Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Alejandra Camacho‐Molina"'
Autor:
Manuel Rosety-Rodríguez, Gabriel Fornieles, Ignacio Rosety, Antonio J. Díaz, Miguel A. Rosety, Alejandra Camacho-Molina, A. Rodríguez-Pareja, A. Tejerina, José Ramón Alvero-Cruz, Francisco J. Ordonez
Publikováno v:
Nutrición Hospitalaria, Vol 28, Iss 6, Pp 1912-1917 (2013)
Introduction: The various diagnostic classifications in the literature concur as regards the important role of abdominal obesity in the onset and progression of metabolic syndrome. Accordingly, this study was aimed at clarifying whether central obesi
Externí odkaz:
https://doaj.org/article/4b9c9236c9de426386c58e89dd6cc239
Autor:
Gabriel Fornieles, Alejandra Camacho-Molina, Miguel A. Rosety, Antonio J. Díaz, Ignacio Rosety, Manuel Rosety-Rodríguez, José Ramón Alvero-Cruz, Manuel Rosety, Francisco J. Ordonez
Publikováno v:
Nutrición Hospitalaria, Vol 28, Iss 6, Pp 1918-1921 (2013)
Introduction: Previous studies have found a significant correlation between parents and offspring regarding overweight and obesity in general population at early life stages. However this issue has received no attention in people with intellectual di
Externí odkaz:
https://doaj.org/article/9dc943ba24a54c76a95f71d45ca90afc
Autor:
Manuel Rosety-Rodríguez, Gabriel Fornieles, Alejandra Camacho-Molina, Ignacio Rosety, Antonio J. Díaz, Miguel A. Rosety, Antonia Rodríguez-Pareja, Francisco J. Ordonez
Publikováno v:
Nutrición Hospitalaria, Vol 28, Iss 5, Pp 1604-1609 (2013)
Fundamento y objetivo: Actualmente se acepta la importancia del estatus proinflamatorio en la fisiopatología del síndrome metabólico. De hecho, ha sido propuesto como diana terapéutica en el manejo clínico de estos pacientes. Por consiguiente es
Externí odkaz:
https://doaj.org/article/d2788a6b5876458cb6f49c4d9e1f0a2b
Autor:
Emilio Israel Wong-Valenzuela, Daniel San Juan, José Santos Zambrano, Alejandra Camacho Molina, Miguel Angel Morales-Morales, Alejandro Lopez-Landa
Publikováno v:
Case Reports in Genetics, Vol 2023 (2023)
Introduction. Monogenic mutations as the cause of recurrent ischemic cerebral small-vessel disease with leukodystrophy are rare. COL4A1 gene mutations are a relatively new etiology of cerebrovascular lesions in young adults; however, any patient has
Externí odkaz:
https://doaj.org/article/666a44e556a34ff59e77ebb4bd4036f7
Autor:
Adriana PerezGrovas‐Saltijeral, Adriana Ochoa‐Morales, Aurelio Jara‐Prado, Rafael Velázquez‐Cruz, Berenice Rivera‐Paredez, David Dávila‐OrtizdeMontellano, Edmar O. Benítez‐Alonso, Mónica Santamaría‐Olmedo, Rosalba Sevilla‐Montoya, Ernesto Marfil‐Marín, Margarita Valdés‐Flores, Leticia Martínez‐Ruano, Alejandra Camacho‐Molina, Alberto Hidalgo‐Bravo
Publikováno v:
European Journal of Neurology. 30:612-621
Juvenile-onset Huntington disease (JHD) is defined when symptoms initiate before 20 years of age. Mechanisms explaining differences between juvenile and adult onset are not fully understood. Our aim was to analyze the distribution of initial symptoms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2115593f24b57e360362b65d56e0a95
https://doi.org/10.1111/ene.15644
https://doi.org/10.1111/ene.15644
Autor:
Aurelio Jara-Prado, Rosalba Sevilla-Montoya, Alejandra Camacho-Molina, Ernesto Marfil-Marin, Adriana Ochoa-Morales, Margarita Valdés-Flores, Adriana PerezGrovas-Saltijeral, Mónica Santamaría-Olmedo, Alberto Hidalgo-Bravo
Publikováno v:
Molecular Neurobiology. 58:6222-6231
Huntington disease (HD) is the most common neurogenetic disorder caused by expansion of the CAG repeat in the HTT gene; nevertheless, the molecular bases of the disease are not fully understood. Non-coding RNAs have demonstrated to be involved in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90a7696439524c763e82940894ec8b20
https://doi.org/10.1007/s12035-021-02536-1
https://doi.org/10.1007/s12035-021-02536-1
Autor:
Alejandra Camacho-Molina, Y. Rodríguez-Agudelo, F. Paz-Rodríguez, M. Chávez-Oliveros, A. Ochoa-Morales, A. Bernal-Pérez, L. Martínez-Ruano
Publikováno v:
Neurología.
Resumen Introduccion La enfermedad de Huntington (EH) es un trastorno neurodegenerativo y hereditario. Gracias al diagnostico predictivo se han descrito caracteristicas clinicas incipientes en la fase prodromica. Objetivo Comparar la ejecucion en tar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2b9766e347bf8282bbb2a984abf11f3
https://doi.org/10.1016/j.nrl.2021.04.015
https://doi.org/10.1016/j.nrl.2021.04.015
Autor:
Alejandra, Camacho Molina, Elvira, Alarcón Manoja, José Ramón, Corzo Gilabert, Daniel, García Gil
Publikováno v:
Emergencias : revista de la Sociedad Espanola de Medicina de Emergencias. 32(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::42af0da8b4bddecbcf7cab8dee75f755
https://pubmed.ncbi.nlm.nih.gov/32395940
https://pubmed.ncbi.nlm.nih.gov/32395940
Autor:
Alejandra Camacho-Molina, Marisol Molina-Medina, Yerye Gibrán Mayén Lobo, José de Jesús Flores-Rivera, Katiuzka Casares-Cruz, Nancy Monroy Jaramillo
Publikováno v:
Molecular Genetics and Metabolism. 129:S37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56cc8838b31fa16d585cfd2a3ef01ece
https://doi.org/10.1016/j.ymgme.2019.11.071
https://doi.org/10.1016/j.ymgme.2019.11.071
Autor:
Alberto Hidalgo-Bravo, Alejandra Camacho-Molina, Antonio Miranda-Duarte, Leticia Martínez-Ruano, Adriana Ochoa-Morales, Aurelio Jara-Prado, Adriana PerezGrovas-Saltijeral
Publikováno v:
Mechanisms of Ageing and Development. 185:111189
Introduction Huntington´s disease (HD) is a neurodegenerative disorder characterized by neuropsychiatric, motor and cognitive manifestations. It is caused by expansion of the trinucleotide CAG on HTT. The molecular bases are not completely understoo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2683f8a14a022871887d904415231420
https://doi.org/10.1016/j.mad.2019.111189
https://doi.org/10.1016/j.mad.2019.111189