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S Valleix

Showing results (1-10 of 21) with videos related to

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La Revue De Medecine Interne|February 13, 2007
[Multisystemic amyloidosis in 2007]G Grateau, S Valleix, P Callard
La Revue De Medecine Interne|July 7, 2001
[Hereditary amyloidosis]G Grateau, S Valleix, M Delpech
Journal Francais D'Ophtalmologie|April 12, 2026
Congenital aniridia with microphthalmia and cataract as unusual ocular features in RAB3GAP1-related Warburg micro syndromeE A Mahler, S Valleix, D Bremond-Gignac
Journal Francais D'Ophtalmologie|October 23, 2020
[Granular dystrophy: Not always easy to classify]B Memmi, S Valleix, T Bourcier, et al.
La Revue De Medecine Interne|July 26, 2000
[Diagnostic strategy in amyloidosis]G Grateau, H Lebrazi, S Valleix, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 24, 2000
A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI gene-R124L and DeltaT125-DeltaE126P Dighiero, S Drunat, F D'Hermies, et al.
La Revue De Medecine Interne|December 30, 2014
[Proteomics, a new tool for an accurate typing of amyloidosis]M Colombat, S Holifanjaniaina, S Onifarasoaniaina, et al.
Journal Francais D'Ophtalmologie|June 6, 2022
[National protocol for diagnosis and care of congenital aniridia: Summary for the attending physician]D Bremond-Gignac, M Robert, A Daruich, et al.
Neurology|July 11, 2001
Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu)E Ellie, F Camou, A Vital, et al.
Annales De Genetique|January 1, 1997
Prevalence, male germ-line origin and new patterns of inversions in haemophilia AS Valleix, K Nafa, N Stieltjes, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
La Revue De Medecine Interne|February 13, 2007
[Multisystemic amyloidosis in 2007]G Grateau, S Valleix, P Callard
La Revue De Medecine Interne|July 7, 2001
[Hereditary amyloidosis]G Grateau, S Valleix, M Delpech
Journal Francais D'Ophtalmologie|April 12, 2026
Congenital aniridia with microphthalmia and cataract as unusual ocular features in RAB3GAP1-related Warburg micro syndromeE A Mahler, S Valleix, D Bremond-Gignac
Journal Francais D'Ophtalmologie|October 23, 2020
[Granular dystrophy: Not always easy to classify]B Memmi, S Valleix, T Bourcier, et al.
La Revue De Medecine Interne|July 26, 2000
[Diagnostic strategy in amyloidosis]G Grateau, H Lebrazi, S Valleix, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 24, 2000
A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI gene-R124L and DeltaT125-DeltaE126P Dighiero, S Drunat, F D'Hermies, et al.
La Revue De Medecine Interne|December 30, 2014
[Proteomics, a new tool for an accurate typing of amyloidosis]M Colombat, S Holifanjaniaina, S Onifarasoaniaina, et al.
Journal Francais D'Ophtalmologie|June 6, 2022
[National protocol for diagnosis and care of congenital aniridia: Summary for the attending physician]D Bremond-Gignac, M Robert, A Daruich, et al.
Neurology|July 11, 2001
Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu)E Ellie, F Camou, A Vital, et al.
Annales De Genetique|January 1, 1997
Prevalence, male germ-line origin and new patterns of inversions in haemophilia AS Valleix, K Nafa, N Stieltjes, et al.
Pageof 3