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Y Nordmann

Showing results (11-20 of 163) with videos related to

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Biochimie|January 1, 1972
[Fructose intolerance]Y Nordmann, F Schapira
Exposes Annuels De Biochimie Medicale|January 1, 1980
[Biosynthesis of heme: regulation; hereditary and experimental porphyrias]B Grandchamp, Y Nordmann
Annales De Medecine Interne|January 1, 1993
[Acute attacks of hepatic porphyria: specific treatment with heme arginate]Y Nordmann, J C Deybach
La Nouvelle Presse Medicale|November 28, 1981
[Familial and sporadic porphyria cutanea symptomatica (author's transl)]H de Verneuil, Y Nordmann
Seminars in Liver Disease|May 1, 1982
Congenital erythropoietic porphyriaY Nordmann, J C Deybach
Human Molecular Genetics|March 1, 1994
Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphismsP Martasek, Y Nordmann, B Grandchamp
La Nouvelle Presse Medicale|June 14, 1975
[Acute intermittent porphyria. Detection of asymptomatic carriers of the genetic defect]B Grandchamp, M Grelier, Y Nordmann
The Biochemical Journal|October 15, 1978
The mitochondrial localization of coproporphyrinogen III oxidaseB Grandchamp, N Phung, Y Nordmann
Acta Medica Scandinavica. Supplementum|January 1, 1972
Hereditary alterations of fructose metabolizing enzymes. Studies on essential fructosuria and on hereditary fructose intoleranceF Schapira, Y Nordmann, C Gregori
Journal De Genetique Humaine|March 1, 1977
[The genetic questionaire: difficult genetic counseling in an unusual type of porphyria (porphyria variegata)]H Husquinet, P Dodinval, Y Nordmann
Pageof 17

Showing results (11-20 of 163) with videos related to

Sort By:
Pageof 17
Biochimie|January 1, 1972
[Fructose intolerance]Y Nordmann, F Schapira
Exposes Annuels De Biochimie Medicale|January 1, 1980
[Biosynthesis of heme: regulation; hereditary and experimental porphyrias]B Grandchamp, Y Nordmann
Annales De Medecine Interne|January 1, 1993
[Acute attacks of hepatic porphyria: specific treatment with heme arginate]Y Nordmann, J C Deybach
La Nouvelle Presse Medicale|November 28, 1981
[Familial and sporadic porphyria cutanea symptomatica (author's transl)]H de Verneuil, Y Nordmann
Seminars in Liver Disease|May 1, 1982
Congenital erythropoietic porphyriaY Nordmann, J C Deybach
Human Molecular Genetics|March 1, 1994
Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphismsP Martasek, Y Nordmann, B Grandchamp
La Nouvelle Presse Medicale|June 14, 1975
[Acute intermittent porphyria. Detection of asymptomatic carriers of the genetic defect]B Grandchamp, M Grelier, Y Nordmann
The Biochemical Journal|October 15, 1978
The mitochondrial localization of coproporphyrinogen III oxidaseB Grandchamp, N Phung, Y Nordmann
Acta Medica Scandinavica. Supplementum|January 1, 1972
Hereditary alterations of fructose metabolizing enzymes. Studies on essential fructosuria and on hereditary fructose intoleranceF Schapira, Y Nordmann, C Gregori
Journal De Genetique Humaine|March 1, 1977
[The genetic questionaire: difficult genetic counseling in an unusual type of porphyria (porphyria variegata)]H Husquinet, P Dodinval, Y Nordmann
Pageof 17