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Jacek Kunicki

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Articles 37
Citations 183
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Recent Articles
1.
Tsegaye B, Kober P, Mossakowska B, Baluszek S, Maksymowicz M, Buchalska B, et al.
J Neuroendocrinol . 2025 Jan; e13492. PMID: 39846216
Gonadotroph neuroendocrine pituitary tumors are among the most common intracranial neoplasms. A notable proportion of these tumors is characterized by invasive growth which hampers the treatment results and worsens prognoses...
2.
Jotanovic J, Boldt H, Burton M, Andersen M, Bengtsson D, Bontell T, et al.
Acta Neuropathol . 2025 Jan; 149(1):4. PMID: 39747763
No abstract available.
3.
Jotanovic J, Boldt H, Burton M, Andersen M, Bengtsson D, Bontell T, et al.
Acta Neuropathol . 2024 Nov; 148(1):68. PMID: 39580368
Aggressive pituitary neuroendocrine tumors (PitNETs)/adenomas are characterized by progressive growth despite surgery and all standard medical therapies and radiotherapy. A subset will metastasize to the brain and/or distant locations and...
4.
Rymuza J, Kober P, Maksymowicz M, Nyc A, Mossakowska B, Woroniecka R, et al.
J Transl Med . 2024 Nov; 22(1):994. PMID: 39497133
Background: Somatotroph neuroendocrine pituitary tumors (sPitNET) are a subtype of pituitary tumors that commonly cause acromegaly. Our study aimed to determine the spectrum of DNA copy number abnormalities (CNAs) in...
5.
Pekul M, Szczepaniak M, Kober P, Rusetska N, Mossakowska B, Baluszek S, et al.
Front Endocrinol (Lausanne) . 2024 Mar; 15:1302667. PMID: 38487343
Introduction: Corticotroph pituitary neuroendocrine tumors (PitNETs) develop from ACTH-producing cells. They commonly cause Cushing's disease (CD), however, some remain clinically silent. Recurrent , , and mutations occur in corticotroph PitNETs....
6.
Tomasik A, Stelmachowska-Banas M, Maksymowicz M, Czajka-Oraniec I, Raczkiewicz D, Zielinski G, et al.
Biomedicines . 2023 Dec; 11(12). PMID: 38137536
The pathologic evaluation of a tumor tissue is an essential part of an acromegaly patient's assessment. This study aimed to analyze the pathologic characteristics of pituitary tumors in patients with...
7.
Rzewuska N, Kunicki J, Pieniak K, Laskus P, Zabielska B, Smolarczyk R, et al.
Eur J Obstet Gynecol Reprod Biol . 2023 Nov; 292:1-7. PMID: 37948928
Background: A few publications have examined the frequency and medical implications of individuals with idiopathic intracranial hypertension (IIH) and polycystic ovarian syndrome (PCOS), but the findings have been inconclusive. IIH...
8.
Kober P, Rymuza J, Baluszek S, Maksymowicz M, Nyc A, Mossakowska B, et al.
Neuroendocrinology . 2023 Sep; 114(1):51-63. PMID: 37699356
Introduction: Growth hormone secretion by sporadic somatotroph neuroendocrine pituitary tumors (PitNETs) is a major cause of acromegaly. These tumors are relatively heterogenous in terms of histopathological and molecular features. Our...
9.
Baluszek S, Kober P, Rusetska N, Wagrodzki M, Mandat T, Kunicki J, et al.
Acta Neuropathol Commun . 2023 Jul; 11(1):113. PMID: 37434245
Chordomas are rare tumors of notochord remnants, occurring mainly in the sacrum and skull base. Despite of their unusually slow growth, chordomas are highly invasive and the involvement of adjacent...
10.
Kober P, Rusetska N, Mossakowska B, Maksymowicz M, Pekul M, Zielinski G, et al.
Front Endocrinol (Lausanne) . 2023 Apr; 14:1124646. PMID: 37065760
Objective: Pituitary neuroendocrine corticotroph tumors commonly cause Cushing's disease (CD) that results from increased adrenocorticotropic hormone (ACTH) secretion by the pituitary tumor and consequent increase of cortisol levels in blood....