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3. Genome Sequencing for Diagnosing Rare Diseases

6. Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies

9. Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome

11. Drowning and Nonfatal Drowning in Children and Adolescents: A Subsequent Retrospective Data Analysis.

12. High association of MOG-IgG antibodies in children with bilateral optic neuritis

14. Parenting stress in families of children with disabilities: Impact of type of disability and assessment of attending paediatricians.

15. Macrocytic Anemia and Mitochondriopathy Resulting from a Defect in Sideroflexin 4

17. Adressen

18. Defining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy

20. Germline AGO2 mutations impair RNA interference and human neurological development

23. Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells

24. Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease

26. MRI of the first event in pediatric acquired demyelinating syndromes with antibodies to myelin oligodendrocyte glycoprotein

27. Cerebrospinal Fluid Protein Concentrations in Hydrocephalus

30. Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study

33. The Role of TRPV1 in Febrile Seizure Susceptibility: Inflammation, Respiratory Alkalosis, and Seizure Threshold.

36. 4. Schädigungen des Gehirns

46. De novo variants in ATP2B1 lead to neurodevelopmental delay

48. Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy

49. Stress, Stress Reduction and Obesity in Childhood and Adolescence.

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