Hasil Pencarian - Dmitrijs Rots

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  1. 1
    The association of FMR1 gene (CGG)n variation with idiopathic female infertility

    The association of FMR1 gene (CGG)n variation with idiopathic female infertility oleh Adele Grasmane, Dmitrijs Rots, Zane Vitina, Valerija Magomedova, Linda Gailite

    Diterbitkan 2019-05-01
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  2. 2
    Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome

    Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome oleh Linda Gailite, Dmitrijs Rots, Ieva Pukite, Gunta Cernevska, Madara Kreile

    Diterbitkan 2018-10-01
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  3. 3
    Exploring disease-specific metabolite signatures in hereditary angioedema patients

    Exploring disease-specific metabolite signatures in hereditary angioedema patients oleh Adine Kanepa, Jingzhi Fan, Jingzhi Fan, Dmitrijs Rots, Dmitrijs Rots, Annija Vaska, Laura Ansone, Monta Briviba, Janis Klovins, Natalja Kurjane, Natalja Kurjane, Kristaps Klavins, Kristaps Klavins

    Diterbitkan 2024-04-01
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  4. 4
    National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia

    National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia oleh Adine Kanepa, Inga Nartisa, Dmitrijs Rots, Linda Gailite, Henriette Farkas, Natalja Kurjane

    Diterbitkan 2023-04-01
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  5. 5
    Genetic Basis of Early Onset Atrial Fibrillation in Patients without Risk Factors

    Genetic Basis of Early Onset Atrial Fibrillation in Patients without Risk Factors oleh Irina Rudaka, Baiba Vilne, Jekaterina Isakova, Oskars Kalejs, Linda Gailite, Dmitrijs Rots

    Diterbitkan 2023-02-01
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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
    A Higher Polygenic Risk Score Is Associated with a Higher Recurrence Rate of Atrial Fibrillation in Direct Current Cardioversion-Treated Patients

    A Higher Polygenic Risk Score Is Associated with a Higher Recurrence Rate of Atrial Fibrillation in Direct Current Cardioversion-Treated Patients oleh Simon Vogel, Irina Rudaka, Dmitrijs Rots, Jekaterīna Isakova, Oskars Kalējs, Kristīne Vīksne, Linda Gailīte

    Diterbitkan 2021-11-01
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  8. 8
    Genetic landscape of preterm birth due to cervical insufficiency: Comprehensive gene analysis and patient next-generation sequencing data interpretation.

    Genetic landscape of preterm birth due to cervical insufficiency: Comprehensive gene analysis and patient next-generation sequencing data interpretation. oleh Ludmila Volozonoka, Dmitrijs Rots, Inga Kempa, Anna Kornete, Dace Rezeberga, Linda Gailite, Anna Miskova

    Diterbitkan 2020-01-01
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  9. 9
    UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays

    UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays oleh Linda Gailite, Alberto Valenzuela-Palomo, Lara Sanoguera-Miralles, Dmitrijs Rots, Madara Kreile, Eladio A. Velasco

    Diterbitkan 2020-03-01
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  10. 10
    Hereditary or acquired? Comprehensive genetic testing assists in stratifying angioedema patients

    Hereditary or acquired? Comprehensive genetic testing assists in stratifying angioedema patients oleh Marija Rozevska, Adine Kanepa, Signe Purina, Linda Gailite, Inga Nartisa, Henriette Farkas, Dmitrijs Rots, Natalja Kurjane

    Diterbitkan 2024-03-01
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  11. 11
    Long-Term Immunological Memory of SARS-CoV-2 Is Present in Patients with Primary Antibody Deficiencies for up to a Year after Vaccination

    Long-Term Immunological Memory of SARS-CoV-2 Is Present in Patients with Primary Antibody Deficiencies for up to a Year after Vaccination oleh Zane Lucane, Baiba Slisere, Lota Ozola, Dmitrijs Rots, Sindija Papirte, Baiba Vilne, Linda Gailite, Natalja Kurjane

    Diterbitkan 2023-02-01
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  12. 12
    Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism

    Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism oleh Ilze Konrade, Ilze Konrade, Julija Zavorikina, Aija Fridvalde, Dmitrijs Rots, Ieva Kalere, Ilze Strumfa, Maija Dambrova, Linda Gailite

    Diterbitkan 2019-01-01
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  13. 13
    P637: A newly derived DNA methylation signature for Koolen de Vries syndrome addresses the diagnostic challenges of the 17q21.31 locus

    P637: A newly derived DNA methylation signature for Koolen de Vries syndrome addresses the diagnostic challenges of the 17q21.31 locus oleh Zain Awamleh, Sanaa Choufani, Dmitrijs Rots, Alexander Dingemans, Juan Dario Ortigoza Escobar, David Koolen, Bert de Vries, Rosanna Weksberg

    Diterbitkan 2024-01-01
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  14. 14
    Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy

    Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy oleh Elina Millere, Elina Millere, Elina Millere, Dmitrijs Rots, Ieva Glazere, Ieva Glazere, Gita Taurina, Natalja Kurjane, Natalja Kurjane, Viktorija Priedite, Linda Gailite, Kaj Blennow, Kaj Blennow, Henrik Zetterberg, Henrik Zetterberg, Henrik Zetterberg, Henrik Zetterberg, Viktorija Kenina, Viktorija Kenina

    Diterbitkan 2021-01-01
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  15. 15
    A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder

    A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder oleh Lot Snijders Blok, Jolijn Verseput, Dmitrijs Rots, Hanka Venselaar, A. Micheil Innes, Connie Stumpel, Katrin Õunap, Karit Reinson, Eleanor G. Seaby, Shane McKee, Barbara Burton, Katherine Kim, Johanna M. van Hagen, Quinten Waisfisz, Pascal Joset, Katharina Steindl, Anita Rauch, Dong Li, Elaine H. Zackai, Sarah E. Sheppard, Beth Keena, Hakon Hakonarson, Andreas Roos, Nicolai Kohlschmidt, Anna Cereda, Maria Iascone, Erika Rebessi, Kristin D. Kernohan, Philippe M. Campeau, Francisca Millan, Jesse A. Taylor, Hanns Lochmüller, Martin R. Higgs, Amalia Goula, Birgitta Bernhard, Danita J. Velasco, Andrew A. Schmanski, Zornitza Stark, Lyndon Gallacher, Lynn Pais, Paul C. Marcogliese, Shinya Yamamoto, Nicholas Raun, Taryn E. Jakub, Jamie M. Kramer, Joery den Hoed, Simon E. Fisher, Han G. Brunner, Tjitske Kleefstra

    Diterbitkan 2023-01-01
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