C Fuchs, G Medici, S Trazzi, L Gennaccaro… - Brain Pathology …, 2019 - europepmc.org
CDKL5 deficiency disorder (CDD) is a rare encephalopathy characterized by early onset epilepsy and severe intellectual disability. CDD is caused by mutations in the X‐linked cyclin …
C Fuchs, G Medici, S Trazzi, L Gennaccaro… - BRAIN …, 2019 - cris.unibo.it
CDKL5 deficiency disorder (CDD) is a rare encephalopathy characterized by early onset epilepsy and severe intellectual disability. CDD is caused by mutations in the X-linked cyclin …
C Fuchs, G Medici, S Trazzi… - Brain pathology …, 2019 - pubmed.ncbi.nlm.nih.gov
CDKL5 deficiency disorder (CDD) is a rare encephalopathy characterized by early onset epilepsy and severe intellectual disability. CDD is caused by mutations in the X-linked cyclin …
C Fuchs, G Medici, S Trazzi, L Gennaccaro… - Brain …, 2019 - search.ebscohost.com
CDKL5 deficiency disorder (CDD) is a rare encephalopathy characterized by early onset epilepsy and severe intellectual disability. CDD is caused by mutations in the X‐linked cyclin …
C Fuchs, G Medici, S Trazzi, L Gennaccaro… - Brain …, 2019 - ncbi.nlm.nih.gov
CDKL5 deficiency disorder (CDD) is a rare encephalopathy characterized by early onset epilepsy and severe intellectual disability. CDD is caused by mutations in the X‐linked cyclin …
C Fuchs, G Medici, S Trazzi, L Gennaccaro, G Galvani… - Brain Pathology, 2019 - cir.nii.ac.jp
CDKL5 deficiency predisposes neurons to cell death through the deregulation of SMAD3 signaling | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …