Us
- Carlos E. Perezcano - Founder | CEO | CSO
- Ángel Ricardi - Medical Coordinator | Corporate Governance
- Mariana Pérez Coria - Medical Director
- Ramón Pérez Martínez - Genetics Medical Doctor
- Arturo Ortega - Scientific Advisor
- Dale Bredesen - ReCODE Medical Advisor
Carlos E. Perezcano
Founder | CEO | CSO
ACADEMIC BACKGROUND
- University Expert in Medical Genetics and Genomics (Universidad Católica de Murcia);
- MSc - Master’s Degree in Precision Medicine and Clinical Genetics (Universidad Politécnica de Valencia)
- MSc - Master’s Degree in Health Law and Medical Liability (IDEJ);
- Fundamentals of Neuroscience – The Electrical Properties of The Neuron (Harvard University);
- Cancer Genomics and Precision Oncology (Harvard Medical School);
- ReCODE Protocol for the Prevention and Reversal of Cognitive Decline, the only protocol that demonstrated for the first time in history that early-stage Dementia is reversible, with results published in the *Journal of Alzheimer Disease*, August 16, 2022;
- PhD - Public Health - 2025;
- PhD - Health Law and Medical Liability - 2026;
- PhD - Psychoanalysis – Neuropsychoanalysis - 2026;
- PhD - Science - Research Development (2025).
AWARDS AND HONORS
On December 16, 2022, he was awarded “Doctor Honoris Causa”, the highest honor an institution can bestow, by a Doctoral Council of over 15 Organizations and Universities, in recognition of his Professional Excellence and Notable Contribution to the Country’s Development.
On October 16, 2023, he was awarded by second time “Doctor Honoris Causa” for his Contribution to Humanity in the Medical and Scientific Progress in the Prevention and Reversal of Cognitive Decline, Alzheimer’s, and Dementia.
RESEARCH AND PUBLICATIONS
-APOE Genotype Distribution in a Mexican Population: A Comparative Study and its Implications for Alzheimer’s and Cardiovascular Disease
Human Biology
2025-04-17 | Preprint | Conceptualization, Writing - original draft, Writing - review & editing, Supervision, Validation
DOI: https://digitalcommons.wayne.edu/humbiol_preprints/228/
Contributors: Carlos E. Perezcano; Andrea Sánchez; Josué Nava.
-Clarifying APOE Genotyping through a Diagnostic Case of ε2/ε4 with Conflicting SNP Interpretation
Genomics 360 – Center for Research in Precision Medicine and Clinical Genomics
Working paper | Conceptualization, Formal analysis, Investigation, Methodology, Supervision, Validation, Writing - original draft, Writing - review & editing
Contributors: Carlos E. Perezcano; Andrea Sánchez; Francisco Javier Borrayo López; Mariana Pérez-Coria
-Metagenomic Functional Approach of the Gastrointestinal Human Microbiome
Genomics 360 – Center for Research in Precision Medicine and Clinical Genomics
Working paper | Conceptualization, Formal analysis, Investigation, Methodology, Supervision, Validation, Writing - original draft, Writing - review & editing
Contributors: Carlos E. Perezcano; Andrea Sánchez; Josué Nava; Mariana Pérez-Coria
-Genetic and Epigenetic Factors in Conversion Disorders (CD): An approach between Molecular Genetics and Affective Neuroscience
Genomics 360 - Center for Research in Precision Medicine and Clinical Genomics
Peer Review | Conceptualization, Formal analysis, Investigation, Methodology, Supervision, Validation, Visualization, Writing - original draft, Writing - review & editing
Contributors: Carlos E. Perezcano; Andrea Sánchez
-Genetic distribution of selected obesity-related SNPs in the FTO, MC4R, DRD2, FABP2, ADRB2, and SH2B1 genes: A pilot study in a Mexico City population
