X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (173) 173
Publication (23) 23
Patent (4) 4
Book / eBook (3) 3
Book Chapter (1) 1
Book Review (1) 1
Conference Proceeding (1) 1
Dissertation (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (89) 89
index medicus (72) 72
male (56) 56
female (48) 48
neurosciences (48) 48
amyotrophic lateral sclerosis (43) 43
clinical neurology (36) 36
middle aged (33) 33
adult (26) 26
aged (25) 25
amyotrophic lateral sclerosis - genetics (22) 22
amyotrophic-lateral-sclerosis (22) 22
animals (22) 22
genetics & heredity (21) 21
als (19) 19
biomarkers (19) 19
disease (19) 19
research (18) 18
neurodegeneration (17) 17
analysis (16) 16
cohort studies (15) 15
neurology (15) 15
diagnosis (14) 14
risk factors (14) 14
cerebrospinal-fluid (13) 13
disease progression (13) 13
proteins (13) 13
psychiatry (13) 13
genetic aspects (12) 12
genetics (12) 12
research article (12) 12
adolescent (11) 11
aged, 80 and over (11) 11
article (11) 11
case-control studies (11) 11
young adult (11) 11
amyotrophic lateral sclerosis - pathology (10) 10
biochemistry & molecular biology (10) 10
care and treatment (10) 10
disease models, animal (10) 10
expression (10) 10
haplotypes (10) 10
multidisciplinary sciences (10) 10
mutation (10) 10
mutations (10) 10
neurofilament proteins - blood (10) 10
neurovetenskaper (10) 10
spinal cord (10) 10
abridged index medicus (9) 9
alleles (9) 9
biology (9) 9
cross-sectional studies (9) 9
longitudinal studies (9) 9
mice (9) 9
physiological aspects (9) 9
amyotrophic lateral sclerosis - diagnosis (8) 8
medical and health sciences (8) 8
medicin och hälsovetenskap (8) 8
medicine (8) 8
mutation - genetics (8) 8
nervous system diseases (8) 8
neurodegenerative diseases (8) 8
neuroscience (8) 8
pathology (8) 8
patients (8) 8
rodents (8) 8
settore bio/18 - genetica (8) 8
superoxide dismutase - genetics (8) 8
amyotrophic lateral sclerosis - blood (7) 7
base sequence (7) 7
clinical trials (7) 7
degeneration (7) 7
developmental prosopagnosia (7) 7
frontotemporal dementia (7) 7
spinal cord - metabolism (7) 7
studies (7) 7
superoxide dismutase (7) 7
amyotrophic lateral sclerosis - metabolism (6) 6
biomarker (6) 6
biomarkers - blood (6) 6
congenital prosopagnosia (6) 6
development and progression (6) 6
europe (6) 6
face recognition (6) 6
gene (6) 6
genetic markers (6) 6
genetic predisposition to disease (6) 6
genetic variation (6) 6
genotype (6) 6
health aspects (6) 6
immunoassay (6) 6
italy (6) 6
markers (6) 6
memory test (6) 6
molecular sequence data (6) 6
motor neuron disease (6) 6
multiple sclerosis (6) 6
multiple-sclerosis (6) 6
neurofilaments (6) 6
neuropsychological tests (6) 6
