Hasil Pencarian - Ieva Micule

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  1. 1
    Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy

    Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy oleh Baiba Lace, Inna Inashkina, Ieva Micule, Inta Vasiljeva, Maruta Solvita Naudina, Jurgis Strautmanis, Janis Stavusis, Eriks Jankevics

    Diterbitkan 2013-01-01
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  2. 2
    Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia

    Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia oleh Arta Katkevica, Madara Kreile, Ieva Grinfelde, Gita Taurina, Ieva Micule, Iveta Dzivite-Krisane, Arta Smite-Laguna, Ieva Malniece

    Diterbitkan 2021-01-01
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  3. 3
    New-Born Screening for Spinal Muscular Atrophy: Results of a Latvian Pilot Study

    New-Born Screening for Spinal Muscular Atrophy: Results of a Latvian Pilot Study oleh Linda Gailite, Olga Sterna, Maija Konika, Aleksejs Isakovs, Jekaterina Isakova, Ieva Micule, Signe Setlere, Mikus Diriks, Madara Auzenbaha

    Diterbitkan 2022-02-01
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  4. 4
    Altered Splicing of <i>LAMP2</i> in a Multigenerational Family from Latvia Affected by Danon Disease

    Altered Splicing of <i>LAMP2</i> in a Multigenerational Family from Latvia Affected by Danon Disease oleh Janis Stavusis, Ieva Micule, Ieva Grinfelde, Anna Zdanovica, Janis Pudulis, Sandra Valeina, Svetlana Sepetiene, Baiba Lace, Inna Inashkina

    Diterbitkan 2024-01-01
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  5. 5
    Case Report: Two Families With HPDL Related Neurodegeneration

    Case Report: Two Families With HPDL Related Neurodegeneration oleh Ieva Micule, Ieva Micule, Baiba Lace, Baiba Lace, Baiba Lace, Nathan T. Wright, Nicolas Chrestian, Jurgis Strautmanis, Mikus Diriks, Janis Stavusis, Dita Kidere, Elfa Kleina, Anna Zdanovica, Nataly Laflamme, Nadie Rioux, Samarth Thonta Setty, Sander Pajusalu, Sander Pajusalu, Sander Pajusalu, Arnaud Droit, Monkol Lek, Serge Rivest, Inna Inashkina

    Diterbitkan 2022-02-01
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  6. 6
    The most common European HINT1 neuropathy variant phenotype and its case studies

    The most common European HINT1 neuropathy variant phenotype and its case studies oleh Marija Rozevska, Dmitrijs Rots, Dmitrijs Rots, Linda Gailite, Ronalds Linde, Stanislavs Mironovs, Maksims Timcenko, Viktors Linovs, Dzintra Locmele, Ieva Micule, Baiba Lace, Viktorija Kenina, Viktorija Kenina, Viktorija Kenina

    Diterbitkan 2023-02-01
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  7. 7
    Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

    Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders oleh Sen Zhao, Yuanqiang Zhang, Sigrun Hallgrimsdottir, Yuzhi Zuo, Xiaoxin Li, Dominyka Batkovskyte, Sen Liu, Hillevi Lindelöf, Shengru Wang, Anna Hammarsjö, Yang Yang, Yongyu Ye, Lianlei Wang, Zihui Yan, Jiachen Lin, Chenxi Yu, Zefu Chen, Yuchen Niu, Huizi Wang, Zhi Zhao, Pengfei Liu, Guixing Qiu, Jennifer E. Posey, Zhihong Wu, James R. Lupski, Ieva Micule, Britt-Marie Anderlid, Ulrika Voss, Dennis Sulander, Ekaterina Kuchinskaya, Ann Nordgren, Ola Nilsson, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Terry Jianguo Zhang, Giedre Grigelioniene, Nan Wu

    Diterbitkan 2022-02-01
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