Genomics 360 - Center for Research in Precision Medicine and Clinical Genomics
Peer Review | Conceptualization, Writing - review & editing, Supervision, Validation
Contributors: Carlos E. Perezcano; Andrea Sánchez; Francisco Javier Borrayo López; Mariana Pérez-Coria
-Personalized Genomic Psychoanalysis (PGP): An Integrative Framework for Mental Health Interventions
Genomics 360 - Center for Research in Precision Medicine and Clinical Genomics
Peer Review | Conceptualization, Investigation, Methodology, Writing - original draft, Writing - review & editing
Contributors: Carlos E. Perezcano; Andrea Sánchez
-Finasteride, Pharmacogenomics, and Suicide Risk: A Public Health Concern
Genomics 360 - Center for Research in Precision Medicine and Clinical Genomics
Peer Review | Conceptualization, Writing - review & editing, Supervision, Validation
Contributors: Carlos E. Perezcano; Francisco Javier Borrayo López; Mariana Pérez-Coria
-Characterization of the cystine/glutamate antiporter in cultured Bergmann glia cells
Neurochemistry International
2017-09 | Journal article | Funding acquisition
DOI: 10.1016/j.neuint.2017.02.011
Part of ISSN: 0197-0186
Contributors: Edna Suárez-Pozos; Zila Martinez-Lozada; Orquidia G. Méndez-Flores; Alain M. Guillem; Luisa C. Hernández-Kelly; Francisco Castelán; Tatiana N. Olivares-Bañuelos; Donaji Chi-Castañeda; Mustapha NAJIMI; Arturo Ortega et al.
-Clock Genes in Glia Cells
ASN Neuro
2016-09 | Journal article | Funding acquisition
Part of ISSN: 1759-0914
Contributors: Donají Chi-Castañeda; Arturo Ortega
-Coupling of glutamate and glucose uptake in cultured Bergmann glial cells
Neurochemistry International
2016-09 | Journal article | Funding acquisition
DOI: 10.1016/j.neuint.2016.05.001
Part of ISSN: 0197-0186
Contributors: Orquidia G Mendez-Flores; Luisa C. Hernández-Kelly; Edna Suárez-Pozos; Mustapha Najimi; Arturo Ortega
-Glutamatergic Transmission: A Matter of Three
Neural Plasticity
2015 | Journal article | Funding acquisition
DOI: 10.1155/2015/787396
Part of ISSN: 2090-5904
Part of ISSN: 1687-5443
Contributors: Zila Martínez-Lozada; Arturo Ortega
-Methylphenidate Increases Glutamate Uptake in Bergmann Glial Cells
Neurochemical Research
2015-11 | Journal article | Funding acquisition
DOI: 10.1007/s11064-015-1721-z
Part of ISSN: 0364-3190
Part of ISSN: 1573-6903
Contributors: Alain M. Guillem; Zila Martínez-Lozada; Luisa C. Hernández-Kelly; Esther López-Bayghen; Bruno López-Bayghen; Oscar A. Calleros; Marco R. Campuzano; Arturo Ortega
-Glutamate-Dependent BMAL1 Regulation in Cultured Bergmann Glia Cells
Neurochemical Research
2015-05 | Journal article | Funding acquisition
DOI: 10.1007/s11064-015-1551-z
Part of ISSN: 0364-3190
Part of ISSN: 1573-6903
Contributors: Donají Chi-Castañeda; Stefan M. Waliszewski; Rossana C. Zepeda; Luisa C. R. Hernández-Kelly; Mario Caba; Arturo Ortega
-Signaling through EAAT-1/GLAST in cultured Bergmann glia cells
Neurochemistry International
2011-11 | Journal article | Funding acquisition
DOI: 10.1016/j.neuint.2011.07.015
Part of ISSN: 0197-0186
Contributors: Zila Martínez-Lozada; Luisa C. Hernández-Kelly; José Aguilera; Esther López-Bayghen; Arturo Ortega
Currently, working on 50+ projects aimed at preventing the negative genetic predisposition of Single Nucleotide Polymorphisms associated with Cognitive Decline, Alzheimer’s, and Dementia. Also developing his research project in Psychoanalysis using the Personalized Genomic Psychoanalysis (PGP), of which he is the Creator.
