E-LIB Suche - Ergebnisse für: Kamoun, P.

1

Endogenous production of hydrogen sulfide in mammals:

Kamoun, P.
Amino Acids. 26 (2004) 3 - p. , 2004

Link: https://doi.org/10.1007/..

2

Les manifestations vasculaires de l'homocystinurie : étude ..:

Simorre, B ; Quéré, I ; Berrut, G...
La Revue de Médecine Interne. 23 (2002) 3 - p. 267-272 , 2002

Link: https://doi.org/10.1016/..

3

Improving the prenatal diagnosis of citrullinemia using cit..:

Chadefaux‐Vekemans, B. ; Rabier, D. ; Chabli, A....
Prenatal Diagnosis. 22 (2002) 6 - p. 456-458 , 2002

Link: https://doi.org/10.1002/..

4

Plasma Lysine Concentration and Availability of 2‐Ketogluta..:

Kamoun, P. ; Richard, V. ; Rabier, D..
Journal of Inherited Metabolic Disease. 25 (2002) 1 - p. 1-6 , 2002

Link: https://doi.org/10.1023/..

5

Mental retardation in Down syndrome: a hydrogen sulfide hpo..:

Kamoun, P.
Medical Hypotheses. 57 (2001) 3 - p. 389-392 , 2001

Link: https://doi.org/10.1054/..

6

Genotype/phenotype correlation in carnitine palmitoyl trans..:

Thuillier, L. ; Sevin, C. ; Demaugre, F....
Neuromuscular Disorders. 10 (2000) 3 - p. 200-205 , 2000

Link: https://doi.org/10.1016/..

7

Genetic hypoglycaemia in infancy and childhood: Pathophysio..:

Saudubray, J. M. ; De Lonlay, P. ; Touati, G....
Journal of Inherited Metabolic Disease. 23 (2000) 3 - p. 197-214 , 2000

Link: https://doi.org/10.1023/..

8

Liver transplantation in urea cycle disorders:

Saudubray, J. M. ; Touati, G. ; Delonlay, P....
European Journal of Pediatrics. 158 (1999) S2 - p. S055-S059 , 1999

Link: https://doi.org/10.1007/..

9

Recognition and management of fatty acid oxidation defects:..:

Saudubray, J. M. ; Martin, D. ; De Lonlay, P....
Journal of Inherited Metabolic Disease. 22 (1999) 4 - p. 487-502 , 1999

Link: https://doi.org/10.1023/..

10

Liver transplantation in propionic acidaemia:

Saudubray, J. M. ; Touati, G. ; Delonlay, P....
European Journal of Pediatrics. 158 (1999) S2 - p. S065-S069 , 1999

Link: https://doi.org/10.1007/..

11

Persistent hypocitrullinaemia as a marker for mtDNA NARP T ..:

Rabier, D. ; Diry, C. ; Rotig, A....
Journal of Inherited Metabolic Disease. 21 (1998) 3 - p. 216-219 , 1998

Link: https://doi.org/10.1023/..

12

Reliability of biochemical parameters used in prenatal diag..:

Merinero, B. ; Pérez-Cerdá, C. ; Garcia, M. J....
Prenatal Diagnosis. 18 (1998) 9 - p. 947-952 , 1998

Link: https://doi.org/10.1002/..

13

Radar observations of three comets and detection of echoes ..:

Kamoun, P. ; Campbell, D. ; Pettengill, G..
Planetary and Space Science. 47 (1998) 1-2 - p. 23-28 , 1998

Link: https://doi.org/10.1016/..

14

Does the polymorphism 677C‐T of the 5,10‐methylenetetrahydr..:

Thuillier, L. ; Chadefaux‐Vekemans, B. ; Bonnefont, J. P....
Journal of Inherited Metabolic Disease. 21 (1998) 8 - p. 812-822 , 1998

Link: https://doi.org/10.1023/..

15

Muscular origin of hyperammonaemia:

Kamoun, P. ; Rabier, D. ; Saudubray, J. M.
European Journal of Pediatrics. 157 (1998) 10 - p. 868-868 , 1998

Link: https://doi.org/10.1007/..