[Weakness of the left hand and pallor in a 21-year-old woman].

[1]  G. Ciccarese,et al.  Changes in neurosyphilis presentation: a survey on 286 patients , 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

[2]  L. Giovanella,et al.  Hashimoto's encephalopathy: A rare proteiform disorder. , 2016, Autoimmunity reviews.

[3]  R. Wevers,et al.  Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man. , 2012, American journal of human genetics.

[4]  P. Prassopoulos,et al.  Basal ganglia hyperintensity on T1‐weighted MRI in rendu–osler–weber disease , 2012, Journal of magnetic resonance imaging : JMRI.

[5]  A. Demetris,et al.  Hereditary Hemorrhagic Telangiectasia of the Liver Complicated by Ischemic Bile Duct Necrosis and Sepsis: Case Report and Review of the Literature , 2010, Digestive Diseases and Sciences.

[6]  J. Roume,et al.  Pancreatic involvement in hereditary hemorrhagic telangiectasia: assessment with multidetector helical CT. , 2010, Radiology.

[7]  A. Stepens,et al.  A Parkinsonian syndrome in methcathinone users and the role of manganese. , 2008, The New England journal of medicine.

[8]  R. Bowler,et al.  Dose–effect relationships between manganese exposure and neurological, neuropsychological and pulmonary function in confined space bridge welders , 2006, Occupational and Environmental Medicine.

[9]  Jun Li,et al.  A case of Hashimoto's encephalopathy: Association with sensory ganglionopathy , 2005, Journal of the Neurological Sciences.

[10]  E. Buscarini,et al.  Liver involvement in hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber disease. , 2005, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

[11]  C. Oppenheim,et al.  Atteintes bilatérales des noyaux gris chez l’adulte , 2005 .

[12]  Wei Zheng,et al.  Manganese toxicity upon overexposure , 2004, NMR in biomedicine.

[13]  J. Wyatt,et al.  The pathology of acute hepatic disintegration in hereditary haemorrhagic telangiectasia , 2003, Histopathology.

[14]  A. Guttmacher,et al.  Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). , 2000, American journal of medical genetics.

[15]  S. Ikeda,et al.  Manganese deposits in patients with biliary atresia after hepatic porto-enterostomy. , 2000, Journal of Pediatric Surgery.

[16]  E. Loza,et al.  Pseudohaemarthrosis: a new manifestation of Osler-Rendu-Weber disease. , 1992, Annals of the rheumatic diseases.

[17]  J. Viallard,et al.  [Hereditary hemorrhagic telangiectasia]. , 2014, La Revue de medecine interne.

[18]  J. Viallard,et al.  Maladie de Rendu-Osler , 2013 .