Isidro Ferrer Abizanda investigador
Ferrer, Isidro (Ferrer Abizanda)
Ferrer, Isidro
VIAF ID: 87866648 (Personal)
Permalink: http://viaf.org/viaf/87866648
Preferred Forms
- 100 1 0 ‡a Ferrer, Isidro
- 100 1 _ ‡a Ferrer, Isidro
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- 100 0 _ ‡a Isidro Ferrer Abizanda ‡c investigador
4xx's: Alternate Name Forms (10)
Works
Title | Sources |
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Alteraciones cuantitativas y morfológicas de las células de Langerhans epidérmicas en pacientes con transplante renal | |
Biopsia endomiocàrdica en miocardiopaties | |
Canvis en l'expressió gènica i en la síntesi de proteïnes produïts per la isquèmia cerebral | |
Contribución a la morfogénesis postnatal del córtex sensorimotor y nervio óptico | |
Desarrollo neuromuscular en la atrofia muscular espinal | |
Differential induction and spread of tau pathology in young PS19 tau transgenic mice following intracerebral injections of pathological tau from Alzheimer's disease or corticobasal degeneration brains | |
Efectos del etanol las dendritas y espinas dendríticas de las neuronas de diferentes regiones cerebrales en el alcoholismo crónico humano del adulto y en el síndrome alcohólico fetal en el niño y en un modelo experimental en la rata | |
Energy metabolism and Protein synthesis in Parkinson's disease and Dementia with Lewy Bodies | |
Envejecimiento cerebral | |
Estudi de les sinucleïnopaties : l'alfa-sinucleïna a la sinapsi i efectes de l'estrès oxidatiu | |
Estudio de la histogénesis de las alteraciones citoarquitec tónicas de la corteza cerebral | |
Evolución de los cambios morfológicos en el hipocampo y en el córtex cerebral de la rata en el estado epiléptico inducido farmacológicamente | |
Expressió de parvalbúmina en el múscul estriat de la rata durant el desenvolupament postnatal i en models experimentals de denervació i degeneració de les fibres musculars | |
Factors patogènics convergents en taupaties | |
Formación y desarrollo de las circunvoluciones cerebrales : estudio morfométrico del desarrollo postnatal de la circunvolución suprasilviana media y de los surcos adyacentes en el gato | |
Guia per a la prevenció i el control de les encefalopaties espongiformes transmissibles | |
Impacto del estrés oxidativo y la disfunción mitocondrial en la homeostasis energética en Adrenoleucodistrofia : implicaciones terapéuticas | |
Implicació del BDNF en malalties neurodegeneratives humanes i en models experimentals in vivo | |
Isquemia cerebral transitoria en el jerbu com a model de malaltia cerebral estudi de neurones inhibidores corticals de circuit local i de mecanismes de mort cel·lular] | |
El mal de les vaques boges: riscos per a la salut : document informatiu per a professionals de la salut | |
Malformacions cerebrals induïdes per radiació | |
Mecanismos inmunológicos involucrados en la patogénia de la esclerosis múltiple | |
Modelling X-linked adrenoleukodystrophy in C. elegans and beyond : a tale of fatty acids and oxidative stress | |
Morfología de las neuronas de la sexta capa de la corteza cerebral : estudio comparativo con el método de Golgi en especies lisencefálicas y girencefálicas, cambios plásticos durante el plegamiento cortical normal y anormal : tesis ... | |
Mort neuronal en l'escorça cerebral de la rata en desenvolupament | |
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions | |
Neuronal pentraxin 1 contributes to the neuronal damage evoked by amyloid-beta and is overexpressed in dystrophic neurites in Alzheimer's brain. | |
Neuropathology of sporadic Parkinson disease before the appearance of parkinsonism: preclinical Parkinson disease | |
Neuroprotective role of trans-resveratrol in a murine model of familial Alzheimer's disease. | |
A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration. | |
NRF2 and RIP140 as new therapeutic targets for X-linked adrenoleukodystrophy (X-ALD) : control of redox/metabolic homeostasis and inflammation | |
Oxidative damage compromises energy metabolism in the axonal degeneration mouse model of X-adrenoleukodystrophy | |
Oxidative Stress in Desminopathies and Myotilinopathies: A Link between Oxidative Damage and Abnormal Protein Aggregation | |
Oxidative stress, mitochondrial and proteostasis malfunction in adrenoleukodystrophy: A paradigm for axonal degeneration | |
Oxidative stress regulates the ubiquitin-proteasome system and immunoproteasome functioning in a mouse model of X-adrenoleukodystrophy. | |
(Patho-)physiological relevance of PINK1-dependent ubiquitin phosphorylation | |
Patologia molecular de les miopaties miofibril·lars | |
Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene. | |
Les plantes i la vegatació del Castell de l'Oreneta : Itinerari botànic | |
Plasma YKL-40 in the spectrum of neurodegenerative dementia | |
Poly(propylene imine) dendrimers with histidine-maltose shell as novel type of nanoparticles for synapse and memory protection | |
The Presence of Human Herpesvirus 6 in the Brain in Health and Disease | |
Prion Protein Interactome: Identifying Novel Targets in Slowly and Rapidly Progressive Forms of Alzheimer's Disease. | |
The Quest for Cellular Prion Protein Functions in the Aged and Neurodegenerating Brain | |
Regulació transcripcional dels receptors d’adenosina en les malalties neurodegeneratives | |
Relevance of host tau in tau seeding and spreading in tauopathies | |
Retraction Note: In situ structural characterization of early amyloid aggregates in Alzheimer's disease transgenic mice and Octodon degus | |
Revealing Adenosine A2A-Dopamine D2 Receptor Heteromers in Parkinson's Disease Post-Mortem Brain through a New AlphaScreen-Based Assay | |
RNA editing alterations define manifestation of prion diseases | |
Role of cellular prion protein in interneuronal amyloid transmission. | |
The serine protease inhibitor neuroserpin is required for normal synaptic plasticity and regulates learning and social behavior | |
Severe alterations in lipid composition of frontal cortex lipid rafts from Parkinson's disease and incidental Parkinson's disease | |
Severe cerebral white matter involvement in a case of dentatorubropallidoluysian atrophy studied at autopsy | |
Sixty years old is the breakpoint of human frontal cortex aging. | |
Specific Metabolomics Adaptations Define a Differential Regional Vulnerability in the Adult Human Cerebral Cortex | |
Spontaneous generation of infectious prion disease in transgenic mice | |
Sporadic Creutzfeldt-Jakob disease with glial PrPRes nuclear and perinuclear immunoreactivity | |
Striatal adenosine A2A receptor expression is controlled by S-adenosyl-L-methionine-mediated methylation | |
The Structure of the Spinal Cord Ependymal Region in Adult Humans Is a Distinctive Trait among Mammals | |
Subtype and regional-specific neuroinflammation in sporadic creutzfeldt-jakob disease | |
Succination of Protein Thiols in Human Brain Aging | |
TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies. | |
Target genes of neuron-restrictive silencer factor are abnormally up-regulated in human myotilinopathy | |
Tau hyperphosphorylation induces oligomeric insulin accumulation and insulin resistance in neurons. | |
Tau-positive nuclear indentations in P301S tauopathy mice. | |
Tauroursodeoxycholic bile acid arrests axonal degeneration by inhibiting the unfolded protein response in X-linked adrenoleukodystrophy | |
TGF-beta1 increases tyrosine hydroxylase expression by a mechanism blocked by BMP-2 in human neuroblastoma SH-SY5Y cells | |
Tomografía computarizada en pediatría | |
Transcriptional network analysis in frontal cortex in Lewy body diseases with focus on dementia with Lewy bodies | |
Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies | |
Transgenic mice overexpressing the full-length neurotrophin receptor TrkC exhibit increased catecholaminergic neuron density in specific brain areas and increased anxiety-like behavior and panic reaction. | |
Tubers from patients with tuberous sclerosis complex are characterized by changes in microtubule biology through ROCK2 signalling. | |
Type-1 cannabinoid receptor activity during Alzheimer's disease progression. | |
Unexpected expression of alpha- and beta-globin in mesencephalic dopaminergic neurons and glial cells | |
Unveiling the olfactory proteostatic disarrangement in Parkinson's disease by proteome-wide profiling | |
Up-regulation of the Kv3.4 potassium channel subunit in early stages of Alzheimer's disease. | |
Upregulation of a small vault RNA (svtRNA2-1a) is an early event in Parkinson disease and induces neuronal dysfunction. | |
VDAC and ERalpha interaction in caveolae from human cortex is altered in Alzheimer's disease. | |
Vías de señalización en enfermedades priónicas | |
Vies de senyalització de mort en neurodegeneració | |
Vivir con el alzheimer | |
Whole genome grey and white matter DNA methylation profiles in dorsolateral prefrontal cortex. | |
YKL40 in sporadic amyotrophic lateral sclerosis: cerebrospinal fluid levels as a prognosis marker of disease progression | |
α-Synuclein accumulates in huntingtin inclusions but forms independent filaments and its deficiency attenuates early phenotype in a mouse model of Huntington's disease. | |
αB-crystallin and HSP27 in glial cells in tauopathies. |