P Canto
Overview
Explore the profile of P Canto including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
26
Citations
253
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0
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Recent Articles
1.
Canto-Cetina T, Silva-Nicanor D, Coral-Vazquez R, Cano-Martinez L, Gonzalez Herrera L, Garcia S, et al.
Climacteric
. 2022 Jul;
25(6):603-608.
PMID: 35866470
Objective: This study aimed to analyze the association between rs3480 and rs16835198 of and their haplotypes with variations in bone mineral density (BMD) and osteopenia/osteoporosis in postmenopausal Mayan-Mestizo women. Methods:...
2.
De Los Santos S, Palma-Flores C, Zentella-Dehesa A, Canto P, Coral-Vazquez R
Nutr Metab Cardiovasc Dis
. 2018 Aug;
28(11):1188-1195.
PMID: 30143409
Background And Aims: Several studies propose that (-)-epicatechin, a flavonol present in high concentration in the cocoa, has cardioprotective effects. This study aimed to evaluate the impact of (-)-epicatechin on...
3.
Garcia S, Coral-Vazquez R, Gallegos-Arreola M, Montes-Almanza L, Canto P, Garcia-Martinez F, et al.
Folia Neuropathol
. 2015 Apr;
53(1):24-8.
PMID: 25909872
The MTHFR gene has been reported as a susceptibility locus for sporadic Parkinson's disease (sPD). The functional variant rs1801133 has been linked to hyperhomocysteinemia and dopaminergic cell death. Among different...
4.
Duchenne muscular dystrophy in a developing country: challenges in management and genetic counseling
Lopez-Hernandez L, Gomez-Diaz B, Escobar-Cedillo R, Gama-Moreno O, Camacho-Molina A, Soto-Valdes D, et al.
Genet Couns
. 2014 Jul;
25(2):129-41.
PMID: 25059011
Background And Objective: Multidisciplinary management of Duchenne Muscular Dystrophy (DMD) has achieved outstanding results in developed nations. We aimed to describe the status of diagnosis and management of DMD in...
5.
Canto P, Munguia P, Soderlund D, Castro J, Mendez J
J Androl
. 2008 Aug;
30(1):41-5.
PMID: 18723471
Kallmann syndrome (KS) is characterized by the association of hypogonadotropic hypogonadism and anosmia or hyposmia. To date, 4 different genes have been identified as responsible for the presence of KS;...
6.
Sanchez-Moreno I, Coral-Vazquez R, Mendez J, Canto P
Mol Hum Reprod
. 2008 May;
14(6):325-30.
PMID: 18453550
SRY directs testicular development. It has been suggested that the only high-mobility group (HMG) box of the SRY is important for the function of this protein; however, other studies have...
7.
Canto P, Vilchis F, Soderlund D, Reyes E, Mendez J
Mol Hum Reprod
. 2006 Jan;
11(11):833-6.
PMID: 16390857
Aetiology of mixed gonadal dysgenesis (MGD) has not been completely elucidated. Molecular analyses have failed to demonstrate the presence of mutations in sex-determining region on Y chromosome (SRY); it has...
8.
Soderlund D, Canto P, Carranza-Lira S, Mendez J
Hum Reprod
. 2005 Feb;
20(4):965-9.
PMID: 15695318
Background: Etiology and inheritance pattern in polycystic ovary syndrome (PCOS) remain uncertain. Granulosa cells from follicles of women with PCOS have little, if any, aromatase (encoded by the CYP19 gene)...
9.
Canto P, Soderlund D, Reyes E, Mendez J
J Clin Endocrinol Metab
. 2004 Sep;
89(9):4480-3.
PMID: 15356051
Mutations of SRY are the cause of complete pure gonadal dysgenesis (PGD) in 10-15% of patients. In the remaining individuals, it has been suggested that mutations in other genes involved...
10.
Soderlund D, Canto P, Mendez J
J Clin Endocrinol Metab
. 2002 Jun;
87(6):2589-92.
PMID: 12050219
Kallmann's syndrome (KS) is characterized by the association of hypogonadotropic hypogonadism and anosmia or hyposmia. Genetic defects have been observed throughout the KAL1 gene, located on the Xp22.3 region, in...