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Johnson, Janel O and Pioro, Erik P and Boehringer, Ashley and Chia, Ruth and Feit, Howard and Renton, Alan E and Pliner, Hannah A and Abramzon, Yevgeniya and Marangi, Giuseppe and Winborn, Brett J and Gibbs, J. Raphael and Nalls, Michael A and Morgan, Sarah and Shoai, Maryam and Hardy, John and Pittman, Alan and Orrell, Richard W and Malaspina, Andrea and Sidle, Katie C and Fratta, Pietro and Harms, Matthew B and Baloh, Robert H and Pestronk, Alan and Weihl, Conrad C and Rogaeva, Ekaterina and Zinman, Lorne and Drory, Vivian E and Borghero, Giuseppe and Mora, Gabriele and Calvo, Andrea and Rothstein, Jeffrey D and Drepper, Carsten and Sendtner, Michael and Singleton, Andrew B and Taylor, J Paul and Cookson, Mark R and Restagno, Gabriella and Sabatelli, Mario and Bowser, Robert and Chio`, Adriano and Traynor, Bryan J and Moglia, Cristina and Cammarosano, Stefania and Canosa, Antonio and Gallo, Sara and Brunetti, Maura and Ossola, Irene and Marinou, Kalliopi and Papetti, Laura and Pisano, Fabrizio and Pinter, Giuseppe Lauria and Conte, Amelia and Luigetti, Marco and Zollino, Marcella and Lattante, Serena and Marangi, Giuseppe and la Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Battistini, Stefania and Ricci, Claudia and Caponnetto, Claudia and Mancardi, Gianluigi and Mandich, Paola and Salvi, Fabrizio and Bartolomei, Ilaria and Mandrioli, Jessica and Sola, Patrizia and Lunetta, Christian and Penco, Silvana and Monsurrò, Maria Rosaria and Conforti, Francesca Luisa and Tedeschi, Gioacchino and Gambardella, Antonio and Quattrone, Aldo and Volanti, Paolo and Floris, Gianluca and Cannas, Antonino and Piras, Valeria and Marrosu, Francesco and Marrosu, Maria Giovanna and Murru, Maria Rita and Pugliatti, Maura and Parish, Leslie D and Sotgiu, Alessandra and Solinas, Giuliana and Ulgheri, Lucia and Ticca, Anna and Simone, Isabella and Logroscino, Giancarlo and Pirisi, Angelo and ITALSGEN
Nature Neuroscience, ISSN 1097-6256, 2014, Volume 17, Issue 5, pp. 664 - 666
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 01/2020, Volume 10, Issue 1, pp. 97 - 12
The lack of biomarkers for an early diagnosis of neurodegenerative disorders (NDs) has hampered the development of therapeutics whose effect would be enhanced... 
WHOLE-BLOOD | ENDOSKELETON | HEMOLYSIS | MULTIDISCIPLINARY SCIENCES | LIGHT-CHAIN | SAMPLES | IMMUNOASSAY | Plasma | Neurodegenerative diseases | Neurodegeneration | Lysis | Biomarkers | Hemoglobin | Amyotrophic lateral sclerosis | Neurofilaments | Filter paper | Drug development
Journal Article
Experimental Brain Research, ISSN 0014-4819, 2018, Volume 237, Issue 3, pp. 673 - 686
Prosopagnosia is a disorder leading to difficulties in recognizing faces. However, recent evidence suggests that individuals with congenital prosopagnosia can... 
Body recognition | Prosopagnosia | Face recognition | Self-recognition | DEVELOPMENTAL PROSOPAGNOSIA | RECOGNITION | PERFORMANCE | FASTER | INVERSION | CHILD | NEUROSCIENCES | PERCEPTION | ASYMMETRIES | SEX-DIFFERENCES | MEMORY TEST | Care and treatment | Genetic disorders | Diagnosis | Research | Self | Face | Advantages | Feet
Journal Article
PLoS ONE, ISSN 1932-6203, 2013, Volume 8, Issue 9, p. e75091
Objective: Neuronal damage is the morphological substrate of persisting neurological disability. Neurofilaments (Nf) are cytoskeletal proteins of neurons and... 
