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1 . Academic Journal
Hereditary or acquired? Comprehensive genetic testing assists in stratifying angioedema patients
저자
by
Marija Rozevska
;
Adine Kanepa
;
Signe Purina
;
Linda Gailite
;
Inga Nartisa
, et al.
소스
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-6 (2024)
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7 . Academic Journal
Exploring disease-specific metabolite signatures in hereditary angioedema patients
저자
by
Adine Kanepa
;
Jingzhi Fan
;
Dmitrijs Rots
;
Annija Vaska
;
Laura Ansone
, et al.
소스
Frontiers in Immunology, Vol 15 (2024)
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7 . Academic Journal
P637: A newly derived DNA methylation signature for Koolen de Vries syndrome addresses the diagnostic challenges of the 17q21.31 locus
저자
by
Zain Awamleh
;
Sanaa Choufani
;
Dmitrijs Rots
;
Alexander Dingemans
;
Juan Dario Ortigoza Escobar
, et al.
소스
Genetics in Medicine Open, Vol 2, Iss , Pp 101543- (2024)
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7 . Academic Journal
National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia
저자
by
Adine Kanepa
;
Inga Nartisa
;
Dmitrijs Rots
;
Linda Gailite
;
Henriette Farkas
, et al.
소스
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-9 (2023)
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7 . Academic Journal
The most common European HINT1 neuropathy variant phenotype and its case studies
저자
by
Marija Rozevska
;
Dmitrijs Rots
;
Linda Gailite
;
Ronalds Linde
;
Stanislavs Mironovs
, et al.
소스
Frontiers in Neurology, Vol 14 (2023)
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7 . Academic Journal
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder
저자
by
Lot Snijders Blok
;
Jolijn Verseput
;
Dmitrijs Rots
;
Hanka Venselaar
;
A. Micheil Innes
, et al.
소스
HGG Advances, Vol 4, Iss 1, Pp 100157- (2023)
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7 . Academic Journal
Genetic Basis of Early Onset Atrial Fibrillation in Patients without Risk Factors
저자
by
Irina Rudaka
;
Baiba Vilne
;
Jekaterina Isakova
;
Oskars Kalejs
;
Linda Gailite
, et al.
소스
Journal of Cardiovascular Development and Disease, Vol 10, Iss 3, p 104 (2023)
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7 . Academic Journal
Long-Term Immunological Memory of SARS-CoV-2 Is Present in Patients with Primary Antibody Deficiencies for up to a Year after Vaccination
저자
by
Zane Lucane
;
Baiba Slisere
;
Lota Ozola
;
Dmitrijs Rots
;
Sindija Papirte
, et al.
소스
Vaccines, Vol 11, Iss 2, p 354 (2023)
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7 . Academic Journal
The association of FMR1 gene (CGG)n variation with idiopathic female infertility
저자
by
Adele Grasmane
;
Dmitrijs Rots
;
Zane Vitina
;
Valerija Magomedova
;
Linda Gailite
.
소스
Archives of Medical Science, Vol 17, Iss 5, Pp 1303-1307 (2019)
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7 . Academic Journal
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome
저자
by
Linda Gailite
;
Dmitrijs Rots
;
Ieva Pukite
;
Gunta Cernevska
;
Madara Kreile
.
소스
BMC Pediatrics, Vol 18, Iss 1, Pp 1-5 (2018)
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