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Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
March 17, 2001
[Signal changes of the bone marrow in MRI under long-term treatment with granulocyte colony-stimulating factors]
A Scherer, V Engelbrecht, P May, et al.
Fortschritte Der Medizin
|
December 20, 1984
[Treatment of the climacteric syndrome. Controlled study of a combination of low-dose clonidine and low-dose conjugated estrogens]
A E Schindler, D Heners, T Pater, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
A patient with alpha-ketoadipic and alpha-aminoadipic aciduria
M Duran, F A Beemer, S K Wadman, et al.
European Journal of Pediatrics
|
November 1, 1979
Clinical, morphological, and biochemical investigations on a patient with an unusual form of neuronal ceroid-lipofuscinosis
K Becker, H H Goebel, L Svennerholm, et al.
Journal of Inherited Metabolic Disease
|
July 4, 2006
Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease
E Simon, R Fingerhut, J Baumkötter, et al.
Journal of Inherited Metabolic Disease
|
October 9, 2007
Description of the mutations in 15 subjects with variant forms of maple syrup urine disease
N Flaschker, O Feyen, S Fend, et al.
Pediatric Research
|
April 1, 1991
Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism
U Wendel, R Baumgartner, S B van der Meer, et al.
Klinische Padiatrie
|
September 1, 1983
[Intermittent maple syrup urine disease in a 12-year-old boy: clinical aspects, diagnosis and treatment]
G Fritsch, U Langenbeck, U Wendel, et al.
Experimental Cell Research
|
June 1, 1973
Studies on the optimal cooling rate for freezing human diploid fibroblasts
H von Böhmer, W Wöhler, U Wendel, et al.
Monatsschrift Fur Kinderheilkunde
|
March 1, 1978
[Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)]
U Wendel, H Przyrembel, K Becker, et al.
Page
of 19
Search research articles
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Showing results (111-120 of 186) with videos related to
Sort By:
Page
of 19
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
March 17, 2001
[Signal changes of the bone marrow in MRI under long-term treatment with granulocyte colony-stimulating factors]
A Scherer, V Engelbrecht, P May, et al.
Fortschritte Der Medizin
|
December 20, 1984
[Treatment of the climacteric syndrome. Controlled study of a combination of low-dose clonidine and low-dose conjugated estrogens]
A E Schindler, D Heners, T Pater, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
A patient with alpha-ketoadipic and alpha-aminoadipic aciduria
M Duran, F A Beemer, S K Wadman, et al.
European Journal of Pediatrics
|
November 1, 1979
Clinical, morphological, and biochemical investigations on a patient with an unusual form of neuronal ceroid-lipofuscinosis
K Becker, H H Goebel, L Svennerholm, et al.
Journal of Inherited Metabolic Disease
|
July 4, 2006
Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease
E Simon, R Fingerhut, J Baumkötter, et al.
Journal of Inherited Metabolic Disease
|
October 9, 2007
Description of the mutations in 15 subjects with variant forms of maple syrup urine disease
N Flaschker, O Feyen, S Fend, et al.
Pediatric Research
|
April 1, 1991
Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism
U Wendel, R Baumgartner, S B van der Meer, et al.
Klinische Padiatrie
|
September 1, 1983
[Intermittent maple syrup urine disease in a 12-year-old boy: clinical aspects, diagnosis and treatment]
G Fritsch, U Langenbeck, U Wendel, et al.
Experimental Cell Research
|
June 1, 1973
Studies on the optimal cooling rate for freezing human diploid fibroblasts
H von Böhmer, W Wöhler, U Wendel, et al.
Monatsschrift Fur Kinderheilkunde
|
March 1, 1978
[Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)]
U Wendel, H Przyrembel, K Becker, et al.
Page
of 19