MEMBERSHIPS
NPSA: New York, USA, Member (Neuropsychoanalysis)
CONFERENCES
"Personalized Genomic Medicine in the Context of the Medical-Legal Revolution" (based on his Doctoral Thesis, setting a precedent for updating Clinical Practice Guidelines in Mexico)
"Advances in Clinical Genetics and Precision Medicine"
"Introduction to Personalized Genomic Psychoanalysis (PGP)"
"Personalized Genomic Medicine – Revolutionizing Medicine and Health Sciences"
COMPANIES AND CENTERS
-Founder and CEO of G3NOMICS 360, a pioneering and leading company in Personalized Genomic Medicine.
-Founder and CEO of the ReCODE Center, specializing in the Prevention and Reversal of Cognitive Decline in Alzheimer’s and Dementia patients.
-Founder and CEO of Personalized Genomic Psychotherapy and Psychoanalysis PGP Specialized Centers.
-Founder and Chairman of Grupo Sangreal.
Ángel Ricardi - Medical Coordinator | Corporate Governance
ACADEMIC BACKGROUND
School of Intermedical Medicine (UNAM)
-Bachelor's Degree in Medical Surgeon Specialty in health projects and management
-Master's Degree in Health Management and Administration (2026)
-Specialized Diploma in Medical Law
-Diploma in management of high-performance teams
-Leader in administrative management of health services, with multifaceted experience in industrial, corporate, insurance and academic environments.
-Specialist in maximizing resource efficiency and leading strategic projects, promoting continuous improvement and the achievement of objectives.
-Results-oriented and with a strategic vision for process optimization.
Mariana Pérez Coria - Medical Director
Academic background:
-Medical Doctor degree: UAEH, Pachuca, Hidalgo, Mexico (2010)
-Specialty in Medical Genetics: Dr. José Eleuterio González University Hospital, HU, UANL, Monterrey, Nuevo León (2014)
-Training stay in Genetic Biochemistry: Hospital Clinic, Barcelona, Spain. (2013)
-PhD in Human Genetics: UDG, Guadalajara, Jalisco, Mexico (2018-2023)
Specialization:
Medical Genetics, UANL.
Subspecialization:
PhD in Human Genetics, UDG.
Member of medical associations:
-Mexican Association of Human Genetics, A.C.: numerary member from 2018 to date.
-Mexican Association for the Study of Congenital Defects, A.C.: member from 2018 to date
-Mexican Council of Human Genetics: current recertification (2021-2026).
Professional experience:
Nuevo León Maternal and Children's Hospital: 6 months (geneticist/outpatient clinic).
Pachuca General Hospital: 4 years (medical geneticist attached to the pediatrics/Interconsultations/outpatient service).
Autonomous University of the State of Hidalgo: 4 years (Professor of the subject of embryology degree Medical Surgeon)
Intermedical University: 4 years (Professor of Clinical Genetics of the Bachelor's Degree in Medical Surgery).
UMAE Pediatrics CMNO, IMSS: 4 years to date (Medical geneticist/Interconsultations/Outpatient consultation/Assistant Professor to the specialty of medical genetics UDG).
Positions Organizations:
-Synod in certification exam for the specialty of Medical Genetics: 2022 and 2023.
-Committee for cochlear implant UMAE pediatrics, IMSS: 2024
Awards and Recognitions:
Recognition as an outstanding Specialist Doctor, IMSS: 2023-2024
Teaching:
-Autonomous University of the State of Hidalgo: 4 years (Professor of the subject of embryology degree Medical Surgeon)
-Intermedical University: 4 years (Professor of the subject of Clinical Genetics of the degree of Medical Surgeon).
-University of the Valley of Mexico: 2 years (Professor of Skin and Annexes in the medical surgeon degree).
-IMSS, UMAE Pediatrics: 4 years to date (Adjunct Professor of the specialty of medical genetics).
