Anna Taczanowska-Niemczuk
Biographic Data
| ID | 8255309 |
|---|---|
| NAME | Anna Taczanowska-Niemczuk |
| GIVEN NAMES | Anna |
| FAMILY NAME | Taczanowska-Niemczuk |
| SIGNATURE | TACZANOWSKA-NIEMCZUK A |
| AFFILIATIONS | Jagiellonian University |
| ORCID | 0009-0009-7280-5557 |
| VERIFIED | Yes |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 3 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2023 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 0 |
Occult Thyroid Cancer in Autoimmune Thyroiditis
Children with AIT may harbor occult PTC even without thyroid gland abnormalities suggestive of malignancy. Comprehensive ultrasound evaluation, including cervical lymph nodes, is vital for early detection and timely treatment
Ultrasound–Histopathological Presentation of Thyroid and Ovary Lesions in Adolescent Patients with Dicer1 Syndrome
Recent advances in genetic evaluation and in histological approaches indicate that MNG/TFND, although rare in the pediatric population, when accompanied by characteristic ultrasound and histopathological features, and by additional features such as androgenization, may warrant assessment also of the DICER1 gene within CPS molecular panel screening
A 4-Year-Old Boy with an Accidentally Detected Mutation in the RET Proto-Oncogene and Mutation in the Gene Encoding the Ryanodine Receptor1 (RyR1)—Case Report
Multiple endocrine neoplasia 2B (MEN2B) is a rare syndrome with prevalence estimated at approximately 0.2 per 100,000; it is caused by mutation of the RET proto-oncogene. MEN2B is characterized by early-onset medullary thyroid carcinoma (MTC), ganglioneuromatosis of the aerodigestive tract, marfanoid habitus, ophthalmologic abnormalities, and pheochromocytoma in adulthood. Mutations in the RyR1 gene manifest clinically in congenital myopathies an…
No prominent works on this page.
A 4-Year-Old Boy with an Accidentally Detected Mutation in the RET Proto-Oncogene and Mutation in the Gene Encoding the Ryanodine Receptor1 (RyR1)—Case Report
Multiple endocrine neoplasia 2B (MEN2B) is a rare syndrome with prevalence estimated at approximately 0.2 per 100,000; it is caused by mutation of the RET proto-oncogene. MEN2B is characterized by early-onset medullary thyroid carcinoma (MTC), ganglioneuromatosis of the aerodigestive tract, marfanoid habitus, ophthalmologic abnormalities, and pheochromocytoma in adulthood. Mutations in the RyR1 gene manifest clinically in congenital myopathies an…
Ultrasound–Histopathological Presentation of Thyroid and Ovary Lesions in Adolescent Patients with Dicer1 Syndrome
Recent advances in genetic evaluation and in histological approaches indicate that MNG/TFND, although rare in the pediatric population, when accompanied by characteristic ultrasound and histopathological features, and by additional features such as androgenization, may warrant assessment also of the DICER1 gene within CPS molecular panel screening
Occult Thyroid Cancer in Autoimmune Thyroiditis
Children with AIT may harbor occult PTC even without thyroid gland abnormalities suggestive of malignancy. Comprehensive ultrasound evaluation, including cervical lymph nodes, is vital for early detection and timely treatment
Internal Medicine (3 works) · Medicine (3 works) · Pathology (3 works) · Thyroid (3 works) · Neuroendocrine Tumor Research Advances (2 works) · Radiology (2 works) · Thyroid Cancer Diagnosis and Treatment (2 works) · Thyroid carcinoma (2 works) · Biology (1 work) · Calcitonin (1 work)