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Brain & Development
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January 20, 2004
Pyruvate dehydrogenase E1alpha subunit deficiency in a female patient: evidence of antenatal origin of brain damage and possible etiology of infantile spasms
Naoko Wada, Toyojiro Matsuishi, Michiko Nonaka, et al.
No to Hattatsu = Brain and Development
|
January 7, 2015
[Successful treatment of epilepsy and circadian rhythm disturbance with levetiracetam in a patient with dentatorubral-pallidoluysian atrophy (DRPLA)]
Shigeaki Hamada, Seishi Shimakawa, Shigeko Satomura, et al.
No to Hattatsu = Brain and Development
|
July 27, 2004
[Case of methylmalonic acidemia presenting clinically Leigh encephalopathy]
Hiromichi Ito, Kenji Mori, Michinori Ito, et al.
Brain & Development
|
March 9, 2011
Transient left temporal lobe lesion in Menkes disease may influence the generation of tonic spasms
Hiromichi Ito, Kenji Mori, Miho Sakata, et al.
Journal of the Neurological Sciences
|
August 7, 2002
Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency
Etsuo Naito, Michinori Ito, Ichiro Yokota, et al.
Clinical Endocrinology
|
October 12, 2004
Plasma adiponectin levels in newborns are higher than those in adults and positively correlated with birth weight
Yumiko Kotani, Ichiro Yokota, Seiko Kitamura, et al.
Brain & Development
|
April 2, 2011
Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene
Yasutoshi Koga, Nataliya Povalko, Koujyu Katayama, et al.
Pediatric Neurology
|
April 17, 2002
Three novel SURF-1 mutations in Japanese patients with Leigh syndrome
Yukiko Ogawa, Etsuo Naito, Michinori Ito, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
August 2, 2005
Stable-isotope dilution gas chromatography-mass spectrometric measurement of 3-hydroxyglutaric acid, glutaric acid and related metabolites in body fluids of patients with glutaric aciduria type 1 found in newborn screening
Yosuke Shigematsu, Ikue Hata, Yukie Tanaka, et al.
Pediatric Neurology
|
August 10, 2005
Thiamine-responsive congenital lactic acidosis: clinical and biochemical studies
Mitsuo Toyoshima, Akira Oka, Yoshiko Egi, et al.
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Search research articles
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Showing results (1-10 of 17) with videos related to
Sort By:
Page
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Brain & Development
|
January 20, 2004
Pyruvate dehydrogenase E1alpha subunit deficiency in a female patient: evidence of antenatal origin of brain damage and possible etiology of infantile spasms
Naoko Wada, Toyojiro Matsuishi, Michiko Nonaka, et al.
No to Hattatsu = Brain and Development
|
January 7, 2015
[Successful treatment of epilepsy and circadian rhythm disturbance with levetiracetam in a patient with dentatorubral-pallidoluysian atrophy (DRPLA)]
Shigeaki Hamada, Seishi Shimakawa, Shigeko Satomura, et al.
No to Hattatsu = Brain and Development
|
July 27, 2004
[Case of methylmalonic acidemia presenting clinically Leigh encephalopathy]
Hiromichi Ito, Kenji Mori, Michinori Ito, et al.
Brain & Development
|
March 9, 2011
Transient left temporal lobe lesion in Menkes disease may influence the generation of tonic spasms
Hiromichi Ito, Kenji Mori, Miho Sakata, et al.
Journal of the Neurological Sciences
|
August 7, 2002
Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency
Etsuo Naito, Michinori Ito, Ichiro Yokota, et al.
Clinical Endocrinology
|
October 12, 2004
Plasma adiponectin levels in newborns are higher than those in adults and positively correlated with birth weight
Yumiko Kotani, Ichiro Yokota, Seiko Kitamura, et al.
Brain & Development
|
April 2, 2011
Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene
Yasutoshi Koga, Nataliya Povalko, Koujyu Katayama, et al.
Pediatric Neurology
|
April 17, 2002
Three novel SURF-1 mutations in Japanese patients with Leigh syndrome
Yukiko Ogawa, Etsuo Naito, Michinori Ito, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
August 2, 2005
Stable-isotope dilution gas chromatography-mass spectrometric measurement of 3-hydroxyglutaric acid, glutaric acid and related metabolites in body fluids of patients with glutaric aciduria type 1 found in newborn screening
Yosuke Shigematsu, Ikue Hata, Yukie Tanaka, et al.
Pediatric Neurology
|
August 10, 2005
Thiamine-responsive congenital lactic acidosis: clinical and biochemical studies
Mitsuo Toyoshima, Akira Oka, Yoshiko Egi, et al.
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of 2