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Clinical Genetics
|
December 1, 1996
CFC syndrome: report of familial cases
M Lecora, G Parenti, G Andria
Clinical Neurology and Neurosurgery
|
January 1, 1983
Electroencephalographic abnormalities in homocystinuria due to cystathionine synthase deficiency
E Del Giudice, S Striano, G Andria
The Journal of Biological Chemistry
|
December 25, 1971
The specific binding of three fragments of staphylococcal nuclease
G Andria, H Taniuchi, J L Cone
The New England Journal of Medicine
|
December 21, 1989
Ultrasonographic detection of arterial disease in treated homocystinuria
P Rubba, F Faccenda, P Strisciuglio, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Protein-bound plasma homocyst(e)ine and identification of heterozygotes for cystathionine-synthase deficiency
R Sartorio, R Carrozzo, L Corbo, et al.
Clinical Genetics
|
July 1, 1978
Atypical expression of beta-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities
G Andria, E Del Giudice, A J Reuser
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
December 15, 1970
[Comparative submicroscopic findings on the isolated brush border of the rat and human intestine]
A Cecio, R V De Masi, G Andria
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
December 15, 1970
[Study of the isolated membranes of the brush border of the rat intestine]
R V De Masi, G Andria, A Cecio
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy
|
January 1, 1991
Dietary treatment of liver glycogenosis
G Andria, G Parenti, P Strisciuglio, et al.
Acta Paediatrica Scandinavica
|
May 1, 1971
Arylamidase activities of brush border membrane of rat intestine
S Auricchio, M Pierro, G Andria, et al.
Page
of 14
Search research articles
Search
Showing results (11-20 of 137) with videos related to
Sort By:
Page
of 14
Clinical Genetics
|
December 1, 1996
CFC syndrome: report of familial cases
M Lecora, G Parenti, G Andria
Clinical Neurology and Neurosurgery
|
January 1, 1983
Electroencephalographic abnormalities in homocystinuria due to cystathionine synthase deficiency
E Del Giudice, S Striano, G Andria
The Journal of Biological Chemistry
|
December 25, 1971
The specific binding of three fragments of staphylococcal nuclease
G Andria, H Taniuchi, J L Cone
The New England Journal of Medicine
|
December 21, 1989
Ultrasonographic detection of arterial disease in treated homocystinuria
P Rubba, F Faccenda, P Strisciuglio, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Protein-bound plasma homocyst(e)ine and identification of heterozygotes for cystathionine-synthase deficiency
R Sartorio, R Carrozzo, L Corbo, et al.
Clinical Genetics
|
July 1, 1978
Atypical expression of beta-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities
G Andria, E Del Giudice, A J Reuser
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
December 15, 1970
[Comparative submicroscopic findings on the isolated brush border of the rat and human intestine]
A Cecio, R V De Masi, G Andria
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
December 15, 1970
[Study of the isolated membranes of the brush border of the rat intestine]
R V De Masi, G Andria, A Cecio
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy
|
January 1, 1991
Dietary treatment of liver glycogenosis
G Andria, G Parenti, P Strisciuglio, et al.
Acta Paediatrica Scandinavica
|
May 1, 1971
Arylamidase activities of brush border membrane of rat intestine
S Auricchio, M Pierro, G Andria, et al.
Page
of 14