Search research articles
Contact Us
Filters
Showing results (21-30 of 34) with videos related to
Page
of 4
Sort By:
Journal of Human Genetics
|
March 27, 2010
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation
Shozo Honda, Koji O Orii, Junya Kobayashi, et al.
Epilepsy Research
|
November 26, 2013
Genetic variations of immunoregulatory genes associated with Rasmussen syndrome
Yukitoshi Takahashi, Yukiko Mogami, June Mine, et al.
Orthopaedic Surgery
|
September 15, 2023
Levodopa-Carbidopa Intestinal Gel Injection for Patient with Severe Parkinson's Disease Followed by Total Hip Arthroplasty: A Case Report and Literature Review
Atsushi Imamura, Gen Kuroyanagi, Takuya Usami, et al.
Digestive Diseases and Sciences
|
September 16, 2006
Recurrent hepatitis C after living donor liver transplantation detected by Tc-99m GSA liver scintigraphy
Masaki Kaibori, Sang Kil Ha-Kawa, Yoichiro Uchida, et al.
Brain & Development
|
September 2, 2014
Effect of levetiracetam in acute encephalitis with refractory, repetitive partial seizures during acute and chronic phase
Riyo Ueda, Yoshiaki Saito, Koyo Ohno, et al.
Clinical & Developmental Immunology
|
December 13, 2006
Vaccination and infection as causative factors in Japanese patients with Rasmussen syndrome: molecular mimicry and HLA class I
Yukitoshi Takahashi, Kazumi Matsuda, Yuko Kubota, et al.
Congenital Anomalies
|
February 18, 2025
Severe pharyngeal stenosis and laryngomalacia in an individual of HNRNPU-related neurodevelopmental disorder associated with a novel nonsense variant
Yusuke Sasaki, Hiroaki Murakami, Yukiko Kuroda, et al.
Clinical Journal of Gastroenterology
|
June 4, 2015
A case of a teenage boy with eosinophilic gastroenteritis with esophageal involvement developing a hemorrhagic duodenal ulcer
Kenji Yamazaki, Tatsuya Sakashita, Hitoshi Iwata, et al.
Brain & Development
|
October 17, 2016
The first report of Japanese patients with asparagine synthetase deficiency
Takahiro Yamamoto, Wakaba Endo, Hidenori Ohnishi, et al.
Brain & Development
|
February 13, 2003
Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L
Naohide Shiroma, Naomi Kanazawa, Zenichiro Kato, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Journal of Human Genetics
|
March 27, 2010
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation
Shozo Honda, Koji O Orii, Junya Kobayashi, et al.
Epilepsy Research
|
November 26, 2013
Genetic variations of immunoregulatory genes associated with Rasmussen syndrome
Yukitoshi Takahashi, Yukiko Mogami, June Mine, et al.
Orthopaedic Surgery
|
September 15, 2023
Levodopa-Carbidopa Intestinal Gel Injection for Patient with Severe Parkinson's Disease Followed by Total Hip Arthroplasty: A Case Report and Literature Review
Atsushi Imamura, Gen Kuroyanagi, Takuya Usami, et al.
Digestive Diseases and Sciences
|
September 16, 2006
Recurrent hepatitis C after living donor liver transplantation detected by Tc-99m GSA liver scintigraphy
Masaki Kaibori, Sang Kil Ha-Kawa, Yoichiro Uchida, et al.
Brain & Development
|
September 2, 2014
Effect of levetiracetam in acute encephalitis with refractory, repetitive partial seizures during acute and chronic phase
Riyo Ueda, Yoshiaki Saito, Koyo Ohno, et al.
Clinical & Developmental Immunology
|
December 13, 2006
Vaccination and infection as causative factors in Japanese patients with Rasmussen syndrome: molecular mimicry and HLA class I
Yukitoshi Takahashi, Kazumi Matsuda, Yuko Kubota, et al.
Congenital Anomalies
|
February 18, 2025
Severe pharyngeal stenosis and laryngomalacia in an individual of HNRNPU-related neurodevelopmental disorder associated with a novel nonsense variant
Yusuke Sasaki, Hiroaki Murakami, Yukiko Kuroda, et al.
Clinical Journal of Gastroenterology
|
June 4, 2015
A case of a teenage boy with eosinophilic gastroenteritis with esophageal involvement developing a hemorrhagic duodenal ulcer
Kenji Yamazaki, Tatsuya Sakashita, Hitoshi Iwata, et al.
Brain & Development
|
October 17, 2016
The first report of Japanese patients with asparagine synthetase deficiency
Takahiro Yamamoto, Wakaba Endo, Hidenori Ohnishi, et al.
Brain & Development
|
February 13, 2003
Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L
Naohide Shiroma, Naomi Kanazawa, Zenichiro Kato, et al.
Page
of 4