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Journal of Geophysical Research. Space Physics
|
March 4, 2016
A summary of the BARREL campaigns: Technique for studying electron precipitation
L A Woodger, A J Halford, R M Millan, et al.
Molecular Genetics & Genomic Medicine
|
October 22, 2014
Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome
Peter M Krawitz, Daniela Schiska, Ulrike Krüger, et al.
Journal of Medical Genetics
|
March 16, 2007
MYO7A mutation screening in Usher syndrome type I patients from diverse origins
T Jaijo, E Aller, M Beneyto, et al.
Techniques in Coloproctology
|
February 1, 2022
"Near-TME": proposed standardisation of the technique for proctectomy in male patients with ulcerative colitis
A Garcia-Granero, G Pellino, D Fletcher-Sanfeliu, et al.
Plant Biology (Stuttgart, Germany)
|
April 4, 2026
Not only reseeder or resprouter plants: Trait syndromes and post-fire responses of three iconic Mediterranean woody species
G Ottaviani, H Beckett, J M Costa-Saura, et al.
Alimentary Pharmacology & Therapeutics
|
September 3, 2010
Maintenance of clinical benefit in Crohn's disease patients after discontinuation of infliximab: long-term follow-up of a single centre cohort
A W G Waugh, S Garg, K Matic, et al.
Journal of Parasitic Diseases : Official Organ of the Indian Society for Parasitology
|
March 2, 2026
Predicting the localized prevalence of ascariasis in the Philippines using bioclimatic and topographical covariates: a case study in Cavite province
Leann Victoria P Roque, Nikki Heherson A Dagamac, Princess Leilene M Millan, et al.
AJNR. American Journal of Neuroradiology
|
April 8, 2022
Antithrombotic Treatment after Carotid Stenting in Patients with Concomitant Atrial Fibrillation
B Pardo-Galiana, M Medina-Rodriguez, M Millan-Vazquez, et al.
Plos One
|
February 25, 2016
Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases
Fiona Blanco-Kelly, María García Hoyos, Miguel Angel Lopez Martinez, et al.
European Journal of Human Genetics : EJHG
|
September 30, 2010
Characterisation of TSC1 promoter deletions in tuberous sclerosis complex patients
Ans M W van den Ouweland, Peter Elfferich, Bernard A Zonnenberg, et al.
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of 12
Search research articles
Search
Showing results (91-100 of 119) with videos related to
Sort By:
Page
of 12
Journal of Geophysical Research. Space Physics
|
March 4, 2016
A summary of the BARREL campaigns: Technique for studying electron precipitation
L A Woodger, A J Halford, R M Millan, et al.
Molecular Genetics & Genomic Medicine
|
October 22, 2014
Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome
Peter M Krawitz, Daniela Schiska, Ulrike Krüger, et al.
Journal of Medical Genetics
|
March 16, 2007
MYO7A mutation screening in Usher syndrome type I patients from diverse origins
T Jaijo, E Aller, M Beneyto, et al.
Techniques in Coloproctology
|
February 1, 2022
"Near-TME": proposed standardisation of the technique for proctectomy in male patients with ulcerative colitis
A Garcia-Granero, G Pellino, D Fletcher-Sanfeliu, et al.
Plant Biology (Stuttgart, Germany)
|
April 4, 2026
Not only reseeder or resprouter plants: Trait syndromes and post-fire responses of three iconic Mediterranean woody species
G Ottaviani, H Beckett, J M Costa-Saura, et al.
Alimentary Pharmacology & Therapeutics
|
September 3, 2010
Maintenance of clinical benefit in Crohn's disease patients after discontinuation of infliximab: long-term follow-up of a single centre cohort
A W G Waugh, S Garg, K Matic, et al.
Journal of Parasitic Diseases : Official Organ of the Indian Society for Parasitology
|
March 2, 2026
Predicting the localized prevalence of ascariasis in the Philippines using bioclimatic and topographical covariates: a case study in Cavite province
Leann Victoria P Roque, Nikki Heherson A Dagamac, Princess Leilene M Millan, et al.
AJNR. American Journal of Neuroradiology
|
April 8, 2022
Antithrombotic Treatment after Carotid Stenting in Patients with Concomitant Atrial Fibrillation
B Pardo-Galiana, M Medina-Rodriguez, M Millan-Vazquez, et al.
Plos One
|
February 25, 2016
Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases
Fiona Blanco-Kelly, María García Hoyos, Miguel Angel Lopez Martinez, et al.
European Journal of Human Genetics : EJHG
|
September 30, 2010
Characterisation of TSC1 promoter deletions in tuberous sclerosis complex patients
Ans M W van den Ouweland, Peter Elfferich, Bernard A Zonnenberg, et al.
Page
of 12