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1. Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

2. Effect of the addition of a mental health specialist for evaluation of undiagnosed patients in centres for rare diseases (ZSE-DUO): a prospective, controlled trial with a two-phase cohort design

4. Cerebrospinal fluid findings in patients with psychotic symptoms—a retrospective analysis

7. Apheresis therapies for NMOSD attacks: A retrospective study of 207 therapeutic interventions

8. Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

11. Efficacy of glatiramer acetate in neuromyelitis optica spectrum disorder: a multicenter retrospective study

12. A Novel, Apparently Silent Variant in MFSD8 Causes Neuronal Ceroid Lipofuscinosis with Marked Intrafamilial Variability

13. Neuromyelitis Optica: Evaluation of 871 Attacks and 1,153 Treatment Courses

14. Defining diagnostic cutoffs in neurological patients for serum very long chain fatty acids (VLCFA) in genetically confirmed X-Adrenoleukodystrophy

17. Confirmation of TACO1 as a Leigh Syndrome Disease Gene in Two Additional Families

18. Apheresis therapies for NMOSD attacks : a retrospective study of 207 therapeutic interventions

19. Immunotherapies in neuromyelitis optica spectrum disorder: efficacy and predictors of response

20. Confirmation of TACO1as a Leigh Syndrome Disease Gene in Two Additional Families

21. The astrocytic response towards invasive meningiomas

23. Confirmation of TACO1 as a Leigh Syndrome Disease Gene in Two Additional Families

24. Dual Guidance Structure for Evaluation of Patients with Unclear Diagnosis in Centers for Rare Diseases (ZSE-DUO): Study Protocol for a Controlled Multi-center Cohort Study

25. Influence of female sex and fertile age on neuromyelitis optica spectrum disorders.

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