Hasil Pencarian - Ieva Grinfelde

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  1. 1
    Treatment of latent tuberculosis in a child with mucopolysaccharidosis type I receiving enzyme replacement therapy: A case report

    Treatment of latent tuberculosis in a child with mucopolysaccharidosis type I receiving enzyme replacement therapy: A case report oleh Lauma Vasilevska, Madara Auzenbaha, Madara Auzenbaha, Ieva Grinfelde, Ieva Grinfelde, Anita Skangale

    Diterbitkan 2022-08-01
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  2. 2
    Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study

    Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study oleh Baiba Lace, Sander Pajusalu, Sander Pajusalu, Sander Pajusalu, Diana Livcane, Ieva Grinfelde, Ieva Grinfelde, Ilze Akota, Ieva Mauliņa, Biruta Barkāne, Janis Stavusis, Inna Inashkina

    Diterbitkan 2022-02-01
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  3. 3
    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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  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 of Inherited Partial AZFa Deletion without Impact on Male Fertility

    Case of Inherited Partial AZFa Deletion without Impact on Male Fertility oleh Baiba Alksere, Dace Berzina, Alesja Dudorova, Una Conka, Santa Andersone, Evija Pimane, Sandra Krasucka, Arita Blumberga, Aigars Dzalbs, Ieva Grinfelde, Natalija Vedmedovska, Violeta Fodina, Juris Erenpreiss

    Diterbitkan 2019-01-01
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  6. 6
    A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia: Case report

    A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia: Case report oleh Baiba Alksere, Liene Kornejeva, Ieva Grinfelde, Aigars Dzalbs, Dace Enkure, Una Conka, Santa Andersone, Arita Blumberga, Liene Nikitina-Zake, Liga Kangare, Ilze Radovica-Spalvina, Inta Vasiljeva, Linda Gailite, Juris Erenpreiss, Violeta Fodina

    Diterbitkan 2021-12-01
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