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Search life-sciences literature (45,104,145 articles, preprints and more)

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Bone Remodeling and Bone Structural Genes in Legg-Calvé-Perthes Disease: The <i>OPG</i> rs2073618 and <i>IL-6</i> rs1800795 Are Associated with High Risk in Mexican Patients.
Cruz-Ortíz BL, Hernández-Zamora E, Reyes-Maldonado E, Rodríguez-Olivas AO, Rubio-Lightbourn J, Martínez-Ramírez CO, Castro-Hernández C, Lezama-Palacios R, Casas-Avila L
DNA Cell Biol, 43(6):288-297, 22 Apr 2024
Cited by: 0 articles | PMID: 38648538
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New Genetic Variants of RUNX2 in Mexican Families Cause Cleidocranial Dysplasia.
Toral López J, Gómez Martinez S, Rivera Vega MDR, Hernández-Zamora E, Cuevas Covarrubias S, Ibarra Castrejón BA, González Huerta LM
Biology (Basel), 13(3):173, 08 Mar 2024
Cited by: 1 article | PMID: 38534443 | PMCID: PMC10968410
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Relevancia de la secuenciación de nueva generación en el diagnóstico de cáncer de mama y dos mutaciones descritas por primera vez en población mexicana.
González-Huerta LM, Hernández-Vázquez A, Toral-López J, Rivera-Vega MDR, Escobar-Gómez M, Hernández-Zamora E
Salud Publica Mex, 65(2 mar-abr), 10 Mar 2023
Cited by: 0 articles | PMID: 38060862
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Prothrombin Time and Coagulation Factor IX as Hemostatic Risk Markers for Legg- Calvé-Perthes Disease.
Hernández-Zamora E, Rodríguez-Olivas AO, Rosales-Cruz E, Galicia-Alvarado MA, Zavala-Hernández C, Reyes-Maldonado E
Clin Appl Thromb Hemost, 29:10760296221151166, 01 Jan 2023
Cited by: 1 article | PMID: 36650707 | PMCID: PMC9869215
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Hemostatic markers and polymorphisms in three Mexican families with Legg-Calvé-Perthes disease.
Rodríguez A, Hernández-Zamora E, Casas-Ávila L, Flores MV, Palacios RAL, Maldonado ER
Research Square, 06 Jul 2022
Cited by: 0 articles | PPR: PPR522546
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Association of Polymorphisms in Estrogen Receptor Genes (ESR1 and ESR2) with Osteoporosis and Fracture-Involvement of Comorbidities and Epistasis.
García-Rojas MD, Palma-Cordero G, Martínez-Ramírez CO, Ponce de León-Suárez V, Valdés-Flores M, Castro-Hernández C, Rubio-Lightbourn J, Hernández-Zamora E, Reyes-Maldonado E, Velázquez-Cruz R, Barredo-Prieto B, Casas-Avila L
DNA Cell Biol, 41(4):437-446, 14 Mar 2022
Cited by: 5 articles | PMID: 35285722
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Increased coagulation factors V, VIII, IX, and homocysteine in Mexican patients with Legg-Calvé-Perthes disease
Hernández-Zamora E, Rodríguez-Olivas AO, Rosales-Cruz E, Zavala-Hernández C, Maldonado ER
Research Square, 28 Feb 2022
Cited by: 0 articles | PPR: PPR463054
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Legg-Calvé-Perthes disease overview.
Rodríguez-Olivas AO, Hernández-Zamora E, Reyes-Maldonado E
Orphanet J Rare Dis, 17(1):125, 15 Mar 2022
Cited by: 14 articles | PMID: 35292045 | PMCID: PMC8922924
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Association of MTHFR rs1801133 and homocysteine with Legg-Calvé-Perthes disease in Mexican patients.
Buendía-Pazarán JG, Hernández-Zamora E, Rodríguez-Olivas AO, Casas-Ávila L, Valdés-Flores M, Reyes-Maldonado E
Orphanet J Rare Dis, 17(1):123, 09 Mar 2022
Cited by: 3 articles | PMID: 35264229 | PMCID: PMC8905721
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Microbial biofilms and their impact on medical areas: physiopathology, diagnosis and treatment.
Ortega-Peña S, Hernández-Zamora E
Bol Med Hosp Infant Mex, 75(2):79-88, 01 Jan 2018
Cited by: 6 articles | PMID: 29658950
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Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.
Cengiz FB, Yilmazer R, Olgun L, Sennaroglu L, Kirazli T, Alper H, Olgun Y, Incesulu A, Atik T, Huesca-Hernandez F, Domínguez-Aburto J, González-Rosado G, Hernandez-Zamora E, Arenas-Sordo ML, Menendez I, Orhan KS, Avci H, Mahdieh N, Bonyadi M, [...] Tekin M
Int J Pediatr Otorhinolaryngol, 101:167-171, 08 Aug 2017
Cited by: 9 articles | PMID: 28964290 | PMCID: PMC5679420
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Coagulation factors, anticoagulant proteins, and plasminogen in Mexican older adults.
Hernández Zamora E, González-Espinosa LO, Zavala-Hernández C, Rosales-Cruz E, Reyes-Maldonado E
