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  1. Book ; Online ; E-Book: Radiation Oncology and Radiotherapy Part C

    Sato, Ai

    2023  

    Author's details Ai Sato [and three others]
    MeSH term(s) Radiotherapy. ; Radiotherapy, Image-Guided. ; Neoplasms/radiotherapy. ; Biomedical Research.
    Keywords Cancer/Radiotherapy
    Subject code 615.842
    Language English
    Size 1 online resource (226 pages)
    Edition First edition.
    Publisher Elsevier Inc
    Publishing place Kidlington, England
    Document type Book ; Online ; E-Book
    Remark Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    ISBN 0-323-99008-8 ; 0-323-99007-X ; 978-0-323-99008-0 ; 978-0-323-99007-3
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

    Full text online

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  2. Article ; Online: Two Ciona sister species are not just complex, but wonderful: A study of maternal mRNAs to safeguard life on earth.

    Sato, Atsuko

    Genesis (New York, N.Y. : 2000)

    2023  Volume 61, Issue 6, Page(s) e23555

    MeSH term(s) Animals ; RNA, Messenger, Stored ; Ciona ; Ciona intestinalis/genetics ; DNA Transposable Elements
    Chemical Substances RNA, Messenger, Stored ; DNA Transposable Elements
    Language English
    Publishing date 2023-09-28
    Publishing country United States
    Document type Letter
    ZDB-ID 2004544-X
    ISSN 1526-968X ; 1526-954X
    ISSN (online) 1526-968X
    ISSN 1526-954X
    DOI 10.1002/dvg.23555
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 2772: Show issues Location:
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  3. Article: [The treatment development for T cell acute lymphoblastic leukemia in children, adolescents, and young adults].

    Sato, Atsushi

    Rinsho ketsueki] The Japanese journal of clinical hematology

    2022  Volume 63, Issue 9, Page(s) 1325–1334

    Abstract: T-cell acute lymphoblastic leukemia (T-ALL) accounts for 10%-15% of pediatric ALL, and its frequency increases during the adolescent and young adult (AYA) periods. The improvements in pediatric T-ALL outcomes have been achieved through the treatment ... ...

    Abstract T-cell acute lymphoblastic leukemia (T-ALL) accounts for 10%-15% of pediatric ALL, and its frequency increases during the adolescent and young adult (AYA) periods. The improvements in pediatric T-ALL outcomes have been achieved through the treatment intensification strategies addressing the cranial radiotherapy omission issue. Furthermore, pediatric-inspired regimens have been adopted for AYA patients with T-ALL, improving outcomes. In Japan, the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) ALL-T11/JALSG T-ALL-211-U trial has been conducted for newly diagnosed patients with T-ALL aged <25 years and has been shown to have excellent outcomes. While early T cell precursor ALL is not an obvious poor prognostic factor in recent treatment strategies for pediatric T-ALL, the minimal residual disease (MRD) has been recognized as the most reliable prognostic indicator. Therefore, MRD is now widely used in T-ALL clinical trials for risk stratification and stem cell transplantation indications. Further progress in the novel therapeutic approaches can potentially improve the outcomes of pediatric and AYA patients with T-ALL.
    MeSH term(s) Adolescent ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Child ; Hematopoietic Stem Cell Transplantation ; Humans ; Neoplasm, Residual ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Precursor T-Cell Lymphoblastic Leukemia-Lymphoma/therapy ; T-Lymphocytes/pathology ; Young Adult
    Language Japanese
    Publishing date 2022-08-31
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 390900-1
    ISSN 0485-1439
    ISSN 0485-1439
    DOI 10.11406/rinketsu.63.1325
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.MO 535: Show issues

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  4. Article: [Treatment strategy for T-cell acute lymphoblastic leukemia in children].

    Sato, Atsushi

    Rinsho ketsueki] The Japanese journal of clinical hematology

    2022  Volume 63, Issue 7, Page(s) 805–815

    Abstract: T-cell acute lymphoblastic leukemia (T-ALL) accounted for approximately 10-15% of pediatric ALL and has often been treated within the same framework as B-cell precursor ALL (BCP-ALL). T-ALL has a poorer prognosis than BCP-ALL. However, improvements have ... ...

