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Paediatric Nursing
|
April 29, 2003
Employing children's nurses?
Sue Price
Paediatric Nursing
|
September 11, 2002
The recruitment and retention of children's nurses
Sue Price
Archives of Disease in Childhood
|
September 20, 2013
Subdural effusions and lack of early pontocerebellar hypoplasia in siblings with RARS2 mutations
Katherina Kastrissianakis, Geetha Anand, Gerardine Quaghebeur, et al.
European Journal of Pediatrics
|
May 8, 2008
Clinical and radiological findings in Schinzel-Giedion syndrome
Mudaffer Al-Mudaffer, Christine Oley, Sue Price, et al.
American Journal of Medical Genetics. Part A
|
April 26, 2017
Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
Andrea C Yu, Regina M Zambrano, Ingrid Cristian, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
May 29, 2003
Vessel caliber and restenosis: a prospective clinical and angiographic study of NIR stent deployment in small and large coronary arteries in the same patient
Peter N Ruygrok, Mark W Webster, Justin J Ardill, et al.
Developmental Medicine and Child Neurology
|
June 9, 2011
Milder phenotypes of glucose transporter type 1 deficiency syndrome
Geetha Anand, Anuruddha Padeniya, Donncha Hanrahan, et al.
American Journal of Medical Genetics. Part A
|
February 1, 2018
Extending the phenotype associated with the CSNK2A1-related Okur-Chung syndrome-A clinical study of 11 individuals
Ceris I Owen, Ramsay Bowden, Michael J Parker, et al.
The American Journal of Cardiology
|
July 20, 2002
Six-month angiographic and 12-month clinical follow-up of MultiLink long (25 to 35 mm) stents for long coronary narrowings in patients with angina pectoris
John A Ormiston, Mark W I Webster, Peter N Ruygrok, et al.
Human Molecular Genetics
|
January 6, 2017
Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders
Jochem M G Evers, Roman A Laskowski, Marta Bertolli, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Paediatric Nursing
|
April 29, 2003
Employing children's nurses?
Sue Price
Paediatric Nursing
|
September 11, 2002
The recruitment and retention of children's nurses
Sue Price
Archives of Disease in Childhood
|
September 20, 2013
Subdural effusions and lack of early pontocerebellar hypoplasia in siblings with RARS2 mutations
Katherina Kastrissianakis, Geetha Anand, Gerardine Quaghebeur, et al.
European Journal of Pediatrics
|
May 8, 2008
Clinical and radiological findings in Schinzel-Giedion syndrome
Mudaffer Al-Mudaffer, Christine Oley, Sue Price, et al.
American Journal of Medical Genetics. Part A
|
April 26, 2017
Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
Andrea C Yu, Regina M Zambrano, Ingrid Cristian, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
May 29, 2003
Vessel caliber and restenosis: a prospective clinical and angiographic study of NIR stent deployment in small and large coronary arteries in the same patient
Peter N Ruygrok, Mark W Webster, Justin J Ardill, et al.
Developmental Medicine and Child Neurology
|
June 9, 2011
Milder phenotypes of glucose transporter type 1 deficiency syndrome
Geetha Anand, Anuruddha Padeniya, Donncha Hanrahan, et al.
American Journal of Medical Genetics. Part A
|
February 1, 2018
Extending the phenotype associated with the CSNK2A1-related Okur-Chung syndrome-A clinical study of 11 individuals
Ceris I Owen, Ramsay Bowden, Michael J Parker, et al.
The American Journal of Cardiology
|
July 20, 2002
Six-month angiographic and 12-month clinical follow-up of MultiLink long (25 to 35 mm) stents for long coronary narrowings in patients with angina pectoris
John A Ormiston, Mark W I Webster, Peter N Ruygrok, et al.
Human Molecular Genetics
|
January 6, 2017
Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders
Jochem M G Evers, Roman A Laskowski, Marta Bertolli, et al.
Page
of 2