Int J Lab Hematol, 39(3):293-300, 06 Mar 2017
Cited by: 1 article | PMID: 28263027
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Risk Factors for Thrombosis Development in Mexican Patients.
Zavala-Hernández C, Hernández-Zamora E, Martínez-Murillo C, Majluf-Cruz A, Vela-Ojeda J, García-Chávez J, Reyes-Maldonado E
Ann Vasc Surg, 29(8):1625-1632, 24 Aug 2015
Cited by: 6 articles | PMID: 26315791
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Characterization of a group unrelated patients with arthrogryposis multiplex congenita.
Valdés-Flores M, Casas-Avila L, Hernández-Zamora E, Kofman S, Hidalgo-Bravo A
J Pediatr (Rio J), 92(1):58-64, 09 Oct 2015
Cited by: 3 articles | PMID: 26453511
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Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Bademci G, Foster J, Mahdieh N, Bonyadi M, Duman D, Cengiz FB, Menendez I, Diaz-Horta O, Shirkavand A, Zeinali S, Subasioglu A, Tokgoz-Yilmaz S, Huesca-Hernandez F, de la Luz Arenas-Sordo M, Dominguez-Aburto J, Hernandez-Zamora E, Montenegro P, Paredes R, Moreta G, [...] Tekin M
Genet Med, 18(4):364-371, 30 Jul 2015
Cited by: 90 articles | PMID: 26226137 | PMCID: PMC4733433
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Anticoagulant proteins in a population of Mexican mestizo donors.
Meillón-García LA, Hernández-Zamora E, Montiel-Manzano G, Zavala-Hernández C, Ramírez-San Juan E, Cesarman-Maus G, Reyes-Maldonado E
Ann Vasc Surg, 29(2):222-226, 24 Nov 2014
Cited by: 1 article | PMID: 25463331
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[Von Willebrand disease. Molecular biology and diagnosis].
Hernández-Zamora E, Zavala-Hernández C, Quintana-González S, Reyes-Maldonado E
Cir Cir, 83(3):255-264, 01 May 2015
Cited by: 2 articles | PMID: 26055290
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[Determination of von Willebrand factor multimers in Mexican population].
Hernández-Zamora E, Zavala-Hernández C, Viveros-Sandoval ME, Ochoa-Rico A, Martínez-Murillo C, Reyes-Maldonado E
Cir Cir, 82(6):607-618, 01 Nov 2014
Cited by: 0 articles | PMID: 25393859
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[The auditory pathway: levels of integration of information and principal neurotransmitters].
Hernández-Zamora E, Poblano A
Gac Med Mex, 150(5):450-460, 01 Sep 2014
Cited by: 6 articles | PMID: 25275847
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Unique spectrum of GJB2 mutations in Mexico.
de la Luz Arenas-Sordo M, Menendez I, Hernández-Zamora E, Sirmaci A, Gutiérrez-Tinajero D, McGetrick M, Murphy-Ruiz P, Leyva-Juárez X, Huesca-Hernández F, Dominguez-Aburto J, Tekin M
Int J Pediatr Otorhinolaryngol, 76(11):1678-1680, 24 Aug 2012
Cited by: 11 articles | PMID: 22925408
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Leiden V factor and spastic cerebral palsy in Mexican children.
Arenas-Sordo Mde L, Zavala-Hernández C, Casiano-Rosas C, Reyes-Maldonado E, Ríos C, Hernández-Zamora E, Del Valle-Cabrera MG, Yamamoto-Furusho JK
Genet Test Mol Biomarkers, 16(8):978-980, 15 May 2012
Cited by: 3 articles | PMID: 22587599
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Single oligoarray-based detection of specific M918T mutation in RET oncogene in multiple endocrine neoplasia type 2B.
Pacheco-Rivera RA, Hernández-Zamora E, González-Yebra B, Beattie K, Maldonado-Rodríguez R, Santiago-Hernández JC, Medrano-Ortiz de Zárate ME, Salcedo M
Clin Exp Med, 11(4):227-234, 21 Jan 2011
Cited by: 0 articles | PMID: 21253810
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Association of resistance to activated protein with the presence of Leiden and Cambridge Factor V mutations in Mexican patients with primary thrombophilia.
Zavala Hernández C, Hernández Zamora E, Martínez Murillo C, Arenas Sordo Mde L, González Orozco AE, Reyes Maldonado E
Cir Cir, 78(2):127-132, 01 Mar 2010
Cited by: 6 articles | PMID: 20478113
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[Diagnosis of the peripheral hereditary neuropathies and its molecular genetics].
Hernández-Zamora E, Arenas-Sordo Mde L
Acta Ortop Mex, 22(4):268-277, 01 Jul 2008
Cited by: 0 articles | PMID: 18979992
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Capillary electrophoresis for the detection of PMP22 gene duplication: study in Mexican patients.
Hernández-Zamora E, de la Luz Arenas-Sordo M, Maldonado-Rodríguez R
Electrophoresis, 29(7):1582-1584, 01 Apr 2008
Cited by: 0 articles | PMID: 18318003
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1-25 of 31 results

