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Stroke
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January 31, 2015
Ischemic stroke phenotype in patients with nonsustained atrial fibrillation
Ethem M Arsava, Demet F Bas, Enver Atalar, et al.
The British Journal of Dermatology
|
September 6, 2019
Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study
A Reimer, M Hess, A Schwieger-Briel, et al.
AJNR. American Journal of Neuroradiology
|
April 20, 2013
Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay
K K Oguz, G Haliloglu, C Temucin, et al.
International Journal of Clinical Pharmacology and Therapeutics
|
February 11, 2009
Modulation of the efficacy of temozolomide and dacarbazine melanoma treatment by DNA-repair factors in vivo and in vitro
L Boeckmann, K-M Thoms, R Gutzmer, et al.
Matrix Biology Plus
|
September 5, 2022
Integrin α3 negative podocytes: A gene expression study
L H Frommherz, S B Sayar, Y Wang, et al.
The British Journal of Dermatology
|
February 10, 2017
A case of mosaicism in ectodermal dysplasia-skin fragility syndrome
I Vázquez-Osorio, N Chmel, E Rodríguez-Díaz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 20, 2024
IL-6 levels dominate the serum cytokine signature of severe epidermolysis bullosa: A prospective cohort study
A Reimer-Taschenbrecker, M Hess, M Davidovic, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
August 3, 2019
Combined anti-inflammatory and low-dose antiproliferative therapy for squamous cell carcinomas in recessive dystrophic epidermolysis bullosa
A Reimer, S Lu, Y He, et al.
The British Journal of Dermatology
|
August 9, 2020
Recurrent MVD mutation in European patients with disseminated porokeratosis
M Saleva-Stateva, K Technau-Hafsi, L Frommherz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 17, 2021
High rate of self-improving phenotypes in children with non-syndromic congenital ichthyosis: case series from south-western Germany
L Frommherz, A Krause, J Kopp, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 90) with videos related to
Sort By:
Page
of 9
Stroke
|
January 31, 2015
Ischemic stroke phenotype in patients with nonsustained atrial fibrillation
Ethem M Arsava, Demet F Bas, Enver Atalar, et al.
The British Journal of Dermatology
|
September 6, 2019
Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study
A Reimer, M Hess, A Schwieger-Briel, et al.
AJNR. American Journal of Neuroradiology
|
April 20, 2013
Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay
K K Oguz, G Haliloglu, C Temucin, et al.
International Journal of Clinical Pharmacology and Therapeutics
|
February 11, 2009
Modulation of the efficacy of temozolomide and dacarbazine melanoma treatment by DNA-repair factors in vivo and in vitro
L Boeckmann, K-M Thoms, R Gutzmer, et al.
Matrix Biology Plus
|
September 5, 2022
Integrin α3 negative podocytes: A gene expression study
L H Frommherz, S B Sayar, Y Wang, et al.
The British Journal of Dermatology
|
February 10, 2017
A case of mosaicism in ectodermal dysplasia-skin fragility syndrome
I Vázquez-Osorio, N Chmel, E Rodríguez-Díaz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 20, 2024
IL-6 levels dominate the serum cytokine signature of severe epidermolysis bullosa: A prospective cohort study
A Reimer-Taschenbrecker, M Hess, M Davidovic, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
August 3, 2019
Combined anti-inflammatory and low-dose antiproliferative therapy for squamous cell carcinomas in recessive dystrophic epidermolysis bullosa
A Reimer, S Lu, Y He, et al.
The British Journal of Dermatology
|
August 9, 2020
Recurrent MVD mutation in European patients with disseminated porokeratosis
M Saleva-Stateva, K Technau-Hafsi, L Frommherz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 17, 2021
High rate of self-improving phenotypes in children with non-syndromic congenital ichthyosis: case series from south-western Germany
L Frommherz, A Krause, J Kopp, et al.
Page
of 9