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Masaya Segawa

Showing results (31-40 of 39) with videos related to

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Neurogenetics|December 17, 2002
Multiple founder effects in Japanese families with primary torsion dystonia harboring the GAG deletion in the Tor1A (DYT1) geneTakeshi Ikeuchi, Yoshiko Nomura, Masaya Segawa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2007
Dopa-responsive dystonia (Segawa disease) -like disease accompanied by mental retardation: a case reportEiichiro Nagata, Arifumi Kosakai, Kortaro Tanaka, et al.
The Journal of Perinatal & Neonatal Nursing|September 10, 2003
Effects of phototherapy in neonates on circadian sleep-wake and saliva cortisol level rhythmsMieko Shimada, Masaya Segawa, Makoto Higurashi, et al.
Journal of the Neurological Sciences|July 24, 2012
Diffuse central hypomyelination presenting as 4H syndrome caused by compound heterozygous mutations in POLR3A encoding the catalytic subunit of polymerase IIIYasuo Terao, Hirotomo Saitsu, Masaya Segawa, et al.
Neuropsychologia|March 23, 2011
Initiation and inhibitory control of saccades with the progression of Parkinson's disease - changes in three major drives converging on the superior colliculusYasuo Terao, Hideki Fukuda, Akihiro Yugeta, et al.
Brain & Development|August 27, 2005
A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizuresKazue Kimura, Takashi Sugawara, Emi Mazaki-Miyazaki, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 14, 2012
Deterioration of horizontal saccades in progressive supranuclear palsyYasuo Terao, Hideki Fukuda, Yuichiro Shirota, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2007
Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brainsMasayuki Itoh, Shuhei Ide, Sachio Takashima, et al.
Kidney International|April 17, 2004
Familial juvenile hyperuricemic nephropathy: detection of mutations in the uromodulin gene in five Japanese familiesEiji Kudo, Naoyuki Kamatani, Osamu Tezuka, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Neurogenetics|December 17, 2002
Multiple founder effects in Japanese families with primary torsion dystonia harboring the GAG deletion in the Tor1A (DYT1) geneTakeshi Ikeuchi, Yoshiko Nomura, Masaya Segawa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2007
Dopa-responsive dystonia (Segawa disease) -like disease accompanied by mental retardation: a case reportEiichiro Nagata, Arifumi Kosakai, Kortaro Tanaka, et al.
The Journal of Perinatal & Neonatal Nursing|September 10, 2003
Effects of phototherapy in neonates on circadian sleep-wake and saliva cortisol level rhythmsMieko Shimada, Masaya Segawa, Makoto Higurashi, et al.
Journal of the Neurological Sciences|July 24, 2012
Diffuse central hypomyelination presenting as 4H syndrome caused by compound heterozygous mutations in POLR3A encoding the catalytic subunit of polymerase IIIYasuo Terao, Hirotomo Saitsu, Masaya Segawa, et al.
Neuropsychologia|March 23, 2011
Initiation and inhibitory control of saccades with the progression of Parkinson's disease - changes in three major drives converging on the superior colliculusYasuo Terao, Hideki Fukuda, Akihiro Yugeta, et al.
Brain & Development|August 27, 2005
A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizuresKazue Kimura, Takashi Sugawara, Emi Mazaki-Miyazaki, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 14, 2012
Deterioration of horizontal saccades in progressive supranuclear palsyYasuo Terao, Hideki Fukuda, Yuichiro Shirota, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2007
Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brainsMasayuki Itoh, Shuhei Ide, Sachio Takashima, et al.
Kidney International|April 17, 2004
Familial juvenile hyperuricemic nephropathy: detection of mutations in the uromodulin gene in five Japanese familiesEiji Kudo, Naoyuki Kamatani, Osamu Tezuka, et al.
Pageof 4