Monoamino oxidase alleles correlate with the presence of essential hypertension among hypogonadic patients

Author:

Royo José Luis1ORCID,Castellano‐Castillo Daniel23,Ruiz‐Galdon Maximiliano1,Molina‐Vega María23,Cardona Fernando23,Tinahones Francisco J.23,Fernández‐García José C.23,Reyes‐Engel Armando1

Affiliation:

1. Department of Surgery, Biochemistry and Immunology School of Medicine University of Malaga Málaga Spain

2. Unidad de Gestión Clínica de Endocrinología y Nutrición del Hospital Virgen de la Victoria Instituto de Investigación Biomédica de Málaga (IBIMA) Universidad de Málaga Málaga Spain

3. Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y la Nutrición, CIBERobn Málaga Spain

Funder

Ministerio de Educación, Cultura y Deporte

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference62 articles.

1. 5 years treatment of arterial hypertension with a monoamine oxidase inhibiter (Marsilid);Abaza A.;Annales De Cardiologie Et D'angeiologie,1968

2. Association of MAOA gene functional promoter polymorphism with CSF dopamine turnover and atypical depression

3. Polymorphisms in genes implicated in dopamine, serotonin and noradrenalin metabolism suggest association with cerebrospinal fluid monoamine metabolite concentrations in psychosis

4. Monoamine oxidase defect in essential arterial hypertension. A single dose pargyline test;Anselmi B.;Monographs in Neural Sciences,1976

5. Proceedings: Monoamine oxidase defect in essential arterial hypertension: “a single dose pargyline test”;Anselmi R.;British Journal of Pharmacology,1974

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