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1.
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.
BMC Pediatr
; 18(1): 317, 2018 10 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-30285761
2.
Influence of IL15 gene variations on the clinical features, treatment response and risk of developing childhood acute lymphoblastic leukemia in Latvian population.
Pediatr Hematol Oncol
; 35(1): 37-44, 2018 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-29528261
3.
Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia.
Case Rep Med
; 2021: 5266820, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34868319
4.
The Fetal Phenotype of Noonan Syndrome Caused by Severe, Cancer-Related PTPN11 Variants.
Am J Case Rep
; 21: e922468, 2020 Jul 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-32794475
5.
X-Linked Lymphoproliferative Disease in Latvia: A Report of Two Clinically Distinct Cases.
Case Rep Med
; 2020: 7108657, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32774386
6.
UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays.
Front Genet
; 11: 169, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32211025
7.
Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia
Asian Pac J Cancer Prev
; 19(1): 91-95, 2018 Jan 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-29373897
8.
Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease.
Mol Genet Genomic Med
; 5(4): 405-409, 2017 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-28717664
9.
Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population.
Arch Med Sci
; 12(3): 479-85, 2016 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27279837
10.
Association between inherited monogenic liver disorders and chronic hepatitis C.
World J Hepatol
; 6(2): 92-7, 2014 Feb 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-24575168
11.
Lack of association between polymorphisms in genes MTHFR and MDR1 with risk of childhood acute lymphoblastic leukemia.
Asian Pac J Cancer Prev
; 15(22): 9707-11, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-25520092
12.
Elevated serum levels of homocysteine as an early prognostic factor of psychiatric disorders in children and adolescents.
Schizophr Res Treatment
; 2012: 373261, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23091720
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