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Neuropediatrics
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August 1, 1992
Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations
I Nelson, G Bonne, F Degoul, et al.
Biochemical and Biophysical Research Communications
|
October 28, 1994
Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) gene
P Seibel, J Lauber, T Klopstock, et al.
Histochemistry
|
January 1, 1990
Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscle
N Romero, C Marsac, M Fardeau, et al.
Annales De Medecine Interne
|
January 1, 1980
[Alopecia, chronic candidodis, mental retardation and repeated ketoacidosic comas curable by biotin administration: multiple carboxylases deficiency (author's transl)]
A Munnich, J M Saudubray, H Ogier, et al.
Neurology
|
April 1, 1987
Phosphorus NMR spectroscopy study of muscular enzyme deficiencies involving glycogenolysis and glycolysis
D Duboc, P Jehenson, S Tran Dinh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 1, 1982
Search for the biochemical basis of biotin dependent multiple carboxylase deficiencies: determination of biotin activation in cultured fibroblasts
M Zamboni, M Gaudry, A Marquet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 26, 1982
Prenatal diagnosis of pyruvate carboxylase deficiency
C Marsac, C Augereau, G Feldman, et al.
Archives Francaises De Pediatrie
|
June 1, 1984
[Characteristics of a case of hepatic fructose-1,6-diphosphatase deficiency]
C Largillière, O Amédée-Manesme, C Marsac, et al.
Pediatric Research
|
January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosis
F X Coude, H Ogier, A Munnich, et al.
Diabetes
|
February 1, 1994
Higher maternal than paternal inheritance of diabetes in GK rats
D Gauguier, I Nelson, C Bernard, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 91) with videos related to
Sort By:
Page
of 10
Neuropediatrics
|
August 1, 1992
Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations
I Nelson, G Bonne, F Degoul, et al.
Biochemical and Biophysical Research Communications
|
October 28, 1994
Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) gene
P Seibel, J Lauber, T Klopstock, et al.
Histochemistry
|
January 1, 1990
Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscle
N Romero, C Marsac, M Fardeau, et al.
Annales De Medecine Interne
|
January 1, 1980
[Alopecia, chronic candidodis, mental retardation and repeated ketoacidosic comas curable by biotin administration: multiple carboxylases deficiency (author's transl)]
A Munnich, J M Saudubray, H Ogier, et al.
Neurology
|
April 1, 1987
Phosphorus NMR spectroscopy study of muscular enzyme deficiencies involving glycogenolysis and glycolysis
D Duboc, P Jehenson, S Tran Dinh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 1, 1982
Search for the biochemical basis of biotin dependent multiple carboxylase deficiencies: determination of biotin activation in cultured fibroblasts
M Zamboni, M Gaudry, A Marquet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 26, 1982
Prenatal diagnosis of pyruvate carboxylase deficiency
C Marsac, C Augereau, G Feldman, et al.
Archives Francaises De Pediatrie
|
June 1, 1984
[Characteristics of a case of hepatic fructose-1,6-diphosphatase deficiency]
C Largillière, O Amédée-Manesme, C Marsac, et al.
Pediatric Research
|
January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosis
F X Coude, H Ogier, A Munnich, et al.
Diabetes
|
February 1, 1994
Higher maternal than paternal inheritance of diabetes in GK rats
D Gauguier, I Nelson, C Bernard, et al.
Page
of 10