Tania Arevalo-Barragan
Mexico City, DIF, Mexico
Last Updated: 09/26/2026
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Found 17 publications
Genetic and molecular approaches for patients with familial hemophagocytic lymphohistiocytosis: a multi-center experience from Mexico.
Journal: Frontiers in immunology
Published: April 07, 2026
Expanding the clinical spectrum of RNU4ATAC-opathies: More frequent and diverse than assumed.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 01, 2025
Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 01, 2025
Expanding the Genetic and Clinical Spectrum of GZF1 -Related Phenotype: A Specific Ocular and Skeletal Disorder Distinguishable From Larsen Syndrome.
Journal: American journal of medical genetics. Part A
Published: August 12, 2025
A Retrospective Study of Clinical and Genetic Features in a Long-Term Cohort of Mexican Children with Alagille Syndrome.
Journal: International journal of molecular sciences
Published: June 07, 2025
A progeria syndrome links DNA hypermethylation to age-related pathology.
Journal: Nature genetics
Published: April 07, 2025
Macular atrophy and focal choroidal excavation in a patient with JAG1- related alagille syndrome.
Journal: Ophthalmic genetics
Published: March 25, 2024
Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency.
Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: October 09, 2023
Dysgerminoma Probably Due to a Novel SOHLH1-pathogenic Variant Causing Familial Ovarian Dysgenesis.
Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: May 05, 2023
Clinical, genetic, and electron microscopy of hair findings in a patient with CDH3 -related hypotrichosis with juvenile macular dystrophy.
Journal: Clinical dysmorphology
Published: February 13, 2023
First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations.
Journal: Molecular syndromology
Published: April 05, 2022
Combined immunodeficiency due to DOCK8 deficiency. State of the art
Journal: Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)
Published: March 20, 2022
Last Updated: 09/26/2026