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Díaz-Ordóñez, Lorena
579  Ergebnisse:
Personensuche X
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1

Familial LCAT Deficiency and Low HDL-C Levels: In silico Ch..:

Ciro Acosta, Sebastian ; Díaz-Ordóñez, Lorena ; Gutierrez-Medina, Juan...
The Application of Clinical Genetics.  17 (2024)  - p. 23-32 , 2024
Link: https://doi.org/10.2147/..
 
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2

Frequency of polymorphisms in the CYP2C9, VKORC1, and CYP4F..:

Giraldo-Ocampo, Sebastian ; Diaz-Ordoñez, Lorena ; Silva-Cuero, Yisther Katherine...
Medicine.  102 (2023)  30 - p. e34204 , 2023
Link: https://doi.org/10.1097/..
 
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3

Case report: Novel frameshift mutation in LAMA2 gene causin..:

Diaz-Lombana, Natalia ; Diaz-Ordoñez, Lorena ; Gutierrez-Medina, Juan David.
Frontiers in Genetics.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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4

Novel mutation in RPGRIP1L gene causing Joubert syndrome: A..:

Duque-Cordoba, Paola Andrea ; Diaz-Ordoñez, Lorena ; Gutierrez-Medina, Juan David.
Medicine.  102 (2023)  47 - p. e35600 , 2023
Link: https://doi.org/10.1097/..
 
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5

Hearing Loss in Patients With Morquio Syndrome: Protocol fo..:

Diaz-Ordoñez, Lorena ; Candelo, Estephania ; Silva-Cuero, Katherine...
JMIR Research Protocols.  11 (2022)  6 - p. e32986 , 2022
Link: https://doi.org/10.2196/..
 
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6

1469. Drug-resistance associated mutations of Human Cytomeg..:

Rosso, Fernando ; Tafur, Eric ; Zapata-Vasquez, Isabel L...
Open Forum Infectious Diseases.  9 (2022)  Supplement_2 - p. , 2022
Link: https://doi.org/10.1093/..
 
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7

A Possible Association Between Zika Virus Infection and CDK..:

Candelo, Estephania ; Sanz, Ana Maria ; Ramirez-Montaño, Diana...
Frontiers in Genetics.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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8

Identification of Nontuberculous Mycobacteria in Drinking W..:

Dávalos, Andrés F. ; Garcia, Pamela K. ; Montoya-Pachongo, Carolina...
International Journal of Environmental Research and Public Health.  18 (2021)  16 - p. 8451 , 2021
Link: https://doi.org/10.3390/..
 
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9

Evaluation of CYP2C19 Gene Polymorphisms in Patients with A..:

Díaz-Ordóñez, Lorena ; Ramírez-Montaño, Diana ; Candelo, Estephania...
Pharmacogenomics and Personalized Medicine.  14 (2021)  - p. 509-520 , 2021
Link: https://doi.org/10.2147/..
 
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10

A Novel Intronic KMT2D Variant as a Cause of Kabuki Syndrom..:

Aristizábal, Erica ; Diaz-Ordóñez, Lorena ; Candelo, Estephania.
The Application of Clinical Genetics.  14 (2021)  - p. 409-416 , 2021
Link: https://doi.org/10.2147/..
 
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11

Expression of BAFF, APRIL, and cognate receptor genes in lu..:

Aguirre-Valencia, David ; Ríos-Serna, Lady J. ; Posso-Osorio, Iván...
Journal of Translational Autoimmunity.  3 (2020)  - p. 100027 , 2020
Link: https://doi.org/10.1016/..
 
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12

Syndromic progressive neurodegenerative disease of infancy ..:

Candelo, Estephania ; Cochard, Léa ; Caicedo-Herrera, Gabriela...
Intractable & Rare Diseases Research.  8 (2019)  3 - p. 187-193 , 2019
Link: https://doi.org/10.5582/..
 
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13

A novel de novo TBX5 mutation in a patient with Holt-Oram s..:

Ríos-Serna, Lady J ; Díaz-Ordoñez, Lorena ; Candelo, Estephania.
The Application of Clinical Genetics.  11 (2018)  - p. 157-162 , 2018
Link: https://doi.org/10.2147/..
 
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14

Familial LCAT Deficiency and Low HDL-C Levels: In silico Ch..:

Ciro Acosta, Sebastian ; Díaz-Ordóñez, Lorena ; Gutierrez-Medina, Juan...
info:eu-repo/semantics/altIdentifier/doi/10.2147/TACG.S438135.  , 2024
Link: https://www.dovepress.co..
 
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15

Case report: Novel frameshift mutation in LAMA2 gene causin..:

Diaz-Lombana, Natalia ; Diaz-Ordoñez, Lorena ; Gutierrez-Medina, Juan David.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319579/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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