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The Journal of Biological Chemistry
|
May 5, 1988
Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagen
A Superti-Furga, E Gugler, R Gitzelmann, et al.
The New England Journal of Medicine
|
March 29, 1984
Prenatal diagnosis of hereditary tyrosinemia
B Steinmann, R Gitzelmann, E A Kvittingen, et al.
Biochimica Et Biophysica Acta
|
January 6, 1970
Localization of rabbit intestinal sucrase with ferritin-antibody conjugates
R Gitzelmann, T Bächi, H Binz, et al.
Genomics
|
August 1, 1993
Complementary DNA sequence and chromosomal mapping of a human proteoglycan-binding cell-adhesion protein (dermatopontin)
A Superti-Furga, M Rocchi, B W Schäfer, et al.
Pediatric Research
|
October 1, 1994
Changes of liver metabolite concentrations in adults with disorders of fructose metabolism after intravenous fructose by 31P magnetic resonance spectroscopy
P Boesiger, R Buchli, D Meier, et al.
Pediatric Research
|
March 1, 1984
Short communication. Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shunt
R Seger, B Steinmann, L Tiefenauer, et al.
Biochemical and Biophysical Research Communications
|
April 30, 1990
Collagen degradation in I-cells is normal
R S Bienkowski, C R Ripley, R Gitzelmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1995
Early and severe sensory loss in three adult siblings with hexosaminidase A and B deficiency (Sandhoff disease)
H Schnorf, R Gitzelmann, N U Bosshard, et al.
European Journal of Pediatrics
|
July 1, 1985
Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting test
P A Dremsek, M Sacher, W Stögmann, et al.
European Journal of Pediatrics
|
May 1, 1985
Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis?
R Gitzelmann, M A Spycher, S Adank, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 117) with videos related to
Sort By:
Page
of 12
The Journal of Biological Chemistry
|
May 5, 1988
Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagen
A Superti-Furga, E Gugler, R Gitzelmann, et al.
The New England Journal of Medicine
|
March 29, 1984
Prenatal diagnosis of hereditary tyrosinemia
B Steinmann, R Gitzelmann, E A Kvittingen, et al.
Biochimica Et Biophysica Acta
|
January 6, 1970
Localization of rabbit intestinal sucrase with ferritin-antibody conjugates
R Gitzelmann, T Bächi, H Binz, et al.
Genomics
|
August 1, 1993
Complementary DNA sequence and chromosomal mapping of a human proteoglycan-binding cell-adhesion protein (dermatopontin)
A Superti-Furga, M Rocchi, B W Schäfer, et al.
Pediatric Research
|
October 1, 1994
Changes of liver metabolite concentrations in adults with disorders of fructose metabolism after intravenous fructose by 31P magnetic resonance spectroscopy
P Boesiger, R Buchli, D Meier, et al.
Pediatric Research
|
March 1, 1984
Short communication. Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shunt
R Seger, B Steinmann, L Tiefenauer, et al.
Biochemical and Biophysical Research Communications
|
April 30, 1990
Collagen degradation in I-cells is normal
R S Bienkowski, C R Ripley, R Gitzelmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1995
Early and severe sensory loss in three adult siblings with hexosaminidase A and B deficiency (Sandhoff disease)
H Schnorf, R Gitzelmann, N U Bosshard, et al.
European Journal of Pediatrics
|
July 1, 1985
Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting test
P A Dremsek, M Sacher, W Stögmann, et al.
European Journal of Pediatrics
|
May 1, 1985
Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis?
R Gitzelmann, M A Spycher, S Adank, et al.
Page
of 12