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Akira Ohtake, San Francisco, US, Union St
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Akira Patrick Ohtake, San Francisco, US, 37th Ave
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Akira Patrick Ohtake, San Francisco, US, California St, Apt 9
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Books & Literature
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of...
doaj.org
Mitochondrial disorders have the highest incidence among congenital metabolic disorders characterized by biochemical respiratory chain complex...
Akira Ohtake | XanEdu Customization Platform
www.academicpub.com
Author: Akira Ohtake. Results. Intractable secretory diarrhea in a Japanese boy with mitochondrial respiratory chain complex I deficiency Springer ...
Oxidative Phosphorylation in Health and Disease - Google Books
books.google.de
Mitochondrial diseases are often hard to diagnose. From the time they were first researched without animal models, patients of mitochondrial diseases were of...
JIMD Reports, Volume Google Books
books.google.de
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously...
Related Documents
CiteSeerX — Analysis of the assembly profiles for mitochondrial- and...
citeseerx.ist.psu.edu
Analysis of the assembly profiles for mitochondrial- and nuclear-DNA ... Akira Ohtake ... the assembly profiles for mitochondrial- and nuclear ...
Deficiency of ECHS 1 causes mitochondrial encephalopathy with cardiac...
www.deepdyve.com
Peter Freisinger , Sandra Eggimann. 3. , Akira Ohtake , Yasushi. Okazaki. 13,14. , Masakazu Kohda , Yoshihito Kishita , Yoshimi Tokuzawa. 14.
Analysis of the Assembly Profiles for Mitochondrial-and ...
citeseerx.ist.psu.edu
Michael Lazarou,1 Matthew McKenzie,1 Akira Ohtake,1,2 David R. Thorburn,3 and Michael T. Ryan1*. Department of Biochemistry, La Trobe University,
EBSCOhost | | Improvements of hypertriglyceridemia and...
web.b.ebscohost.com
Hironori Nagasaka & Ken-ichi Hirano & Akira Ohtake &. Takashi Miida & Tomozumi Takatani & Kei Murayama &. Tohru Yorifuji & Kunihiko Kobayashi &.
Scientific Publications
COQ4 Mutations Cause a Broad Spectrum of Mitochondrial Disorders...
www.sciencedirect.com
Gloria Brea-Calvo,,; Tobias B. Haack,,,; Daniela Karall,,; Akira Ohtake,; Federica Invernizzi,; Rosalba Carrozzo,; Laura Kremer,,; Sabrina Dusi, ...
Publications
A case of transient neonatal citrullinemia | SpringerLink
link.springer.com
A male infant with transient citrullinemia is described. Initially, he was found to have hypertyrosinemia and hypermethioninemia upon routine neonatal scre
Mitochondrial Protein Complexes and Disease
www.amdf.org.au
Mitochondrial Protein Complexes and Disease Dr Matthew McKenzie (Head) ... Akira Ohtake (Saitama University) Kei Murayama (Chiba Children’s Hospital)
Reports & Statements
Expression analysis of two mutant human ornithine transcarbamylases...
www.nature.com
Expression analysis of two mutant human ornithine transcarbamylases ... Akira Ohtake · Masataka Mori · Hiroo Niimi Received: July 25, Accepted: ...
JapanSylvian.com • View topic - 'Glowing Enigmas' Photographic...
www.japansylvian.com
Then, leading British painter, Russell Mills (and Russell, Akira Ohtake and friendly relationship with Brian Eno is well known) in collaboration ...
Compound heterozygous GFM2 mutations with Leigh syndrome complicated...
www.nature.com
Original Article
Miscellaneous
Akira Ohtake | Saitama Medical University - Academia.edu
saitama-med.academia.edu
Academia.edu is a place to share and follow research.
ASMRM Shinagawa JP - Bioblast
www.bioblast.at
ASMRM Shinagawa JP. Shinagawa JP, Oct Akira Ohtake, Department of Pediatrics, Saitama Medical University Listed under MitoGlobal Events.
A unique mutation of ALK2, G356D, found in a patient with...
www.infona.pl
... Kohei Miyazono, Konosuke Nakayama, Akira Nanba, Hiroshi Tomoda, Yasushi Okazaki, Akira Ohtake, Hiromi Oda, Ichiro Owan, ...[ more ].
Compound heterozygous GFM2 mutations with Leigh syndrome complicated...
scifeeds.com
Defects in the mitochondrial translation apparatus can impair energy production in affected tissues and organs. Most components of this apparatus are encoded...
Hypertrophic trigeminal nerves: Moustache sign Khadilkar SV, Visana...
www.neurologyindia.com
Neurol India is an peer-reviewed biomedical periodical of Neurological Society of India.
JCI - NDUFS6 mutations are a novel cause of lethal neonatal...
www.jci.org
Denise M. Kirby,1,2,3 Renato Salemi,1 Canny Sugiana,1,3Akira Ohtake,4 Lee Parry,1 Katrina M. Bell,1 Edwin P. Kirk,5 Avihu Boneh,1,2,3 ...
Johannes A Mayr - Publications List
publicationslist.org
Gloria Brea-Calvo, Tobias B Haack, Daniela Karall, Akira Ohtake, Federica Invernizzi, Rosalba Carrozzo, Laura Kremer, Sabrina Dusi, Christine Fauth, Sabine ...
Masashi Tanaka - Publications List
publicationslist.org
Hirofumi Komaki, Yutaka Nishigaki, Noriyuki Fuku, Hiroko Hosoya, Kei Murayama, Akira Ohtake, Yu-Ichi Goto, Hiroyuki Wakamoto, Yasutoshi Koga, Masashi ...
PLOS Genetics: Publishing science, accelerating research
journals.plos.org
... Takuya Fushimi, Masaru Shimura, Keiko Kaiho-Ichimoto, Hiroko Harashima, Taro Yamazaki, Masato Mori, Kei Murayama, Akira Ohtake, Yasushi Okazaki.
ポスター発表 – 第5回生命医薬情報学連合大会（IIBMP2016）
www.jsbi.org
... Mizuno, Atsuko Imai, Akihiro Nakaya, Tomoko Hirata, Yukiko Yatsuka, Nurun Borna, Hiroko Harashima, Kei Murayama, Akira Ohtake and Yasushi Okazaki.
第8回日本ミトコンドリア学会年会
www.j-mit.org
Masato Mori 1), Tamako Goto 1), Hiroko Harashima 2), Kei Murayama 3), Akira Ohtake 2), Mariko Y Momoi 1) (Department of Pediatrics, Jichi Medical University ...
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