Emiy Yokoyama-Rebollar
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Explore the profile of Emiy Yokoyama-Rebollar including associated specialties, affiliations and a list of published articles.
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9
Citations
18
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Recent Articles
1.
Guerra E, Beutelspacher-Fernandez K, Silva-Estrada J, Santa-Ana-Bayona M, Martinez-Dominguez P, Agredano-Chavez C, et al.
JACC Case Rep
. 2024 Nov;
29(19):102603.
PMID: 39484323
This paper presents the case of a 14-year-old boy with Danon disease exhibiting exclusive cardiac involvement, initially suspected as hypertrophic cardiomyopathy. Significant deterioration raised suspicion of an alternative etiology. A...
2.
Zarate-Mondragon F, Alcantara-Garcia R, Belmont-Martinez L, Consuelo-Sanchez A, Fernandez-Hernandez L, Flores-Calderon J, et al.
Bol Med Hosp Infant Mex
. 2024 Jul;
81(Supl 1):1-13.
PMID: 39009030
Introduction: Tyrosinemia type 1 is a rare disease with autosomal recessive inheritance, featuring various clinical manifestations. These may encompass acute neonatal liver failure, neonatal cholestatic syndrome, chronic hepatitis, cirrhosis, hepatocellular...
3.
Gamez-Gonzalez L, Xochihua-Diaz L, Ramirez-Lopez M, Colmenero-Rascon M, Yokoyama-Rebollar E, Hernandez-Santiago I, et al.
Pediatr Allergy Immunol Pulmonol
. 2023 Jul;
36(3):119-121.
PMID: 37466470
The etiology of Kawasaki disease (KD) and its precise genetic basics remain unknown. Genetic variants affecting immunity have been found in some patients. The occurrence of KD in siblings is...
4.
Corona-Rivera J, Zenteno J, Lopez-Perez L, Yokoyama-Rebollar E, Villarroel C, Barragan-Arevalo T, et al.
Mol Syndromol
. 2023 Apr;
14(2):143-151.
PMID: 37064331
Introduction: -related neurodevelopmental disorder (related NDD) is caused by pathogenic variants in the gene and is characterized by a distinctive facial appearance, intellectual disability, speech delay, seizures, feeding difficulties, cryptorchidism,...
5.
Carrillo-Tapia E, Espinosa-Padilla S, Perez-Perez D, Gonzalez-Serrano M, Berron-Ruiz L, Espinosa-Rosales F, et al.
Genet Test Mol Biomarkers
. 2022 Apr;
26(4):220-227.
PMID: 35394812
Fragment analysis of exon 1 of the human androgen receptor, known as HUMARA, is a polymerase chain reaction (PCR)-based method for detecting X-linked agammaglobulinemia (XLA) carriers. This method takes advantage...
6.
Landero-Huerta D, Vigueras-Villasenor R, Taja-Chayeb L, Garcia-Andrade F, Arechaga-Ocampo E, Yokoyama-Rebollar E, et al.
J Pediatr Endocrinol Metab
. 2021 Apr;
34(7):843-849.
PMID: 33838085
Objectives: Cryptorchidism is the most common genitourinary birth defect in live newborn males and is considered as an important risk factor for testicular germ cell tumors and infertility. The Androgen...
7.
Landero-Huerta D, Vigueras-Villasenor R, Yokoyama-Rebollar E, Garcia-Andrade F, Rojas-Castaneda J, Herrera-Montalvo L, et al.
Front Cell Dev Biol
. 2020 Aug;
8:762.
PMID: 32850863
Allelic variants in genes implicated in the development of testicular germ cell tumor (TGCT) could be present in patients with cryptorchidism (CO). Currently; the mechanisms explaining this relationship are still...
8.
Landero-Huerta D, Vigueras-Villasenor R, Yokoyama-Rebollar E, Arechaga-Ocampo E, Rojas-Castaneda J, Jimenez-Trejo F, et al.
Front Biosci (Landmark Ed)
. 2017 Feb;
22(7):1073-1098.
PMID: 28199193
Testicular germ cell cancer (TGCT) is the most common malignancy among young adult males, which has become important due to its increased incidence and mortality in the population worldwide. The...
9.
Yokoyama-Rebollar E, Ruiz-Herrera A, Lieberman-Hernandez E, Del Castillo-Ruiz V, Sanchez-Sandoval S, Avila-Flores S, et al.
Mol Cytogenet
. 2015 Apr;
8:27.
PMID: 25901183
Background: The 15q11q13 region is subject to imprinting and is involved in various structural rearrangements. Less than 1% of Angelman Syndrome patients are due to translocations involving 15q11q13. These translocations...