Kalmon D Post
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Explore the profile of Kalmon D Post including associated specialties, affiliations and a list of published articles.
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44
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973
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Recent Articles
1.
Freda P, Bruce J, Jin Z, Kostadinov J, Khandji A, Cremers S, et al.
J Clin Endocrinol Metab
. 2024 Jul;
PMID: 38986012
Purpose: Long-term GH/IGF-1 excess could increase risk of cancer in acromegaly, but individual levels of these hormones do not relate to this risk. Therefore, we newly investigated longitudinally-measured IGF-1 levels...
2.
Devarajan A, Vasan V, Dullea J, Zhang J, Vasa D, Schupper A, et al.
Neurosurgery
. 2024 Feb;
95(2):392-399.
PMID: 38421190
Background And Objectives: Pituitary adenomas (PAs) are the most common intrasellar tumor. Clinically relevant adenomas have a prevalence of 1 per 1000 in the general population. Transsphenoidal surgery (TSS) is...
3.
Carr M, Zimering J, Beroza J, Melillo A, Kellner C, Mocco J, et al.
J Neurosurg
. 2022 Mar;
137(5):1544-1552.
PMID: 35276643
The Department of Neurosurgery's residency program at The Mount Sinai Hospital was founded in 1946. The department has its origins in 1914 as a division of general surgery, with Charles...
4.
Lakomkin N, Van Gompel J, Post K, Cho S, Lee J, Hadjipanayis C
J Neurooncol
. 2021 Feb;
151(3):403-413.
PMID: 33611707
Purpose: Resection of pituitary adenomas presents a number of unique challenges in neuro-oncology. The proximity of these lesions to key vascular and endocrine structures as well as the need to...
5.
Uzilov A, Taik P, Cheesman K, Javanmard P, Ying K, Roehnelt A, et al.
J Clin Endocrinol Metab
. 2020 Nov;
106(3):826-842.
PMID: 33221858
Context: Pituitary corticotroph adenomas are rare tumors that can be associated with excess adrenocorticotropin (ACTH) and adrenal cortisol production, resulting in the clinically debilitating endocrine condition Cushing disease. A subset...
6.
Freda P, Bruce J, Reyes-Vidal C, Singh S, DeLeon Y, Jin Z, et al.
Pituitary
. 2020 Oct;
24(2):170-183.
PMID: 33124000
Context: Outcome of acromegaly surgery is assessed by IGF-1 and glucose-suppressed GH, but whether the latter provides additional clinically relevant information when IGF-1 is normal is unclear. The role of...
7.
Brown T, Cheesman K, Post K
AACE Clin Case Rep
. 2020 Sep;
6(5):e221-e224.
PMID: 32984525
Objective: To describe an unusual presentation of a patient with recurrent pituitary apoplexy of an adenoma that switched phenotypes from a nonfunctioning, or silent gonadotroph adenoma (SGA), to a silent...
8.
Freda P, Bruce J, Khandji A, Jin Z, Hickman R, Frey E, et al.
J Endocr Soc
. 2020 Apr;
4(4):bvaa021.
PMID: 32258955
Context: Clinically nonfunctioning pituitary adenomas (CNFPAs) typically remain undetected until mass effect symptoms develop. However, currently, head imaging is performed commonly for many other indications, which may increase incidental discovery...
9.
Uzilov A, Cheesman K, Fink M, Newman L, Pandya C, Lalazar Y, et al.
Cold Spring Harb Mol Case Stud
. 2017 May;
3(3):a001602.
PMID: 28487882
Cushing's disease (CD) is caused by pituitary corticotroph adenomas that secrete excess adrenocorticotropic hormone (ACTH). In these tumors, somatic mutations in the gene have been identified as recurrent and pathogenic...
10.
Shah N, Ruiz H, Zafar U, Post K, Buettner C, Geer E
Clin Endocrinol (Oxf)
. 2016 Sep;
86(1):68-74.
PMID: 27630017
Context: Inflammation contributes to the development of metabolic and cardiovascular disease. Cushing's disease (CD), a state of chronic glucocorticoid (GC) excess characterized by visceral obesity and insulin resistance, may be...