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Lancet (London, England)
|
November 18, 1978
Systematic neonatal screening for Duchenne muscular dystrophy
C Dellamonica, J M Robert, J Cotte, et al.
La Nouvelle Presse Medicale
|
April 21, 1979
[Systematic neonatal screening for Duchenne muscular dystrophy]
C Dellamonica, J M Robert, J Cotte, et al.
Archives Francaises De Pediatrie
|
August 1, 1981
[Plasma concentrations of amino acids, urea nitrogen and ammonia in 1 to 2 month-old low birth weight premature infant (author's transl)]
L Sann, D Rigal, P Divry, et al.
Journal De Genetique Humaine
|
March 1, 1981
[Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience]
H Plauchu, C Dellamonica, B Pascal, et al.
Acta Paediatrica Scandinavica
|
November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood
P Divry, M David, N Gregersen, et al.
Pathologie-Biologie
|
December 15, 2004
[The computer-assisted management programs for antibiotic therapies in connection with an application in geriatrics]
C Obez, A-M Barisic, W Chatelier, et al.
Annales De Pediatrie
|
October 1, 1987
[Reference values for serum transferrin in newborn infants and children]
G Plomteux, C Charlier, A Albert, et al.
Annales De Biologie Clinique
|
January 1, 1987
[Reference values of serum transferrin in newborn infants, children and adults]
G Plomteux, C Charlier, A Albert, et al.
Journal De Genetique Humaine
|
August 1, 1987
[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)]
H Plauchu, M P Cordier, H N Carrier, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Lancet (London, England)
|
November 18, 1978
Systematic neonatal screening for Duchenne muscular dystrophy
C Dellamonica, J M Robert, J Cotte, et al.
La Nouvelle Presse Medicale
|
April 21, 1979
[Systematic neonatal screening for Duchenne muscular dystrophy]
C Dellamonica, J M Robert, J Cotte, et al.
Archives Francaises De Pediatrie
|
August 1, 1981
[Plasma concentrations of amino acids, urea nitrogen and ammonia in 1 to 2 month-old low birth weight premature infant (author's transl)]
L Sann, D Rigal, P Divry, et al.
Journal De Genetique Humaine
|
March 1, 1981
[Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience]
H Plauchu, C Dellamonica, B Pascal, et al.
Acta Paediatrica Scandinavica
|
November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood
P Divry, M David, N Gregersen, et al.
Pathologie-Biologie
|
December 15, 2004
[The computer-assisted management programs for antibiotic therapies in connection with an application in geriatrics]
C Obez, A-M Barisic, W Chatelier, et al.
Annales De Pediatrie
|
October 1, 1987
[Reference values for serum transferrin in newborn infants and children]
G Plomteux, C Charlier, A Albert, et al.
Annales De Biologie Clinique
|
January 1, 1987
[Reference values of serum transferrin in newborn infants, children and adults]
G Plomteux, C Charlier, A Albert, et al.
Journal De Genetique Humaine
|
August 1, 1987
[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)]
H Plauchu, M P Cordier, H N Carrier, et al.
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of 2