Publication/lectures:
-Cardiac rhabdomyomas. Presentation of tuberous sclerosis. Case Report, Arch Inv Mat Inf, 2013, V, 1, 30-33 New Mutation in the RAB27A Gene in a Mexican Family with Griscelli Syndrome Type 2, Dermatol Pediatr Latinoam, 2013, 11, 2, 68-71
-Identification of novel mutations in Mexican patients with Aarskog–Scott syndrome, Molecular Genetics & Genomic Medicine, 2015, 3, 3, 197–202
-Genotypes and Haplotypes in the AXIN2 and TCF7L2 Genes are Associated with Susceptibility and With Clinicopathological Characteristics in Breast Cancer Patients, Rosales-Reynoso, M. A. et al., British Journal of Biomedical Science, 2022, 79, 10211, 01/25/22
-Sex differences in fetal kidney reprogramming: the case in the reninangiotensin system, Pérez-Coria M, Vázquez-Rivera GE, Gómez-García EF, Mendoza-Carrera F, Pediatr Nephrol, 2023, 08/12/23
-Association of KLOTHO gene variants with metabolic and renal function parameters in Mexican patients living with type 2 diabetes, MendozaCarrera F, Farías-Basulto A, Gómez-García EF, Rizo de la Torre LDC, CuetoManzano AM, Cortés-Sanabria L, Pérez-Coria M, Vázquez-Rivera GE, J Diabetes Metab Disord, 2024, 04/23/24
-Effects of polycystic ovary syndrome on embryonic development, 2020 Academic Sessions of the Mexican Association for the Study of Congenital Defects, Faculty of Medicine, UANL, Monterrey, Nuevo León, 08/12/20
-Renal fetal reprogramming, epigenetic aspects, 2022 academic sessions of the Mexican association for the study of congenital defects, Faculty of Medicine, UANL, -Monterrey, Nuevo León, 02/09/22
-Diagnostic Odyssey in Rare Diseases: Challenges Beyond the Exome, Academic Sessions of the Society of Graduates, Students and Alumni of the Doctorate in Human Genetics, UDG, Guadalajara, Jalisco: 29/02/2024
Ramón Pérez Martínez - Medical Doctor
Academic background:
Bachelor's Degree in Military Medicine
Specialty in Medical Genetics
Specialization:
Medical Genetics
Member of Medical Associations:
National College of Military Physicians
Mexican Association of Human Genetics
Mexican Council of Genetics
Mexican College of Medical Geneticists
Member of the Genetics chapter of the Mexican College of Gynecology-Obstetrics
Professional experience:
Ministry of National Defense for 37 years with the following positions:
Leader of the Health Platoon of 22/o. Infantry Battalion of Ciudad Ixtepec, Oaxaca, from February 5, 1993 to December 1, 1995.
Leader of the Health Platoon of the 13/o. Motorized Cavalry Regiment of Ciudad Ixtepec, Oaxaca, from December 1, 1995 to August 31, 1998.
Chief of the Auxiliary Diagnostic and Treatment Services of the Regional Military Hospital of San Luis Potosí from December 30, 1998 to May 15, 2001.
Head of the Urology Service of the Regional Military Hospital of San Luis Potosí from May 16, 2001 to May 1, 2005.
Head of the Emergency Service from September 1, 2001 to December 30, 2005.
Chief of the Health Section of the Regional Military Hospital of San Luis Potosí from September 1, 2001 to March 31, 2007.
Secretary of the Clinical Records Committee of the Regional Military Hospital of San Luis Potosí from October 1, 2005 to March 31, 2007.
Head of the Research Group of the Technical Section of the General Directorate of Military Health from 1 April 2007 to 28 February 2008.
Head of the Research Department of the Medical Specialties Unit of the Ministry of National Defense from June 7, 2011 to 2015.
Head of teaching and research of the medical specialties unit of the army Mexico City 2015 to 2021
President of the Clinical Research Ethics Committee of the Medical Specialties Unit of the Ministry of National Defense from July 21, 2011 to 2021.
