Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis (Purpura papulosa haemorrhagica Hebrae)
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Gastrointestinal involvement in Fabry disease. So important, yet often neglected.Fabry disease and the skin: data from FOS, the Fabry outcome survey.Angiokeratomas of Fabry successfully treated with intense pulsed light.[Globosides as key players in the pathophysiology of Shiga toxin-associated acute kidney failure and Fabry disease].Depletion of globosides and isoglobosides fully reverts the morphologic phenotype of Fabry diseaseEnzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923-2016).Angiokeratoma circumscriptum: a case report and review of the literature.Fabry's disease. A brief review in connection with a Scandinavian survey.Fabry disease: recent advances in enzyme replacement therapy.Fabry disease - underestimated in the differential diagnosis of multiple sclerosis?Newborn screening for lysosomal storage disorders.Fabry disease, enzyme replacement therapy and the significance of antibody responses.Difficulties and barriers in diagnosing Fabry disease: what can be learnt from the literature?Perspectives in Pediatric Pathology, Chapter 21. Testicular Pathology in Heritable Metabolic Disease.Fabry's disease: an example of cardiorenal syndrome type 5.Characterization and phosphoproteomic analysis of a human immortalized podocyte model of Fabry disease generated using CRISPR/Cas9 technology.Angiokeratoma serpiginosum.Early markers of Fabry disease revealed by proteomics.Cardiac Fabry's disease: an unusual cause of left ventricular hypertrophy.Pathomechanisms of renal Fabry disease.Fabry's disease: otoneurologic findings in twelve members of one family.Caveolin-associated accumulation of globotriaosylceramide in the vascular endothelium of alpha-galactosidase A null mice.Fabry disease: a morphologic study of 11 cases.Postmortem diagnosis of Fabry disease with acromegaly and a unique vasculopathy.Quantitative dysmorphology assessment in Fabry disease.[Anterior segment findings with far-reaching consequences].Enzyme replacement therapy in orphan and ultra-orphan diseases: the limitations of standard economic metrics as exemplified by Fabry-Anderson disease.
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Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis (Purpura papulosa haemorrhagica Hebrae)
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 1898
@uk
name
Ein Beitrag zur Kenntniss der ...... papulosa haemorrhagica Hebrae)
@en
Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis
@nl
type
label
Ein Beitrag zur Kenntniss der ...... papulosa haemorrhagica Hebrae)
@en
Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis
@nl
prefLabel
Ein Beitrag zur Kenntniss der ...... papulosa haemorrhagica Hebrae)
@en
Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis
@nl
P356
P1476
Ein Beitrag zur Kenntniss der ...... papulosa haemorrhagica Hebrae)
@en
P2093
P2888
P304
P356
10.1007/BF01986897
P577
1898-12-01T00:00:00Z
P6179
1024643089