Search Results - "de Marco, Luiz Armando"
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1
PTEN expression in patients with carcinoma of the cervix and its association with p53, Ki-67 and CD31
Published in Revista Brasileira de ginecologia e obstetrícia (01-05-2014)“…To investigate protein expression and mutations in phosphatase and tensin homolog (PTEN) in patients with stage IB cervical squamous cell carcinoma (CSCC) and…”
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2
Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract
Published in Jornal de pediatria (01-01-2014)“…to determine the frequency of different phenotypes for congenital anomalies of the kidney and urinary tract (CAKUT) in a Brazilian sample, and to evaluate the…”
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3
No BRAF p.V600E mutation detection in ameloblastoma liquid biopsy-based analysis by ddPCR
Published in Oral oncology (01-02-2024)Get full text
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4
Genetic Variations in AMPK , FOXO3A , and POMC Increase the Risk of Extreme Obesity
Published in Journal of obesity (2024)“…Genetic variability significantly impacts metabolism, weight gain, and feeding behaviors, predisposing individuals to obesity. This study explored how…”
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5
Whole-exome sequencing as a diagnostic tool for distal renal tubular acidosis
Published in Jornal de pediatria (01-11-2015)“…Distal renal tubular acidosis (dRTA) is characterized by metabolic acidosis due to impaired renal acid excretion. The aim of this study was to demonstrate the…”
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6
Loss of heterozygosity of the PTCH gene in ameloblastoma
Published in Human pathology (01-08-2012)“…Summary Ameloblastoma is a locally aggressive benign neoplasm derived from odontogenic epithelium, with high recurrence rates. Alterations in the Sonic…”
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7
PAX2 Polymorphisms and Congenital Abnormalities of the Kidney and Urinary Tract in a Brazilian Pediatric Population: Evidence for a Role in Vesicoureteral Reflux
Published in Molecular diagnosis & therapy (01-08-2014)“…Background and Objectives Congenital anomalies of the kidney and urinary tract (CAKUT) are common genetic malformations. Since the PAX2 gene has a role in…”
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8
Associations between polymorphic variants of the tryptophan hydroxylase 2 gene and obsessive-compulsive disorder
Published in Revista brasileira de psiquiatria (01-06-2011)“…A substantial body of evidence suggests that obsessive-compulsive disorder has a genetic component, and substantial candidate genes for the disorder have been…”
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9
Obsessive-compulsive disorder and 5-HTTLPR
Published in Revista brasileira de psiquiatria (01-09-2009)Get full text
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10
Molecular medicine: a path towards a personalized medicine
Published in Revista brasileira de psiquiatria (01-03-2012)“…Psychiatric disorders are among the most common human illnesses; still, the molecular and cellular mechanisms underlying their complex pathophysiology remain…”
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11
Familial hyperparathyroidism: Surgical outcome after 30 years of follow-up in 3 families with germline HRPT2 mutations
Published in Surgery (01-02-2009)Get full text
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12
Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract
Published in Jornal de Pediatria (Versão em Português) (01-01-2014)“…To determine the frequency of different phenotypes for congenital anomalies of the kidney and urinary tract (CAKUT) in a Brazilian sample, and to evaluate the…”
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13
Importance of genetic polymorphisms in the response to age-related macular degeneration treatment
Published in Revista Brasileira de Oftalmologia (01-06-2012)“…Age-related macular degeneration (AMD) is a degenerative disorder that affects the central retina and involves the Bruch's membrane, the retinal pigment…”
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14
Catechol-O-methyltransferase genetic variant associated with the risk of Alzheimer's disease in a Brazilian population
Published in Dementia and geriatric cognitive disorders (01-01-2012)“…The aim of the present study was to examine the association between polymorphism in the catechol-O-methyltransferase(COMT) gene and Alzheimer's disease (AD) in…”
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15
Adenoid ameloblastoma harbors beta-catenin mutations
Published in Modern pathology (01-11-2022)“…Adenoid ameloblastoma is a very rare benign epithelial odontogenic tumor characterized microscopically by epithelium resembling conventional ameloblastoma,…”
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16
EVALUATION OF TERT PROMOTER HOTSPOT MUTATIONS IN AMELOBLASTOMA AND AMELOBLASTIC CARCINOMA
Published in Oral surgery, oral medicine, oral pathology and oral radiology (01-07-2023)“…Ameloblastoma is a benign, locally destructive, and infiltrative neoplasm. Ameloblastic carcinoma (AC) is a rare malignant tumor that arises either de novo or…”
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17
The Effect of a Muscle Weight-Bearing and Aerobic Exercise Program on the Body Composition, Muscular Strength, Biochemical Markers, and Bone Mass of Obese Patients Who Have Undergone Gastric Bypass Surgery
Published in Obesity surgery (01-08-2017)“…Background The effect of an exercise program on the body composition, muscular strength (MS), biochemical markers, and bone mineral density (BMD) of…”
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18
Selective visuoconstructional impairment following mild COVID-19 with inflammatory and neuroimaging correlation findings
Published in Molecular psychiatry (01-02-2023)“…People recovered from COVID-19 may still present complications including respiratory and neurological sequelae. In other viral infections, cognitive impairment…”
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19
Analysis of KRAS, BRAF, and EGFR mutational status in respiratory epithelial adenomatoid hamartoma (REAH)
Published in Journal of oral pathology & medicine (01-07-2023)“…Background Respiratory epithelial adenomatoid hamartoma (REAH) is a sinonasal glandular overgrowth arising from the surface respiratory epithelium and…”
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20
Predictive analysis between cytokine profile and Aβ42, p‐Tau, and p‐Tau/Aβ42 levels in the cerebrospinal fluid of older adults with and without cognitive impairment
Published in Alzheimer's & dementia (01-12-2023)“…Background The immune system activation observed in Alzheimer’s disease (AD) pathology contributes to its pathogenesis. It is proposed that ongoing…”
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