Chief of Genetics at the Medical Specialties Unit of the Mexican Army from March 1, 2011 to 2021.
Positions Organizations:
President of the Clinical Research Ethics Committee of the Medical Specialties Unit of the Ministry of National Defense from July 21, 2011 to 202.
Member of the Pharmacovigilance Committee of the Medical Specialties Unit of the Ministry of National Defense, from 2012 to 2021.
Member of the Quality and Patient Safety Committee from March 2017 to 2021.
Member of the Genetics Chapter of the Mexican College of Specialists in Gynecology and Obstetrics 2017-2018
Member of the National Commission for the Analysis, Evaluation, Registration and Monitoring of Rare Diseases instituted from July 2016 to 2021
Awards and Recognitions:
Rank of Captain 1st in the Mexican National Army September 1990
Degree of Major Medical Surgeon in the Mexican National Army September 1991
Rank of Lieutenant Colonel Medical Surgeon In The Mexican National Army September 2021
Medal of Perseverance Fifth Class awarded by the Mexican National Army November 1995
Fourth Class Perseverance Medal awarded by the Mexican National Army November 2000
Third Class Perseverance Medal Awarded by the Mexican National Army November 2005
Second Class Perseverance Medal Awarded by the Mexican National Army November 2010
First Class Perseverance Medal Awarded by the Mexican National Army November 2015
Special Perseverance Medal Awarded by the Mexican National Army November 2020
Diploma of Recognition for Services for 8 years and 5 months at the regional military hospital of San Luis Potosí, showing camaraderie, loyalty and accentuated professionalism in the performance of their work 2007
Recognition for having collaborated in obtaining the National Award for Quality in Health in the Medical Specialties Unit in its 2010 Edition granted by the Ministry of Health.
Recognition for carrying out Actions Aimed at Quality and Warmth, during the month of January 2014, in the medical specialties unit of the Ministry of National Defense.
Recognition for her valuable participation in the Certification of "Labor Equality and Non-Discrimination 2018" of the Medical Specialties Unit.
Recognition for his enthusiasm, dedication and professionalism, in the daily activities as Head of the Department of Teaching and Research of the Medical Specialties Unit of the Ministry of National Defense, during the period from March 1, 2011 to December 1, 2020, contributing to the well-being and care of the user.
Teaching:
MORE THAN 20 TEACHING POSITIONS, AMONG WHICH WE CAN MENTION:
ASSOCIATE PROFESSOR OF THE MILITARY SCHOOL OF HEALTH GRADUATES IN THE SUBJECT OF EMBRYOLOGY OF THE RESIDENCY PROGRAM IN GYNECOLOGY-OBSTETRICS, Women's Specialties Clinic, School Year 2012-2021
FULL PROFESSOR OF THE MILITARY SCHOOL OF HEALTH GRADUATES IN THE SUBJECT OF GENETICS OF THE RESIDENCY PROGRAM IN GYNECOLOGY-OBSTETRICS, Women's Specialties Clinic, School Year 2012-2021
Publication / conferences:
"SPEAKER OF THE CARDIOPULMONARY RESUSCITATION (CPR) WORKSHOP COURSE" Place: Hospital Militar de San Luís Potosí, S. L. P. Date: April 26, 2004. Organized by: The Teaching Headquarters of the Military Hospital of San Luis Potosí, S. L. P. Credits: 2.1 Continuing Medical Education Credits.
GUEST PROFESSOR AT THE MEDICAL GENETICS SEMINAR WITH THE TOPIC "BIOLOGICAL BASES, TERMINOLOGY AND MODELS OF INHERITANCE" Place: Pediatric Hospital of Coyoacán, Organized by: The Head of Teaching of the Pediatric Hospital of Coyoacán. June 26, 2009
ASSOCIATE PROFESSOR AT THE PAEDIATRIC CONFERENCE AT THE CENTRAL MILITARY HOSPITAL LECTURE: NEWS IN GENETICS Place: Aula Magna of the Central Military Hospital, organised by the Department of Teaching and Research of the Central Military Hospital, Period: from 18 to 20 June 2013
SPEAKER OF THE XIV COURSE ON CURRENT AFFAIRS IN LABORATORY TECHNIQUES PRESENTATION: INBORN ERRORS OF METABOLISM, CONGENITAL METABOLOPATHY. Place: auditorium of the Dental Specialties Unit Organized by: the Teaching and Research Area of the Medical Specialties Unit, Period: October 17, 2013.
