New Articles From Orphanet Journal of Rare Diseases

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases LETTER TO THE EDITOR PIGO deficiency: palmoplantar keratoderma and novel mutations Marie-Anne Morren, Jaak Jaeken, Gepke Visser, Isabelle Salles, Chris Van Geet, Ilenia Simeoni, Ernest Turro and Kathleen Freson Orphanet Journal of Rare Diseases 2017, 12:101 | Published on: 25 May 2017 Full Text | PDF RESEARCH Whipple’s disease mimicking rheumatoid arthritis can cause misdiagnosis and treatment failure Cornelia Glaser, Siegbert Rieg, Thorsten Wiech, Christine Scholz, Dominique Endres, Oliver Stich, Peter Hasselblatt, Walter Geißdörfer, Christian Bogdan, Annerose Serr, Georg Häcker, Reinhard E. Voll, Jens Thiel and Nils Venhoff Orphanet Journal of Rare Diseases 2017, 12:99 | Published on: 25 May 2017 Full Text | PDF POSITION STATEMENT A plea to provide best evidence in trials under sample-size restrictions: the example of pioglitazone to resolve leukoplakia and erythroplakia in Fanconi anemia patients Florian Lasch, Kristina Weber, Mwe Mwe Chao and Armin Koch Orphanet Journal of Rare Diseases 2017, 12:102 | Published on: 25 May 2017 Full Text | PDF RESEARCH Depression in patients with SAPHO syndrome and its relationship with brain activity and connectivity Jie Lu, Yanping Duan, Zhentao Zuo, Wenrui Xu, Xuewei Zhang, Chen Li, Rong Xue, Hanzhang Lu and Weihong Zhang Orphanet Journal of Rare Diseases 2017, 12:103 | Published on: 25 May 2017 Full Text | PDF REVIEW Therapeutic strategies to address neuronal nitric oxide synthase deficiency and the loss of nitric oxide bioavailability in Duchenne Muscular Dystrophy Cara A. Timpani, Alan Hayes and Emma Rybalka Orphanet Journal of Rare Diseases 2017, 12:100 | Published on: 25 May 2017 Full Text | PDF

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