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European Journal of Pediatrics
|
February 1, 1981
Glycogenosis type Ib. Further evidence for a membrane disease
J Schaub, K Bartholomé, D Feist, et al.
Klinische Wochenschrift
|
September 15, 1981
[Morphological and biochemical studies on glycogenosis type V (McArdle) (author's transl)]
D Pongratz, J Schaub, C Koppenwallner, et al.
European Journal of Pediatrics
|
May 1, 1982
Hypocalcemic myopathy in idiopathic hypoparathyroidism
K Kruse, W Scheunemann, W Baier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 14, 1983
Prenatal diagnosis of galactosemia and properties of galactose-1-phosphate uridyltransferase in erythrocytes of galactosemic variants as well as in human fetal and adult organs
Y S Shin, W Endres, M Rieth, et al.
Die Medizinische Welt
|
November 23, 1979
[Wolman's disease (Wolman's syndrome)]
W Permanetter, J Müller-Höcker, G Hübner, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1971
[Secondary cystathioninuria]
W Endres, J Schaub, H J Bremer, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Trace element excess in PKU diets?
E Sievers, H D Oldigs, K Dörner, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
January 1, 1992
Longitudinal zinc balances in breast-fed and formula-fed infants
E Sievers, H D Oldigs, K Dörner, et al.
Deutsche Medizinische Wochenschrift (1946)
|
May 29, 1970
[Intestinal lymphangiectasis]
P Peller, J Schaub, H Zobel, et al.
Journal of Trace Elements and Electrolytes in Health and Disease
|
March 1, 1990
Urinary zinc excretion in infancy
E Sievers, H D Oldigs, K Dörner, et al.
Page
of 19
Search research articles
Search
Showing results (51-60 of 190) with videos related to
Sort By:
Page
of 19
European Journal of Pediatrics
|
February 1, 1981
Glycogenosis type Ib. Further evidence for a membrane disease
J Schaub, K Bartholomé, D Feist, et al.
Klinische Wochenschrift
|
September 15, 1981
[Morphological and biochemical studies on glycogenosis type V (McArdle) (author's transl)]
D Pongratz, J Schaub, C Koppenwallner, et al.
European Journal of Pediatrics
|
May 1, 1982
Hypocalcemic myopathy in idiopathic hypoparathyroidism
K Kruse, W Scheunemann, W Baier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 14, 1983
Prenatal diagnosis of galactosemia and properties of galactose-1-phosphate uridyltransferase in erythrocytes of galactosemic variants as well as in human fetal and adult organs
Y S Shin, W Endres, M Rieth, et al.
Die Medizinische Welt
|
November 23, 1979
[Wolman's disease (Wolman's syndrome)]
W Permanetter, J Müller-Höcker, G Hübner, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1971
[Secondary cystathioninuria]
W Endres, J Schaub, H J Bremer, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Trace element excess in PKU diets?
E Sievers, H D Oldigs, K Dörner, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
January 1, 1992
Longitudinal zinc balances in breast-fed and formula-fed infants
E Sievers, H D Oldigs, K Dörner, et al.
Deutsche Medizinische Wochenschrift (1946)
|
May 29, 1970
[Intestinal lymphangiectasis]
P Peller, J Schaub, H Zobel, et al.
Journal of Trace Elements and Electrolytes in Health and Disease
|
March 1, 1990
Urinary zinc excretion in infancy
E Sievers, H D Oldigs, K Dörner, et al.
Page
of 19