Ariadna González-Del Angel (A González-Del-Angel)

Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 18

Top Topics

Intellectual Disability

Systemic Lupus Erythematosus

Top Venues

Children (Basel, Switzerland)

American journal of medical genetics. Part A

Journal of cutaneous pathology

This page only lists publications with an associated author ORCID identifier.

Publications

Miguel Angel Alcántara-Ortigoza, Ana Luisa Rodríguez-Lozano, Bernardette Estandia-Ortega, Ariadna González-Del Angel, Luisa Díaz García, Francisco Eduardo Rivas-Larrauri, Ruth Guadalupe Nájera-Velázquez
Does the esv3587290 Copy Number Variation in the VANGL1 Gene Differ as a Genetic Factor for Developing Nephritis in Mexican Childhood-Onset Systemic Lupus Erythematosus Patients? Children (Basel, Switzerland) 11 (6) (2024)
Miguel Angel Alcántara-Ortigoza, Ana Luisa Rodríguez-Lozano, Bernardette Estandia-Ortega, Ariadna González-Del Angel, Luisa Díaz García, Francisco Eduardo Rivas-Larrauri, Ruth Guadalupe Nájera-Velázquez
Does the esv3587290 Copy Number Variation in the VANGL1 Gene Differ as a Genetic Factor for Developing Nephritis in Mexican Childhood-Onset Systemic Lupus Erythematosus Patients? Children (Basel, Switzerland) 11 (6) (2024)
Ariadna González-Del Angel, Adriana Ruiz-Herrera, Nancy Leticia Hernández-Martínez, Carlos G Todd-Quiñones, Lourdes Carola Durán-McKinster, Patricia Herrera-Mora, Miguel Angel Alcántara-Ortigoza
Uncommon Large and Bilateral Fibrous Cephalic Plaques in a Patient with TSC2 -Related Tuberous Sclerosis Complex. Children (Basel, Switzerland) 10 (10) (2023)
Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel, Isabel Ibarra-González, Liliana Fernández-Hernández, Sara Guillén-López, Lizbeth Alejandra López-Mejía, Cynthia Fernández-Lainez
In Silico Structural Protein Evaluation of the Phenylalanine Hydroxylase p.(Tyr77His) Variant Associated with Benign Hyperphenylalaninemia as Identified through Mexican Newborn Screening. Children (Basel, Switzerland) 10 (12) (2023)
Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel, Isabel Ibarra-González, Liliana Fernández-Hernández, Sara Guillén-López, Lizbeth Alejandra López-Mejía, Cynthia Fernández-Lainez
In Silico Structural Protein Evaluation of the Phenylalanine Hydroxylase p.(Tyr77His) Variant Associated with Benign Hyperphenylalaninemia as Identified through Mexican Newborn Screening. Children (Basel, Switzerland) 10 (12) (2023)
Ariadna González-Del Angel, Miguel Angel Alcántara-Ortigoza, Sandra Ramos, Carolina Algara-Ramírez, Marco Antonio Hernández-Hernández, Lorenza Saenger-Rivas
Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis. International journal of molecular sciences 24 (19) (2023)
Bernardette Estandia-Ortega, Miriam Erandi Reyna-Fabián, José Antonio Velázquez-Aragón, Ariadna González-Del Angel, Liliana Fernández-Hernández, Miguel Angel Alcántara-Ortigoza
The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes. Life (Basel, Switzerland) 12 (11) (2022)
David Apam-Garduño, Jorge Cazarín-Barrientos, Nancy Leticia Hernández-Martínez, Miriam Erandi Reyna-Fabián, Mario Magaña, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel, María Refugio Rivera-Vega
Clinical, pathological, and molecular correlation of folliculocystic and collagen hamartoma: A new potential diagnostic criterion for tuberous sclerosis complex? Journal of cutaneous pathology (2022)
Bernardette Estandia-Ortega, Liliana Fernández-Hernández, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel
Proposed clinical approach and imaging studies in families with oculo-auriculo-vertebral spectrum to assess variable expressivity. American journal of medical genetics. Part A 188 (5) (2022)
Liliana Fernández-Hernández, Miriam Erandi Reyna-Fabián, Miguel Angel Alcántara-Ortigoza, Carmen Aláez-Verson, Luis L Flores-Lagunes, Karol Carrillo-Sánchez, Ariadna González-Del Angel
Unusual Clinical Manifestations in a Mexican Patient with Sanfilippo B Syndrome. Diagnostics (Basel, Switzerland) 12 (5) (2022)
Marcela Vela Amieva, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel, Leticia Belmont-Martínez, Carlos López-Candiani, Isabel Ibarra-González
Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening. Orphanet journal of rare diseases 16 (1) (2021)
Miguel Angel Alcántara-Ortigoza, Iraís Sánchez-Verdiguel, Liliana Fernández-Hernández, Sergio Enríquez-Flores, Aidy González-Núñez, Nancy Leticia Hernández-Martínez, Carmen Sánchez, Ariadna González-Del Angel
Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR. Children (Basel, Switzerland) 8 (6) (2021)
Marcela Vela Amieva, Miguel Angel Alcántara-Ortigoza, Isabel Ibarra-González, Ariadna González-Del Angel, Liliana Fernández-Hernández, Sara Guillén-López, Lizbeth Alejandra López-Mejía, Rosa Itzel Carrillo-Nieto, Leticia Belmont-Martínez, Cynthia Fernández-Lainez
An Updated PAH Mutational Spectrum of Phenylketonuria in Mexican Patients Attending a Single Center: Biochemical, Clinical-Genotyping Correlations. Genes 12 (11) (2021)
Edna Morán-Villaseñor, Maria Del Mar Saéz de Ocariz, A Torrelo, J I Arostegui, Marco Antonio Yamazaki-Nakashimada, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel, José Antonio Velázquez-Aragón, G López-Herrera, L Berrón-Ruiz, Maria Teresa García-Romero
Expanding the clinical features of autoinflammation and phospholipase Cγ2-associated antibody deficiency and immune dysregulation by description of a novel patient. Journal of the European Academy of Dermatology and Venereology : JEADV 33 (12) (2019)
Ariadna González-Del Angel, Rocío Rius, Miguel A Alcántara-Ortigoza, Elaine Spector, Victoria Del Castillo, Luis Enrique Mata-García
Further delineation of achondroplasia-hypochondroplasia complex with long-term survival. American journal of medical genetics. Part A 176 (5) (2019)
Miguel Angel Alcántara-Ortigoza, Miriam Erandi Reyna-Fabián, Ariadna González-Del Angel, Bernardette Estandia-Ortega, Cesárea Bermúdez-López, Gabriela Marisol Cruz-Miranda, Matilde Ruíz-García
Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular Dystrophy with A Normal Multiplex Polymerase Chain Reaction DMD Gene Result: A Study Including Targeted Next-Generation Sequencing. Genes 10 (11) (2019)
Alan Caro-Contreras, Miguel A Alcántara-Ortigoza, Juan F Ahumada-Pérez, Ariadna González-Del Angel
Molecular analysis provides further evidence that Chitayat syndrome is caused by the recurrent p.(Tyr89Cys) pathogenic variant in the ERF gene. American journal of medical genetics. Part A 179 (1) (2018)
Ariadna González-Del Angel, Alan Caro-Contreras, Miguel Angel Alcántara-Ortigoza, Sandra Ramos, Roberto Cruz-Alcívar, Paola Moyers-Pérez
Unique association of hypochondroplasia with craniosynostosis and cleft palate in a Mexican family. American journal of medical genetics. Part A 176 (1) (2017)