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J Boisse

Showing results (1-10 of 12) with videos related to

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Canadian Medical Association Journal|August 7, 1971
[New etiologic approach to periodic ketoacidosis in children]J Boisse
Annales De Biologie Clinique|January 1, 1973
[Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer]J Boisse, N Moatti
Annales De Biologie Clinique|January 1, 1974
[Therapeutic trials in amino acid disorders]J M Saudubray, J Boisse
La Presse Medicale|November 21, 1970
[How to detect avoidable mental retardation?]J Boisse, H Brissaud, A Lemonnier, et al.
Annales De Pediatrie|February 2, 1971
[Treatment of phenylketonuria. Principles, management and importance of a phenylalanine-free protein hydrolysate]J Boisse, J M Saudubray, T Cathy, et al.
Archives Francaises De Pediatrie|June 1, 1972
[Study of a case of methylmalonic acidemia of neonatal onset. Therapeutic value of peritoneal dialysis. Discussion of vitamin B 12 sensitivity]J M Saudubray, J Boisse, C Charpentier, et al.
Annales De Pediatrie|January 2, 1971
[Methylmalonic acidemia. A new cause of severe ketoacidosis. Study of a case]J Boisse, R Perelman, J C Rudler, et al.
La Presse Medicale|February 20, 1971
[Evaluation of the activity of a phenylketonuria detection center. Analysis of the results of 500,000 tests]J Barbesier, J Boisse, C Charpentier, et al.
Annales De Pediatrie|June 1, 1972
[Treatment of phenylketonuria with a new phenylalanine-free protein hydrolysate (Albumaid XP). II. Practical application and effect on weight, height and bone development in 21 days]J M Saudubray, J Boisse, J Strouck, et al.
Pediatrie|January 1, 1970
[Rubinstein-Taybi syndrome. Discussion of incomplete and familial forms]F Hayem, J Boisse, M O Rethore, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Canadian Medical Association Journal|August 7, 1971
[New etiologic approach to periodic ketoacidosis in children]J Boisse
Annales De Biologie Clinique|January 1, 1973
[Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer]J Boisse, N Moatti
Annales De Biologie Clinique|January 1, 1974
[Therapeutic trials in amino acid disorders]J M Saudubray, J Boisse
La Presse Medicale|November 21, 1970
[How to detect avoidable mental retardation?]J Boisse, H Brissaud, A Lemonnier, et al.
Annales De Pediatrie|February 2, 1971
[Treatment of phenylketonuria. Principles, management and importance of a phenylalanine-free protein hydrolysate]J Boisse, J M Saudubray, T Cathy, et al.
Archives Francaises De Pediatrie|June 1, 1972
[Study of a case of methylmalonic acidemia of neonatal onset. Therapeutic value of peritoneal dialysis. Discussion of vitamin B 12 sensitivity]J M Saudubray, J Boisse, C Charpentier, et al.
Annales De Pediatrie|January 2, 1971
[Methylmalonic acidemia. A new cause of severe ketoacidosis. Study of a case]J Boisse, R Perelman, J C Rudler, et al.
La Presse Medicale|February 20, 1971
[Evaluation of the activity of a phenylketonuria detection center. Analysis of the results of 500,000 tests]J Barbesier, J Boisse, C Charpentier, et al.
Annales De Pediatrie|June 1, 1972
[Treatment of phenylketonuria with a new phenylalanine-free protein hydrolysate (Albumaid XP). II. Practical application and effect on weight, height and bone development in 21 days]J M Saudubray, J Boisse, J Strouck, et al.
Pediatrie|January 1, 1970
[Rubinstein-Taybi syndrome. Discussion of incomplete and familial forms]F Hayem, J Boisse, M O Rethore, et al.
Pageof 2