Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Pampols

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1996
Glycerol trioleate/glycerol trierucate therapy in X-linked adrenoleukodystrophy: saturated and unsaturated fatty acids in blood cells. Implications for the follow-upM Ruiz, T Pampols, M Girós
Neurology|February 1, 1974
Infantile Gaucher's disease: A biochemical studyF González-Sastre, T Pampols, J Sabater
Archivos De Neurobiologia|May 1, 1978
[Effects of malnutrition on the maturity of the C.N.S. III. Evolution of the largest lipid fractions and gangliosides]F González Sastre, T Pampols, J Sabater
Prenatal Diagnosis|July 1, 1997
ALDP expression in fetal cells and its application in prenatal diagnosis of X-linked adrenoleukodystrophyM Ruiz, M J Coll, T Pampols, et al.
Revista Clinica Espanola|July 1, 1978
[Localization of beta-hexosaminidase activity in the serum proteinogram]J Codina, F González Sastre, T Pampols, et al.
Anales Espanoles De Pediatria|October 1, 1977
[GM2 gangliosidosis diagnosis and carriers detection by fractionation of N-acetyl-beta-D-hexosaminidase by electrophoresis on cellulose acetate gel (author's transl)]T Pampols, M L Girós, F González Sastre, et al.
Anales Espanoles De Pediatria|November 15, 1984
[Sandhoff disease]M Herrera Martín, F Montejo Iglesias, T Pampols, et al.
Acta Neurologica Scandinavica|June 1, 1993
Diagnosis of X-adrenoleucodystrophy phenotypic variantsF Coria, M A García-Viejo, J A Delgado, et al.
Medicina Clinica|March 10, 1979
[Gm1 gangliosidosis types 1 and 2 (author's transl)]I Ferrer, J Vila Torres, E Fernández Alvarez, et al.
Anales Espanoles De Pediatria|February 15, 1984
[Sandhoff's disease (GM2 gangliosidosis, type II). Presentation of a case with a clinical and biochemical study. Carrier detection]T Rodríguez Costa, T Pampols, F Gonzalez-Sastre, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|January 1, 1996
Glycerol trioleate/glycerol trierucate therapy in X-linked adrenoleukodystrophy: saturated and unsaturated fatty acids in blood cells. Implications for the follow-upM Ruiz, T Pampols, M Girós
Neurology|February 1, 1974
Infantile Gaucher's disease: A biochemical studyF González-Sastre, T Pampols, J Sabater
Archivos De Neurobiologia|May 1, 1978
[Effects of malnutrition on the maturity of the C.N.S. III. Evolution of the largest lipid fractions and gangliosides]F González Sastre, T Pampols, J Sabater
Prenatal Diagnosis|July 1, 1997
ALDP expression in fetal cells and its application in prenatal diagnosis of X-linked adrenoleukodystrophyM Ruiz, M J Coll, T Pampols, et al.
Revista Clinica Espanola|July 1, 1978
[Localization of beta-hexosaminidase activity in the serum proteinogram]J Codina, F González Sastre, T Pampols, et al.
Anales Espanoles De Pediatria|October 1, 1977
[GM2 gangliosidosis diagnosis and carriers detection by fractionation of N-acetyl-beta-D-hexosaminidase by electrophoresis on cellulose acetate gel (author's transl)]T Pampols, M L Girós, F González Sastre, et al.
Anales Espanoles De Pediatria|November 15, 1984
[Sandhoff disease]M Herrera Martín, F Montejo Iglesias, T Pampols, et al.
Acta Neurologica Scandinavica|June 1, 1993
Diagnosis of X-adrenoleucodystrophy phenotypic variantsF Coria, M A García-Viejo, J A Delgado, et al.
Medicina Clinica|March 10, 1979
[Gm1 gangliosidosis types 1 and 2 (author's transl)]I Ferrer, J Vila Torres, E Fernández Alvarez, et al.
Anales Espanoles De Pediatria|February 15, 1984
[Sandhoff's disease (GM2 gangliosidosis, type II). Presentation of a case with a clinical and biochemical study. Carrier detection]T Rodríguez Costa, T Pampols, F Gonzalez-Sastre, et al.
Pageof 2