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M JEUNE

Showing results (51-60 of 75) with videos related to

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Pediatrie|July 1, 1979
[Puberty in congenital hypothyroidism. Apropos of 95 cases]M David, C Augay, M Sempé, et al.
La Presse Medicale|January 30, 1971
[Blood insulin in phenylketonuric patients before and after diet therapy]M Jeune, M David, A Ruitton, et al.
Archives Francaises De Pediatrie|February 1, 1977
[Albright's type II osteodystrophy and hypothyroidism due to TSH deficiency. Apropos of a case in a child]M David, J J Madjar, D Floret, et al.
Annales De Pediatrie|February 2, 1970
[Urinary infection and congenital adrenal hyperplasia: 14 cases]M David, J Bertrand, P Mollard, et al.
Annales De Pediatrie|February 2, 1970
[Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy]M Jeune, C Collombel, M Michel, et al.
Archives Francaises De Pediatrie|February 1, 1980
[XY pure gonadal dysgenesis. Two cases report (author's transl)]J P Feït, M David, E de Peretti, et al.
Pediatrie|January 1, 1974
[2 infants born of a mother with phenylketonuria. Failure of a low phenylalanine diet during the 2d pregnancy]M Bovier-Lapierre, C Saint-Dizier, F Freycon, et al.
La Nouvelle Presse Medicale|April 28, 1979
[Combined test for assessment of anterior pituitary function using glucagon-propranolol, TRH and LHRH (author's transl)]J P Feït, M David, A Chopard, et al.
Archives Francaises De Pediatrie|May 1, 1979
[Oculocraniosomatic neuromuscular disease]J P Feit, H Carrier, M David, et al.
Pediatrie|December 1, 1978
[Systematic screening for congenital hypothyroidism by determination of TSH in dried blood samples: results of experience during a 21-month period]M David, C Dorche, M O Rolland, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
Pediatrie|July 1, 1979
[Puberty in congenital hypothyroidism. Apropos of 95 cases]M David, C Augay, M Sempé, et al.
La Presse Medicale|January 30, 1971
[Blood insulin in phenylketonuric patients before and after diet therapy]M Jeune, M David, A Ruitton, et al.
Archives Francaises De Pediatrie|February 1, 1977
[Albright's type II osteodystrophy and hypothyroidism due to TSH deficiency. Apropos of a case in a child]M David, J J Madjar, D Floret, et al.
Annales De Pediatrie|February 2, 1970
[Urinary infection and congenital adrenal hyperplasia: 14 cases]M David, J Bertrand, P Mollard, et al.
Annales De Pediatrie|February 2, 1970
[Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy]M Jeune, C Collombel, M Michel, et al.
Archives Francaises De Pediatrie|February 1, 1980
[XY pure gonadal dysgenesis. Two cases report (author's transl)]J P Feït, M David, E de Peretti, et al.
Pediatrie|January 1, 1974
[2 infants born of a mother with phenylketonuria. Failure of a low phenylalanine diet during the 2d pregnancy]M Bovier-Lapierre, C Saint-Dizier, F Freycon, et al.
La Nouvelle Presse Medicale|April 28, 1979
[Combined test for assessment of anterior pituitary function using glucagon-propranolol, TRH and LHRH (author's transl)]J P Feït, M David, A Chopard, et al.
Archives Francaises De Pediatrie|May 1, 1979
[Oculocraniosomatic neuromuscular disease]J P Feit, H Carrier, M David, et al.
Pediatrie|December 1, 1978
[Systematic screening for congenital hypothyroidism by determination of TSH in dried blood samples: results of experience during a 21-month period]M David, C Dorche, M O Rolland, et al.
Pageof 8