Bonnet D - Search Results

1

Cardiomyopathies in propionic aciduria are reversible after liver transplantation.

Romano S, Valayannopoulos V, Touati G, Jais JP, Rabier D, de Keyzer Y, Bonnet D, de Lonlay P. Romano S, et al. Among authors: bonnet d. J Pediatr. 2010 Jan;156(1):128-34. doi: 10.1016/j.jpeds.2009.07.002. J Pediatr. 2010. PMID: 19818452

2

Efficiency of metabolic screening in childhood cardiomyopathies.

Bonnet D, de Lonlay P, Gautier I, Rustin P, Rötig A, Kachaner J, Acar P, LeBidois J, Munnich A, Sidi D. Bonnet D, et al. Eur Heart J. 1998 May;19(5):790-3. doi: 10.1053/euhj.1997.0818. Eur Heart J. 1998. PMID: 9717014

3

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.

Iserin L, de Lonlay P, Viot G, Sidi D, Kachaner J, Munnich A, Lyonnet S, Vekemans M, Bonnet D. Iserin L, et al. Among authors: bonnet d. Eur J Pediatr. 1998 Nov;157(11):881-4. doi: 10.1007/s004310050959. Eur J Pediatr. 1998. PMID: 9835429

4

Recognition and management of fatty acid oxidation defects: a series of 107 patients.

Saudubray JM, Martin D, de Lonlay P, Touati G, Poggi-Travert F, Bonnet D, Jouvet P, Boutron M, Slama A, Vianey-Saban C, Bonnefont JP, Rabier D, Kamoun P, Brivet M. Saudubray JM, et al. Among authors: bonnet d. J Inherit Metab Dis. 1999 Jun;22(4):488-502. doi: 10.1023/a:1005556207210. J Inherit Metab Dis. 1999. PMID: 10407781 Review.

5

Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.

Bonnet D, Martin D, Pascale De Lonlay, Villain E, Jouvet P, Rabier D, Brivet M, Saudubray JM. Bonnet D, et al. Circulation. 1999 Nov 30;100(22):2248-53. doi: 10.1161/01.cir.100.22.2248. Circulation. 1999. PMID: 10577999

6

[Metabolic and genetic investigations in childhood cardiomyopathies].

Bonnet D, Rustin P, Rötig A, de Lonlay P, Viot G, Munnich A, Sidi D. Bonnet D, et al. Arch Mal Coeur Vaiss. 1999 Nov;92(11):1509-14. Arch Mal Coeur Vaiss. 1999. PMID: 10598230 Review. French.

7

[A rare cause of cardiomyopathy in childhood: propionic acidosis. Three case reports].

Ou P, Touati G, Fraisse A, Sidi D, Kachaner J, Saudubray JM, Bonnet D. Ou P, et al. Among authors: bonnet d. Arch Mal Coeur Vaiss. 2001 May;94(5):531-3. Arch Mal Coeur Vaiss. 2001. PMID: 11434026 French.

8

Conotruncal heart defects in three patients with congenital disorder of glycosylation type Ia (CDG Ia).

Romano S, Bajolle F, Valayannopoulos V, Lyonnet S, Colomb V, de Baracé C, Vouhe P, Pouard P, Vuillaumier-Barrot S, Dupré T, de Keyzer Y, Sidi D, Seta N, Bonnet D, de Lonlay P. Romano S, et al. Among authors: bonnet d. J Med Genet. 2009 Apr;46(4):287-8. doi: 10.1136/jmg.2008.057620. J Med Genet. 2009. PMID: 19357119 No abstract available.

9

Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases.

Mahlaoui N, Minard-Colin V, Picard C, Bolze A, Ku CL, Tournilhac O, Gilbert-Dussardier B, Pautard B, Durand P, Devictor D, Lachassinne E, Guillois B, Morin M, Gouraud F, Valensi F, Fischer A, Puel A, Abel L, Bonnet D, Casanova JL. Mahlaoui N, et al. Among authors: bonnet d. J Pediatr. 2011 Jan;158(1):142-8, 148.e1. doi: 10.1016/j.jpeds.2010.07.027. Epub 2010 Sep 16. J Pediatr. 2011. PMID: 20846672

10

Laronidase for cardiopulmonary disease in Hurler syndrome 12 years after bone marrow transplantation.

Valayannopoulos V, de Blic J, Mahlaoui N, Stos B, Jaubert F, Bonnet D, Fischer A, de Lonlay P. Valayannopoulos V, et al. Among authors: bonnet d. Pediatrics. 2010 Nov;126(5):e1242-7. doi: 10.1542/peds.2009-2843. Epub 2010 Oct 25. Pediatrics. 2010. PMID: 20974778

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