1 2

Search life-sciences literature (45,104,145 articles, preprints and more)

Search results

Bone Remodeling and Bone Structural Genes in Legg-Calvé-Perthes Disease: The <i>OPG</i> rs2073618 and <i>IL-6</i> rs1800795 Are Associated with High Risk in Mexican Patients.

New Genetic Variants of RUNX2 in Mexican Families Cause Cleidocranial Dysplasia.

Relevancia de la secuenciación de nueva generación en el diagnóstico de cáncer de mama y dos mutaciones descritas por primera vez en población mexicana.

Prothrombin Time and Coagulation Factor IX as Hemostatic Risk Markers for Legg- Calvé-Perthes Disease.

Hemostatic markers and polymorphisms in three Mexican families with Legg-Calvé-Perthes disease.

Association of Polymorphisms in Estrogen Receptor Genes (ESR1 and ESR2) with Osteoporosis and Fracture-Involvement of Comorbidities and Epistasis.

Increased coagulation factors V, VIII, IX, and homocysteine in Mexican patients with Legg-Calvé-Perthes disease

Legg-Calvé-Perthes disease overview.

Association of MTHFR rs1801133 and homocysteine with Legg-Calvé-Perthes disease in Mexican patients.

Microbial biofilms and their impact on medical areas: physiopathology, diagnosis and treatment.

Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.

Coagulation factors, anticoagulant proteins, and plasminogen in Mexican older adults.

Risk Factors for Thrombosis Development in Mexican Patients.

Characterization of a group unrelated patients with arthrogryposis multiplex congenita.

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.

Anticoagulant proteins in a population of Mexican mestizo donors.

[Von Willebrand disease. Molecular biology and diagnosis].

[Determination of von Willebrand factor multimers in Mexican population].

[The auditory pathway: levels of integration of information and principal neurotransmitters].

Unique spectrum of GJB2 mutations in Mexico.

Leiden V factor and spastic cerebral palsy in Mexican children.

Single oligoarray-based detection of specific M918T mutation in RET oncogene in multiple endocrine neoplasia type 2B.

Association of resistance to activated protein with the presence of Leiden and Cambridge Factor V mutations in Mexican patients with primary thrombophilia.

[Diagnosis of the peripheral hereditary neuropathies and its molecular genetics].

Capillary electrophoresis for the detection of PMP22 gene duplication: study in Mexican patients.

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