Clinical and pidigree study on familial cases of West syndrome in Japan
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-10-01
著者
-
SUGAI Kenji
National Center Hospital for Mental, Nervous and Muscular Disorders, National Center of Neurology an
-
Fukuyama Yukio
Child Neurological Institute
-
Ishikawa Akashi
Sapporo City Hospital
-
Sugai Kenji
National Center Hospital For Mental Nervous And Muscular Disorders National Center For Neurology And
-
Sugai Kenji
National Center Hospital For Mental Nervous And Muscular Disorders National Center Of Neurology And
-
Hirano Satoru
Ryokuseikai Hospital
-
YASUDA Kimiko
Chiba Prefectural Rehabilitation Center
-
FUJIMOTO Shinji
Nagoya City University
-
OHTSU Mayu
Tokyo Women's Medical University
-
OHTA Hodaka
Okayama University
-
OGAWA Atsushi
Fukuoka University
-
HAMANO Shin-ichiroh
Saitama Children's Medical Center
-
YOSHIOKA Hiroshi
Kyoto Prefectural University of Medicine
-
SEKI Tohru
Keioh University
-
ITOKAZU Naoya
Miyazaki Medical University
-
TAWA Ritsuko
Ehime Prefectural Niihama Hospital
-
Ohtsu Mayu
Tokyo Women's Medical University
-
Hamano Shin-ichiroh
Saitama Children's Medical Center
関連論文
- Single Nucleotide Polymorphisms and Haplotypes of CYP1A2 in a Japanese Population
- Twenty-six Novel Single Nucleotide Polymorphisms and their Frequencies of the NR113 (CAR) Gene in a Japanese Population
- Eleven Novel Single Nucleotide Polymorphisms in the NR1I2 (PXR) Gene, Four of which Induce Non-synonymous Amino Acid Alterations
- Effect of NaClO Treatment on Bonding to Root Canal Dentin Using a New Evaluation Method
- Rasmussen Syndrome : Multifocal Spread of Inflammation Suggested from MRI and PET Findings
- Myoclonic-astatic epilepsy of early childhood - clinical and EEG analysis of myoclonic-astatic seizures, and discussions on the nosology of the syndrome
- Severe myoclonic epilepsy in infants - a review based on the Tokyo Women's Medical University series of 84 cases
- Clinical and pidigree study on familial cases of West syndrome in Japan
- Molecular genetic study in Japanese patients with Alexander disease : a novel mutation, R79L
- Siblings of Schwartz-Jampel Syndrome with abnormal muscle computed tomographic findings
- A study of ring 20 chromosome karyotype with epilepsy
- Bibliography of congenital muscular dystrophies : Series V (2001)
- History of clinical identification of West syndrome - in quest after the classic
- Clinical analysis of West syndrome associated with phenylketonuria
- Introduction to Pies and Beardsmore's article
- Thank you for everything-Preface and remarks
- Preface
- Proceedings of the Third Annual Meeting of the Study Group on Seizures in Infancy and Early Childhood, Tokyo, December 18,1999