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The Oncologist
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March 30, 2016
Novel Treatments for Rare Cancers: The U.S. Orphan Drug Act Is Delivering-A Cross-Sectional Analysis
Clemens Stockklausner, Anette Lampert, Georg F Hoffmann, et al.
Orphanet Journal of Rare Diseases
|
May 14, 2016
Novel treatments for rare rheumatologic disorders: analysis of the impact of 30 years of the US orphan drug act
Thomas Lutz, Anette Lampert, Georg F Hoffmann, et al.
Orphanet Journal of Rare Diseases
|
April 22, 2015
Pressure for drug development in lysosomal storage disorders - a quantitative analysis thirty years beyond the US orphan drug act
Konstantin Mechler, William K Mountford, Georg F Hoffmann, et al.
Pediatric Neurology
|
October 1, 2015
Recurrent Stroke-Like Episodes in FBXL4-Associated Early-Onset Mitochondrial Encephalomyopathy
Darius Ebrahimi-Fakhari, Angelika Seitz, Stefan Kölker, et al.
Pediatric Research
|
October 30, 2013
Emerging role of autophagy in pediatric neurodegenerative and neurometabolic diseases
Darius Ebrahimi-Fakhari, Lara Wahlster, Georg F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
September 20, 2012
Screening for congenital disorders of glycosylation in the first weeks of life
Christian Thiel, Dorothea Meßner-Schmitt, Georg F Hoffmann, et al.
International Journal of Methods in Psychiatric Research
|
November 19, 2016
Defining the hidden evidence in autism research. Forty per cent of rigorously designed clinical trials remain unpublished - a cross-sectional analysis
Konstantin Mechler, Georg F Hoffmann, Ralf W Dittmann, et al.
Plos One
|
August 25, 2016
Thirty Years of Orphan Drug Legislation and the Development of Drugs to Treat Rare Seizure Conditions: A Cross Sectional Analysis
Jan Henje Döring, Anette Lampert, Georg F Hoffmann, et al.
Annals of African Medicine
|
October 25, 2017
Iron and vitamin D levels among autism spectrum disorders children
Abdulbari Bener, Azhar O Khattab, Dinesh Bhugra, et al.
Molecular Genetics and Metabolism
|
February 5, 2013
Pitfalls in phenylalanine loading test in the diagnosis of dopa-responsive dystonia
Thomas Opladen, Georg F Hoffmann, Andrea A Kühn, et al.
Page
of 39
Search research articles
Search
Showing results (31-40 of 381) with videos related to
Sort By:
Page
of 39
The Oncologist
|
March 30, 2016
Novel Treatments for Rare Cancers: The U.S. Orphan Drug Act Is Delivering-A Cross-Sectional Analysis
Clemens Stockklausner, Anette Lampert, Georg F Hoffmann, et al.
Orphanet Journal of Rare Diseases
|
May 14, 2016
Novel treatments for rare rheumatologic disorders: analysis of the impact of 30 years of the US orphan drug act
Thomas Lutz, Anette Lampert, Georg F Hoffmann, et al.
Orphanet Journal of Rare Diseases
|
April 22, 2015
Pressure for drug development in lysosomal storage disorders - a quantitative analysis thirty years beyond the US orphan drug act
Konstantin Mechler, William K Mountford, Georg F Hoffmann, et al.
Pediatric Neurology
|
October 1, 2015
Recurrent Stroke-Like Episodes in FBXL4-Associated Early-Onset Mitochondrial Encephalomyopathy
Darius Ebrahimi-Fakhari, Angelika Seitz, Stefan Kölker, et al.
Pediatric Research
|
October 30, 2013
Emerging role of autophagy in pediatric neurodegenerative and neurometabolic diseases
Darius Ebrahimi-Fakhari, Lara Wahlster, Georg F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
September 20, 2012
Screening for congenital disorders of glycosylation in the first weeks of life
Christian Thiel, Dorothea Meßner-Schmitt, Georg F Hoffmann, et al.
International Journal of Methods in Psychiatric Research
|
November 19, 2016
Defining the hidden evidence in autism research. Forty per cent of rigorously designed clinical trials remain unpublished - a cross-sectional analysis
Konstantin Mechler, Georg F Hoffmann, Ralf W Dittmann, et al.
Plos One
|
August 25, 2016
Thirty Years of Orphan Drug Legislation and the Development of Drugs to Treat Rare Seizure Conditions: A Cross Sectional Analysis
Jan Henje Döring, Anette Lampert, Georg F Hoffmann, et al.
Annals of African Medicine
|
October 25, 2017
Iron and vitamin D levels among autism spectrum disorders children
Abdulbari Bener, Azhar O Khattab, Dinesh Bhugra, et al.
Molecular Genetics and Metabolism
|
February 5, 2013
Pitfalls in phenylalanine loading test in the diagnosis of dopa-responsive dystonia
Thomas Opladen, Georg F Hoffmann, Andrea A Kühn, et al.
Page
of 39