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Alcántara-Ortigoza, Miguel A.
98  Ergebnisse:
Personensuche X
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1

Does the esv3587290 Copy Number Variation in the VANGL1 Gen..:

Alcántara-Ortigoza, Miguel ; Rodríguez-Lozano, Ana ; Estandía-Ortega, Bernardette...
Children.  11 (2024)  6 - p. 712 , 2024
Link: https://doi.org/10.3390/..
 
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2

Functional characterization of the p.(Gln195His) or Tainan ..:

Alcántara-Ortigoza, Miguel A. ; Hernández-Ochoa, Beatriz ; González-del Angel, Ariadna...
Clinical Biochemistry.  109-110 (2022)  - p. 64-73 , 2022
Link: https://doi.org/10.1016/..
 
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3

TSC2/PKD1 contiguous gene syndrome, with emphasis on a case..:

Reyna-Fabián, Miriam E. ; Alcántara-Ortigoza, Miguel A. ; Hernández-Martínez, Nancy L....
Nefrología (English Edition).  40 (2020)  1 - p. 91-98 , 2020
Link: https://doi.org/10.1016/..
 
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4

First comprehensive TSC1/TSC2 mutational analysis in Mexica..:

Reyna-Fabián, Miriam E. ; Hernández-Martínez, Nancy L. ; Alcántara-Ortigoza, Miguel A....
Scientific Reports.  10 (2020)  1 - p. , 2020
Link: https://doi.org/10.1038/..
 
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5

TSC2/PKD1 contiguous gene syndrome, with emphasis on a case..:

Reyna-Fabián, Miriam E. ; Alcántara-Ortigoza, Miguel A. ; Hernández-Martínez, Nancy L....
Nefrología.  40 (2020)  1 - p. 91-98 , 2020
Link: https://doi.org/10.1016/..
 
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6

Screening of IRF6 Variants in Patients Subjected to Genetic..:

Velázquez-Aragón, José A. ; Angel, Ariadna González-del ; Alcántara-Ortigoza, Miguel A...
The Cleft Palate-Craniofacial Journal.  58 (2020)  9 - p. 1128-1134 , 2020
Link: https://doi.org/10.1177/..
 
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7

Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1..:

Alcántara-Ortigoza, Miguel A. ; De Rubens-Figueroa, Jesús ; Reyna-Fabian, Miriam E....
Pediatric Cardiology.  36 (2015)  7 - p. 1551-1551 , 2015
Link: https://doi.org/10.1007/..
 
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8

Effects of Fructans from Mexican Agave in Newborns Fed with..:

López-Velázquez, Gabriel ; Parra-Ortiz, Minerva ; Mora, Ignacio...
Nutrients.  7 (2015)  11 - p. 8939-8951 , 2015
Link: https://doi.org/10.3390/..
 
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9

Successful stem cell transplantation in a child with chroni..:

Scheffler-Mendoza, Selma C. ; Yamazaki-Nakashimada, Marco A. ; Olaya-Vargas, Alberto...
Clinical Immunology.  154 (2014)  2 - p. 112-115 , 2014
Link: https://doi.org/10.1016/..
 
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10

Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in..:

Alcántara-Ortigoza, Miguel A. ; De Rubens-Figueroa, Jesús ; Reyna-Fabian, Miriam E....
Pediatric Cardiology.  36 (2014)  4 - p. 802-808 , 2014
Link: https://doi.org/10.1007/..
 
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11

Mucopolysaccharidosis type II in a female carrying a hetero..:

Piña-Aguilar, Raul E. ; Zaragoza-Arévalo, Gerardo R. ; Rau, Isabella...
European Journal of Medical Genetics.  56 (2013)  3 - p. 159-162 , 2013
Link: https://doi.org/10.1016/..
 
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12

In Silico Structural Protein Evaluation of the Phenylalanin..:

Vela-Amieva, Marcela ; Alcántara-Ortigoza, Miguel Angel ; González-del Angel, Ariadna...
Children.  10 (2023)  12 - p. 1865 , 2023
Link: https://doi.org/10.3390/..
 
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13

Unusual Trisomy X Phenotype Associated with a Concurrent He..:

González-del Angel, Ariadna ; Alcántara-Ortigoza, Miguel Angel ; Ramos, Sandra...
International Journal of Molecular Sciences.  24 (2023)  19 - p. 14643 , 2023
Link: https://doi.org/10.3390/..
 
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14

Uncommon Large and Bilateral Fibrous Cephalic Plaques in a ..:

González-del Angel, Ariadna ; Ruiz-Herrera, Adriana ; Hernández-Martínez, Nancy Leticia...
Children.  10 (2023)  10 - p. 1614 , 2023
Link: https://doi.org/10.3390/..
 
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15

The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum..:

Estandia-Ortega, Bernardette ; Reyna-Fabián, Miriam Erandi ; Velázquez-Aragón, José Antonio...
Life.  12 (2022)  11 - p. 1723 , 2022
Link: https://doi.org/10.3390/..
 
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