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

1

194. Reparación de la válvula mitral mediante un nuevo anil..:

Gómez Vidal, M. ; Sáez de Ibarra, J.I. ; Perier, P....
Cirugía Cardiovascular. 19 (2012) 2 - p. 230 , 2012

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

2

Extracorporeal Circulation as an Additional Method for Cere..:

Guibaud, J.P. ; Roques, X. ; Laborde, N....
Journal of Cardiac Surgery. 19 (2004) 5 - p. 415-419 , 2004

Link: https://doi.org/10.1111/..

3

Hémocompatibilité et biomatériaux:

Guibaud, J.P. ; Forestier, F. ; Janvier, G.
ITBM-RBM. 23 (2002) - p. 22-26 , 2002

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

4

Outcome of 21 Children with Hurler Syndrome Transplanted fr..:

Souillet, G ; Guffon, N ; Maire, I..
Pediatric Research. 45 (1999) - p. 770-770 , 1999

Link: https://doi.org/10.1203/..

5

Follow-up of nine patients with Hurler syndrome after bone ..:

Guffon, N. ; Souillet, G. ; Maire, I...
The Journal of Pediatrics. 133 (1998) 1 - p. 119-125 , 1998

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

6

Mutations in the pterin-4α-carbinolamine dehydratase ( PCBD..:

Thöny, B. ; Neuheiser, F. ; Kierat, L....
Human Genetics. 103 (1998) 2 - p. 162-167 , 1998

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

7

Étude des acylcarnitines plasmatiques par spectrométrie de ..:

Delolme, F ; Vianey-Saban, C ; Guffon, N...
Archives de Pédiatrie. 4 (1997) 9 - p. 819-826 , 1997

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

8

Diagnosis of inborn errors of metabolism by acylcarnitine p..:

Vianey‐Saban, C. ; Guffon, N. ; Delolne, F....
Journal of Inherited Metabolic Disease. 20 (1997) 3 - p. 411-414 , 1997

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

9

Juvenile metachromatic leukodystrophy: neurological outcome..:

Guffon, N. ; Souillet, G. ; Maire, I....
Journal of Inherited Metabolic Disease. 18 (1995) 2 - p. 159-161 , 1995

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

10

A new neonatal case ofN‐acetylglutamate synthase deficiency..:

Guffon, N. ; Vianey‐Saban, C. ; Bourgeois, J....
Journal of Inherited Metabolic Disease. 18 (1994) 1 - p. 61-65 , 1994

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

11

Human cultured myoblasts: A model for the diagnosis of mito..:

Dumoulin, R. ; Mandon, G. ; Collombet, J. M....
Journal of Inherited Metabolic Disease. 16 (1993) 3 - p. 545-547 , 1993

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

12

2‐Ketoglutarate dehydrogenase deficiency, a rare cause of p..:

Guffon, N. ; Lopez‐Mediavilla, C. ; Dumoulin, R....
Journal of Inherited Metabolic Disease. 16 (1993) 5 - p. 821-830 , 1993

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

13

Farber disease: an ultrastructural study: Report of a case ..:

Zappatini-Tommasi, L. ; Dumontel, C. ; Guibaud, P..
Virchows Archiv A Pathological Anatomy and Histopathology. 420 (1992) 3 - p. 281-290 , 1992

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

14

Isolated 3‐methylcrotonyl‐CoA carboxylase deficiency in a 1..:

Rolland, M. O. ; Divry, P. ; Zabot, M. T....
Journal of Inherited Metabolic Disease. 14 (1991) 5 - p. 838-839 , 1991

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

15

Early prenatal diagnosis of propionic acidaemia with simult..:

Rolland, M. O. ; Divry, P. ; Mandon, G....
Journal of Inherited Metabolic Disease. 13 (1990) 3 - p. 345-348 , 1990

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