Alan Conejo-Cardenas
Mexico City, DIF, Mexico
Last Updated: 09/26/2026
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Found 21 publications
Arthrogryposis With CNS Involvement in AFF3-Related KINSSHIP Syndrome: A Detailed Phenotypic Characterization From a Mexican Patient and Review of the Literature.
Journal: American journal of medical genetics. Part A
Published: May 27, 2026
Geographic and Socioeconomic Determinants of Treatment Abandonment in Pediatric Acute Leukemia: A Cohort Study in South-Central Mexico.
Journal: Cancer control : journal of the Moffitt Cancer Center
Published: January 16, 2026
Cytogenomic description of a Mexican cohort with differences in sex development.
Journal: Molecular cytogenetics
Published: February 16, 2024
The muscle regeneration marker FOXP3 is associated with muscle injury in Duchenne muscular dystrophy.
Journal: Brain & development
Published: December 13, 2023
Risk factors in the origin of Down syndrome
Journal: Revista medica del Instituto Mexicano del Seguro Social
Published: November 16, 2022
Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries.
Journal: Genes
Published: August 11, 2022
Natural history of circulating miRNAs in Duchenne disease: Association with muscle injury and metabolic parameters.
Journal: Acta neurologica Scandinavica
Published: May 12, 2022
Pro-inflammatory monocytes are increased in Duchenne muscular dystrophy and suppressed with omega-3 fatty acids: A double-blind, randomized, placebo-controlled pilot study.
Journal: European journal of neurology
Published: August 18, 2021
Multiple Organ Failure Associated with SARS-CoV-2 Infection in a Child with Down Syndrome: Is Trisomy 21 Associated with an Unfavourable Clinical Course?
Journal: Case reports in pediatrics
Published: August 09, 2021
Clinical, radiological, and molecular diagnosis of progressive fibrodysplasia ossificans.
Journal: Boletin medico del Hospital Infantil de Mexico
Published: May 03, 2021
The lag of genetic counseling in Mexico
Journal: Revista medica del Instituto Mexicano del Seguro Social
Published: March 05, 2021
Tumorous congenital calcinosis cutis associated with early childhood epileptic encephalopathy with a pathogenic FGF12 gene variant.
Journal: Boletin medico del Hospital Infantil de Mexico
Published: November 13, 2020
Last Updated: 09/26/2026