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Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
June 22, 2021
[Childhood emergencies-worsening healthcare bottlenecks for children in a systematic long-term analysis of the EMS system in a German metropolis]
F Hoffmann, M Landeg, W Rittberg, et al.
Der Unfallchirurg
|
October 13, 2020
[Development of a new module for the TraumaRegister DGU<sup>®</sup> : Better collation of the sequelae of severe injuries during pregnancy]
H Trentzsch, A Weißleder, T Annecke, et al.
European Journal of Pediatrics
|
October 26, 2020
Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis-implications for process quality and patient care
Gwendolyn Gramer, Inken Brockow, Christiane Labitzke, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2012
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1. From blood spot to screening result
J Gerard Loeber, Peter Burgard, Martina C Cornel, et al.
The European Journal of Neuroscience
|
August 3, 2002
NMDA receptor activation and respiratory chain complex V inhibition contribute to neurodegeneration in d-2-hydroxyglutaric aciduria
Stefan Kölker, Verena Pawlak, Barbara Ahlemeyer, et al.
Stem Cell Research
|
February 18, 2019
Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-A
Dominic Lenz, Christian Staufner, Selina Wächter, et al.
BMJ Case Reports
|
June 21, 2011
Pyridoxal phosphate-dependent neonatal epileptic encephalopathy
S Bagci, J Zschocke, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
August 19, 2007
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 gene
O Y Al-Dirbashi, K K Abu-Amero, A F Alswaid, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
August 16, 2011
Estimating the SF-6D value set for a population-based sample of Brazilians
Luciane N Cruz, Suzi A Camey, Juliana F Hoffmann, et al.
Neurochemistry International
|
February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)
S W Sauer, S Kölker, G F Hoffmann, et al.
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of 108
Search research articles
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Showing results (611-620 of 1,073) with videos related to
Sort By:
Page
of 108
Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
June 22, 2021
[Childhood emergencies-worsening healthcare bottlenecks for children in a systematic long-term analysis of the EMS system in a German metropolis]
F Hoffmann, M Landeg, W Rittberg, et al.
Der Unfallchirurg
|
October 13, 2020
[Development of a new module for the TraumaRegister DGU<sup>®</sup> : Better collation of the sequelae of severe injuries during pregnancy]
H Trentzsch, A Weißleder, T Annecke, et al.
European Journal of Pediatrics
|
October 26, 2020
Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis-implications for process quality and patient care
Gwendolyn Gramer, Inken Brockow, Christiane Labitzke, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2012
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1. From blood spot to screening result
J Gerard Loeber, Peter Burgard, Martina C Cornel, et al.
The European Journal of Neuroscience
|
August 3, 2002
NMDA receptor activation and respiratory chain complex V inhibition contribute to neurodegeneration in d-2-hydroxyglutaric aciduria
Stefan Kölker, Verena Pawlak, Barbara Ahlemeyer, et al.
Stem Cell Research
|
February 18, 2019
Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-A
Dominic Lenz, Christian Staufner, Selina Wächter, et al.
BMJ Case Reports
|
June 21, 2011
Pyridoxal phosphate-dependent neonatal epileptic encephalopathy
S Bagci, J Zschocke, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
August 19, 2007
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 gene
O Y Al-Dirbashi, K K Abu-Amero, A F Alswaid, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
August 16, 2011
Estimating the SF-6D value set for a population-based sample of Brazilians
Luciane N Cruz, Suzi A Camey, Juliana F Hoffmann, et al.
Neurochemistry International
|
February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)
S W Sauer, S Kölker, G F Hoffmann, et al.
Page
of 108