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

D P Germain

Showing results (21-30 of 49) with videos related to

Pageof 5
Sort By:
La Revue De Medecine Interne|January 8, 2011
[Fabry disease: enzymatic screening using dried blood spots on filter paper]E Caudron, D P Germain, P Prognon
La Revue De Medecine Interne|January 8, 2011
X-linked inheritance and its implication in the diagnosis and management of female patients in Fabry diseaseD P Germain, K Benistan, L Angelova
La Revue De Medecine Interne|January 8, 2011
[Azoospermia as a new feature of Fabry disease]D Lacombe, D P Germain, A Papaxanthos-Roche
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Eighth International Symposium on Lysosomal Storage DiseasesA B Mehta, D P Germain, R Martin
Mutation Research|October 16, 2001
Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to algluceraseD P Germain, C R Kaneski, R O Brady
La Revue De Medecine Interne|January 8, 2011
[Vestibular and cochlear manifestations in Fabry's disease]D Malinvaud, D P Germain, K Benistan, et al.
Biochemical and Biophysical Research Communications|July 29, 2000
Homozygosity for the R1268Q mutation in MRP6, the pseudoxanthoma elasticum gene, is not disease-causingD P Germain, J Perdu, V Remones, et al.
Human Mutation|November 3, 2000
Identification of two polymorphisms (c189G>C; c190T>C) in exon 2 of the human MRP6 gene (ABCC6) by screening of Pseudoxanthoma elasticum patients: possible sequence correction?D P Germain, V Remones, J Perdu, et al.
La Revue De Medecine Interne|January 18, 2006
[The cochlea in Fabry disease: a sensorineural hearing loss model of vascular origin?]D Malinvaud, P Avan, D P Germain, et al.
Nephrologie & Therapeutique|May 17, 2021
Screening for Fabry disease in male patients with end-stage renal disease in western FranceC Vigneau, D P Germain, D Larmet, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
La Revue De Medecine Interne|January 8, 2011
[Fabry disease: enzymatic screening using dried blood spots on filter paper]E Caudron, D P Germain, P Prognon
La Revue De Medecine Interne|January 8, 2011
X-linked inheritance and its implication in the diagnosis and management of female patients in Fabry diseaseD P Germain, K Benistan, L Angelova
La Revue De Medecine Interne|January 8, 2011
[Azoospermia as a new feature of Fabry disease]D Lacombe, D P Germain, A Papaxanthos-Roche
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Eighth International Symposium on Lysosomal Storage DiseasesA B Mehta, D P Germain, R Martin
Mutation Research|October 16, 2001
Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to algluceraseD P Germain, C R Kaneski, R O Brady
La Revue De Medecine Interne|January 8, 2011
[Vestibular and cochlear manifestations in Fabry's disease]D Malinvaud, D P Germain, K Benistan, et al.
Biochemical and Biophysical Research Communications|July 29, 2000
Homozygosity for the R1268Q mutation in MRP6, the pseudoxanthoma elasticum gene, is not disease-causingD P Germain, J Perdu, V Remones, et al.
Human Mutation|November 3, 2000
Identification of two polymorphisms (c189G>C; c190T>C) in exon 2 of the human MRP6 gene (ABCC6) by screening of Pseudoxanthoma elasticum patients: possible sequence correction?D P Germain, V Remones, J Perdu, et al.
La Revue De Medecine Interne|January 18, 2006
[The cochlea in Fabry disease: a sensorineural hearing loss model of vascular origin?]D Malinvaud, P Avan, D P Germain, et al.
Nephrologie & Therapeutique|May 17, 2021
Screening for Fabry disease in male patients with end-stage renal disease in western FranceC Vigneau, D P Germain, D Larmet, et al.
Pageof 5