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Diagnostic Cytopathology
|
February 22, 2012
Familial mesothelioma in first degree relatives
Alexandra M Kalogeraki, Dimitrios J Tamiolakis, Eleni D Lagoudaki, et al.
Annals of Hematology
|
December 4, 2008
The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter
Christos Chassanidis, Angelos Kalamaras, Marios Phylactides, et al.
Neurology
|
December 15, 2004
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALS
J M Graham, N Papadakis, J Evans, et al.
Scientific Reports
|
March 1, 2020
Α 10-gigawatt attosecond source for non-linear XUV optics and XUV-pump-XUV-probe studies
I Makos, I Orfanos, A Nayak, et al.
Pharmacogenomics
|
August 9, 2019
Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients
Apostolos Stratopoulos, Alexandra Kolliopoulou, Kariofyllis Karamperis, et al.
Journal of Clinical Pharmacy and Therapeutics
|
August 24, 2017
Patients' intention to consume prescribed and non-prescribed medicines: A study based on the theory of planned behaviour in selected European countries
A Kamekis, A Bertsias, J Moschandreas, et al.
OTA International : the Open Access Journal of Orthopaedic Trauma
|
August 8, 2024
Rehabilitation after musculoskeletal injury: European perspective
Michael Kelly, Richard L Donovan, Zoe H Dailiana, et al.
Nature Genetics
|
March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Belinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 68) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 68 results.
Diagnostic Cytopathology
|
February 22, 2012
Familial mesothelioma in first degree relatives
Alexandra M Kalogeraki, Dimitrios J Tamiolakis, Eleni D Lagoudaki, et al.
Annals of Hematology
|
December 4, 2008
The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter
Christos Chassanidis, Angelos Kalamaras, Marios Phylactides, et al.
Neurology
|
December 15, 2004
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALS
J M Graham, N Papadakis, J Evans, et al.
Scientific Reports
|
March 1, 2020
Α 10-gigawatt attosecond source for non-linear XUV optics and XUV-pump-XUV-probe studies
I Makos, I Orfanos, A Nayak, et al.
Pharmacogenomics
|
August 9, 2019
Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients
Apostolos Stratopoulos, Alexandra Kolliopoulou, Kariofyllis Karamperis, et al.
Journal of Clinical Pharmacy and Therapeutics
|
August 24, 2017
Patients' intention to consume prescribed and non-prescribed medicines: A study based on the theory of planned behaviour in selected European countries
A Kamekis, A Bertsias, J Moschandreas, et al.
OTA International : the Open Access Journal of Orthopaedic Trauma
|
August 8, 2024
Rehabilitation after musculoskeletal injury: European perspective
Michael Kelly, Richard L Donovan, Zoe H Dailiana, et al.
Nature Genetics
|
March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Belinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Page
of 7