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B Cagianut

Showing results (11-20 of 20) with videos related to

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Schweizerische Medizinische Wochenschrift|April 2, 1977
[Juvenile diabetes, tapeto-retinal degeneration, neurogenic hearing disorder (Alström syndrome), associated with congenital dyserythropoietic type III anemia]B Cagianut, P Hochstrasser, K Rhyner
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1972
[Ocular and general abnormalities in classical trisomy]B Cagianut, G Molz, K Theiler
Helvetica Chimica Acta|October 29, 2010
The formation of furan-2,5-dicarboxylic acid from d-glucuron and d-galacturonic acid in humans; a new way of breaking down carbohydratesB FLASCHENTRAGER, B CAGIANUT, F MEIER
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1981
[Hereditary retinal degeneration: new experimental aspects]B Cagianut, A Huwyler, M Kutter, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 1, 1980
[Dysplasia opticoseptalis]B Cagianut, P Sigg, W Isler, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1985
Studies on hereditary retinal degeneration. The rd gene in the mouseB Cagianut, G Sandri, P Zilla, et al.
Klinische Wochenschrift|September 17, 1984
Decreased thiosulfate sulfur transferase (rhodanese) in Leber's hereditary optic atrophyB Cagianut, H P Schnebli, K Rhyner, et al.
Klinische Monatsblatter Fur Augenheilkunde|July 1, 1982
[Thiosulfate-sulfur transferase deficiency in Leber's hereditary optic atrophy ]B Cagianut, H P Schnebli, K Rhyner, et al.
Lancet (London, England)|October 31, 1981
Thiosulphate-sulphur transferase (rhodanese) deficiency in Leber's hereditary optic atrophyB Cagianut, K Rhyner, W Furrier, et al.
Anatomy and Embryology|December 22, 1976
A new allele of ocular retardation: early development and morphogenetic cell deathK Theiler, D S Varnum, J H Nadeau, et al.
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Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Schweizerische Medizinische Wochenschrift|April 2, 1977
[Juvenile diabetes, tapeto-retinal degeneration, neurogenic hearing disorder (Alström syndrome), associated with congenital dyserythropoietic type III anemia]B Cagianut, P Hochstrasser, K Rhyner
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1972
[Ocular and general abnormalities in classical trisomy]B Cagianut, G Molz, K Theiler
Helvetica Chimica Acta|October 29, 2010
The formation of furan-2,5-dicarboxylic acid from d-glucuron and d-galacturonic acid in humans; a new way of breaking down carbohydratesB FLASCHENTRAGER, B CAGIANUT, F MEIER
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1981
[Hereditary retinal degeneration: new experimental aspects]B Cagianut, A Huwyler, M Kutter, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 1, 1980
[Dysplasia opticoseptalis]B Cagianut, P Sigg, W Isler, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1985
Studies on hereditary retinal degeneration. The rd gene in the mouseB Cagianut, G Sandri, P Zilla, et al.
Klinische Wochenschrift|September 17, 1984
Decreased thiosulfate sulfur transferase (rhodanese) in Leber's hereditary optic atrophyB Cagianut, H P Schnebli, K Rhyner, et al.
Klinische Monatsblatter Fur Augenheilkunde|July 1, 1982
[Thiosulfate-sulfur transferase deficiency in Leber's hereditary optic atrophy ]B Cagianut, H P Schnebli, K Rhyner, et al.
Lancet (London, England)|October 31, 1981
Thiosulphate-sulphur transferase (rhodanese) deficiency in Leber's hereditary optic atrophyB Cagianut, K Rhyner, W Furrier, et al.
Anatomy and Embryology|December 22, 1976
A new allele of ocular retardation: early development and morphogenetic cell deathK Theiler, D S Varnum, J H Nadeau, et al.
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