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Kei Murayama

Juntendo University

SCHOLARLY PAPERS

2

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167

TOTAL CITATIONS

0

Scholarly Papers (2)

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1.

Successful Diagnosis of Sengers Syndrome Using a Comprehensive Genomic Analysis

Number of pages: 20 Posted: 29 Jan 2024
Kohta Nakamura, Yukiko Yatsuka, Sachie Naito, Akira Hasegawa, Takeya Kasukawa, Atsushi Kondo, Yoshihito Kishita, Yohei Sugiyama, Takanori Onuki, Tomohiro Ebihara, Tomoko Tsuruoka, Takuya Fushimi, Akira Ohtake, Kei Murayama, Atsuko Imai-Okazaki and Yasushi Okazaki
Juntendo University, Juntendo University, JCHO Funabashi Central Hospital, RIKEN Center for Integrative Medical Sciences, RIKEN Center for Integrative Medical Sciences, RIKEN Center for Integrative Medical Sciences, Kindai University, Juntendo University - Juntendo University Hospital, Chiba Children's Hospital, Chiba Children's Hospital, Chiba Children's Hospital, Chiba Children's Hospital, Saitama Medical University, Juntendo University, Juntendo University and Juntendo University
Downloads 117 (608,822)

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mitochondrial disease, mitochondrial DNA depletion syndrome, mitochondrial respiratory chain complex deficiencies, Sengers Syndrome, Genetic analysis

2.

Focal Segmental Glomerulosclerosis with a Mutation in the Mitochondrially Encoded Nadh Dehydrogenase 5 Gene: A Case Report

Number of pages: 30 Posted: 20 Dec 2022
Tsukasa Naganuma, Toshiyuki Imasawa, Ikuo Nukui, Masakiyo Wakasugi, Hiroshi Kitamura, Yukiko Yatsuka, Yoshihito Kishita, Yasushi Okazaki, Kei Murayama and Yoshimi Jinguji
affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, Juntendo University, Kindai University, Juntendo University, Juntendo University and affiliation not provided to SSRN
Downloads 50 (1,063,489)

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focal segmental glomerulosclerosis, mitochondrial nephropathy, NADH dehydrogenase 5, Complex I, case report