature Genetics|September 7, 2001
Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherinE Sprecher, R Bergman, G Richard, et al.
The British Journal of Dermatology|March 2, 2018
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotypeD Vodo, O Sarig, D Jeddah, et al.
Clinical and Experimental Dermatology|September 29, 2018
Grover disease and bullous pemphigoid: a clinicopathological study of six casesE Ellenbogen, S Geller, S Azrielant, et al.
Neurology|March 17, 1999
Limitations of quantitative sensory testing when patients are biased toward a bad outcomeD Yarnitsky, E Sprecher, R Zaslansky, et al.
Clinical and Experimental Dermatology|July 20, 2020
Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin BJ Mohamad, L Samuelov, L Malki, et al.
Neurobiology of Aging|June 11, 2015
Amyloid burden is associated with self-reported sleep in nondemented late middle-aged adultsKate E Sprecher, Barbara B Bendlin, Annie M Racine, et al.
Neurology|July 7, 2017
Poor sleep is associated with CSF biomarkers of amyloid pathology in cognitively normal adultsKate E Sprecher, Rebecca L Koscik, Cynthia M Carlsson, et al.
Pageof 20

Showing results (171-180 of 200) with videos related to

Sort By:
Pageof 20
The British Journal of Dermatology|April 14, 2020
Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndromeD J Ralser, S Kumar, O Borisov, et al.
Clinical and Experimental Dermatology|November 15, 2020
Molecular epidemiology of pachyonychia congenita in the Israeli populationM Pavlovsky, A Peled, L Samuelov, et al.
Diabetes Care|April 24, 2001
Type 1 diabetes environmental factors and correspondence analysis of HLA class II genes in the Yemenite Jewish community in IsraelN Weintrob, E Sprecher, S Israel, et al.
Nature Genetics|September 7, 2001
Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherinE Sprecher, R Bergman, G Richard, et al.
The British Journal of Dermatology|March 2, 2018
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotypeD Vodo, O Sarig, D Jeddah, et al.
Clinical and Experimental Dermatology|September 29, 2018
Grover disease and bullous pemphigoid: a clinicopathological study of six casesE Ellenbogen, S Geller, S Azrielant, et al.
Neurology|March 17, 1999
Limitations of quantitative sensory testing when patients are biased toward a bad outcomeD Yarnitsky, E Sprecher, R Zaslansky, et al.
Clinical and Experimental Dermatology|July 20, 2020
Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin BJ Mohamad, L Samuelov, L Malki, et al.
Neurobiology of Aging|June 11, 2015
Amyloid burden is associated with self-reported sleep in nondemented late middle-aged adultsKate E Sprecher, Barbara B Bendlin, Annie M Racine, et al.
Neurology|July 7, 2017
Poor sleep is associated with CSF biomarkers of amyloid pathology in cognitively normal adultsKate E Sprecher, Rebecca L Koscik, Cynthia M Carlsson, et al.
Pageof 20