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Wiener Klinische Wochenschrift
|
January 1, 1992
[Diagnosis of inborn errors of metabolism: necessity or luxury?]
S Stöckler
The Journal of Pediatrics
|
December 5, 1997
Creatine deficiency syndromes: a new perspective on metabolic disorders and a diagnostic challenge
S Stöckler-Ipsiroglu
Wiener Klinische Wochenschrift
|
January 1, 1992
[Strategies for the diagnosis of lysosomal storage diseases: symptoms, methods and samples]
E Paschke, S Stöckler
Wiener Klinische Wochenschrift
|
February 14, 1997
Guanidinoacetate methyltransferase deficiency: a newly recognized inborn error of creatine biosynthesis
S Stöckler, F Hanefeld
Lancet (London, England)
|
September 21, 1996
Creatine replacement therapy in guanidinoacetate methyltransferase deficiency, a novel inborn error of metabolism
S Stöckler, F Hanefeld, J Frahm
The Journal of Pediatrics
|
August 1, 1990
Clearance of toxic metabolites during therapy for inborn errors of metabolism
E Ring, G Zobel, S Stöckler
Wiener Klinische Wochenschrift
|
January 1, 1992
[Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers]
B Molzer, S Stöckler, H Bernheimer
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 8, 2000
Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism
J Ilas, A Mühl, S Stöckler-Ipsiroglu
Klinische Padiatrie
|
September 1, 1989
[Congenital metabolic diseases as a cause of acute illnesses in the neonatal period]
S Stöckler, O S Ipsiroglu, E Paschke
Wiener Klinische Wochenschrift
|
September 1, 1989
[Pregnancy and neonatal screening in Austria]
S Stöckler, O S Ipsiroglu, M Häusler
Page
of 8
Search research articles
Search
Showing results (1-10 of 71) with videos related to
Sort By:
Page
of 8
Wiener Klinische Wochenschrift
|
January 1, 1992
[Diagnosis of inborn errors of metabolism: necessity or luxury?]
S Stöckler
The Journal of Pediatrics
|
December 5, 1997
Creatine deficiency syndromes: a new perspective on metabolic disorders and a diagnostic challenge
S Stöckler-Ipsiroglu
Wiener Klinische Wochenschrift
|
January 1, 1992
[Strategies for the diagnosis of lysosomal storage diseases: symptoms, methods and samples]
E Paschke, S Stöckler
Wiener Klinische Wochenschrift
|
February 14, 1997
Guanidinoacetate methyltransferase deficiency: a newly recognized inborn error of creatine biosynthesis
S Stöckler, F Hanefeld
Lancet (London, England)
|
September 21, 1996
Creatine replacement therapy in guanidinoacetate methyltransferase deficiency, a novel inborn error of metabolism
S Stöckler, F Hanefeld, J Frahm
The Journal of Pediatrics
|
August 1, 1990
Clearance of toxic metabolites during therapy for inborn errors of metabolism
E Ring, G Zobel, S Stöckler
Wiener Klinische Wochenschrift
|
January 1, 1992
[Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers]
B Molzer, S Stöckler, H Bernheimer
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 8, 2000
Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism
J Ilas, A Mühl, S Stöckler-Ipsiroglu
Klinische Padiatrie
|
September 1, 1989
[Congenital metabolic diseases as a cause of acute illnesses in the neonatal period]
S Stöckler, O S Ipsiroglu, E Paschke
Wiener Klinische Wochenschrift
|
September 1, 1989
[Pregnancy and neonatal screening in Austria]
S Stöckler, O S Ipsiroglu, M Häusler
Page
of 8