| 1 | Findings in ear tomography study from patients with oculo-auriculo-vertebral syndrome. | 1ᵉʳ autor: Arenas-Sordo, MD, Barradas-Hernández, I, Peñuelas-Romero, JK, Del Real-Martínez, KA, et al. | 2024 | EUROPEAN JOURNAL OF HUMAN GENETICS | WoS-id: 001407868900604
| 0 | 0 |
| 2 | Findings in ear tomography study from patients with oculo-auriculo-vertebral syndrome | 1ᵉʳ autor: Arenas-Sordo, MD, Barradas-Hernández, I, Peñuelas-Romero, JK, Del Real-Martínez, KA, et al. | 2024 | EUROPEAN JOURNAL OF HUMAN GENETICS | WoS-id: 001421430500863
| 0 | 0 |
| 3 | Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment | Coautor: Arenas-Sordo M.L., Bahena, Paulina, Daftarian, Narsis, Maroofian, Reza, et al. | 2022 | HUMAN GENETICS | WoS-id: 000663490900001
Scopus-id: 2-s2.0-85108260882
| 10 | 9 |
| 4 | Next generation sequencing of a genes panel for the study of Mexican patients with global developmental delay | 1ᵉʳ autor: de la Luz Arenas-Sordo, Maria, Linares-Mendoza, Paola, Penuelas-Romero, Karina, Martinez-Martinez, Javier | 2022 | EUROPEAN JOURNAL OF HUMAN GENETICS | WoS-id: 000779367701095
| 0 | 0 |
| 5 | Usefulness of Cerebral Palsy Curves in Mexican Patients: A Cross-Sectional Study | Coautor: Arenas-Sordo M.L., Viñals-Labañino C.P., Velazquez-Bustamante A.E., Vargas-Santiago S.I. | 2019 | J CHILD NEUROL | WoS-id: 000464498500007
Scopus-id: 2-s2.0-85062772586
| 1 | 4 |
| 6 | Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort | Coautor: Arenas-Sordo M.D.L.L., Cengiz F.B., Yilmazer R., Olgun L., et al. | 2017 | INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY | WoS-id: 000413713100030
Scopus-id: 2-s2.0-85030111743
| 16 | 17 |
| 7 | Clinical features of 149 patients with facio-auriculo-vertebral spectrum [Manifestaciones clínicas de 149 pacientes con espectro facio-aurículo-vertebral] | 2ᵒ autor y autor de correspondencia: Arenas-Sordo M.L., Muñoz-Pedroza L.A. | 2013 | Acta Otorrinolaringologica Espanola | Scopus-id: 2-s2.0-84884231704
| 0 | 11 |
| 8 | Leiden V Factor and Spastic Cerebral Palsy in Mexican Children | 1ᵉʳ autor: Arenas-Sordo, MDLL, Zavala-Hernández C., Casiano-Rosas C., Reyes-Maldonado E., et al. | 2012 | GENETIC TESTING AND MOLECULAR BIOMARKERS | WoS-id: 000308303200028
Scopus-id: 2-s2.0-84865680181
| 5 | 8 |
| 9 | Unique spectrum of GJB2 mutations in Mexico | 1ᵉʳ autor: Arenas-Sordo, MD, Menendez I., Hernández-Zamora E., Sirmaci A., et al. | 2012 | INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY | WoS-id: 000311463500028
Scopus-id: 2-s2.0-84867692443
| 16 | 19 |
| 10 | Association of resistance to activated protein with the presence of Leiden and Cambridge Factor V mutations in Mexican patients with primary thrombophilia | Coautor: Arenas Sordo M.L., Zavala Hernández C., Hernández Zamora E., Martínez Murillo C., et al. | 2010 | CIRUGIA Y CIRUJANOS | WoS-id: 000277312000005
Scopus-id: 2-s2.0-79958126298
| 6 | 9 |
| 11 | Association of Leiden and Cambridge factor V coagulation mutations and activated protein C resistance (APCR) in Mexican patients with primary thrombophilia [Asociación de la RPCA con mutaciones Leiden y Cambridge del factor V de la coagulac | Coautor: De La Luz Arenas-Sordo M., Zavala-Hernández C., Hernández-Zamora E., Martínez-Murillo C., et al. | 2010 | CIRUGIA Y CIRUJANOS | Scopus-id: 2-s2.0-79251498625
| 0 | 1 |
| 12 | Capillary electrophoresis, a new diagnostic tool [La electroforesis capilar como una nueva estrategia en la medicina y el diagnóstico clínico] | 2ᵒ autor: Arenas-Sordo M.L., Magaña J.J., Gómez R. | 2009 | REVISTA MEDICA DE CHILE | WoS-id: 000269566900014
Scopus-id: 2-s2.0-70350026462
| 1 | 2 |
| 13 | Microarray design using virtual hybridization to study variations in REP-CMT1A sites [Diseño de microsondas mediante hibridación virtual para el estudio de variantes en los sitios REP-CMT1A] | 2ᵒ autor: Arenas-Sordo M.D.L.L., Hernández-Zamora E., Maldonado-Rodríguez R. | 2008 | GACETA MEDICA DE MEXICO | WoS-id: 000254328300001
Scopus-id: 2-s2.0-50849124145
| 1 | 1 |
| 14 | Capillary electrophoresis for the detection of PMP22 gene duplication: Study in Mexican patients | 2ᵒ autor: Arenas-Sordo, MD, Hernández-Zamora E., Maldonado-Rodríguez R. | 2008 | Electrophoresis | WoS-id: 000255146600023