SPEAKER AT THE PROGRAM OF HEALTH REGULATIONS FOR PUBLIC SERVANTS 2013, PRESENTATION: OFFICIAL MEXICAN STANDARD NOM-234-SSA1-2003, USE OF CLINICAL FIELDS FOR CLINICAL CYCLES AND UNDERGRADUATE INTERNSHIP Place: Aula Magna of the Medical Specialties Unit, organized by: the Teaching and Research Area of the Medical Specialties Unit, Period: December 17, 2013
ASSOCIATE PROFESSOR AT THE II PEDIATRIC CONFERENCE OF THE CENTRAL MILITARY HOSPITAL, PRESENTATION: METACHROMATIC LEUKODYSTROPHY, GENETIC DIAGNOSTIC APPROACH, Place: Aula Magna of the Central Military Hospital, Organized by the Department of Teaching and Research of the Central Military Hospital, Period: June 3 to 5, 2014
SPEAKER AT THE 2014 CONTINUING MEDICAL EDUCATION PROGRAM OF THE MEDICAL SPECIALTIES UNIT, PRESENTATION: CLINICAL RESEARCH ETHICS COMMITTEE Place: Aula Magna of the Medical Specialties Unit, organized by: the Teaching and Research Area of the Medical Specialties Unit, Period: August 9, 2014
SPEAKER AT THE 2014 CONTINUING MEDICAL EDUCATION PROGRAM OF THE MEDICAL SPECIALTIES UNIT, PRESENTATION: LINES OF RESEARCH, Place: Aula Magna of the Medical Specialties Unit, organized by: the Teaching and Research Area of the Medical Specialties Unit, Period: August 30, 2014
SPEAKER OF THE XV COURSE ON CURRENT AFFAIRS IN LABORATORY TECHNIQUES PRESENTATION: PREIMPLANTATION GENETIC DIAGNOSIS. Place: auditorium of the Dental Specialties Unit, Organized by: the Teaching and Research Area of the Medical Specialties Unit, Period: from October 15 to 17, 2014.
SPEAKER OF THE XVI COURSE ON CURRENT AFFAIRS IN LABORATORY TECHNIQUES PRESENTATION: MUTATIONS AND METABOLIC BLOCKADE IN INBORN ERRORS OF METABOLISM. Place: auditorium of the Dental Specialties Unit Organized by: the Teaching and Research Area of the Medical Specialties Unit, Period: from October 14 to 16, 2015.
SPEAKER OF THE XVII COURSE ON CURRENT AFFAIRS IN CLINICAL LABORATORY TECHNIQUES, PRESENTATION: TOP GENETIC DISEASES. Place: auditorium of the Dental Specialties Unit Organized by: the Teaching and Research Area of the Medical Specialties Unit, Period: October 13, 2016.
