Zobrazeno 1 - 10
of 180
pro vyhledávání: '"Kenzo Takeshita"'
Autor:
Kenzo Takeshita, Yoshihiro Maegaki, Kousaku Ohno, Gen Nishimura, Atsushi Ieshima, Hiroaki Ehara, Yasushi Utsunomiya
Publikováno v:
American Journal of Medical Genetics Part A. :973-978
We describe a Japanese brother and sister with Martsolf syndrome. They had short stature, severe mental retardation, cataract, hypogonadism, craniofacial dysmorphism, and bone and joint symptoms including scoliosis, lax finger joints, and talipes val
Neuropsychological profiles of patients with 2q37.3 deletion associated with developmental dyspraxia
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (8)
Patients with 2q37 deletions manifest brachydactyly mental retardation syndrome (BDMR). Recent advances in human molecular research have revealed that alterations in the histone deacetylase 4 gene (HDAC4) are responsible for the clinical manifestatio
Autor:
Ayumi Seki, Kenzo Takeshita, Tatsuya Koeda, Shuji Sugihara, Yoshiharu Hirata, Masayuki Kamba, Toshihide Ogawa
Publikováno v:
Brain and Development. 23:312-316
A functional magnetic resonance imaging (fMRI) study during Japanese 'kana' readings was performed on Japanese dyslexic children. Five dyslexic children (aged 9-12 years) and five healthy children (aged 9-11 years) were investigated. The fMRI examina
Publikováno v:
Brain and Development. 23:58-61
A Japanese girl with peculiar leukoencephalopathy was reported. Following normal development until 1 year of age, she showed progressive neurological deterioration with ataxia, epilepsy, pyramidal tract signs and choreic movement. Serial brain comput
Autor:
Kenzo Takeshita, Kyoichi Ohtani
Publikováno v:
Congenital Anomalies. 40:269-274
In detecting changes of the occurrence of birth malformation it is important to indicate the prevalence of environmental hazards. The Tottori Monitoring System for Birth Defects (TOM) is a small regional system covering 6,000 births yearly which was
Autor:
Sumimasa Yamashita, Kenzo Takeshita, Robert A. Good, Kenji Nihei, Toshiro Hara, Nobuo Koide, Hideo Aiba
Publikováno v:
Journal of Neurovirology. 6:121-126
Live measles virus-specific T helper 1/T helper 2-cytokine productions by peripheral blood mononuclear cells in response to live measles, mumps or varicella virus were measured in 15 patients with subacute sclerosing panencephalitis and 15 controls b
Publikováno v:
Headache: The Journal of Head and Face Pain. 39:280-286
Twenty women with migraine were evaluated by EEG coherence analysis. In comparison with controls, the migrainous subjects showed lower interhemispheric coherence values at C3-C4 for the delta band (P=0.0030) and at F3-F4 (P=0.0055) and C3-C4 (P=0.001
Publikováno v:
Brain and Development. 21:184-191
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by epilepsy, mental retardation and hamartomatous lesions in multiple organs. It has been shown that the genes responsible for TSC, TSC1 and TSC2, act as tumor suppresso
Publikováno v:
Clinica Chimica Acta. 279:47-54
1H NMR spectroscopy is a promising method for the analysis of physiological fluids in clinical medicine. In the course of screening the urine of patients by 1D- and pulsed-field gradient 2D 1H NMR spectroscopy at 500 MHz, we encountered a case with a
Publikováno v:
Pediatric Neurology. 19:199-203
The authors studied the epidemiology of spina bifida in Tottori Prefecture, Japan, from 1976 to 1995. Thirty-four patients (16 men and 18 women) were registered in this study. Consanguineous marriages, familial occurrence, and abnormalities in prenat