Effect of counseling to improve compliance in Mexican women receiving depot-medroxyprogesterone acetate TEC De Cetina, P Canto, MO Luna Contraception 63 (3), 143-146, 2001 | 201 | 2001 |
Mutations in the Desert hedgehog (DHH) Gene in Patients with 46,XY Complete Pure Gonadal Dysgenesis P Canto, D Soderlund, E Reyes, JP Mendez The Journal of Clinical Endocrinology & Metabolism 89 (9), 4480-4483, 2004 | 196 | 2004 |
Gonadoblastoma in Turner syndrome patients with nonmosaic 45, X karyotype and Y chromosome sequences P Canto, S Kofman-Alfaro, AL Jiménez, D Söderlund, C Barrón, E Reyes, ... Cancer genetics and cytogenetics 150 (1), 70-72, 2004 | 99 | 2004 |
A heterozygous mutation in the desert hedgehog gene in patients with mixed gonadal dysgenesis P Canto, F Vilchis, D Söderlund, E Reyes, JP Mendez Molecular human reproduction 11 (11), 833-836, 2005 | 88 | 2005 |
A novel mutation of the insulin-like 3 gene in patients with cryptorchidism P Canto, I Escudero, D Söderlund, E Nishimura, S Carranza-Lira, ... Journal of human genetics 48 (2), 86-90, 2003 | 82 | 2003 |
Methylenetetrahydrofolate Reductase C677T and glutathione S− transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women P Canto, T Canto-Cetina, R Juárez-Velázquez, H Rosas-Vargas, ... Hypertension Research 31 (5), 1015-1019, 2008 | 80 | 2008 |
Mutations of the 5α‐reductase type 2 gene in eight Mexican patients from six different pedigrees with 5α‐reductase‐2 deficiency P Canto, F Vilchis, B Chávez, O Mutchinick, J Imperato‐McGinley, ... Clinical endocrinology 46 (2), 155-160, 1997 | 75 | 1997 |
Identification of missense mutations in the SRD5A2 gene from patients with steroid 5α‐reductase 2 deficiency Vilchis, Méndez, Canto, Lieberman, Chávez Clinical endocrinology 52 (3), 383-387, 2000 | 72 | 2000 |
Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1 P Canto, P Munguia, D Söderlund, JJ Castro, JP Mendez Journal of andrology 30 (1), 41-45, 2009 | 69 | 2009 |
A novel homozygous mutation in the second transmembrane domain of the gonadotrophin releasing hormone receptor gene D Söderlund, P Canto, E De La Chesnaye, A Ulloa‐Aguirre, JP Mendez Clinical endocrinology 54 (4), 493-498, 2001 | 64 | 2001 |
Risk factors and impact on bone mineral density in postmenopausal Mexican mestizo women D Rojano-Mejía, G Aguilar-Madrid, G López-Medina, L Cortes-Espinosa, ... Menopause 18 (3), 302-306, 2011 | 59 | 2011 |
No evidence of mutations in the P450 aromatase gene in patients with polycystic ovary syndrome D Söderlund, P Canto, S Carranza-Lira, JP Mendez Human Reproduction 20 (4), 965-969, 2005 | 59 | 2005 |
A mutation in the 5′ non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism P Canto, E de la Chesnaye, M López, A Cervantes, B Chávez, F Vilchis, ... The Journal of Clinical Endocrinology & Metabolism 85 (5), 1908-1911, 2000 | 59 | 2000 |
Bone mineral density in postmenopausal Mexican-Mestizo women with normal body mass index, overweight, or obesity JP Méndez, D Rojano-Mejía, J Pedraza, RM Coral-Vázquez, R Soriano, ... Menopause 20 (5), 568-572, 2013 | 57 | 2013 |
Frequency of Y chromosomal material in Mexican patients with Ullrich‐Turner syndrome M López, P Canto, M Aguinaga, L Torres, A Cervantes, G Alfaro, ... American journal of medical genetics 76 (2), 120-124, 1998 | 57 | 1998 |
(–)‐Epicatechin improves mitochondrial‐related protein levels and ameliorates oxidative stress in dystrophic δ‐sarcoglycan null mouse striated muscle I Ramirez‐Sanchez, S De los Santos, S Gonzalez‐Basurto, P Canto, ... The FEBS journal 281 (24), 5567-5580, 2014 | 52 | 2014 |
Identification of three novel mutations in the KAL1 gene in patients with Kallmann syndrome D Soderlund, P Canto, JP Méndez The Journal of Clinical Endocrinology & Metabolism 87 (6), 2589-2592, 2002 | 48 | 2002 |
Mutational analysis of the luteinizing hormone receptor gene in two individuals with Leydig cell tumors P Canto, D Söderlund, G Ramón, E Nishimura, JP Méndez American journal of medical genetics 108 (2), 148-152, 2002 | 47 | 2002 |
Molecular Analysis of the SRD5A2 in 46,XY Subjects With Incomplete Virilization: The P212R Substitution of the Steroid 5α‐Reductase 2 May Constitute an … F Vilchis, L Ramos, JP Méndez, S Benavides, P Canto, B Chávez Journal of andrology 31 (4), 358-364, 2010 | 45 | 2010 |
Immunodetection analysis of muscular dystrophies in Mexico B Gómez‐Díaz, H Rosas‐Vargas, B Roque‐Ramírez, P Meza‐Espinoza, ... Muscle & nerve 45 (3), 338-345, 2012 | 43 | 2012 |