    Abstract T-cell acute lymphoblastic leukemia (T-ALL) accounted for approximately 10-15% of pediatric ALL and has often been treated within the same framework as B-cell precursor ALL (BCP-ALL). T-ALL has a poorer prognosis than BCP-ALL. However, improvements have been achieved through treatment intensification strategies using dexamethasone, L-asparaginase, and nelarabine, thereby reducing cranial irradiation. Furthermore, T-ALL-specific treatment protocols have been introduced based on these advancements. The JPLSG ALL-T11/JALSG T-ALL-211-U trial in Japan has been conducted from 2011 to 2017 for newly diagnosed patients with T-ALL under the age of 25 years. The trial included minimal residual disease-based treatment stratification and treatment intensification as described above and has shown excellent outcomes. Recently, new therapeutic agents have been actively developed for T-ALL. Thus, targeted therapy development based on new findings is expected in the future.
    MeSH term(s) Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Asparaginase/therapeutic use ; Child ; Humans ; Neoplasm, Residual ; Precursor T-Cell Lymphoblastic Leukemia-Lymphoma/drug therapy
    Chemical Substances Asparaginase (EC 3.5.1.1)
    Language Japanese
    Publishing date 2022-08-03
    Publishing country Japan
    Document type Clinical Trial ; Journal Article
    ZDB-ID 390900-1
    ISSN 0485-1439
    ISSN 0485-1439
    DOI 10.11406/rinketsu.63.805
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Cultural persistence and the 'herbal medicine paradox': Evidence from European data.

    Costa-Font, Joan / Sato, Azusa

    Journal of health psychology

    2024  , Page(s) 13591053241237031

    Abstract: The use of herbal or traditional medicines has survived the proliferation of modern medicine. The phenomenon has been labeled as the 'herbal medicines paradox' (HMP). We study whether such HMP hypothesis can be explained by the persistence of attitudes ... ...

    Abstract The use of herbal or traditional medicines has survived the proliferation of modern medicine. The phenomenon has been labeled as the 'herbal medicines paradox' (HMP). We study whether such HMP hypothesis can be explained by the persistence of attitudes across cultural boundaries. We undertake a secondary analysis of individual-level migration data to test the persistence of the use of herbal medicines in relation to norms in the person's country of birth (or home country). We study the association between attitudes towards herbal medicine treatments of both first (
    Language English
    Publishing date 2024-04-02
    Publishing country England
    Document type Journal Article
    ZDB-ID 2021897-7
    ISSN 1461-7277 ; 1359-1053
    ISSN (online) 1461-7277
    ISSN 1359-1053
    DOI 10.1177/13591053241237031
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  6. Article: [Neuronal Intranuclear Inclusion Disease(NIID)].

    Sato, Aki

    No shinkei geka. Neurological surgery

    2021  Volume 49, Issue 2, Page(s) 419–424

    Abstract: Neuronal intranuclear inclusion disease(NIID)is a progressive neurodegenerative condition characterized by eosinophilic hyaline intranuclear inclusions in neuronal and other somatic cells. Since 2011, when skin biopsy was proven to be a diagnostic tool, ... ...

    Abstract Neuronal intranuclear inclusion disease(NIID)is a progressive neurodegenerative condition characterized by eosinophilic hyaline intranuclear inclusions in neuronal and other somatic cells. Since 2011, when skin biopsy was proven to be a diagnostic tool, the incidence of NIID has been increasing. Its symptoms include dementia, muscle weakness, and sensory or autonomic disturbance. MRI shows hyperintense lesions of the subcortical white matter, especially on the U-fiber. These findings persist and continue to worsen for years.
    MeSH term(s) Biopsy ; Humans ; Intranuclear Inclusion Bodies ; Magnetic Resonance Imaging ; Neurodegenerative Diseases/diagnostic imaging
    Language Japanese
    Publishing date 2021-03-24
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 197053-7
    ISSN 1882-1251 ; 0301-2603
    ISSN (online) 1882-1251
    ISSN 0301-2603
    DOI 10.11477/mf.1436204408
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: [Mild Encephalopathy with Reversible Splenial Lesion(MERS)].

    Sato, Aki

    No shinkei geka. Neurological surgery

    2021  Volume 49, Issue 2, Page(s) 413–417

    Abstract: Mild encephalitis/encephalopathy with a reversible splenial lesion(MERS)is a clinically and radiologically benign condition that has been described within the past two decades. MRI findings include isolated symmetrical ovoid lesions of the splenium with ... ...

