Search research articles
Contact Us
Filters
Showing results (91-100 of 147) with videos related to
Page
of 15
Sort By:
Pediatrics
|
April 22, 2018
Imaging in Pediatric Concussion: A Systematic Review
Julia Schmidt, Kathryn S Hayward, Katlyn E Brown, et al.
Canadian Journal of Occupational Therapy. Revue Canadienne D'Ergotherapie
|
May 15, 2023
Quality of Physical Activity Participation Among Adults with Disabilities Through Pandemic Restriction
Gordon Tao, Gurkaran Singh, Ethan Simpson, et al.
Journal of Virology
|
October 17, 2014
Tetramer enrichment reveals the presence of phenotypically diverse hepatitis C virus-specific CD8+ T cells in chronic infection
Katja Nitschke, Tobias Flecken, Julia Schmidt, et al.
Experimental Dermatology
|
November 11, 2014
Hair follicle targeting, penetration enhancement and Langerhans cell activation make cyanoacrylate skin surface stripping a promising delivery technique for transcutaneous immunization with large molecules and particle-based vaccines
Annika Vogt, Sabrina Hadam, Iliane Deckert, et al.
Human Molecular Genetics
|
January 31, 2022
Single-cell transcription profiles in Bloom syndrome patients link BLM deficiency with altered condensin complex expression signatures
Ipek Ilgin Gönenc, Alexander Wolff, Julia Schmidt, et al.
Trials
|
November 7, 2013
Comparison of error-based and errorless learning for people with severe traumatic brain injury: study protocol for a randomized control trial
Tamara Ownsworth, Jennifer Fleming, Robyn Tate, et al.
Human Genetics
|
January 24, 2024
Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromes
Julia Schmidt, Silke Kaulfuß, Hagen Ott, et al.
European Journal of Human Genetics : EJHG
|
October 11, 2021
Familial cleft tongue caused by a unique translation initiation codon variant in TP63
Julia Schmidt, Gudrun Schreiber, Janine Altmüller, et al.
Scientific Reports
|
March 9, 2022
A novel single-cell RNA-sequencing approach and its applicability connecting genotype to phenotype in ageing disease
Orr Shomroni, Maren Sitte, Julia Schmidt, et al.
Clinical and Translational Allergy
|
February 28, 2019
Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedema
Andreas Recke, Elisabeth G Massalme, Uta Jappe, et al.
Page
of 15
Search research articles
Search
Showing results (91-100 of 147) with videos related to
Sort By:
Page
of 15
Pediatrics
|
April 22, 2018
Imaging in Pediatric Concussion: A Systematic Review
Julia Schmidt, Kathryn S Hayward, Katlyn E Brown, et al.
Canadian Journal of Occupational Therapy. Revue Canadienne D'Ergotherapie
|
May 15, 2023
Quality of Physical Activity Participation Among Adults with Disabilities Through Pandemic Restriction
Gordon Tao, Gurkaran Singh, Ethan Simpson, et al.
Journal of Virology
|
October 17, 2014
Tetramer enrichment reveals the presence of phenotypically diverse hepatitis C virus-specific CD8+ T cells in chronic infection
Katja Nitschke, Tobias Flecken, Julia Schmidt, et al.
Experimental Dermatology
|
November 11, 2014
Hair follicle targeting, penetration enhancement and Langerhans cell activation make cyanoacrylate skin surface stripping a promising delivery technique for transcutaneous immunization with large molecules and particle-based vaccines
Annika Vogt, Sabrina Hadam, Iliane Deckert, et al.
Human Molecular Genetics
|
January 31, 2022
Single-cell transcription profiles in Bloom syndrome patients link BLM deficiency with altered condensin complex expression signatures
Ipek Ilgin Gönenc, Alexander Wolff, Julia Schmidt, et al.
Trials
|
November 7, 2013
Comparison of error-based and errorless learning for people with severe traumatic brain injury: study protocol for a randomized control trial
Tamara Ownsworth, Jennifer Fleming, Robyn Tate, et al.
Human Genetics
|
January 24, 2024
Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromes
Julia Schmidt, Silke Kaulfuß, Hagen Ott, et al.
European Journal of Human Genetics : EJHG
|
October 11, 2021
Familial cleft tongue caused by a unique translation initiation codon variant in TP63
Julia Schmidt, Gudrun Schreiber, Janine Altmüller, et al.
Scientific Reports
|
March 9, 2022
A novel single-cell RNA-sequencing approach and its applicability connecting genotype to phenotype in ageing disease
Orr Shomroni, Maren Sitte, Julia Schmidt, et al.
Clinical and Translational Allergy
|
February 28, 2019
Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedema
Andreas Recke, Elisabeth G Massalme, Uta Jappe, et al.
Page
of 15