Multi-institutional study on the correlation between chromosomal abnormalities and epilepsy
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J. Tohyama | H. Hattori | T. Kanda | Y. Yamori | Naoko Yoshida | Haruyo Hirota | T. Okuno | O. Kanazawa | M. Sasagawa | Noriyuki Akasaka | Masatoshi Ito | M. Yoshioka | T. Kumada | T. Fujii | K. Mutoh | T. Miyajima | Hideki Amagane | Kenichiro Kobayashi | T. Go | Y. Hamada | Takanori Kamimura | Rieko Tanaka
[1] J. Roger,et al. Epileptic Syndromes in Infancy, Childhood and Adolescence , 2005 .
[2] J. Stephenson. Autonomic seizures in 18q- syndrome , 2005, Brain and Development.
[3] Wang-Tso Lee,et al. Electroclinical characteristics of seizures—comparing Prader-Willi syndrome with Angelman syndrome , 2005, Brain and Development.
[4] S. G. Boyd,et al. The EEG in early diagnosis of the Angelman (Happy Puppet) syndrome , 1988, European Journal of Pediatrics.
[5] E. Niebuhr. The cri du chat syndrome , 1978, Human Genetics.
[6] T. Okuno,et al. [Intractable epilepsy (apneic seizure) in an infant with 18q deletion syndrome]. , 2003, No to hattatsu = Brain and development.
[7] I. Scheffer,et al. Chromosomal Abnormalities and Epilepsy: A Review for Clinicians and Gene Hunters , 2002, Epilepsia.
[8] A. Battaglia,et al. Wolf-Hirschhorn (4p-) syndrome. , 2005, Advances in pediatrics.
[9] A. Schinzel,et al. Chromosome imbalances associated with epilepsy. , 2001, American journal of medical genetics.
[10] G. Ayala,et al. Chromosome Abnormalities and Epilepsy , 2001, Epilepsia.
[11] W. Oertel,et al. Autonomic Seizures Versus Syncope in 18q‐ Deletion Syndrome: A Case Report , 2000, Epilepsia.
[12] R. Olsen,et al. Angelman syndrome: Correlations between epilepsy phenotypes and genotypes , 1998, Annals of neurology.
[13] 井上有史. Ring chromosome 20 and nonconvulsive status epilepticus: A new epileptic syndrome(環状20番染色体と非けいれん発作重延: 新しいてんかん症候群) , 1998 .
[14] A. Battaglia,et al. The inv dup(15) syndrome , 1997, Neurology.
[15] H. Stroink,et al. Evolution of Epilepsy and EEG Findings in Angelman Syndrome , 1997, Epilepsia.
[16] R. Guerrini,et al. Early Clinical and EEG Features of Infantile Spasms in Down Syndrome , 1996, Epilepsia.
[17] L. Minotti,et al. 4p‐ Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern , 1995, Epilepsia.
[18] G. Lanzi,et al. Seizure and EEG Patterns in Angelman's Syndrome , 1995, Journal of child neurology.
[19] R. Pauli,et al. Investigation of thermoregulatory characteristics in patients with Prader-Willi syndrome. , 1994, American journal of medical genetics.
[20] Jean Aicardi,et al. Diseases of the Nervous System in Childhood , 1993 .
[21] A. Chudley,et al. Recognizable behavioral and somatic phenotype in patients with proximal interstitial 18q deletion: report on a new affected child and follow-up on the original reported familial cases. , 1992, American journal of medical genetics.
[22] G. Sekhon,et al. Monosomy 18q12.1----21.1: a recognizable aneuploidy syndrome? Report of a patient and review of the literature. , 1992, American journal of medical genetics.
[23] A. Aylsworth,et al. Neurological aspects of del(1q) syndrome. , 1991, American journal of medical genetics.
[24] K. Wisniewski,et al. SEIZURES IN CHILDREN WITH DOWN SYNDROME: ETIOLOGY, CHARACTERISTICS AND OUTCOME , 1991, Developmental medicine and child neurology.
[25] S. Pueschel,et al. Seizure disorders in Down syndrome. , 1991, Archives of neurology.
[26] K. Takeshita,et al. Chromosome abnormalities and epileptic seizures , 1988, Japanese Journal of Human Genetics.
[27] H. Gastaut,et al. LISSENCEPHALY(AGYRIA‐PACHYGYRIA): CLINICAL FINDINGS AND SERIAL EEG STUDIES , 1987 .
[28] R. Pauli,et al. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome. , 1986, American journal of medical genetics.
[29] Y. Kuroki,et al. Epilepsy in childhood down syndrome , 1984, Brain and Development.
[30] I. Forsman,et al. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]. , 1979, American journal of medical genetics.
[31] W. E. Nelson. Textbook of Pediatrics , 1969 .
[32] T. Clendenin. Chromosomal abnormalities. , 1966, Clinical obstetrics and gynecology.