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The British Journal of Dermatology
|
April 14, 2020
Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndrome
D J Ralser, S Kumar, O Borisov, et al.
Clinical and Experimental Dermatology
|
November 15, 2020
Molecular epidemiology of pachyonychia congenita in the Israeli population
M 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 Israel
N 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-cadherin
E Sprecher, R Bergman, G Richard, et al.
The British Journal of Dermatology
|
March 2, 2018
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype
D Vodo, O Sarig, D Jeddah, et al.
Clinical and Experimental Dermatology
|
September 29, 2018
Grover disease and bullous pemphigoid: a clinicopathological study of six cases
E Ellenbogen, S Geller, S Azrielant, et al.
Neurology
|
March 17, 1999
Limitations of quantitative sensory testing when patients are biased toward a bad outcome
D 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 B
J 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 adults
Kate 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 adults
Kate E Sprecher, Rebecca L Koscik, Cynthia M Carlsson, et al.
Page
of 20
Search research articles
Search
Showing results (171-180 of 200) with videos related to
Sort By:
Page
of 20
The British Journal of Dermatology
|
April 14, 2020
Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndrome
D J Ralser, S Kumar, O Borisov, et al.
Clinical and Experimental Dermatology
|
November 15, 2020
Molecular epidemiology of pachyonychia congenita in the Israeli population
M 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 Israel
N 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-cadherin
E Sprecher, R Bergman, G Richard, et al.
The British Journal of Dermatology
|
March 2, 2018
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype
D Vodo, O Sarig, D Jeddah, et al.
Clinical and Experimental Dermatology
|
September 29, 2018
Grover disease and bullous pemphigoid: a clinicopathological study of six cases
E Ellenbogen, S Geller, S Azrielant, et al.
Neurology
|
March 17, 1999
Limitations of quantitative sensory testing when patients are biased toward a bad outcome
D 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 B
J 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 adults
Kate 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 adults
Kate E Sprecher, Rebecca L Koscik, Cynthia M Carlsson, et al.
Page
of 20