Lista de obras - Marta Fichna - Dominio Público Uruguay

A coding variant in NLRP1 is associated with autoimmune Addison's disease.

artículo científico publicado en 2010

A genome-wide association study on medulloblastoma

artículo científico publicado en 2020

Adrenal hypoplasia congenita - an uncommon reason of primary adrenal insufficiency

artículo científico publicado en 2010

Amiodarone-induced thyrotoxicosis in a case of Eisenmenger's syndrome.

artículo científico publicado en 2013

Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts

artículo científico publicado en 2014

Association of polymorphisms and haplotypes of the NBN gene with laryngeal cancer and multiple primary tumors of the head and neck.

artículo científico publicado en 2011

Autoantibodies against zinc transporter 8 are related to age and metabolic state in patients with newly diagnosed autoimmune diabetes

artículo científico publicado en 2018

Changes in total and acylated ghrelin levels during mitotane treatment in patients with adrenocortical carcinoma

artículo científico publicado en 2019

Cumulative effect of IFIH1 variants and increased gene expression associated with type 1 diabetes.

artículo científico publicado en 2014

Determination of 21-hydroxylase autoantibodies: inter-laboratory concordance in the Euradrenal International Serum Exchange Program

artículo científico publicado en 2015

Diagnostic value of selected biochemical markers in the detection of recurrence of medullary thyroid cancer - comparison of calcitonin, procalcitonin, chromogranin A, and carcinoembryonic antigen

artículo científico publicado en 2017

Elevated serum RANTES chemokine levels in autoimmune Addison disease.

artículo científico publicado en 2018

Env gene expression of human endogenous retrovirus-k and human endogenous retrovirus-w in childhood acute leukemia cells

artículo científico publicado en 2013

FKBP5 polymorphism is associated with insulin resistance in children and adolescents with obesity

artículo científico publicado en 2016

Functional variants of gene encoding folate metabolizing enzyme and methotrexate-related toxicity in children with acute lymphoblastic leukemia.

artículo científico publicado en 2015

Glucocorticoids and beta-cell function

artículo científico publicado en 2017

Hypogonadotropic hypogonadism due to GnRH receptor mutation in a sibling.

artículo científico publicado en 2011

Impact of Month of Birth on the Risk of Development of Autoimmune Addison's Disease

scientific article published on 30 August 2016

Increased risk of endocrine autoimmunity in first-degree relatives of patients with autoimmune Addison's disease

artículo científico publicado en 2020

Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease--an association study and expression analysis

artículo científico publicado en 2014

MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes

artículo científico publicado en 2016

Metabolic assessment of hydrocortisone replacement therapy in patients with primary adrenocortical insufficiency

artículo científico publicado el 1 de enero de 2011

No evidence for association of the polymorphisms in NLRP1 gene with type 1 diabetes in Poland

scientific article published on 03 March 2011

Non-Classic Disorder of Adrenal Steroidogenesis and Clinical Dilemmas in 21-Hydroxylase Deficiency Combined with Backdoor Androgen Pathway. Mini-Review and Case Report ⬇️

artículo científico publicado en 2020

PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients

artículo científico publicado en 2010

Pneumocystis pneumonia in children - the relevance of chemoprophylaxis in different groups of immunocompromised and immunocompetent paediatric patients

artículo científico publicado en 2015

Polymorphic variant at the IL2 region is associated with type 1 diabetes and may affect serum levels of interleukin-2.

artículo científico publicado en 2013

Polymorphic variants of the HSD11B1 gene may be involved in adverse metabolic effects of glucocorticoid replacement therapy in Addison's disease

artículo científico publicado en 2016

Polymorphic variants of the IL2RA gene and susceptibility to type 1 diabetes in the Polish population.

artículo científico publicado en 2011

Polymorphisms in microRNA target sites modulate risk of lymphoblastic and myeloid leukemias and affect microRNA binding

artículo científico publicado en 2014

Polymorphisms in the interferon-induced helicase (IFIH1) locus and susceptibility to Addison's disease

artículo científico publicado en 2013

Polymorphisms of the Toll-Like Receptor-3 Gene in Autoimmune Adrenal Failure and Type 1 Diabetes in Polish Patients.

artículo científico publicado en 2015

Positive autoantibodies to ZnT8 indicate elevated risk for additional autoimmune conditions in patients with Addison's disease

artículo científico publicado en 2016

Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay.

artículo científico publicado en 2014

STAT4 sequence variant and elevated gene expression are associated with type 1 diabetes in Polish children

scientific article published on 01 January 2020

Screening for associated autoimmune disorders in Polish patients with Addison's disease.

artículo científico publicado en 2010

Serum Visfatin does not seem to be a Useful Marker to Guide Glucocorticoid Substitution in Adrenal Insufficiency

scientific article published on 06 April 2020

Steroid replacement in primary adrenal failure does not appear to affect circulating adipokines

artículo científico publicado en 2014

Susceptibility loci in lung cancer and COPD: association of IREB2 and FAM13A with pulmonary diseases.

