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Pediatric Pulmonology
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November 29, 2022
German newborn screening for Cystic fibrosis: Parental perspectives and suggestions for improvements
Simon Gapp, Sven F Garbade, Patrik Feyh, et al.
Neuropediatrics
|
March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestations
B Assmann, R Hackler, V Peters, et al.
Plos Neglected Tropical Diseases
|
October 23, 2008
Use of genomic DNA as an indirect reference for identifying gender-associated transcripts in morphologically identical, but chromosomally distinct, Schistosoma mansoni cercariae
Jennifer M Fitzpatrick, Anna V Protasio, Andrew J McArdle, et al.
Molecular Genetics and Metabolism
|
November 17, 2022
Detection of early cardiac disease manifestation in propionic acidemia - Results of a monocentric cross-sectional study
Alexander Kovacevic, Sven F Garbade, Friederike Hörster, et al.
Children (Basel, Switzerland)
|
January 21, 2023
Evaluation of Right Ventricular Function in Patients with Propionic Acidemia-A Cross-Sectional Study
Alexander Kovacevic, Sven F Garbade, Friederike Hörster, et al.
The Journal of Experimental Medicine
|
November 21, 2001
The role of interleukin (IL)-10 in the persistence of Leishmania major in the skin after healing and the therapeutic potential of anti-IL-10 receptor antibody for sterile cure
Y Belkaid, K F Hoffmann, S Mendez, et al.
Neuropediatrics
|
August 18, 2001
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiency
M Baethmann, U Wendel, G F Hoffmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 24, 2004
Normal dopaminergic and serotonergic metabolites in cerebrospinal fluid and blood of restless legs syndrome patients
Karin Stiasny-Kolster, J Carsten Möller, Johannes Zschocke, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiency
S Kölker, P Burgard, J G Okun, et al.
Brain : a Journal of Neurology
|
December 31, 2015
Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism
Darius Ebrahimi-Fakhari, Afshin Saffari, Lara Wahlster, et al.
Page
of 126
Search research articles
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Showing results (711-720 of 1,255) with videos related to
Sort By:
Page
of 126
Pediatric Pulmonology
|
November 29, 2022
German newborn screening for Cystic fibrosis: Parental perspectives and suggestions for improvements
Simon Gapp, Sven F Garbade, Patrik Feyh, et al.
Neuropediatrics
|
March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestations
B Assmann, R Hackler, V Peters, et al.
Plos Neglected Tropical Diseases
|
October 23, 2008
Use of genomic DNA as an indirect reference for identifying gender-associated transcripts in morphologically identical, but chromosomally distinct, Schistosoma mansoni cercariae
Jennifer M Fitzpatrick, Anna V Protasio, Andrew J McArdle, et al.
Molecular Genetics and Metabolism
|
November 17, 2022
Detection of early cardiac disease manifestation in propionic acidemia - Results of a monocentric cross-sectional study
Alexander Kovacevic, Sven F Garbade, Friederike Hörster, et al.
Children (Basel, Switzerland)
|
January 21, 2023
Evaluation of Right Ventricular Function in Patients with Propionic Acidemia-A Cross-Sectional Study
Alexander Kovacevic, Sven F Garbade, Friederike Hörster, et al.
The Journal of Experimental Medicine
|
November 21, 2001
The role of interleukin (IL)-10 in the persistence of Leishmania major in the skin after healing and the therapeutic potential of anti-IL-10 receptor antibody for sterile cure
Y Belkaid, K F Hoffmann, S Mendez, et al.
Neuropediatrics
|
August 18, 2001
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiency
M Baethmann, U Wendel, G F Hoffmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 24, 2004
Normal dopaminergic and serotonergic metabolites in cerebrospinal fluid and blood of restless legs syndrome patients
Karin Stiasny-Kolster, J Carsten Möller, Johannes Zschocke, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiency
S Kölker, P Burgard, J G Okun, et al.
Brain : a Journal of Neurology
|
December 31, 2015
Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism
Darius Ebrahimi-Fakhari, Afshin Saffari, Lara Wahlster, et al.
Page
of 126