Scopus-id: 2-s2.0-42149093137
| 2 | 2 |
| 15 | Diagnosis of the peripheral hereditary neuropathies and its molecular genetics [El diagnóstico de las neuropatías periféricas hereditarias y la genética molecular.] | 2ᵒ autor y autor de correspondencia: Arenas-Sordo M.L., Hernández-Zamora E. | 2008 | Acta ortopédica mexicana | Scopus-id: 2-s2.0-58149398063
| 0 | 0 |
| 16 | Molecular study of a family with gene PMP22 duplication and large phenotypic variability [Estudio molecular de una familia con duplicación del gen PMP22 y gran variabilidad fenotípica] | 1ᵉʳ autor: De La Luz Arenas-Sordo M., Hernández-Zamora E., Gómez-Ortega R., Valdés-Flores M., et al. | 2008 | CIRUGIA Y CIRUJANOS | Scopus-id: 2-s2.0-77956277675
| 0 | 0 |
| 17 | Strategies for clinical and molecular diagnosis of Charcot-Marie-Tooth 1A. Study in Mexican patients [Estrategias para el diagnóstico clínico y molecular de Charcot-Marie-Tooth 1A. Estudio en pacientes mexicanos] | 2ᵒ autor: Arenas-Sordo M.D.L.L., Hernández-Zamor E., Escobar-Cedillo R.E., González-Huerta N.C., et al. | 2007 | GACETA MEDICA DE MEXICO | WoS-id: 000254327800005
Scopus-id: 2-s2.0-42949120755
| 2 | 2 |
| 18 | Surgical treatment for scoliosis. Minimal evolution control at 5 years [Tratamiento quirúrgico de la escoliosis. Control de evolución mínimo de 5 años.] | Coautor: Arenas-Sordo M.L., Rosales-Olivares L.M., García J., Miramontes-Martínez V.P., et al. | 2007 | CIRUGIA Y CIRUJANOS | WoS-id: 000258334400007
Scopus-id: 2-s2.0-35748956791
| 3 | 4 |
| 19 | Liofilizado de fibrina combinado con injerto óseo autólogo en artrodesis posterolateral. Estudio en conejos de Nueva Zelanda. | Coautor: Arenas-Sordo M.L., Zárate-Kalfópulos B., Estrada-Villaseñor E., Lecona-Buitrón H., et al. | 2007 | CIRUGIA Y CIRUJANOS | WoS-id: 000258334800009
Scopus-id: 2-s2.0-47049111944
| 5 | 8 |
| 20 | Percutaneous biopsy evaluation in the diagnosis of thoracic and lumbar vertebral destruction syndrome [Evaluación de la biopsia percutánea en el diagnóstico del síndrome de destrucción vertebral tóracico y lumbar.] | Coautor: Arenas-Sordo M.L., Rosales-Olivares L.M., Valle-Cerna I., Alpizar-Aguirre A., et al. | 2007 | CIRUGIA Y CIRUJANOS | Scopus-id: 2-s2.0-53049088227
| 0 | 5 |
| 21 | Von Recklinghausen disease [Enfermedad de von Recklinghausen] | 2ᵒ autor y autor de correspondencia: Arenas-Sordo M.D.L.L., Barrios B.C.A. | 2007 | MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL | Scopus-id: 2-s2.0-34547597689
| 0 | 0 |
| 22 | Cockayne's syndrome: a case report. Literature review. | 1ᵉʳ autor: Arenas-Sordo M.L., Hernández-Zamora E., Montoya-Pérez L.A., Aldape-Barrios B.C. | 2006 | MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL | Scopus-id: 2-s2.0-33745927133
| 0 | 18 |
| 23 | Cockayne's syndrome: A case report. Literature review [Síndrome de Cockayne: Informe de un caso. Revisión de la literatura] | 1ᵉʳ autor: De La Luz Arenas Sordo M., Hernández Zamora E., Montoya Pérez L.A., Aldape Barrios B.C. | 2006 | MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL | Scopus-id: 2-s2.0-33745102021
| 0 | 4 |
| 24 | Molecular analysis of the NDP gene in two families with Norrie disease | Coautor: Arenas-Sordo M.L., Rivera-Vega M.R., Chiñas-Lopez S., Jimenez Vaca A.L., et al. | 2005 | ACTA OPHTHALMOL SCAN | WoS-id: 000227969600013
Scopus-id: 2-s2.0-17644415353
| 7 | 9 |
| 25 | An 8q21 deletion in a patient with comorbid psychosis and mental retardation | 2ᵒ autor: De La Luz Arenas-Sordo M., Urraca N., Ortiz-Domínguez A., Martínez A., et al. | 2005 | Cns Spectrums | WoS-id: 000236752600009
Scopus-id: 2-s2.0-28944451905
| 4 | 6 |
| 26 | Incontinentia pigmenti (IP2): familiar case report with affected men. Literature review. | 1ᵉʳ autor: Arenas-Sordo M.L., Vallejo-Vega B., Hernández-Zamora E., Gálvez-Rosas A., et al. | 2005 | MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL | Scopus-id: 2-s2.0-33644790596
| 0 | 16 |
| 27 | Periodontal disease in Noonan's syndrome [Enfermedad periodontal en el síndrome de Noonan.] | 2ᵒ autor: Arenas-Sordo M.L., Torres-Carmona M.A., Saavedra-Ontiveros D., Sánchez-Guerrero M.C. | 1991 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-0026144391
| 0 | 11 |
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