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Journal of Inherited Metabolic Disease
|
May 10, 2002
Tetrahydrobiopterin responsiveness in phenylketonuria. Two new cases and a review of molecular genetic findings
U Lässker, J Zschocke, N Blau, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
July 1, 1993
[Williams-Beuren syndrome in combination with celiac disease]
R Pankau, C J Partsch, A Gosch, et al.
Annals of Hematology
|
April 23, 2003
Neutrophil aggregates in a 13-year-old girl: a rare hematological phenomenon
A Claviez, H-A Horst, R Santer, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 17, 2002
Laboratory signs of activated coagulation are common in Henoch-Schönlein purpura
K Brendel-Müller, A Hahn, R Schneppenheim, et al.
Pediatric Radiology
|
January 1, 1991
Computed tomography in superior mesenteric artery syndrome
R Santer, C Young, T Rossi, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 1, 1996
Williams-Beuren syndrome and celiac disease
R Santer, R Pankau, J Schaub, et al.
Archives of Disease in Childhood
|
June 27, 2000
Hereditary fructose intolerance and alpha(1) antitrypsin deficiency
G Hillebrand, R Schneppenheim, H D Oldigs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Decreased activity of respiratory-chain enzymes in glutaric aciduria type II
R Santer, A Claass, M Krawinkel, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
December 1, 1993
Urinary excretion of epidermal growth factor and transforming growth factor-alpha in breast-fed and formula-fed infants
R Santer, P Borlinghaus, E Sievers, et al.
Endocrine-Related Cancer
|
December 8, 2009
Interleukin-6 trans-signalling differentially regulates proliferation, migration, adhesion and maspin expression in human prostate cancer cells
Frédéric R Santer, Kamilla Malinowska, Zoran Culig, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 110) with videos related to
Sort By:
Page
of 11
Journal of Inherited Metabolic Disease
|
May 10, 2002
Tetrahydrobiopterin responsiveness in phenylketonuria. Two new cases and a review of molecular genetic findings
U Lässker, J Zschocke, N Blau, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
July 1, 1993
[Williams-Beuren syndrome in combination with celiac disease]
R Pankau, C J Partsch, A Gosch, et al.
Annals of Hematology
|
April 23, 2003
Neutrophil aggregates in a 13-year-old girl: a rare hematological phenomenon
A Claviez, H-A Horst, R Santer, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 17, 2002
Laboratory signs of activated coagulation are common in Henoch-Schönlein purpura
K Brendel-Müller, A Hahn, R Schneppenheim, et al.
Pediatric Radiology
|
January 1, 1991
Computed tomography in superior mesenteric artery syndrome
R Santer, C Young, T Rossi, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 1, 1996
Williams-Beuren syndrome and celiac disease
R Santer, R Pankau, J Schaub, et al.
Archives of Disease in Childhood
|
June 27, 2000
Hereditary fructose intolerance and alpha(1) antitrypsin deficiency
G Hillebrand, R Schneppenheim, H D Oldigs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Decreased activity of respiratory-chain enzymes in glutaric aciduria type II
R Santer, A Claass, M Krawinkel, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
December 1, 1993
Urinary excretion of epidermal growth factor and transforming growth factor-alpha in breast-fed and formula-fed infants
R Santer, P Borlinghaus, E Sievers, et al.
Endocrine-Related Cancer
|
December 8, 2009
Interleukin-6 trans-signalling differentially regulates proliferation, migration, adhesion and maspin expression in human prostate cancer cells
Frédéric R Santer, Kamilla Malinowska, Zoran Culig, et al.
Page
of 11