Suchergebnisse

PubPharm (38)

31

Whipple’s disease mimicking rheumatoid arthritis can cause misdiagnosis and treatment failure

sonderdruck aus: Orphanet journal of rare diseases | 2017

von Glaser, C. | Rieg, S. | Wiech, T. | +8

32

Mudd’s disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes

sonderdruck aus: Orphanet journal of rare diseases | 2015

von Chien, Y. | Abdenur, J. | Baronio, F. | +1

33

Targeting epidermal lipids for treatment of Mendelian disorders of cornification

sonderdruck aus: Orphanet journal of rare diseases | 2014

von Kiritsi, D. | Schauer, F. | Wölfle, U. | +3

34

Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency

sonderdruck aus: Orphanet journal of rare diseases | 2014

von Grünert, S.

35

Bullous pemphigoid in infants: characteristics, diagnosis and treatment

sonderdruck aus: Orphanet journal of rare diseases | 2014

von Schwieger-Briel, A. | Möllmann, C. | Mattulat, B. | +4

36

RARE-Bestpractices: a platform for sharing best practices for the management of rare diseases

sonderdruck aus: Orphanet journal of rare diseases | 2014

von Taruscio, D. | Schünemann, H. | Meerpohl, J. | +3

37

Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice

sonderdruck aus: Orphanet journal of rare diseases | 2014

von Mayorandan, S. | Spiekerkötter, U. | Das, A.

38

The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseases

sonderdruck aus: Orphanet journal of rare diseases | 2013

von Rodger, S. | Lochmüller, H. | Tassoni, A. | +3