X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4991) 4991
Publication (446) 446
Newsletter (140) 140
Book Chapter (61) 61
Book Review (59) 59
Book / eBook (13) 13
Conference Proceeding (7) 7
Data Set (5) 5
Magazine Article (3) 3
Dissertation (2) 2
Reference (2) 2
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (4019) 4019
male (2575) 2575
female (2387) 2387
clinical neurology (1896) 1896
index medicus (1711) 1711
adult (1571) 1571
middle aged (1556) 1556
magnetic resonance imaging (1224) 1224
ataxia (1123) 1123
neurosciences (1076) 1076
cerebellar ataxia (1045) 1045
aged (922) 922
cerebellar ataxia - diagnosis (852) 852
child (754) 754
adolescent (714) 714
diagnosis (696) 696
diagnosis, differential (689) 689
cerebellum (619) 619
neurology (602) 602
mutation (526) 526
child, preschool (499) 499
cerebellum - pathology (475) 475
research (456) 456
cerebellar ataxia - etiology (448) 448
atrophy (439) 439
cerebellar-ataxia (411) 411
pediatrics (404) 404
cerebellar ataxia - genetics (394) 394
surgery (372) 372
genetic aspects (363) 363
cerebellar diseases - diagnosis (359) 359
spinocerebellar ataxia (347) 347
disease (341) 341
pedigree (341) 341
brain - pathology (336) 336
phenotype (325) 325
genetics & heredity (318) 318
animals (314) 314
brain (313) 313
tomography, x-ray computed (307) 307
psychiatry (306) 306
care and treatment (302) 302
infant (292) 292
syndrome (274) 274
children (273) 273
young adult (264) 264
cerebellar ataxia - physiopathology (258) 258
risk factors (241) 241
patients (235) 235
gene (232) 232
cerebellar ataxia - pathology (227) 227
genetics (225) 225
cerebellar ataxia - complications (222) 222
health aspects (219) 219
spinocerebellar ataxias - genetics (219) 219
medicine & public health (218) 218
medicine (208) 208
analysis (207) 207
medical research (207) 207
article (202) 202
nervous system diseases (201) 201
age of onset (199) 199
neurologic examination (198) 198
mutations (197) 197
disease progression (196) 196
treatment outcome (196) 196
medicine, general & internal (195) 195
aged, 80 and over (186) 186
dominant cerebellar-ataxia (186) 186
degeneration (185) 185
neuroimaging (185) 185
multiple system atrophy (182) 182
nervous system (181) 181
follow-up studies (177) 177
medicine, experimental (177) 177
retrospective studies (177) 177
case report (173) 173
ataxia - diagnosis (171) 171
cerebellar diseases - pathology (168) 168
mri (162) 162
case studies (161) 161
disorders (161) 161
cerebellar neoplasms - diagnosis (159) 159
antibodies (158) 158
cerebellum - physiopathology (154) 154
spinocerebellar ataxias - diagnosis (154) 154
age (151) 151
severity of illness index (151) 151
cerebellar (149) 149
physiological aspects (149) 149
cerebellum - abnormalities (148) 148
acute disease (146) 146
cerebellar diseases - complications (146) 146
clinical-features (144) 144
cerebellar atrophy (143) 143
usage (142) 142
cerebellar neoplasms - pathology (140) 140
dna mutational analysis (140) 140
development and progression (138) 138
features (138) 138
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (4585) 4585
Japanese (148) 148
German (129) 129
French (122) 122
Spanish (106) 106
Russian (23) 23
Polish (22) 22
Italian (16) 16
Czech (11) 11
Dutch (6) 6
Portuguese (6) 6
Turkish (6) 6
Chinese (5) 5
Norwegian (5) 5
Korean (4) 4
Romanian (3) 3
Swedish (3) 3
Croatian (2) 2
Hungarian (2) 2
Icelandic (1) 1
Serbian (1) 1
Slovak (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Renaud, Mathilde and Tranchant, Christine and Martin, Juan Vicente Torres and Mochel, Fanny and Synofzik, Matthis and van de Warrenburg, Bart and Pandolfo, Massimo and Koenig, Michel and Kolb, Stefan A and Anheim, Mathieu and Alonso, Isabel and Azzedine, Hamid and Barbot, Clara and Bereau, Matthieu and Berkovic, Sam and Bernard, Geneviéve and Bindoff, Laurence A and Bompaire, Flavie and Bonneau, Dominique and Bonneau, Patrizia and Boycott, Kym M and Bras, Jose and Brais, Bernard and Brigatti, Karlla W and Cameron, Jillian and Chamova, Teodora and Choquet, Karine and Delague, Valérie and Denizeau, Philippe and Dotti, Maria Teresa and El‐Euch, Ghada and Elmalik, Salah A and Federico, Antonio and Fiskerstrand, Torunn and Gagnon, Cynthia and Guerreiro, Rita and Guissart, Claire and Hassin‐Baer, Sharon and Heimdal, Ketil Riddervold and Héron, Bénédicte and Isohanni, Pirjo and Kalaydijeva, Luba and Kawarai, Toshitaka and Koht, Jeanette Aimee and Lai, Szu‐Chia and Piana, Roberta La and Lecocq, Claire and Linnankivi, Tarja and Lönnqvist, Tuula and Lu, Chin‐Song and Maas, Roderick and Mahlaoui, Nizar and Mallaret, Martial and Marelli, Cecilia and Mariotti, Caterina and Mathieu, Jean and Méneret, Aurélie and Mignarri, Andrea and Monin, Marie Lorraine and Montaut, Solveig and Nanetti, Lorenzo and Nadjar, Yann and Poujois, Aurélia and Salih, Mustafa A and Sousa, Sergio and Stanier, Philip and Stoppa‐Lyonnet, Dominique and Strauss, Kevin and Tallaksen, Chantal and Tarnopolsky, Mark and Tinant, Nadége and Tournev, Ivailo and Topaloglu, Haluk and Varhaug, Kristin Nielsen and Woimant, France and Wolf, Nicole I and Yahalom, Gilad and Yoon, Grace and Young, Millie and RADIAL Working Grp and RADIAL Working Group and the RADIAL Working Group
Annals of Neurology, ISSN 0364-5134, 12/2017, Volume 82, Issue 6, pp. 892 - 899
Objective Differential diagnosis of autosomal recessive cerebellar ataxias can be challenging. A ranking algorithm named RADIAL that predicts the molecular... 
