Juan Fernando Ortiz
Overview
Explore the profile of Juan Fernando Ortiz including associated specialties, affiliations and a list of published articles.
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44
Citations
190
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Recent Articles
1.
Aguirre A, Astudillo Moncayo O, Mosquera J, Muyolema Arce V, Gallegos C, Ortiz J, et al.
Cureus
. 2023 Jul;
15(6):e39903.
PMID: 37404420
Facioscapulohumeral muscular dystrophy (FSHD) is the third most common type of muscular dystrophy. This disease presents as a slowly progressive asymmetric muscle weakness that involves the facial, scapular, and upper...
2.
Aguirre A, Vivanco R, Ortiz J, Rozen V, InsuastI W, Fiallos J, et al.
Cureus
. 2023 Jun;
15(5):e39237.
PMID: 37337500
CANOMAD, characterized by chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M (IgM) paraprotein, cold agglutinins, and disialosyl antibodies, encompasses a clinical, radiological, and laboratory diagnosis. CANOMAD is a rare condition, with fewer...
3.
Argudo J, Astudillo Moncayo O, Insuasti W, Garofalo G, Aguirre A, Encalada S, et al.
Cureus
. 2023 Jan;
14(12):e32709.
PMID: 36686069
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a mitochondrial disease that lacks a definitive treatment. Lately, there has been an increased interest in the scientific community about...
4.
Patel U, Mehta N, Patel A, Patel N, Ortiz J, Khurana M, et al.
Cureus
. 2022 Nov;
14(9):e29694.
PMID: 36321004
Few studies have thoroughly evaluated the neuro-invasive effect of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which may contribute to a wide range of sequelae from mild long-term effects...
5.
Ayala I, Aziz S, Argudo J, Yepez M, Camacho M, Ojeda D, et al.
Brain Sci
. 2022 Aug;
12(8).
PMID: 36009103
Ataxia is a constellation of symptoms that involves a lack of coordination, imbalance, and difficulty walking. Hereditary ataxia occurs when a person is born with defective genes, and this degenerative...
6.
Sen M, Moncayo J, Kelley M, Suarez Salazar D, Tenemaza M, Camacho M, et al.
Cureus
. 2022 Aug;
14(7):e27029.
PMID: 35989745
Alien limb phenomenon (ALP) is a clinical finding seen in numerous neurological disorders, including Creutzfeldt-Jakob disease (CJD). We aimed to conduct a systematic review to update advances in understanding the...
7.
Understanding Protein Protocadherin-19 (PCDH19) Syndrome: A Literature Review of the Pathophysiology
Moncayo J, Ayala I, Argudo J, Aguirre A, Parwani J, Pachano A, et al.
Cureus
. 2022 Jul;
14(6):e25808.
PMID: 35822151
PCDH19 syndrome is a monogenic epilepsy related to the protein protocadherin-19 (PCDH19) gene, which encodes for a protein important for brain development. The protein also seems to regulate gamma-aminobutyric acid...
8.
Pulvinar Sign, Stroke and Their Relationship with Fabry Disease: A Systematic Review and Metanalysis
Ortiz J, Solis M, Ali S, Khurana M, Moncayo J, Kothari N, et al.
Neurol Int
. 2022 Jun;
14(2):497-505.
PMID: 35736622
Background: Fabry disease (FD) is the second most common lysosomal storage disorder. This disorder affects multiple systems that include the cardiac, renal, and nervous system. The pulvinar sign (PS) is...
9.
Pacheco K, Ortiz J, Parwani J, Cruz C, Yepez M, Buj M, et al.
Neurol Int
. 2022 Jun;
14(2):488-496.
PMID: 35736621
(1) Background: Reversible cerebral vasoconstriction syndrome (RCVS) encompasses a clinical and radiological diagnosis characterized by recurrent thunderclap headache, with or without focal deficits due to multifocal arterial vasoconstriction and dilation....
10.
Patel U, Patel N, Khurana M, Parulekar A, Patel A, Ortiz J, et al.
Neurol Int
. 2022 Jun;
14(2):441-452.
PMID: 35736618
Introduction: Tobacco use is one of the most significant risk factors for stroke. Besides traditional cigarettes and combustible products, the use of e-cigarettes and electronic nicotine delivery products has been...