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2. Detection of Common Arrhythmias by the Watch-PAT: Expression of Electrical Arrhythmias by Pulse Recording

3. Watch-PAT is Useful in the Diagnosis of Sleep Apnea in Patients with Atrial Fibrillation

4. Ginkgo biloba extract EGb 761® alleviates neurosensory symptoms in patients with dementia: a meta-analysis of treatment effects on tinnitus and dizziness in randomized, placebo-controlled trials

7. Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire

9. Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire

11. Genetik / Pränatale Diagnostik

15. D5.8 Submitted open access papers on comparative analysis of the resilience of farming systems across the EU and their delivery of private and public goods, and the impacts of future scenarios, improved strategies and policy options

23. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

28. Atypical periodic paralysis and myalgia: A novel RYR1 phenotype

29. Ginkgo biloba extract EGb 761® alleviates neurosensory symptoms in patients with dementia: a meta-analysis of treatment effects on tinnitus and dizziness in randomized, placebo-controlled trials

33. PS1004 PTC299 IS A NOVEL DHODH INHIBITOR FOR USE IN TREATMENT OF AML

34. Uniparental Disomy of Chromosome 2 Unmasks New ITGA6 Recessive Mutation and Results in a Lethal Junctional Epidermolysis Bullosa in a Newborn

38. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

39. Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors

41. 814 Uniparental inheritance of junctional epidermolysis bullosa (JEB) through mutation of ITGA6 and trisomic rescue

42. Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial

43. Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease

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