Gailite L - Search Results

1

Kohlschütter-Tönz syndrome: Case report with novel feature and detailed review of features associated with ROGDI variants.

Liepina L, Kalnina ML, Micule I, Gailite L, Rots D, Kalnina J, Strautmanis J, Celmina M. Liepina L, et al. Among authors: gailite l. Am J Med Genet A. 2022 Apr;188(4):1263-1279. doi: 10.1002/ajmg.a.62613. Epub 2021 Dec 23. Am J Med Genet A. 2022. PMID: 34939736 Review.

2

Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia.

Kreile M, Rots D, Zarina A, Rautiainen L, Visnevska-Preciniece Z, Kovalova Z, Gailite L. Kreile M, et al. Among authors: gailite l. Asian Pac J Cancer Prev. 2018 Jan 27;19(1):91-95. doi: 10.22034/APJCP.2018.19.1.91. Asian Pac J Cancer Prev. 2018. PMID: 29373897 Free PMC article.

3

Influence of IL15 gene variations on the clinical features, treatment response and risk of developing childhood acute lymphoblastic leukemia in Latvian population.

Rots D, Kreile M, Nikulshin S, Kovalova Z, Gailite L. Rots D, et al. Among authors: gailite l. Pediatr Hematol Oncol. 2018 Feb;35(1):37-44. doi: 10.1080/08880018.2018.1440334. Epub 2018 Mar 12. Pediatr Hematol Oncol. 2018. PMID: 29528261 Clinical Trial.

4

Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.

Gailite L, Rots D, Pukite I, Cernevska G, Kreile M. Gailite L, et al. BMC Pediatr. 2018 Oct 3;18(1):317. doi: 10.1186/s12887-018-1285-6. BMC Pediatr. 2018. PMID: 30285761 Free PMC article.

5

Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism.

Konrade I, Zavorikina J, Fridvalde A, Rots D, Kalere I, Strumfa I, Dambrova M, Gailite L. Konrade I, et al. Among authors: gailite l. Front Endocrinol (Lausanne). 2019 Jan 17;9:795. doi: 10.3389/fendo.2018.00795. eCollection 2018. Front Endocrinol (Lausanne). 2019. PMID: 30705665 Free PMC article.

6

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

Gailite L, Valenzuela-Palomo A, Sanoguera-Miralles L, Rots D, Kreile M, Velasco EA. Gailite L, et al. Front Genet. 2020 Mar 6;11:169. doi: 10.3389/fgene.2020.00169. eCollection 2020. Front Genet. 2020. PMID: 32211025 Free PMC article.

7

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

Volozonoka L, Rots D, Kempa I, Kornete A, Rezeberga D, Gailite L, Miskova A. Volozonoka L, et al. Among authors: gailite l. PLoS One. 2020 Mar 26;15(3):e0230771. doi: 10.1371/journal.pone.0230771. eCollection 2020. PLoS One. 2020. PMID: 32214361 Free PMC article.

8

Clinical and neurophysiological spectrum of polyneuropathies in children.

Millere E, Gribuste L, Kazaine I, Strautmanis J, Gailite L, Kenina V. Millere E, et al. Among authors: gailite l. Neurol Neurochir Pol. 2020;54(5):466-470. doi: 10.5603/PJNNS.a2020.0068. Epub 2020 Sep 17. Neurol Neurochir Pol. 2020. PMID: 32939748

9

Plasma neurofilament light chain as a potential biomarker in Charcot-Marie-Tooth disease.

Millere E, Rots D, Simrén J, Ashton NJ, Kupats E, Micule I, Priedite V, Kurjane N, Blennow K, Gailite L, Zetterberg H, Kenina V. Millere E, et al. Among authors: gailite l. Eur J Neurol. 2021 Mar;28(3):974-981. doi: 10.1111/ene.14689. Epub 2021 Jan 6. Eur J Neurol. 2021. PMID: 33340200

10

Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy.

Millere E, Rots D, Glazere I, Taurina G, Kurjane N, Priedite V, Gailite L, Blennow K, Zetterberg H, Kenina V. Millere E, et al. Among authors: gailite l. Front Neurol. 2021 Jan 20;11:586610. doi: 10.3389/fneur.2020.586610. eCollection 2020. Front Neurol. 2021. PMID: 33551952 Free PMC article.

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