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Biochemical and Biophysical Research Communications
|
April 20, 1999
Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatches
D P Germain, L Poenaru
Clinical Genetics
|
January 10, 2003
Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patients
M Senechal, D P Germain
La Revue De Medecine Interne
|
April 29, 2006
Phenotype variations in Gaucher disease
P Mistry, D P Germain
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 27, 2014
[Genetic aspects of mucopolysaccharidoses]
D Lacombe, D P Germain
La Revue De Medecine Interne
|
January 30, 2008
[Therapeutic objectives in Gaucher disease]
P Mistry, D P Germain
Human Mutation
|
January 4, 2001
Identification of novel polymorphisms in the pM5 and MRP1 (ABCC1) genes at locus 16p13.1 and exclusion of both genes as responsible for pseudoxanthoma elasticum
J Perdu, D P Germain
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
February 8, 2003
Endothelial markers and homocysteine in patients with classic Fabry disease
K Demuth, D P Germain
La Revue De Medecine Interne
|
April 29, 2006
Therapeutic goals in Gaucher disease
P Mistry, D P Germain
Archives of Pediatrics & Adolescent Medicine
|
January 1, 1997
Pathological case of the month. Pseudoxanthoma elasticum
D P Germain, F M Pope
International Journal of Clinical Pharmacology and Therapeutics
|
December 31, 2009
Pharmacological chaperone therapy by active-site-specific chaperones in Fabry disease: in vitro and preclinical studies
D P Germain, J-Q Fan
Page
of 5
Search research articles
Search
Showing results (11-20 of 49) with videos related to
Sort By:
Page
of 5
Biochemical and Biophysical Research Communications
|
April 20, 1999
Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatches
D P Germain, L Poenaru
Clinical Genetics
|
January 10, 2003
Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patients
M Senechal, D P Germain
La Revue De Medecine Interne
|
April 29, 2006
Phenotype variations in Gaucher disease
P Mistry, D P Germain
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 27, 2014
[Genetic aspects of mucopolysaccharidoses]
D Lacombe, D P Germain
La Revue De Medecine Interne
|
January 30, 2008
[Therapeutic objectives in Gaucher disease]
P Mistry, D P Germain
Human Mutation
|
January 4, 2001
Identification of novel polymorphisms in the pM5 and MRP1 (ABCC1) genes at locus 16p13.1 and exclusion of both genes as responsible for pseudoxanthoma elasticum
J Perdu, D P Germain
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
February 8, 2003
Endothelial markers and homocysteine in patients with classic Fabry disease
K Demuth, D P Germain
La Revue De Medecine Interne
|
April 29, 2006
Therapeutic goals in Gaucher disease
P Mistry, D P Germain
Archives of Pediatrics & Adolescent Medicine
|
January 1, 1997
Pathological case of the month. Pseudoxanthoma elasticum
D P Germain, F M Pope
International Journal of Clinical Pharmacology and Therapeutics
|
December 31, 2009
Pharmacological chaperone therapy by active-site-specific chaperones in Fabry disease: in vitro and preclinical studies
D P Germain, J-Q Fan
Page
of 5