about
Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomasPathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.Association between polymorphisms in the TSHR gene and Graves' orbitopathy.13-cis-retinoic acid re-differentiation therapy and recombinant human thyrotropin-aided radioiodine treatment of non-Functional metastatic thyroid cancer: a single-center, 53-patient phase 2 study.Occurrence of phaeochromocytoma tumours in RET mutation carriers - a single-centre study.Presentation of points of general discussion and voting among the speakers of the European Thyroid Association-Cancer Research Network (ETA-CRN) meeting in Lisbon, 2009, entitled "European comments to ATA medullary thyroid cancer guidelines".A registry-based study of thyroid paraganglioma: histological and genetic characteristics.Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study.[Evaluation of effects of L-thyroxine therapy in differentiated thyroid carcinoma on the cardiovascular system --prospective study]Recombinant human TSH-aided radioiodine treatment of advanced differentiated thyroid carcinoma: a single-centre study of 54 patients.[131I-MIBG therapy in the treatment of pheochromocytoma in children--own experiences].Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention.Guidelines of Polish National Societies Diagnostics and Treatment of Thyroid Carcinoma. 2018 Update.[131-I MIBG therapy of malignant pheochromocytoma and paraganglioma tumors - a single center study.]Molecular classification of pituitary adenomas: in search for criteria useful for high-throughput studies.The penetrance of MEN2 pheochromocytoma is not only determined by RET mutations.rs3827440, a nonsynonymous single nucleotide polymorphism within GPR174 gene in X chromosome, is associated with Graves' disease in Polish Caucasian population.Comparison of clinical examination with orbital MRI evaluation in patients with thyroid orbitopathy - do we need imaging and when?Interaction of HLA-DRB1 alleles with CTLA-4 in the predisposition to Graves' disease: the impact of DRB1*07Association of CD40 gene polymorphism (C-1T) with susceptibility and phenotype of Graves' diseasePreventive medicine of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumorsRadioactive iodine (RAI) treatment of hyperthyroidism is safe in patients with Graves' orbitopathy--a prospective study
P50
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P50
description
Polish endocrinologist
@en
Pools onderzoekster
@nl
inchríneolaí Polannach
@ga
polska lekarka, endokrynolog
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name
K Hasse-Lazar
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K Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
@cs
Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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K Hasse-Lazar
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K Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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K Hasse-Lazar
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K Hasse-Lazar
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K Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
@es
Kornelia Hasse-Lazar
@ga
Kornelia Hasse-Lazar
@gl
Kornelia Hasse-Lazar
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Kornelia Hasse-Lazar
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P214
P106
P1153
23496418200
P1412
P1559
Kornelia Hasse-Lazar
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P21
P214
P27
P31
P496
0000-0002-6430-0980
P735
P7859
viaf-311805168