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Page 1
Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chain.
Chabrol B, Sigaudy S, Paquis V, Montfort MF, Giudicelli H, Pellissier JF, Millet V, Mancini J, Philip N. Chabrol B, et al. Among authors: montfort mf. Am J Med Genet. 1997 Oct 17;72(2):222-6. doi: 10.1002/(sici)1096-8628(19971017)72:2<222::aid-ajmg18>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9382147
Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlation.
Aquaron R, Bergé-Lefranc JL, Pellissier JF, Montfort MF, Mayan M, Figarella-Branger D, Coquet M, Serratrice G, Pouget J. Aquaron R, et al. Among authors: montfort mf. Neuromuscul Disord. 2007 Mar;17(3):235-41. doi: 10.1016/j.nmd.2006.12.014. Epub 2007 Feb 26. Neuromuscul Disord. 2007. PMID: 17324573
Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case report.
Vialettes BH, Paquis-Flucklinger V, Pelissier JF, Bendahan D, Narbonne H, Silvestre-Aillaud P, Montfort MF, Righini-Chossegros M, Pouget J, Cozzone PJ, Desnuelle C. Vialettes BH, et al. Among authors: montfort mf. Diabetes Care. 1997 Nov;20(11):1731-7. doi: 10.2337/diacare.20.11.1731. Diabetes Care. 1997. PMID: 9353617
Thyroglobulins of cyclostomes and an elasmobranch.
Suzuki S, Gorbman A, Rolland M, Montfort MF, Lissitzky S. Suzuki S, et al. Among authors: montfort mf. Gen Comp Endocrinol. 1975 May;26(1):56-69. doi: 10.1016/0016-6480(75)90215-4. Gen Comp Endocrinol. 1975. PMID: 1132667 No abstract available.
Efficiency of thyroglobulin as a thyroid hormone-forming protein.
Rolland M, Montfort MF, Lissitzky S. Rolland M, et al. Among authors: montfort mf. Biochim Biophys Acta. 1973 Apr 20;303(2):338-47. doi: 10.1016/0005-2795(73)90365-6. Biochim Biophys Acta. 1973. PMID: 4710237 No abstract available.