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12. BRAT1 mutations are associated with infantile epileptic encephalopathy, mitochondrial dysfunction, and survival into childhood. Issue 9 (9th June 2016)

15. De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy. Issue 3 (28th November 2018)

16. Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas. (15th January 2019)

17. Early Loss of Pericytes and Perivascular Stromal Cell-Induced Scar Formation after Stroke. Issue 3 (March 2013)

18. Endoplasmic reticulum‐stress and unfolded protein response‐activation in immune‐mediated necrotizing myopathy. (15th June 2022)

19. Enlarging the Nosological Spectrum of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids (HDLS). (16th March 2014)

20. Eosinophilic fasciitis (Shulman syndrome)—recognition of the histological spectrum allows for new insights into possible pathomechanisms. (20th September 2022)