Maria Claudia Nogueira Zerbini
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Explore the profile of Maria Claudia Nogueira Zerbini including associated specialties, affiliations and a list of published articles.
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54
Citations
411
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Recent Articles
11.
Brondani V, Lacombe A, Mariani B, Montenegro L, Soares I, Bezerra-Neto J, et al.
Int J Mol Sci
. 2021 Jan;
22(3).
PMID: 33513905
Adrenocortical carcinoma (ACC) is a rare malignancy that is associated with a dismal prognosis. Pan-genomic studies have demonstrated the involvement of and genes in adrenocortical tumorigenesis. Our aims were to...
12.
Tanno F, Srougi V, Almeida M, Ide Yamauchi F, Coelho F, Nishi M, et al.
J Endocr Soc
. 2020 Jul;
4(8):bvaa083.
PMID: 32724871
Purpose: This prospective study presents the results of a new approach in the treatment of primary macronodular adrenal hyperplasia (PMAH), with simultaneous total adrenalectomy of the larger adrenal gland and...
13.
Williams T, Gomez-Sanchez C, Rainey W, Giordano T, Lam A, Marker A, et al.
J Clin Endocrinol Metab
. 2020 Jul;
106(1):42-54.
PMID: 32717746
Objective: Develop a consensus for the nomenclature and definition of adrenal histopathologic features in unilateral primary aldosteronism (PA). Context: Unilateral PA is the most common surgically treated form of hypertension....
14.
Bernardi Bertonha F, Bando S, Ferreira L, Chaccur P, Vinhas C, Zerbini M, et al.
PLoS One
. 2020 Apr;
15(4):e0227547.
PMID: 32294112
The human thymus suffers a transient neonatal involution, recovers and then starts a process of decline between the 1st and 2nd years of life. Age-related morphological changes in thymus were...
15.
Conceicao B, Cavalcante I, Kremer J, Auricino T, Bento E, Zerbini M, et al.
Arch Endocrinol Metab
. 2020 Apr;
64(4):390-401.
PMID: 32267363
Objective To analyze the morphological and functional characteristics of primary macronodular adrenal hyperplasia (PMAH) nodules carrying or not carrying ARMC5 mutations and the consequences of the presence of mutations in...
16.
Brondani V, Montenegro L, Lacombe A, Magalhaes B, Nishi M, de Assis Funari M, et al.
Cancers (Basel)
. 2020 Mar;
12(3).
PMID: 32156018
Adrenocortical cancer is a rare malignant neoplasm associated with a dismal prognosis. Identification of the molecular pathways involved in adrenal tumorigenesis is essential for a better understanding of the disease...
17.
Mariani B, Nishi M, Wanichi I, Brondani V, Lacombe A, Charchar H, et al.
Front Endocrinol (Lausanne)
. 2020 Mar;
11:36.
PMID: 32117062
Germline mutations are considered to be the main genetic cause of primary macronodular adrenal hyperplasia (PMAH). PMAH is associated with high variability of cortisol secretion caused from subclinical hypercortisolism to...
18.
Lacombe A, Soares I, Mariani B, Nishi M, Bezerra-Neto J, Charchar H, et al.
Cancers (Basel)
. 2020 Jan;
12(1).
PMID: 31963898
Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with an unfavorable prognosis. Despite the poor prognosis in the majority of patients, no improvements in treatment strategies have been achieved. Therefore,...
19.
de Campos F, Felipe-Silva A, Zerbini M
Autops Case Rep
. 2019 Sep;
3(3):11-19.
PMID: 31528614
Anaplastic large cell lymphoma (ALCL), described less than 30 years ago by Karl Lennert and Herald Stein in Kiel, West Germany, is a T-cell or null non-Hodgkin lymphoma, with distinctive...
20.
Veloso J, Siqueira S, Zerbini M
Autops Case Rep
. 2019 Sep;
3(1):23-28.
PMID: 31528594
Rosai-Dorfman disease (RDD) or Sinus histiocytosis with massive lymphadenopathy is a rare and benign histiocytic proliferative disorder first described by Juan Rosai and Ronald Dorfman in 1969, whose etiology remains...