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ABOUT JoVE

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Simone Schröder

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Nature Communications|November 12, 2021

Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathyMatthias Kettwig, Katharina Ternka, Kristin Wendland, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017

FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variantsDiana Mitter, Milka Pringsheim, Marc Kaulisch, et al.

Annals of Clinical and Translational Neurology|April 26, 2019

Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- miceMilka Pringsheim, Diana Mitter, Simone Schröder, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Nature Communications|November 12, 2021

Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathyMatthias Kettwig, Katharina Ternka, Kristin Wendland, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017

FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variantsDiana Mitter, Milka Pringsheim, Marc Kaulisch, et al.

Annals of Clinical and Translational Neurology|April 26, 2019

Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- miceMilka Pringsheim, Diana Mitter, Simone Schröder, et al.

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