CONFERENCE: OFFICIAL MEXICAN STANDARD 234-SSA 2003 USE OF CLINICAL FIELDS AND UNDERGRADUATE INTERNSHIP DATE: OCTOBER 6, 2018 VENUE: MEDICAL SPECIALTIES UNIT ORGANIZED: BY THE TEACHING AND RESEARCH DEPARTMENT OF THE MEDICAL SPECIALTIES UNIT
CONFERENCE: CLINICAL REVIEW AND LABORATORY DIAGNOSIS OF SHCWARTZ, JAMPEL AND HUNTER SYNDROMES, DATE: OCTOBER 12, 2018, VENUE: DENTAL SPECIALTIES UNIT XIX CONGRESS OF NEWS IN DIAGNOSTIC TECHNIQUES IN CLINICAL LABORATORY 2018 ORGANIZED: BY THE DEPARTMENT OF TEACHING AND RESEARCH OF THE MEDICAL SPECIALTIES UNIT
CONFERENCE: DUCHENNE MUSCULAR DYSTROPHY DATE: 10-OCTOBER-2019 VENUE: DENTAL SPECIALTIES UNIT XX EVENT: CONGRESS OF NEWS IN DIAGNOSTIC TECHNIQUES IN CLINICAL LABORATORY 2019 ORGANIZED: BY THE DEPARTMENT OF TEACHING AND RESEARCH OF THE MEDICAL SPECIALTIES UNIT
CONFERENCE: GAUCHER DISEASE DATE: NOVEMBER 26, 2019 VENUE: MILITARY HOSPITAL FOR WOMEN'S SPECIALTIES AND NEONATOLOGY EVENT: 1ST CONFERENCE ON RARE DISEASES IN PEDIATRICS WITHIN THE FRAMEWORK OF THE IX CONGRESS OF THE MILITARY HOSPITAL FOR WOMEN'S SPECIALTIES AND NEONATOLOGY 2019 ORGANIZED: BY THE DEPARTMENT OF TEACHING AND RESEARCH OF THE MILITARY HOSPITAL FOR WOMEN'S SPECIALTIES AND NEONATOLOGY
PUBLISHED ARTICLES.
A Delta-Sarcoglycan Gene Polymorphism as a Risk Factor for Hypertrophic Cardiomyopathy, REVISTA: GENETIC TESTING AND MOLECULAR BIOMARKERS AÑO: Agosto 2012, Vol. 16, No. 8: 855-8582012
Neurodevelopmental delay secondary to pituitary stem dysgenesis clinical presentation of two cases, JOURNAL: MEXICAN JOURNAL OF NEUROSURGERY, YEAR: November-December 2014, 15(S3):S35
Miller Dieker syndrome, importance of determining genetic mutation and description of a case. JOURNAL: MEXICAN JOURNAL OF NEUROSURGERY, YEAR: November-December 2014, 15(S3):S35
Impact of Enzyme Replacement Therapy (ERT) for six months in a patient with early-onset Pompe disease, JOURNAL: MEXICAN JOURNAL OF NEUROSURGERY YEAR: November-December 2014, 15(S3):S10
Description of a patient with infantile onset Pompe disease after 45 months of enzyme replacement therapy EVENTO: Annual WORLD Symposium 2018 Abstracts, REVISTA: Molecular Genetics and Metabolism 123 (2018) S15–S153 Número de trabajo 330
"PREVALENCE OF PITUITARY STEM DYSGENESIS IN THE POPULATION ENTITLED UNDER 15 YEARS OF AGE IN THE MILITARY HEALTH SECTOR: DESCRIPTION OF 3 CASES" XXIV Annual Meeting of the Mexican Society of Pediatric Neurology A.C. From 20 to 23 May 2015
"PREVALENCE OF WILLIAMS SYNDROME IN THE POPULATION UNDER 15 YEARS OF AGE IN THE MILITARY SECTOR DESCRIPTION OF 3 CASES", XXIV Annual Meeting of the Mexican Society of Pediatric Neurology A.C. From 20 to 23 May 2015
NEURODEVELOPMENTAL DELAY SECONDARY TO PITUITARY STEM DYSGENESIS CLINICAL PRESENTATION OF TWO CASES, MEXICAN JOURNAL OF NEUROSURGERY, November-December 2014, 15(S3):S35
MILLER DIEKER SYNDROME IMPORTANCE OF GENETIC MUTATION AND CASE DESCRIPTION. REVISTA MEXICANA DE NEUROCIRUGÍA (MEXICAN JOURNAL OF NEUROSURGERY), November-December 2014, 15(S3):S35
CASE SERIES: PRADER-WILLI SYNDROME WITH MOLECULAR AND CYTOGENETIC DIAGNOSIS IN THE MEDICAL SPECIALTIES UNIT REVISTA DE SANIDAD MILITAR VOL 72 NUMS 3-4 MAY-AUGUST 2018 PP 258-263
METHYLMALONIC ACIDEMIA; REPORT OF THE FIRST CASE IN MEXICO MANAGED WITH CARGLUMIC ACID, MEXICAN JOURNAL OF ENDOCRINOLOGY, METABOLISM AND NUTRITION REV MEX ENDOCRINOL METAB NUTR. 2021; 8: 158-63
Arturo Ortega - Scientific Advisor
Doctor of Science in Neurobiology (PhD), 1991
The Weizmann Institute of Science, Rehovot, Israel
National Researcher Level III
LINES OF RESEARCH
Glutamic acid is the main excitatory neurotransmitter in the central nervous system. It exerts its actions by activating membrane receptors and transporters, whose over-activation is linked to neuronal death, a phenomenon known as excitotoxicity. In my laboratory we are interested in elucidating the glutamate-activated signaling cascades that regulate gene expression and are associated with neurodegenerative processes.
