Search research articles
Contact Us
Filters
Showing results (51-60 of 61) with videos related to
Page
of 7
Sort By:
Scandinavian Journal of Gastroenterology
|
February 24, 2001
Sustained virological response in chronic hepatitis C patients after a 6- and a 36-month interferon-alpha2b treatment schedule: a multicenter, randomized, controlled study
M Damen, C J Weegink, E P Mauser-Bunschoten, et al.
American Journal of Human Genetics
|
October 23, 1997
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
P D'Adamo, L Fassone, A Gedeon, et al.
Neuromuscular Disorders : NMD
|
February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
M R Davis, E Haan, H Jungbluth, et al.
Molecular Psychiatry
|
February 11, 2015
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy
G McMichael, M N Bainbridge, E Haan, et al.
Molecular Psychiatry
|
February 25, 2015
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
B W M van Bon, B P Coe, R Bernier, et al.
American Journal of Human Genetics
|
December 13, 2006
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation
M Upadhyaya, S M Huson, M Davies, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients
T Roscioli, G Elakis, T C Cox, et al.
Research Square
|
August 13, 2025
Cross-tissue omics-guided drug repurposing triangulates novel targetable mechanisms for Alzheimer's disease and candidate genetic biomarkers for treatment stratification
Sathyaseelan Chakkarai, Michal Sadowski, Qiong Yang, et al.
Molecular Psychiatry
|
August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females
E E Palmer, T Stuhlmann, S Weinert, et al.
Acta Anaesthesiologica Scandinavica
|
October 8, 2021
Rapid Evaluation of Coronavirus Illness Severity (RECOILS) in intensive care: Development and validation of a prognostic tool for in-hospital mortality
Drago Plečko, Nicolas Bennett, Johan Mårtensson, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 61) with videos related to
Sort By:
Page
of 7
Scandinavian Journal of Gastroenterology
|
February 24, 2001
Sustained virological response in chronic hepatitis C patients after a 6- and a 36-month interferon-alpha2b treatment schedule: a multicenter, randomized, controlled study
M Damen, C J Weegink, E P Mauser-Bunschoten, et al.
American Journal of Human Genetics
|
October 23, 1997
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
P D'Adamo, L Fassone, A Gedeon, et al.
Neuromuscular Disorders : NMD
|
February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
M R Davis, E Haan, H Jungbluth, et al.
Molecular Psychiatry
|
February 11, 2015
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy
G McMichael, M N Bainbridge, E Haan, et al.
Molecular Psychiatry
|
February 25, 2015
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
B W M van Bon, B P Coe, R Bernier, et al.
American Journal of Human Genetics
|
December 13, 2006
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation
M Upadhyaya, S M Huson, M Davies, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients
T Roscioli, G Elakis, T C Cox, et al.
Research Square
|
August 13, 2025
Cross-tissue omics-guided drug repurposing triangulates novel targetable mechanisms for Alzheimer's disease and candidate genetic biomarkers for treatment stratification
Sathyaseelan Chakkarai, Michal Sadowski, Qiong Yang, et al.
Molecular Psychiatry
|
August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females
E E Palmer, T Stuhlmann, S Weinert, et al.
Acta Anaesthesiologica Scandinavica
|
October 8, 2021
Rapid Evaluation of Coronavirus Illness Severity (RECOILS) in intensive care: Development and validation of a prognostic tool for in-hospital mortality
Drago Plečko, Nicolas Bennett, Johan Mårtensson, et al.
Page
of 7