CEREBELLAR-ATAXIA | PHENOTYPE | DISORDERS | MUTATIONS | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | Cerebellum | Sensitivity analysis | Cerebellar ataxia | Scoring | Patients | Genetic screening | Literature reviews | Sensitivity | Ranking | Algorithms | Magnetic resonance imaging | Predictions | Fingers & toes | Biomarkers | Ataxia | Electromyography | Bioindicators | Differential diagnosis | Diagnosis | EMG
Journal Article
Journal Article
Journal Article
ARQUIVOS DE NEURO-PSIQUIATRIA, ISSN 0004-282X, 03/2019, Volume 77, Issue 3, pp. 184 - 193
Cerebellar ataxia is a common finding in neurological practice and has a wide variety of causes, ranging from the chronic and slowly-progressive cerebellar... 
PSYCHIATRY | Cerebellar ataxia | CLASSIFICATION | SYMPTOMS | OPSOCLONUS-MYOCLONUS | cerebellar diseases | NEUROSCIENCES | cerebellum | DEFICIENCY | DEGENERATION | FEATURES | Cerebellum | Edema | Cerebral infarction | Nutrient deficiency | Vitamin deficiency | Ataxia | Differential diagnosis | Hemorrhage | Metabolic disorders | cerebelo | Ataxia cerebelar | doenças cerebelares
Journal Article
Current Opinion in Neurology, ISSN 1350-7540, 08/2009, Volume 22, Issue 4, pp. 419 - 429
Journal Article
Journal of Neuroinflammation, ISSN 1742-2094, 09/2015, Volume 12, Issue 1, p. 168
Serological testing for anti-neural autoantibodies is important in patients presenting with idiopathic cerebellar ataxia, since these autoantibodies may... 
Anti-Nb | Autoantibodies | Paraneoplastic cerebellar degeneration | Inositol 1,4,5-trisphosphate receptor 1 (ITPR1, I3PR) antibodies | Cerebellar degeneration-related protein 2-like (CDR2L) antibodies | Protein kinase gamma (PKCγ) antibodies | Cerebellitis | Rho GTPase activating protein 26 (ARHGAP26, GRAF) antibodies | Voltage-gated calcium channel (VGCC) antibodies | Anti-AP3B2 | Delta notch-like epidermal growth factor-related receptor (DNER) antibodies | Homer-3 antibodies | Anti-Ca | Anti-Tr | Autoimmune cerebellar ataxia | Purkinje cell antibody 2 (PCA-2) | Purkinje cells | Metabotropic glutamate receptor 1 (mGluR1) antibodies | Cerebellar degeneration-related protein 2 (CDR2) antibodies | Glutamate receptor delta2 (GluRδ2) antibodies | Neuronal adaptin-like protein (beta-NAP) antibodies | Anti-Yo | Carbonic anhydrase-related protein VIII (CARP VIII) antibodies | Anti-Sj | HUMAN TUMOR-IMMUNITY | PARANEOPLASTIC NEUROLOGICAL SYNDROMES | IMMUNOLOGY | RECOMBINANT YO PROTEIN | CEREBROSPINAL-FLUID | FACTOR-RELATED RECEPTOR | DEGENERATION-ASSOCIATED ANTIGEN | CENTRAL-NERVOUS-SYSTEM | STIFF-PERSON SYNDROME | Protein kinase gamma (PKC gamma) antibodies | NEUROSCIENCES | HODGKINS-DISEASE | NEUROMYELITIS-OPTICA | Glutamate receptor delta2 (GluR delta 2) antibodies | Adaptor Protein Complex 3 - immunology | Autoantibodies - metabolism | Cerebellar Ataxia - metabolism | Nerve Tissue Proteins - immunology | Humans | Purkinje Cells | Adaptor Protein Complex beta Subunits - immunology | Cerebellar Ataxia - diagnosis | Receptors, Cell Surface - immunology | Cerebellar Ataxia - immunology | Immunohistochemistry | Autoimmunity | Antigens | Calcium channels | Prognosis | Cerebellar ataxia | Forecasts and trends | B cells | Glutamate | Diagnosis | Health aspects | Protein kinases
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 09/2011, Volume 1233, Issue 1, pp. 139 - 147
Journal Article