HEAVY-CHAIN | MULTIPLE-SCLEROSIS | BRAIN-INJURY | AXONAL DAMAGE MARKERS | SUBUNIT PNF-H | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GUILLAIN-BARRE-SYNDROME | NF-H | AMYOTROPHIC-LATERAL-SCLEROSIS | CEREBROSPINAL-FLUID NEUROFILAMENT | Guillain-Barre Syndrome - cerebrospinal fluid | Immunoassay | Electrochemical Techniques | Humans | Middle Aged | Amyotrophic Lateral Sclerosis - diagnosis | Male | Biomarkers - blood | Luminescent Measurements | Alzheimer Disease - cerebrospinal fluid | Amyotrophic Lateral Sclerosis - blood | Case-Control Studies | Alzheimer Disease - diagnosis | Neurofilament Proteins - blood | Guillain-Barre Syndrome - diagnosis | Amyotrophic Lateral Sclerosis - cerebrospinal fluid | Aged, 80 and over | Guillain-Barre Syndrome - blood | Adult | Female | Aged | Alzheimer Disease - blood | Development and progression | Amyotrophic lateral sclerosis | Nervous system diseases | Cytoskeletal proteins | Guillain-Barre syndrome | Alzheimer's disease | Drugs | Neuroprotection | Neurosciences | Nuclear magnetic resonance--NMR | Disease | Laboratories | Central nervous system | Clinical trials | Chains | Systematic review | Cerebrospinal fluid | Blood | Proteins | Neurodegeneration | Light | Neurofilaments | Longitudinal studies | Light levels | Medical research | Immunoglobulins | Neurodegenerative diseases | Electrochemiluminescence | Dentistry | Patients | Substrates | Blood levels | Neurological diseases | Medicine | Serum levels | Neurology | Brain research | Hospitals | Correlation analysis | Neurological complications | Structural damage | Biomarkers | Cytoskeleton | Nuclear magnetic resonance | NMR
Journal Article
by Nicolas, Aude and Kenna, Kevin P and Renton, Alan E and Ticozzi, Nicola and Faghri, Faraz and Chia, Ruth and Dominov, Janice A and Kenna, Brendan J and Nalls, Mike A and Keagle, Pamela and Rivera, Alberto M and van Rheenen, Wouter and Murphy, Natalie A and van Vugt, Joke J.F.A and Geiger, Joshua T and Van der Spek, Rick A and Pliner, Hannah A and Shankaracharya and Smith, Bradley N and Marangi, Giuseppe and Topp, Simon D and Abramzon, Yevgeniya and Gkazi, Athina Soragia and Eicher, John D and Kenna, Aoife and Logullo, Francesco O and Simone, Isabella and Logroscino, Giancarlo and Salvi, Fabrizio and Bartolomei, Ilaria and Borghero, Giuseppe and Murru, Maria Rita and Costantino, Emanuela and Pani, Carla and Puddu, Roberta and Caredda, Carla and Piras, Valeria and Tranquilli, Stefania and Cuccu, Stefania and Corongiu, Daniela and Melis, Maurizio and Milia, Antonio and Marrosu, Francesco and Marrosu, Maria Giovanna and Floris, Gianluca and Cannas, Antonino and Capasso, Margherita and Caponnetto, Claudia and Mancardi, Gianluigi and Origone, Paola and Mandich, Paola and Conforti, Francesca L and Mora, Gabriele and Marinou, Kalliopi and Sideri, Riccardo and Penco, Silvana and Mosca, Lorena and Lunetta, Christian and Pinter, Giuseppe Lauria and Corbo, Massimo and Riva, Nilo and Carrera, Paola and Volanti, Paolo and Mandrioli, Jessica and Fini, Nicola and Fasano, Antonio and Tremolizzo, Lucio and Arosio, Alessandro and Ferrarese, Carlo and Trojsi, Francesca and Tedeschi, Gioacchino and Monsurrò, Maria Rosaria and Piccirillo, Giovanni and Femiano, Cinzia and Ticca, Anna and Ortu, Enzo and La Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Sabatelli, Mario and Zollino, Marcella and Conte, Amelia and Luigetti, Marco and Lattante, Serena and Marangi, Giuseppe and Santarelli, Marialuisa and Petrucci, Antonio and Pugliatti, Maura and Pirisi, Angelo and Parish, Leslie D and Occhineri, Patrizia and Giannini, Fabio and Battistini, Stefania and Benigni, Michele and Cau, Tea B and Loi, Daniela and Calvo, Andrea and Moglia, Cristina and Brunetti, Maura and Barberis, Marco and ... and Project MinE ALS Sequencing Consortium and ALS Sequencing Consortium and Genomic Translation for ALS Care (GTAC) Consortium and NYGC ALS Consortium and ITALSGEN Consortium and Answer ALS Foundation and Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium and SLAGEN Consortium and French ALS Consortium and Genomic Translation ALS Care GTAC and Clinical Res ALS Related Disorders and Project MinE ALS Sequencing Consor and Answer ALS Fdn and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Neuron, ISSN 0896-6273, 03/2018, Volume 97, Issue 6, pp. 1268 - 1283.e6
Journal Article