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No to Hattatsu = Brain and Development|December 10, 2013
[The association of hypocarnitinemia with enteral diets and antiepileptic drugs in children and adults with severe physical and mental disabilities]Akiko Wakisaka, Yo Niida, Shinya Yamada, et al.Ophthalmology|December 6, 2005
Amniotic membrane transplantation in acute phase of toxic epidermal necrolysis with severe corneal involvementAkira Kobayashi, Tsuyoshi Yoshita, Kazuhisa Sugiyama, et al.Journal of Human Genetics|February 8, 2013
Mutational analysis of TSC1 and TSC2 in Japanese patients with tuberous sclerosis complex revealed higher incidence of TSC1 patients than previously reportedYo Niida, Akiko Wakisaka, Takanori Tsuji, et al.Brain & Development|July 26, 2011
A case of acute encephalopathy with hemophagocytic lymphohistiocytosis and clonal T-cell expansionTaizo Wada, Kashiku Nishiura, Mondo Kuroda, et al.Cancer Genetics and Cytogenetics|October 11, 2005
Inactivation patterns of NF2 and DAL-1/4.1B (EPB41L3) in sporadic meningiomaFabio Nunes, Yiping Shen, Yo Niida, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|November 14, 2017
Diffusion tensor imaging and magnetic resonance spectroscopy in a patient with adult onset tuberous sclerosis complexHidehiro Ishikawa, Atsushi Niwa, Masaru Asahi, et al.American Journal of Medical Genetics. Part A|March 9, 2007
Clinical and molecular cytogenetic characterization of two patients with non-mutational aberrations of the FMR2 geneShozo Honda, Shin Hayashi, Mitsuhiro Kato, et al.The Tokai Journal of Experimental and Clinical Medicine|June 20, 2025
Multifocal Micronodular Pneumocyte Hyperplasia and Osteosclerotic Lesions in a Patient with Tuberous Sclerosis Complex Misdiagnosed with Lung AdenocarcinomaMasami Ishimaru, Hiroto Takiguchi, Saya Miyahara, et al.Frontiers in Oncology|June 6, 2022
Genomics of Tumor Origin and Characteristics for Adenocarcinoma and Malignant Pleural Mesothelioma: A Case ReportKatsuo Usuda, Yo Niida, Masahito Ishikawa, et al.Atherosclerosis Plus|April 14, 2025
A male patient with pseudoxanthoma elasticum caused by isodisomy of chromosome 16 containing a nonsense variant of the ABCC6 gene: A quarter-century treatment experienceMinoru Wakasa, Chihiro Nakagawa, Taka-Aki Takamura, et al.Pageof 10