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/vufind/Search/Results?lookfor=%22Akiyama%2C+Nana%22&type=Person&sort=year
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PubPharm (16)
1
Patient survey on cancer genomic medicine in Japan under the national health insurance system
enthalten in:
Cancer science
| 2024
von
Kage, H.
|
Akiyama, N.
|
Chang, H.
| +20
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2
Patient survey on cancer genomic medicine in Japan under the national health insurance system
enthalten in:
Cancer Science
| 2024
von
Kage, H.
|
Akiyama, N.
|
Chang, H.
| +20
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3
Human resources for administrative work to carry out a comprehensive genomic profiling test in Japan
enthalten in:
Cancer science
| 2023
von
Kage, H.
|
Oda, K.
|
Muto, M.
| +17
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4
Severe spinal cord hypoplasia due to a novel ATAD3A compound heterozygous deletion
enthalten in:
Molecular genetics and metabolism reports
| 2022
von
Ebihara, T.
|
Nagatomo, T.
|
Sugiyama, Y.
| +16
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5
Nonsyndromic arteriopathy and aortopathy and vascular Ehlers-Danlos syndrome causing COL3A1 variants
enthalten in:
American journal of medical genetics. Part A
| 2022
von
Yagi, H.
|
Takeda, N.
|
Amiya, E.
| +7
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6
Prenatal Diagnosis of Severe Mitochondrial Diseases Caused by Nuclear Gene Defects: A Study in Japan
enthalten in:
ResearchSquare.com
| 2022
von
Akiyama, N.
|
Shimura, M.
|
Yamazaki, T.
| +16
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7
Clinical and molecular basis of hepatocerebral mitochondrial DNA depletion syndrome in Japan: Evaluation of outcomes after liver transplantation
enthalten in:
ResearchSquare.com
| 2022
von
Shimura, M.
|
Kuranobu, N.
|
Ogawa-Tominaga, M.
| +21
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8
Clinical and molecular basis of hepatocerebral mitochondrial DNA depletion syndrome in Japan: Evaluation of outcomes after liver transplantation
enthalten in:
ResearchSquare.com
| 2022
von
Shimura, M.
|
Kuranobu, N.
|
Ogawa-Tominaga, M.
| +21
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9
Neonatal-onset mitochondrial disease : clinical features, molecular diagnosis and prognosis
enthalten in:
Archives of disease in childhood. Fetal and neonatal edition
| 2022
von
Ebihara, T.
|
Nagatomo, T.
|
Sugiyama, Y.
| +17
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10
Nonsyndromic arteriopathy and aortopathy and vascular Ehlers–Danlos syndrome causing COL3A1 variants
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2022
von
Yagi, H.
|
Takeda, N.
|
Amiya, E.
| +7
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Orphanet journal of rare diseases
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American Journal of Medical Genetics Part C: Se...
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Archives of disease in childhood. Fetal and neo...
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Journal Article
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570
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DGUOK
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Liver transplantation
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MICOS13
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MPV17
3
Mitochondrial DNA maintenance defects
3
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3
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2
DNA, Mitochondrial
2
Research Support, Non-U.S. Gov't
2
cancer genomic medicine
2
comprehensive genomic profiling
1
ALT, alanine aminotransferase
1
AST, aspartate transaminase
1
ATAD3
1
ATAD3A, ATPase family AAA-domain containing pro...
1
ATAD3B, ATPase family AAA-domain containing pro...
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2024
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