artículo científico publicado en 2015

The role of antithyroglobulin, antiperoxidase and anti-TSH receptor autoantibodies in amiodarone-induced thyrotoxicosis and amiodarone-induced hypothyroidism (A two-center study)

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

artículo científico publicado en 2008

Upregulation of FOXO3 in New-Onset Type 1 Diabetes Mellitus

artículo científico publicado en 2020

Vitamin D deficiency and thyroid autoantibody fluctuations in patients with Graves' disease - A mere coincidence or a real relationship?

scientific article published on 26 December 2019

miR-487a-3p upregulated in type 1 diabetes targets CTLA4 and FOXO3

artículo científico publicado en 2018

Lista de obras de Marta Fichna

A coding variant in NLRP1 is associated with autoimmune Addison's disease.

A genome-wide association study on medulloblastoma

Adrenal hypoplasia congenita - an uncommon reason of primary adrenal insufficiency

Amiodarone-induced thyrotoxicosis in a case of Eisenmenger's syndrome.

Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts

Association of polymorphisms and haplotypes of the NBN gene with laryngeal cancer and multiple primary tumors of the head and neck.

Autoantibodies against zinc transporter 8 are related to age and metabolic state in patients with newly diagnosed autoimmune diabetes

Changes in total and acylated ghrelin levels during mitotane treatment in patients with adrenocortical carcinoma

Cumulative effect of IFIH1 variants and increased gene expression associated with type 1 diabetes.

Determination of 21-hydroxylase autoantibodies: inter-laboratory concordance in the Euradrenal International Serum Exchange Program

Diagnostic value of selected biochemical markers in the detection of recurrence of medullary thyroid cancer - comparison of calcitonin, procalcitonin, chromogranin A, and carcinoembryonic antigen

Elevated serum RANTES chemokine levels in autoimmune Addison disease.

Env gene expression of human endogenous retrovirus-k and human endogenous retrovirus-w in childhood acute leukemia cells

FKBP5 polymorphism is associated with insulin resistance in children and adolescents with obesity

Functional variants of gene encoding folate metabolizing enzyme and methotrexate-related toxicity in children with acute lymphoblastic leukemia.

Glucocorticoids and beta-cell function

Hypogonadotropic hypogonadism due to GnRH receptor mutation in a sibling.

Impact of Month of Birth on the Risk of Development of Autoimmune Addison's Disease

Increased risk of endocrine autoimmunity in first-degree relatives of patients with autoimmune Addison's disease

Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease--an association study and expression analysis

MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes

Metabolic assessment of hydrocortisone replacement therapy in patients with primary adrenocortical insufficiency

No evidence for association of the polymorphisms in NLRP1 gene with type 1 diabetes in Poland

Non-Classic Disorder of Adrenal Steroidogenesis and Clinical Dilemmas in 21-Hydroxylase Deficiency Combined with Backdoor Androgen Pathway. Mini-Review and Case Report ⬇️

PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients

Pneumocystis pneumonia in children - the relevance of chemoprophylaxis in different groups of immunocompromised and immunocompetent paediatric patients

Polymorphic variant at the IL2 region is associated with type 1 diabetes and may affect serum levels of interleukin-2.

Polymorphic variants of the HSD11B1 gene may be involved in adverse metabolic effects of glucocorticoid replacement therapy in Addison's disease

Polymorphic variants of the IL2RA gene and susceptibility to type 1 diabetes in the Polish population.

Polymorphisms in microRNA target sites modulate risk of lymphoblastic and myeloid leukemias and affect microRNA binding

Polymorphisms in the interferon-induced helicase (IFIH1) locus and susceptibility to Addison's disease

Polymorphisms of the Toll-Like Receptor-3 Gene in Autoimmune Adrenal Failure and Type 1 Diabetes in Polish Patients.

Positive autoantibodies to ZnT8 indicate elevated risk for additional autoimmune conditions in patients with Addison's disease

Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay.

STAT4 sequence variant and elevated gene expression are associated with type 1 diabetes in Polish children

Screening for associated autoimmune disorders in Polish patients with Addison's disease.

Serum Visfatin does not seem to be a Useful Marker to Guide Glucocorticoid Substitution in Adrenal Insufficiency

Steroid replacement in primary adrenal failure does not appear to affect circulating adipokines

Susceptibility loci in lung cancer and COPD: association of IREB2 and FAM13A with pulmonary diseases.

The role of antithyroglobulin, antiperoxidase and anti-TSH receptor autoantibodies in amiodarone-induced thyrotoxicosis and amiodarone-induced hypothyroidism (A two-center study)

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

Upregulation of FOXO3 in New-Onset Type 1 Diabetes Mellitus

Vitamin D deficiency and thyroid autoantibody fluctuations in patients with Graves' disease - A mere coincidence or a real relationship?

miR-487a-3p upregulated in type 1 diabetes targets CTLA4 and FOXO3