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Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure
Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure
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Results 1-10 of 15 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
5-Oct-2022
Alanyl-tRNA synthetase 1 gene variants in hereditary neuropathy genotype and phenotype overview
Setlere, Signe
;
Jurcenko, Marija
;
Gailite, Linda
;
Rots, Dmitrijs
;
Kenina, Viktorija
;
Department of Doctoral Studies
;
Scientific Laboratory of Molecular Genetics
;
Department of Biology and Microbiology
Mar-2022
New-Born Screening for Spinal Muscular Atrophy : Results of a Latvian Pilot Study
Gailite, Linda
;
Sterna, Olga
;
Konika, Maija
;
Isakovs, Aleksejs
;
Isakova, Jekaterina
;
Micule, Ieva
;
Setlere, Signe
;
Diriks, Mikus
;
Auzenbaha, Madara
;
Scientific Laboratory of Molecular Genetics
2023
The most common European HINT1 neuropathy variant phenotype and its case studies
Rozevska, Marija
;
Rots, Dmitrijs
;
Gailite, Linda
;
Linde, Ronalds
;
Mironovs, Stanislavs
;
Timcenko, Maksims
;
Linovs, Viktors
;
Locmele, Dzintra
;
Micule, Ieva
;
Lace, Baiba
;
Kenina, Viktorija
;
Scientific Laboratory of Molecular Genetics
23-Jun-2021
GJB1 Gene Analysis in Two Extended Families with X-Linked Charcot-Marie-Tooth Disease
Kovale, Sabine
;
Terauda, Ruta
;
Millere, Elina
;
Taurina, Gita
;
Murmane, Daiga
;
Isakova, Jekaterina
;
Kenina, Viktorija
;
Gailite, Linda
;
Scientific Laboratory of Molecular Genetics
22-Apr-2022
A systematic review and standardized clinical validity assessment of genes involved in female reproductive failure
Volozonoka, Ludmila
;
Miskova, Anna
;
Kornejeva, Liene
;
Kempa, Inga
;
Bargatina, Veronika
;
Gailite, Linda
;
Scientific Laboratory of Molecular Genetics
;
Department of Obstetrics and Gynaecology
16-Jun-2022
Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia
Lace, Baiba
;
Micule, Ieva
;
Kenina, Viktorija
;
Setlere, Signe
;
Strautmanis, Jurgis
;
Kazaine, Inese
;
Taurina, Gita
;
Murmane, Daiga
;
Grinfelde, Ieva
;
Kornejeva, Liene
;
Krumina, Zita
;
Sterna, Olga
;
Radovica-Spalvina, Ilze
;
Vasiljeva, Inta
;
Gailite, Linda
;
Stavusis, Janis
;
Livcane, Diana
;
Kidere, Dita
;
Malniece, Ieva
;
Inashkina, Inna
;
Rīga Stradiņš University
;
Scientific Laboratory of Molecular Genetics
2019
Novel variant of the androgen receptor gene in a patient with complete androgen insensitivity syndrome and polyorchidism
Konrade, Ilze
;
Zavorikina, Julija
;
Fridvalde, Aija
;
Rots, Dmitrijs
;
Kalere, Ieva
;
Strumfa, Ilze
;
Dambrova, Maija
;
Gailite, Linda
;
Department of Internal Diseases
;
Scientific Laboratory of Molecular Genetics
;
Faculty of Pharmacy
;
Department of Pathology
;
Department of Human Physiology and Biochemistry
3-Oct-2018
Case report : Multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome
Gailite, Linda
;
Rots, Dmitrijs
;
Pukite, Ieva
;
Cernevska, Gunta
;
Kreile, Madara
;
Scientific Laboratory of Molecular Genetics
Dec-2021
A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia : Case report
Alksere, Baiba
;
Kornejeva, Liene
;
Grinfelde, Ieva
;
Dzalbs, Aigars
;
Enkure, Dace
;
Conka, Una
;
Andersone, Santa
;
Blumberga, Arita
;
Nikitina-Zake, Liene
;
Kangare, Liga
;
Radovica-Spalvina, Ilze
;
Vasiljeva, Inta
;
Gailite, Linda
;
Erenpreiss, Juris
;
Fodina, Violeta
;
Rīga Stradiņš University
Jun-2022
Dentalni status i parodontološko zdravlje pacijenata s fenilketonurijom u Latviji
Abola, Iveta
;
Emulina, Darta Elizabete
;
Skadins, Ingus
;
Brinkmane, Anda
;
Gailite, Linda
;
Auzenbaha, Madara
;
Scientific Laboratory of Molecular Genetics
;
Department of Conservative Dentistry and Oral Health
;
Department of Biology and Microbiology
Discover
Author
5
Kenina, Viktorija
4
Rots, Dmitrijs
3
Auzenbaha, Madara
3
Kornejeva, Liene
3
Micule, Ieva
3
Setlere, Signe
2
Abola, Iveta
2
Brinkmane, Anda
2
Dzivite-Krisane, Iveta
2
Emulina, Darta Elizabete
.
next >
Subject
6
3.1 Basic medicine
4
Clinical Neurology
4
SDG 3 - Good Health and Well-being
3
Obstetrics and Gynaecology
2
1.6 Biological sciences
2
Endocrinology
2
Genetics(clinical)
2
PCOS
2
Pediatrics, Perinatology, and Chi...
2
phenylketonuria
.
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Date issued
2
2023
6
2022
4
2021
1
2020
1
2019
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2018