Suchergebnisse - "Fossati, Barbara"

PubPharm (75)

31

Prevalence of cutaneous comorbidities in psoriatic patients and their impact on quality of life

enthalten in: European journal of dermatology : EJD | 2019

von Caldarola, G. | De Simone, C. | Talamonti, M. | +5

32

Prevalence of cutaneous comorbidities in psoriatic patients and their impact on quality of life

enthalten in: European journal of dermatology | 2019

von Caldarola, G. | De Simone, C. | Talamonti, M. | +5

33

Aberrant insulin receptor expression is associated with insulin resistance and skeletal muscle atrophy in myotonic dystrophies

enthalten in: PloS one | 2019

von Renna, L. | Bosè, F. | Brigonzi, E. | +3

34

TNNT2 Missplicing in Skeletal Muscle as a Cardiac Biomarker in Myotonic Dystrophy Type 1 but Not in Myotonic Dystrophy Type 2

enthalten in: Frontiers in neurology | 2019

von Bosè, F. | Renna, L. | Fossati, B. | +7

35

Emerging treatment options for the treatment of moderate to severe plaque psoriasis and psoriatic arthritis : evaluating bimekizumab and its therapeutic potential

enthalten in: Psoriasis (Auckland, N.Z.) | 2019

von Chiricozzi, A. | De Simone, C. | Fossati, B. | +1

ErratumIn: Psoriasis (Auckl). 2019 Aug 15;9:73-74. - PMID 31616625

36

Incidence of amplification failure in DMPK allele due to allelic dropout event in a diagnostic laboratory

enthalten in: Clinica chimica acta; international journal of clinical chemistry | 2018

von De Siena, C. | Cardani, R. | Brigonzi, E. | +5

37

Eight years after an international workshop on myotonic dystrophy patient registries : case study of a global collaboration for a rare disease

enthalten in: Orphanet journal of rare diseases | 2018

von Wood, L. | Bassez, G. | Bleyenheuft, C. | +36

ErratumIn: Orphanet J Rare Dis. 2019 Aug 15;14(1):199. - PMID 31416449

38

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

enthalten in: Orphanet journal of rare diseases | 2018

von Wood, L. | Bassez, G. | Bleyenheuft, C. | +36

39

SCN4A as modifier gene in patients with myotonic dystrophy type 2

enthalten in: Scientific reports | 2018

von Binda, A. | Renna, L. | Bosè, F. | +7

40

Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy : A Case Report With Critical Therapeutical Implications and Review of the Literature

enthalten in: Frontiers in neurology | 2018

von Cavalli, M. | Fossati, B. | Vitale, R. | +6