    Abstract Mild encephalitis/encephalopathy with a reversible splenial lesion(MERS)is a clinically and radiologically benign condition that has been described within the past two decades. MRI findings include isolated symmetrical ovoid lesions of the splenium with a high-intensity signal on DWI and decreased apparent diffusion coefficient. These findings have been associated with viral infections, epilepsy, antiepileptic drug usage, and metabolic disturbances, among others. These conditions may present with severe clinical features, such as consciousness disturbance or cytokine storm; however, patients usually recover completely with optimal treatment. Some pathological conditions with splenic lesions, such as Marchiafava-Bignami disease, may be irreversible. Therefore, diseases with splenic lesions require careful attention.
    MeSH term(s) Brain Diseases/diagnostic imaging ; Brain Diseases/drug therapy ; Corpus Callosum/diagnostic imaging ; Diffusion Magnetic Resonance Imaging ; Encephalitis/diagnostic imaging ; Encephalitis/drug therapy ; Humans ; Magnetic Resonance Imaging
    Language Japanese
    Publishing date 2021-03-24
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 197053-7
    ISSN 1882-1251 ; 0301-2603
    ISSN (online) 1882-1251
    ISSN 0301-2603
    DOI 10.11477/mf.1436204407
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: [Autoimmune Encephalitis/Meningitis].

    Sato, Aki

    No shinkei geka. Neurological surgery

    2021  Volume 49, Issue 2, Page(s) 401–406

    Abstract: Less than half of the cases of autoimmune encephalitis have brain MRI abnormalities; however, some patterns of MRI findings help diagnosis. Usually, DWI and FLAIR images reveal hyperintensity lesions in the cortical or subcortical regions or the ... ...

    Abstract Less than half of the cases of autoimmune encephalitis have brain MRI abnormalities; however, some patterns of MRI findings help diagnosis. Usually, DWI and FLAIR images reveal hyperintensity lesions in the cortical or subcortical regions or the cerebellum and/or the brainstem. Hyperintensity lesions in the limbic cortex on DWI suggest NMDAR encephalitis. RA or polychondritis-related meningitis show bright dot or linear signals on the convexities on DWI. Area postrema syndrome is a typical form of neuromyelitis optica. These conditions need to be diagnosed promptly for effective treatment.
    MeSH term(s) Encephalitis/diagnostic imaging ; Hashimoto Disease/diagnostic imaging ; Humans ; Magnetic Resonance Imaging ; Meningitis/diagnostic imaging
    Language Japanese
    Publishing date 2021-03-24
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 197053-7
    ISSN 1882-1251 ; 0301-2603
    ISSN (online) 1882-1251
    ISSN 0301-2603
    DOI 10.11477/mf.1436204405
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: [Creutzfeldt-Jakob Disease].

    Sato, Aki

    No shinkei geka. Neurological surgery

    2021  Volume 49, Issue 2, Page(s) 407–412

    Abstract: Sporadic Creutzfeldt-Jacob disease(sCJD)is a prion disease presenting with subacute or rapidly progressive dementia with a poor prognosis. Asymmetrical cortical lesions with thalamic involvement are found in sCJD cases, which is similar distribution to ... ...

    Abstract Sporadic Creutzfeldt-Jacob disease(sCJD)is a prion disease presenting with subacute or rapidly progressive dementia with a poor prognosis. Asymmetrical cortical lesions with thalamic involvement are found in sCJD cases, which is similar distribution to status epileptics, but the lesions are not observed in the limbic systems, and they rarely occur in the precentral gyrus. Characteristically, hyperintense abnormal findings are more prominent on DWI than on FLAIR and T2WI. 19.9% of CJD is genetic CJD(gCJD), and CJD with a mutation of codon 180 from valine to isoleucine(V180I)accounts for 40% of gCJD in Japan. Patients with this type of gCJD rarely have a family history because of the low penetration rate. The age of onset is usually later, and its clinical symptoms deteriorate more slowly than sCJD. DWI shows abnormal cortical hyperintense signals(cortical ribboning).
    MeSH term(s) Creutzfeldt-Jakob Syndrome/diagnostic imaging ; Creutzfeldt-Jakob Syndrome/epidemiology ; Humans ; Japan ; Magnetic Resonance Imaging ; Mutation
    Language Japanese
    Publishing date 2021-03-24
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 197053-7
    ISSN 1882-1251 ; 0301-2603
    ISSN (online) 1882-1251
    ISSN 0301-2603
    DOI 10.11477/mf.1436204406
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Atypical azygos continuation of the caudal vena cava in a dog.

    Masuyama, A / Sato, A / Murakami, M

    The Journal of small animal practice

    2023  Volume 65, Issue 2, Page(s) 150

    MeSH term(s) Dogs ; Animals ; Vena Cava, Inferior/diagnostic imaging ; Longitudinal Studies
    Language English
    Publishing date 2023-10-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 410743-3
    ISSN 1748-5827 ; 0022-4510 ; 1748-5827
    ISSN (online) 1748-5827
    ISSN 0022-4510 ; 1748-5827
    DOI 10.1111/jsap.13686
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