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Page 1
[Isolated agenesia of pulmonary artery].
Boudard I, Mely L, Labbé A, Bellon G, Chabrol B, Dubus JC. Boudard I, et al. Among authors: chabrol b. Arch Pediatr. 2004 Sep;11(9):1078-82. doi: 10.1016/j.arcped.2004.04.026. Arch Pediatr. 2004. PMID: 15350999 French.
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy.
Bannwarth S, Procaccio V, Rouzier C, Fragaki K, Poole J, Chabrol B, Desnuelle C, Pouget J, Azulay JP, Attarian S, Pellissier JF, Gargus JJ, Abdenur JE, Mozaffar T, Calvas P, Labauge P, Pages M, Wallace DC, Lambert JC, Paquis-Flucklinger V. Bannwarth S, et al. Among authors: chabrol b. Mitochondrion. 2008 Mar;8(2):136-45. doi: 10.1016/j.mito.2007.10.008. Epub 2007 Nov 6. Mitochondrion. 2008. PMID: 18078792
[Juvenile dermatomyositis: diagnosis and treatment].
Gissinger-Prévot S, Figarella-Branger D, Mancini J, Chabrol B. Gissinger-Prévot S, et al. Among authors: chabrol b. Arch Pediatr. 2008 Jan;15(1):50-3. doi: 10.1016/j.arcped.2007.08.025. Epub 2007 Dec 27. Arch Pediatr. 2008. PMID: 18164188 French.
[Epileptic seizures in childhood: from seizure type to diagnosis].
Milh M, Ticus I, Villeneuve N, Hugonencq C, Mancini J, Chabrol B. Milh M, et al. Among authors: chabrol b. Arch Pediatr. 2008 Feb;15(2):216-22. doi: 10.1016/j.arcped.2007.11.007. Epub 2008 Jan 14. Arch Pediatr. 2008. PMID: 18248967 French.
[GLUT-1 deficiency syndrome or De Vivo disease: a case report].
Ticus I, Cano A, Villeneuve N, Milh M, Mancini J, Chabrol B. Ticus I, et al. Among authors: chabrol b. Arch Pediatr. 2008 Aug;15(8):1296-9. doi: 10.1016/j.arcped.2008.04.024. Epub 2008 Jun 16. Arch Pediatr. 2008. PMID: 18556184 French.
343 results