RESEARCH TOPICS
Participation of glial cells: astrocytes, oligodendrocytes and microglia in the regulation of glutamatergic neurotransmission. Translational control. Learning and memory.
AWARDS & DISTINCTIONS
-Member of the Inter-American Cooperation Committee, American Society for Neurochemistry 2017-2021 (Inter-American Cooperation Committee) https://www.asneurochem.org/Committees
-Member of the Committee of Young Latin American Investigators (American Society for Neurochemistry https://www.asneurochem.org/Committees
-Member of the Evaluation Committee of the Commission of Biological Sciences of Cells and Molecules - Type Working Team of the Fund for Scientific and Technological Research (FONCyT) of the Republic of Argentina.
-Member of the Evaluation Committee of the first stage of the 13th Edition of the awards for the best postgraduate theses. General Directorate of Research and Postgraduate Studies, Autonomous University of Aguascalientes, June 2021.
-Member of the Board of the American Society for Neurochemistry https://www.asneurochem.org/Leadership
Evaluation committees, technical committees and editorial committees
Miembro del Comité Editorial de Journal of Neurochemistryhttps://onlinelibrary.wiley.com/page/journal/14714159/homepage/editorialboard.html
Member of the Editorial Board of ASN Neurohttp://us.sagepub.com/en-us/nam/journal/asn-neuro#editorial-board
Member of the Editorial Board of Neurochemical Researchhttps://www.springer.com/journal/11064/editors
Member of the Editorial Board of Advances in Neurobiologyhttps://link.springer.com/bookseries/8787
Miembro del Comité Editorial de Neurochemistry Internationalhttps://www.journals.elsevier.com/neurochemistry-international/editorial-board
Miembro del Comité Editorial Frontiers in Neurosciencehttps://www.frontiersin.org/journals/neuroscience#editorial-board
Miembro Editor académico en BioMed Research International in Cell Biologyhttps://www.hindawi.com/journals/bmri/editors/
Dale Bredesen - ReCODE Medical Advisor
Dr. Dale Bredesen is an internationally renowned neuroscientist, known for his work on the mechanisms of neurodegenerative diseases such as Alzheimer's disease. A graduate of Caltech, he earned his medical degree at Duke University Medical Center and completed his neurology residency at the University of California, San Francisco. He subsequently worked in the laboratory of Nobel Laureate Stanley Prusiner at UCSF as an NIH postdoctoral fellow. He has held faculty positions at UCSF, UCLA, and UC San Diego. He directed the Program on Aging at the Burnham Institute before joining the Buck Institute in 1998 as its founding president and CEO. Dr. Bredesen has contributed significantly to the understanding and treatment of diseases such as Alzheimer's, being a pioneer in the development of innovative therapeutic approaches.
Experience
With over 10 years of experience in the field, you will receive the treatment you need.
Professional
We have up-to-date training and certifications, as well as prestigious publications in specialized magazines.
Confidentiality
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Reliability
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