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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 disease
D 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 Diseases
A 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 alglucerase
D 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-causing
D 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 France
C Vigneau, D P Germain, D Larmet, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 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 disease
D 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 Diseases
A 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 alglucerase
D 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-causing
D 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 France
C Vigneau, D P Germain, D Larmet, et al.
Page
of 5