Carlos Alcalde Martín
A5081905231- Classical Antiquity Studies
- Organic Chemistry Synthesis Methods
- Joseph Conrad and Literature
- Historical Art and Architecture Studies
- Cultural and Mythological Studies
- Early Modern Spanish Literature
- Kawasaki Disease and Coronary Complications
- Metabolism and Genetic Disorders
- Chemical synthesis and alkaloids
- Marine Sponges and Natural Products
- Coronary Artery Anomalies
- Cardiac Structural Anomalies and Repair
- Folate and B Vitamins Research
- Classical Philosophy and Thought
- Diet and metabolism studies
- Lysosomal Storage Disorders Research
- Glycogen Storage Diseases and Myoclonus
- Literary and Cultural Studies
- Historical, Religious, and Philosophical Studies
- Photographic and Visual Arts
- Mitochondrial Function and Pathology
- Cardiac electrophysiology and arrhythmias
- Literature, Culture, and Aesthetics
- Medical and Health Sciences Research
- Archaeological and Historical Studies
Hospital Universitario Río Hortega
2003-2020
Universidad de Málaga
2008-2019
AVM Faculdade Integrada
2014
University of Coimbra
2014
San Antonio College
2014
Centro Universitário Belas Artes de São Paulo
2014
Universidad de Granada
1997
Mucopolysaccharidosis type II (MPS II) is an inherited X-linked disease associated with a deficiency in the enzyme iduronate 2-sulfatase due to gene (IDS) mutations. Recent studies MPS carriers did not find clinical involvement, but these were mainly performed by anamnesis and patients' self-reported description of signs symptoms. So although it rare heterozygous carriers, investigations other types disorders suggest that some manifestations may be possibility. The aim this study was...
Kawasaki disease is a self-limiting acute vasculitis that affects small and medium-sized vessels, the most common cause of acquired heart in children our environment. Up to 25% untreated patients develop coronary aneurysms. It suspected an infectious agent may be trigger disease, but causative still unknown. Based on previous evidence, recommendations are proposed for diagnosis, treatment long-term management these patients, order unify criteria. The diagnosis must quick, based easy-to-use...
Benign convulsions with mild gastroenteritis (CwG) are a rare diagnosis in Western countries, and it is characterized by afebrile seizures, almost times more than once, during without severe hydroelectrolitic affection. The most frequent implied virus rotavirus. This benign disease, spite of cluster neither complementary explorations nor antiepileptic treatment required.Seven cases between 6 27 months aged CwG due to rotavirus reported.Four patients had one seizure, all were generalized...
Retrospective analysis of the neurodevelopment in first two years life patients with severe congenital heart disease.Out 89 disease 19 were excluded due to a history prematurity and/or chromosomopathy, four ischemic stroke and lack medical history. Denver Test (DT) results at 2, 6, 12, 15 18 months, motor, language social interaction fields achieved.59.4% male 40.6% female. The mean age undergoing extracorporeal membrane oxygenation pathological DT months was 3 compared 11.88 those normal...
Although with early treatment phenylketonuria patients may have average intelligence levels, it is important to optimize the nutritional management maintain adequate phenylalanine so that can develop their intellectal potential free of abnormalities in daily activities due deficits cognitive executive functions. This study presents a series 26 patients, diagnosed and treated early, who underwent psychometric evaluation together determinations along lives, at time doing tests. A trend...
Background . Multiple acyl-CoA dehydrogenase deficiency is an autosomal recessive disorder of the amino acid metabolism and fatty oxidation due to electron transfer protein or ubiquinone oxidoreductase. The clinical picture ranges from a severe neonatal lethal presentation late myopathic forms responsive riboflavin. Up now, there no effective treatment for form, which exhibits metabolic acidosis, hyperammonemia, hypoketotic hypoglycemia, rhabdomyolysis. We present case child who has had good...
On the numerous occasions in which Plutarch mentions places, monuments, objects or events his Parallel Lives, there are few examples we assured that he had seen those personally, either because states so outright uses formulaic expressions indicates experience, can deduce it from descriptions and comments.In this paper study value of author’s findings own eyewitness testimony. A key aspect is role eye witness testimony discussions nature characters its relationship with other elements...
Las ilustraciones de Picasso a las Metamorfosis Ovidio evidencian la tradición clásica en distintos aspectos: tema centrado el hombre, iconografía, estilo y espíritu. Tienen un rasgo fundamental los mitos, libertad tratamiento que les da permanente vitalidad actualidad.