viernes, 26 de mayo de 2017

New Articles From Orphanet Journal of Rare Diseases


New Articles For BioMed Central:

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

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

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

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

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


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