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Antimicrobial Agents and Chemotherapy
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February 5, 2025
Guidelines vs mindlines: a qualitative investigation of how clinicians' beliefs influence the application of rapid molecular diagnostics in intensive care
Sarah-Jane F Stewart, Alyssa M Pandolfo, Yogini Jani, et al.
European Journal of Neurology
|
January 15, 2014
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood
B P C van de Warrenburg, J van Gaalen, S Boesch, et al.
Neurology
|
March 23, 2007
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3
P Hedera, M A Blair, E Andermann, et al.
The Journal of Nutrition, Health & Aging
|
January 13, 2012
A systematic review of the literature concerning the relationship between obesity and mortality in the elderly
L M Donini, C Savina, E Gennaro, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
July 8, 2014
Assessing the appropriateness of the level of care for morbidly obese subjects: validation of the CASCO-R scale
L M Donini, R Dalle Grave, E Di Flaviano, et al.
International Journal of Obesity (2005)
|
April 21, 2010
Metabolic or bariatric surgery? Long-term effects of malabsorptive vs restrictive bariatric techniques on body composition and cardiometabolic risk factors
C Lubrano, S Mariani, M Badiali, et al.
The Journal of Antimicrobial Chemotherapy
|
November 16, 2023
UK clinicians' attitudes towards the application of molecular diagnostics to guide antibiotic use in ICU patients with pneumonias: a quantitative study
Sarah-Jane F Stewart, Alyssa M Pandolfo, Zoe Moon, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish population
E Monrós, J Cañizares, M D Moltó, et al.
Human Molecular Genetics
|
August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles
L Montermini, E Andermann, M Labuda, et al.
Nature Genetics
|
December 1, 1996
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13
T D Taylor, M Litt, P Kramer, et al.
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of 12
Search research articles
Search
Showing results (91-100 of 116) with videos related to
Sort By:
Page
of 12
Antimicrobial Agents and Chemotherapy
|
February 5, 2025
Guidelines vs mindlines: a qualitative investigation of how clinicians' beliefs influence the application of rapid molecular diagnostics in intensive care
Sarah-Jane F Stewart, Alyssa M Pandolfo, Yogini Jani, et al.
European Journal of Neurology
|
January 15, 2014
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood
B P C van de Warrenburg, J van Gaalen, S Boesch, et al.
Neurology
|
March 23, 2007
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3
P Hedera, M A Blair, E Andermann, et al.
The Journal of Nutrition, Health & Aging
|
January 13, 2012
A systematic review of the literature concerning the relationship between obesity and mortality in the elderly
L M Donini, C Savina, E Gennaro, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
July 8, 2014
Assessing the appropriateness of the level of care for morbidly obese subjects: validation of the CASCO-R scale
L M Donini, R Dalle Grave, E Di Flaviano, et al.
International Journal of Obesity (2005)
|
April 21, 2010
Metabolic or bariatric surgery? Long-term effects of malabsorptive vs restrictive bariatric techniques on body composition and cardiometabolic risk factors
C Lubrano, S Mariani, M Badiali, et al.
The Journal of Antimicrobial Chemotherapy
|
November 16, 2023
UK clinicians' attitudes towards the application of molecular diagnostics to guide antibiotic use in ICU patients with pneumonias: a quantitative study
Sarah-Jane F Stewart, Alyssa M Pandolfo, Zoe Moon, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish population
E Monrós, J Cañizares, M D Moltó, et al.
Human Molecular Genetics
|
August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles
L Montermini, E Andermann, M Labuda, et al.
Nature Genetics
|
December 1, 1996
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13
T D Taylor, M Litt, P Kramer, et al.
Page
of 12