[HTML] frontiersin.org

[HTML][HTML] Functional and structural impairments in the perirhinal cortex of a mouse model of CDKL5 deficiency disorder are rescued by a TrkB agonist

E Ren, V Roncacé, S Trazzi, C Fuchs… - Frontiers in Cellular …, 2019 - frontiersin.org
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-linked
neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …
被引用次数：37 相关文章

Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist

E Ren, V Roncacé, S Trazzi, C Fuchs… - Frontiers in Cellular …, 2019 - search.proquest.com
Abstract Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-
linked neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …

Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist

E Ren, V Roncacé, S Trazzi, C Fuchs… - … : New Insights Into …, 2020 - books.google.com
Edited by: Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-
linked neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …
[HTML] nih.gov

[HTML][HTML] Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist

E Ren, V Roncacé, S Trazzi, C Fuchs… - Frontiers in Cellular …, 2019 - ncbi.nlm.nih.gov
Abstract Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-
linked neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …
[PDF] unibo.it

[PDF][PDF] Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist

E Ren, V Roncacé, S Trazzi, C Fuchs, G Medici… - cris.unibo.it
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-linked
neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …

Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist

E Ren, V Roncacé, S Trazzi, C Fuchs… - Frontiers in cellular …, 2019 - pubmed.ncbi.nlm.nih.gov
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-linked
neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …
[PDF] academia.edu

[PDF][PDF] Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist

E Ren, V Roncacé, S Trazzi, C Fuchs, G Medici… - academia.edu
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-linked
neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …

Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist.

E Ren, V Roncacé, S Trazzi, C Fuchs… - Frontiers in Cellular …, 2019 - europepmc.org
Abstract Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-
linked neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …

Functional and Structural Impairments in the Perirhinal Cortex of a Mouse Model of CDKL5 Deficiency Disorder Are Rescued by a TrkB Agonist.

E Ren, V Roncacé, S Trazzi, C Fuchs… - Frontiers in Cellular …, 2019 - europepmc.org
Abstract Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-
linked neurodevelopmental encephalopathy caused by mutations in the CDKL5 gene and …