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American Journal of Human Genetics
|
November 1, 1996
Molecular analysis of a GM2-activator deficiency in two patients with GM2-gangliosidosis AB variant
U Schepers, G Glombitza, T Lemm, et al.
Journal of Inherited Metabolic Disease
|
October 17, 2006
Sudden deterioration in nonclassical infantile-onset Pompe disease responding to alglucosidase alfa infusion therapy: a case report
S I Pascual-Pascual, P Rubio, L Albajara, et al.
The Science of the Total Environment
|
June 17, 2006
Modeling of soiling based on silica-soda-lime glass exposure at six European sites
A Ionescu, R-A Lefèvre, A Chabas, et al.
Anales Espanoles De Pediatria
|
October 1, 1987
[Mucolipidosis II or "I-cell disease" in the newborn infant. 2 new cases]
I Tamés, A Gracía, A Aladro, et al.
Anales Espanoles De Pediatria
|
November 1, 1977
[Fucosidosis type 2. A new case (author's transl)]
J M Santolaya, M Hernández, A Chabas, et al.
Archives of Disease in Childhood
|
March 1, 1996
Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome
M Pineda, C Pavia, M A Vilaseca, et al.
The Science of the Total Environment
|
November 13, 2020
Multi O- and S-isotopes as tracers of black crusts formation under volcanic and non-volcanic atmospheric conditions in Sicily (Italy)
A Aroskay, E Martin, S Bekki, et al.
Archivos De Neurobiologia
|
May 1, 1988
[Mucopolysaccharidosis VII: familial study]
J A Moreno, M Aleu, A Chabas, et al.
American Journal of Human Genetics
|
October 1, 1995
A pseudodeficiency allele (D152N) of the human beta-glucuronidase gene
R Vervoort, M R Islam, W Sly, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 25, 2008
[Alpha-mannosidosis]
F M Pérez Fernández, R Camino-León, E López Laso, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
American Journal of Human Genetics
|
November 1, 1996
Molecular analysis of a GM2-activator deficiency in two patients with GM2-gangliosidosis AB variant
U Schepers, G Glombitza, T Lemm, et al.
Journal of Inherited Metabolic Disease
|
October 17, 2006
Sudden deterioration in nonclassical infantile-onset Pompe disease responding to alglucosidase alfa infusion therapy: a case report
S I Pascual-Pascual, P Rubio, L Albajara, et al.
The Science of the Total Environment
|
June 17, 2006
Modeling of soiling based on silica-soda-lime glass exposure at six European sites
A Ionescu, R-A Lefèvre, A Chabas, et al.
Anales Espanoles De Pediatria
|
October 1, 1987
[Mucolipidosis II or "I-cell disease" in the newborn infant. 2 new cases]
I Tamés, A Gracía, A Aladro, et al.
Anales Espanoles De Pediatria
|
November 1, 1977
[Fucosidosis type 2. A new case (author's transl)]
J M Santolaya, M Hernández, A Chabas, et al.
Archives of Disease in Childhood
|
March 1, 1996
Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome
M Pineda, C Pavia, M A Vilaseca, et al.
The Science of the Total Environment
|
November 13, 2020
Multi O- and S-isotopes as tracers of black crusts formation under volcanic and non-volcanic atmospheric conditions in Sicily (Italy)
A Aroskay, E Martin, S Bekki, et al.
Archivos De Neurobiologia
|
May 1, 1988
[Mucopolysaccharidosis VII: familial study]
J A Moreno, M Aleu, A Chabas, et al.
American Journal of Human Genetics
|
October 1, 1995
A pseudodeficiency allele (D152N) of the human beta-glucuronidase gene
R Vervoort, M R Islam, W Sly, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 25, 2008
[Alpha-mannosidosis]
F M Pérez Fernández, R Camino-León, E López Laso, et al.
Page
of 3