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Noriko Aida

Showing results (31-40 of 112) with videos related to

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American Journal of Medical Genetics. Part A|May 13, 2006
Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndromeToshiyuki Yamamoto, Kiyoko Sameshima, Ken-ichi Sekido, et al.
Pediatric Neurology|January 19, 2016
Effectiveness of Corticosteroid Therapy for Acute Neurological Symptoms in Incontinentia PigmentiSeiichi Tomotaki, Jun Shibasaki, Yuki Yunoki, et al.
Scientific Reports|January 18, 2020
White matter microstructural changes in tuberous sclerosis: Evaluation by neurite orientation dispersion and density imaging (NODDI) and diffusion tensor imagesToshiaki Taoka, Noriko Aida, Yuta Fujii, et al.
Plos One|December 7, 2013
Neonatal brain metabolite concentrations: an in vivo magnetic resonance spectroscopy study with a clinical MR system at 3 TeslaMoyoko Tomiyasu, Noriko Aida, Mamiko Endo, et al.
The Journal of Pediatrics|August 15, 2021
Comparison of Predictive Values of Magnetic Resonance Biomarkers Based on Scan Timing in Neonatal Encephalopathy Following Therapeutic HypothermiaJun Shibasaki, Tetsu Niwa, Aurélie Piedvache, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 14, 2015
Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutationYumi Asakura, Koji Muroya, Junko Hanakawa, et al.
American Journal of Medical Genetics. Part A|October 21, 2015
Elevation of neuron specific enolase and brain iron deposition on susceptibility-weighted imaging as diagnostic clues for beta-propeller protein-associated neurodegeneration in early childhood: Additional case report and review of the literatureKyoko Takano, Naoko Shiba, Keiko Wakui, et al.
Pediatric Blood & Cancer|January 6, 2010
A prospective study of a long-term follow-up of an observation program for neuroblastoma detected by mass screeningMio Tanaka, Hisato Kigasawa, Keisuke Kato, et al.
Brain & Development|January 21, 2020
Blended phenotype of AP4E1 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15Hiroaki Murakami, Tomoko Uehara, Yoshinori Tsurusaki, et al.
Pediatric Neurology|October 13, 2014
Clinical characteristics and outcomes of Möbius syndrome in a children's hospitalKiyoshi Matsui, Ai Kataoka, Atsuko Yamamoto, et al.
Pageof 12

Showing results (31-40 of 112) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics. Part A|May 13, 2006
Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndromeToshiyuki Yamamoto, Kiyoko Sameshima, Ken-ichi Sekido, et al.
Pediatric Neurology|January 19, 2016
Effectiveness of Corticosteroid Therapy for Acute Neurological Symptoms in Incontinentia PigmentiSeiichi Tomotaki, Jun Shibasaki, Yuki Yunoki, et al.
Scientific Reports|January 18, 2020
White matter microstructural changes in tuberous sclerosis: Evaluation by neurite orientation dispersion and density imaging (NODDI) and diffusion tensor imagesToshiaki Taoka, Noriko Aida, Yuta Fujii, et al.
Plos One|December 7, 2013
Neonatal brain metabolite concentrations: an in vivo magnetic resonance spectroscopy study with a clinical MR system at 3 TeslaMoyoko Tomiyasu, Noriko Aida, Mamiko Endo, et al.
The Journal of Pediatrics|August 15, 2021
Comparison of Predictive Values of Magnetic Resonance Biomarkers Based on Scan Timing in Neonatal Encephalopathy Following Therapeutic HypothermiaJun Shibasaki, Tetsu Niwa, Aurélie Piedvache, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 14, 2015
Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutationYumi Asakura, Koji Muroya, Junko Hanakawa, et al.
American Journal of Medical Genetics. Part A|October 21, 2015
Elevation of neuron specific enolase and brain iron deposition on susceptibility-weighted imaging as diagnostic clues for beta-propeller protein-associated neurodegeneration in early childhood: Additional case report and review of the literatureKyoko Takano, Naoko Shiba, Keiko Wakui, et al.
Pediatric Blood & Cancer|January 6, 2010
A prospective study of a long-term follow-up of an observation program for neuroblastoma detected by mass screeningMio Tanaka, Hisato Kigasawa, Keisuke Kato, et al.
Brain & Development|January 21, 2020
Blended phenotype of AP4E1 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15Hiroaki Murakami, Tomoko Uehara, Yoshinori Tsurusaki, et al.
Pediatric Neurology|October 13, 2014
Clinical characteristics and outcomes of Möbius syndrome in a children's hospitalKiyoshi Matsui, Ai Kataoka, Atsuko Yamamoto, et al.
Pageof 12