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Annales De Biologie Clinique
|
January 28, 1999
[Molecular genetics of the remethylation of homocysteine]
A Chango, F Parrot-Roulaud, J Nicolas
Thyroid : Official Journal of the American Thyroid Association
|
January 26, 2000
Homocysteine, hypothyroidism, and effect of thyroid hormone replacement
B Catargi, F Parrot-Roulaud, C Cochet, et al.
Pediatric Research
|
July 1, 1992
Mitochondrial myopathy studies on permeabilized muscle fibers
T Letellier, M Malgat, M Coquet, et al.
Archives Francaises De Pediatrie
|
June 1, 1993
[Coffin-Lowry syndrome and hyperprolinemia]
D Lacombe, F Parrot-Roulaud, J F Castell, et al.
Intensive Care Medicine
|
January 1, 1992
Inborn errors of metabolism (IEM) revealed by Reye's syndrome (RS)
M Fayon, M Carre, F Parrot-Roulaud, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Fatal neonatal hepatocellular deficiency with lactic acidosis: a defect of the respiratory chain
F Parrot-Roulaud, M Carre, T Lamirau, et al.
Pediatrie
|
January 1, 1992
[Beta-ketothiolase deficiency: a case of ketoacidosis with hyperglycinemia]
C Elleau, F Parrot-Roulaud, Y Perel, et al.
Presse Medicale (Paris, France : 1983)
|
November 5, 1997
[Cerebral vascular complication of hyperhomocysteinemia. Controlling thromboembolic complications with folates]
M Candito, P Bedoucha, D Jambou, et al.
Gastroenterology
|
October 1, 1992
Fatal neonatal liver failure and mitochondrial cytopathy: an observation with antenatal ascites
M Fayon, T Lamireau, P Bioulac-Sage, et al.
The Journal of Pediatrics
|
December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onset
V Cormier, P Rustin, J P Bonnefont, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Annales De Biologie Clinique
|
January 28, 1999
[Molecular genetics of the remethylation of homocysteine]
A Chango, F Parrot-Roulaud, J Nicolas
Thyroid : Official Journal of the American Thyroid Association
|
January 26, 2000
Homocysteine, hypothyroidism, and effect of thyroid hormone replacement
B Catargi, F Parrot-Roulaud, C Cochet, et al.
Pediatric Research
|
July 1, 1992
Mitochondrial myopathy studies on permeabilized muscle fibers
T Letellier, M Malgat, M Coquet, et al.
Archives Francaises De Pediatrie
|
June 1, 1993
[Coffin-Lowry syndrome and hyperprolinemia]
D Lacombe, F Parrot-Roulaud, J F Castell, et al.
Intensive Care Medicine
|
January 1, 1992
Inborn errors of metabolism (IEM) revealed by Reye's syndrome (RS)
M Fayon, M Carre, F Parrot-Roulaud, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Fatal neonatal hepatocellular deficiency with lactic acidosis: a defect of the respiratory chain
F Parrot-Roulaud, M Carre, T Lamirau, et al.
Pediatrie
|
January 1, 1992
[Beta-ketothiolase deficiency: a case of ketoacidosis with hyperglycinemia]
C Elleau, F Parrot-Roulaud, Y Perel, et al.
Presse Medicale (Paris, France : 1983)
|
November 5, 1997
[Cerebral vascular complication of hyperhomocysteinemia. Controlling thromboembolic complications with folates]
M Candito, P Bedoucha, D Jambou, et al.
Gastroenterology
|
October 1, 1992
Fatal neonatal liver failure and mitochondrial cytopathy: an observation with antenatal ascites
M Fayon, T Lamireau, P Bioulac-Sage, et al.
The Journal of Pediatrics
|
December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onset
V Cormier, P Rustin, J P Bonnefont, et al.
Page
of 2