Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Juan M. González-Toledo"'
Autor:
Emilia M. Carmona-Calero, Juan M. González-Toledo, Luis G. Hernández-Abad, Agustin Castañeyra-Perdomo, Ibrahim González-Marrero
Publikováno v:
Children, Vol 9, Iss 12, p 1966 (2022)
Hydrocephalus is a central nervous system condition characterized by CSF buildup and ventricular hypertrophy. It is divided into two types: communicative and non-communicating hydrocephalus. Congenital hydrocephalus has been linked to several changes
Externí odkaz:
https://doaj.org/article/4bb39cfc3ecf47a5baa747afa41a0f55
Autor:
Agustín Castañeyra-Perdomo, Ibrahim González-Marrero, Juan M. González-Toledo, Luis G. Hernández-Abad, Leandro Castañeyra-Ruiz, Emilio Gonzalez-Arnay, Emilia M. Carmona-Calero
Publikováno v:
Human Pathology: Case Reports, Vol 15, Iss , Pp 29-32 (2019)
Holoprosencephaly (HPE) is a birth defect that occurs during the first weeks of pregnancy and as a result the prosencephalon does not clearly divide in diencephalon, two halves of the telencephalon and lateral ventricles in the brain of the fetus and
Externí odkaz:
https://doaj.org/article/be7e9fab0a9240dab6273b3abceedf90
Autor:
Ibrahim González-Marrero, Leandro Castañeyra-Ruiz, Juan M. González-Toledo, Agustín Castañeyra-Ruiz, Hector de Paz-Carmona, Rafael Castro, Juan R. Hernandez-Fernaud, Agustín Castañeyra-Perdomo, Emilia M. Carmona-Calero
Publikováno v:
International Journal of Hypertension, Vol 2013 (2013)
The aim of the present work is to analyze the cerebrospinal fluid proteomic profile, trying to find possible biomarkers of the effects of hypertension of the blood to CSF barrier disruption in the brain and their participation in the cholesterol and
Externí odkaz:
https://doaj.org/article/7b27671ba11146e99026b59166916219
Autor:
Emilia M. Carmona-Calero, Ibrahim González-Marrero, Luis G. Hernández-Abad, J.A. Hernandez-Garcia, Juan M. González-Toledo, Leandro Castañeyra-Ruiz, Agustín Castañeyra-Perdomo, E. Gonzalez-Davila
Publikováno v:
Neurología.
INTRODUCTION The relationship between the entorhinal cortex and the hippocampus has been studied by different authors, who have highlighted the importance of grid cells, place cells, and the trisynaptic circuit in the processes that they regulate: th
Autor:
Emilio González-Arnay, Ibrahim González-Marrero, Luis G. Hernández-Abad, Leandro Castañeyra-Ruiz, Agustín Castañeyra-Perdomo, Juan M. González-Toledo, Emilia M. Carmona-Calero
Publikováno v:
Human Pathology: Case Reports, Vol 15, Iss, Pp 29-32 (2019)
Holoprosencephaly (HPE) is a birth defect that occurs during the first weeks of pregnancy and as a result the prosencephalon does not clearly divide in diencephalon, two halves of the telencephalon and lateral ventricles in the brain of the fetus and
Autor:
Ibrahim González-Marrero, Agustín Castañeyra-Perdomo, María Castañeyra-Ruiz, Agustín Castañeyra-Ruiz, Emilia M. Carmona-Calero, Nélida Rancel-Torres, Leandro Castañeyra-Ruiz, Héctor de Paz-Carmona, Juan M. González-Toledo
Publikováno v:
Advances in Endocrinology. 2014:1-6
The syndrome of inappropriate antidiuretic hormone (SIADH) is a disease characterized by hyponatremia and hyperosmolarity of urine where vasopressin and angiotensin II are implicated in the alteration of salt water balance and cardiovascular and bloo
Autor:
Maria L. Ruiz-Mayor, Juan M. González-Toledo, Leandro Castañeyra-Ruiz, Ibrahim González-Marrero, Héctor de Paz-Carmona, Agustín Castañeyra-Perdomo, Emilia M. Carmona-Calero, Agustín Castañeyra-Ruiz
Publikováno v:
The Open Pathology Journal. 6:1-7
The Syndrome of Inappropriate Antidiuretic Hormone (SIADH) is a disease characterized by hyponatremia and hyperosmolality of urine, and where vasopressin, angiotensin II and catecholamines are implicated in salt water balance, cardiovascular and bloo
Autor:
Leandro Castañeyra-Ruiz, Juan M. González-Toledo, Agustín Castañeyra-Ruiz, Lidia Ruiz-Mayor, Emilia M. Carmona-Calero, Héctor de Paz-Carmona, Agustín Castañeyra-Perdomo, Ibrahim González-Marrero
Publikováno v:
Neuroscience and Medicine. :60-64
High blood pressure produces ventricular dilation, variations in circumventricular organs and changes in the cerebrospinal fluid compositions. On the other hand, chronic hypertension in spontaneously hypertensive rats can cause changes in the integri
Autor:
María Castañeyra-Ruiz, Ibrahim González-Marrero, Agustín Castañeyra-Ruiz, Juan M. González-Toledo, Agustín Castañeyra-Perdomo, Emilia M. Carmona-Calero, Leandro Castañeyra-Ruiz
Publikováno v:
Medical Hypotheses. 82:74-76
Kallmann syndrome (KS) is a genetic disorder which combines hypogonadotropic hypogonadism and anosmia. Hypogonadism is characterized by the absence or reduced levels of gonadotropin-releasing hormone and anosmia due to olfactory bulb aplasia. KS trea
Autor:
Emilia M. Carmona-Calero, Juan M. González-Toledo, Paloma Fernández-Rodríguez, H. De Paz-Carmona, Agustín Castañeyra-Ruiz, M. L. Ruiz-Mayor, Ibrahim González-Marrero, Agustín Castañeyra-Perdomo, Leandro Castañeyra-Ruiz
Publikováno v:
Anatomia, Histologia, Embryologia. 38:282-285
Reissner's fibre (RF) is formed by the polymerization of the glycoprotein secreted by the subcommissural organ (SCO). The SCO also secretes soluble glycoprotein into the cerebrospinal fluid (CSF); variations in RF and SCO have been reported in hydroc