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[Complications of autism].
de Pontual L, Heulin M, Charles E, Héron B, Zylberberg P. de Pontual L, et al. Among authors: heron b. Arch Pediatr. 2015 May;22(5 Suppl 1):179-80. doi: 10.1016/S0929-693X(15)30089-0. Arch Pediatr. 2015. PMID: 26112580 French. No abstract available.
[Diagnosis of metabolic coma in children].
Poggi-Travert F, Héron B, Billette de Villemeur T, Spada M, Jouvet P, Charpentier C, Rabier D, Kamoun P, Saudubray JM. Poggi-Travert F, et al. Among authors: heron b. Arch Pediatr. 1994 Sep;1(9):843-51. Arch Pediatr. 1994. PMID: 7842129 Review. French.
Phenotypic characterization of seven individuals with Marbach-Schaaf neurodevelopmental syndrome.
Marbach F, Lipska-Ziętkiewicz BS, Knurowska A, Michaud V, Margot H, Lespinasse J, Tran Mau Them F, Coubes C, Park J, Grosch S, Roggia C, Grasshoff U, Kalsner L, Denommé-Pichon AS, Afenjar A, Héron B, Keren B, Caro P, Schaaf CP. Marbach F, et al. Among authors: heron b. Am J Med Genet A. 2022 Sep;188(9):2627-2636. doi: 10.1002/ajmg.a.62884. Epub 2022 Jul 5. Am J Med Genet A. 2022. PMID: 35789103
Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
Rabier D, Diry C, Rotig A, Rustin P, Heron B, Bardet J, Parvy P, Ponsot G, Marsac C, Saudubray JM, Munnich A, Kamoun P. Rabier D, et al. Among authors: heron b. J Inherit Metab Dis. 1998 Jun;21(3):216-9. doi: 10.1023/a:1005391300203. J Inherit Metab Dis. 1998. PMID: 9686360 No abstract available.
139 results