Catalogo Prodotti UNIBA

Catalogo Prodotti UNIBA: [154961] Home page macrotipologia

Sfoglia

N.D. 0

1 Contributo su Rivista 92057
- 1.1 Articolo in rivista 84777
- 1.2 Recensione in rivista 2175
- 1.3 Scheda bibliografica 507
- 1.4 Nota a sentenza 1080
- 1.5 Abstract in rivista 3341
- 1.6 Traduzione in rivista 177

2 Contributo in Volume 26766
- 2.1 Contributo in volume (Capitolo o Saggio) 23965
- 2.2 Prefazione/Postfazione 808
- 2.3 Breve introduzione 297
- 2.4 Voce (in dizionario o enciclopedia) 1089
- 2.5 Traduzione in volume 284
- 2.6 Recensione in volume 38
- 2.7 Schede di catalogo 285

3 Libro 4596
- 3.1 Monografia o trattato scientifico 4073
- 3.2 Concordanza 5
- 3.3 Indice 21
- 3.4 Bibliografia 25
- 3.5 Edizione critica 129
- 3.6 Pubblicazione di fonti inedite 16
- 3.7 Commento scientifico 64
- 3.8 Traduzione di libro 263

4 Contributo in Atti di Convegno (Proceeding) 26995
- 4.1 Contributo in Atti di convegno 20271
- 4.2 Abstract in Atti di convegno 5753
- 4.3 Poster 971

5 Altro 1904
- 5.01 Composizione 0
- 5.02 Disegno 1
- 5.03 Design 2
- 5.04 Performance 8
- 5.05 Esposizione 23
- 5.06 Mostra 33
- 5.07 Manufatto 1
- 5.08 Prototipo d'arte e relativi progetti 0
- 5.09 Cartografia 74
- 5.10 Banca dati 70
- 5.11 Software 29
- 5.12 Altro 1663

6 Brevetti 275
- 6.1 Brevetto 275

7 Curatele 2082
- 7.1 Curatela 2082

8 Tesi di dottorato 289
- 8.1 Tesi di dottorato 289

Prodotti recenti

Pathophysiological mechanisms of oromandibular dystonia

Oromandibular dystonia (OMD) is a rare form of focal idiopathic dystonia. OMD was clinically identified at the beginning of the 20th century, and the main clinical features have been progressively described over the years. However, OMD has several peculiarities that still remain unexplained, including the high rate of oral trauma, which is often related to the onset of motor symptoms. The purpose of this paper was to formulate a hypothesis regarding the pathophysiology of OMD, starting from t...

Does epilepsy contribute to the clinical phenotype of C9orf72 mutation in fronto-temporal dementia?

C9orf72 mutation is the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) worldwide. Recently, several reports of patients with FTD who carried the C9orf72 mutation and also manifested epilepsy have been published, since seizures occur in FTD at a higher rate than in the general population, the possible association between epilepsy and C9orf72 mutation remains to be clarified. In the attempt to understand whether epilepsy contributes to the phe...

Longitudinal evaluation of patients with isolated head tremor

Introduction: Isolated head tremor, a pathological condition characterized by head tremor without dystonic postures or tremor in other body parts, has recently been suggested to be a form of dystonia. It is however still unclear whether isolated head tremor precedes dystonia or remains unmodified overtime. Methods: We enrolled 20 patients with isolated head tremor. For each patient, we assessed videos recorded at enrollment and after 5 years. The videotapes were reviewed by two independent ex...

Neurofilament assessment in patients with cervical dystonia

We evaluated levels of serum neurofilament light chains (NfL), a known biomarker of neuroaxonal damage, in patients with cervical dystonia (CD) and healthy controls (HCs). CD patients had normal NfL levels supporting the hypothesis that CD may be considered as a functional network disorder rather than as a neurodegenerative disease.

Olfactory hallucinations in Parkinson's disease patients and the role of their evaluation in clinical practice

none

Scopri

Accesso al fulltext

no fulltext120567
reserved16332
open16223
partially open1815
embargoed14
restricted7
mixed3