Familial pernicious chronic intestinal pseudo-obstruction with a mitochondrial DNA A3243G mutation, Intern Med, vol.56, pp.1089-1093, 2017. ,
DOI : 10.2169/internalmedicine.56.7753
URL : https://www.jstage.jst.go.jp/article/internalmedicine/56/9/56_56.7753/_pdf
Mitochondrial neuropathies": A survey from the large cohort of the Italian Network, Neuromuscul Disord, vol.26, pp.272-276, 2016. ,
URL : https://hal.archives-ouvertes.fr/hal-02086938
Pontocerebellar hypoplasia type 6: A British case with PEHO-like features, Am J Med Genet A, vol.152, pp.2079-2084, 2010. ,
DOI : 10.1002/ajmg.a.33531
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?, J Neurol, vol.261, pp.504-510, 2014. ,
Gastrointestinal manifestations of mitochondrial disorders: a systematic review, Therap Adv Gastroenterol, vol.10, pp.142-154, 2017. ,
DOI : 10.1177/1756283x16666806
URL : http://europepmc.org/articles/pmc5330602?pdf=render
, The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license
, The Japanese Society of Internal Medicine Intern Med, vol.57, pp.769-770, 2018.