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Correction: Imaging of parotid anomalies in infants and children.
Chalard F, Hermann AL, Elmaleh-Bergès M, le Pointe HD. Chalard F, et al. Insights Imaging. 2022 May 6;13(1):86. doi: 10.1186/s13244-022-01231-6. Insights Imaging. 2022. PMID: 35523911 Free PMC article. No abstract available.
Imaging of parotid anomalies in infants and children.
Chalard F, Hermann AL, Elmaleh-Bergès M, Ducou le Pointe H. Chalard F, et al. Insights Imaging. 2022 Feb 24;13(1):27. doi: 10.1186/s13244-022-01166-y. Insights Imaging. 2022. PMID: 35201515 Free PMC article. Review.
SOX10 mutations mimic isolated hearing loss.
Pingault V, Faubert E, Baral V, Gherbi S, Loundon N, Couloigner V, Denoyelle F, Noël-Pétroff N, Ducou Le Pointe H, Elmaleh-Bergès M, Bondurand N, Marlin S. Pingault V, et al. Clin Genet. 2015 Oct;88(4):352-9. doi: 10.1111/cge.12506. Epub 2014 Nov 6. Clin Genet. 2015. PMID: 25256313
Leigh's disease due to a new mutation in the PDHX gene.
Schiff M, Miné M, Brivet M, Marsac C, Elmaleh-Bergés M, Evrard P, Ogier de Baulny H. Schiff M, et al. Ann Neurol. 2006 Apr;59(4):709-14. doi: 10.1002/ana.20818. Ann Neurol. 2006. PMID: 16566017
Early-onset hyperargininaemia: a severe disorder?
Schiff M, Benoist JF, Cardoso ML, Elmaleh-Bergès M, Forey P, Santiago J, Ogier de Baulny H. Schiff M, et al. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S175-8. doi: 10.1007/s10545-009-1137-5. Epub 2009 Apr 20. J Inherit Metab Dis. 2009. PMID: 19381865
Further delineation of the 17p13.3 microdeletion involving YWHAE but distal to PAFAH1B1: four additional patients.
Schiff M, Delahaye A, Andrieux J, Sanlaville D, Vincent-Delorme C, Aboura A, Benzacken B, Bouquillon S, Elmaleh-Berges M, Labalme A, Passemard S, Perrin L, Manouvrier-Hanu S, Edery P, Verloes A, Drunat S. Schiff M, et al. Eur J Med Genet. 2010 Sep-Oct;53(5):303-8. doi: 10.1016/j.ejmg.2010.06.009. Epub 2010 Jul 3. Eur J Med Genet. 2010. PMID: 20599530
64 results