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Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia.
- Published in:
- 2016
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- Publication type:
- letter
HPCA-related dystonia: Too rare to be found?
- Published in:
- 2016
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- Publication type:
- letter
De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
- Published in:
- Movement Disorders, 2014, v. 29, n. 9, p. 1190, doi. 10.1002/mds.25876
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- Publication type:
- Article
Cognitive impairment in multiple system atrophy: A position statement by the neuropsychology task force of the MDS multiple system atrophy (MODIMSA) study group.
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- Movement Disorders, 2014, v. 29, n. 7, p. 857, doi. 10.1002/mds.25880
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- Publication type:
- Article
Cognitive Impairment in Multiple System Atrophy: A Position Statement by the Neuropsychology Task Force of the MDS Multiple System Atrophy (MODIMSA) Study Group.
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- Movement Disorders, 2014, v. 29, p. 857, doi. 10.1002/mds.25880
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- Publication type:
- Article
White matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutations.
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- Movement Disorders, 2013, v. 28, n. 6, p. 772, doi. 10.1002/mds.25397
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- Publication type:
- Article
Status dystonicus: Predictors of outcome and progression patterns of underlying disease.
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- Movement Disorders, 2012, v. 27, n. 6, p. 783, doi. 10.1002/mds.24981
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- Publication type:
- Article
Quality of life in patients with treated and clinically stable Wilson's disease.
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- Movement Disorders, 2011, v. 26, n. 8, p. 1503, doi. 10.1002/mds.23608
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- Publication type:
- Article
Reply: MRI measurements of brain stem structures in patients with Richardson's syndrome, progressive supranuclear palsy-parkinsonism, and Parkinson's disease.
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- Movement Disorders, 2011, v. 26, n. 8, p. 1575, doi. 10.1002/mds.23702
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- Publication type:
- Article
MRI measurements of brainstem structures in patients with Richardson's syndrome, progressive supranuclear palsy-parkinsonism, and Parkinson's disease.
- Published in:
- Movement Disorders, 2011, v. 26, n. 2, p. 247, doi. 10.1002/mds.23293
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- Publication type:
- Article
Impaired insulin sensitivity and secretion in normoglycemic patients with spinocerebellar ataxia type 1.
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- Movement Disorders, 2010, v. 25, n. 12, p. 1976, doi. 10.1002/mds.23176
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- Publication type:
- Article
Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.
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- Movement Disorders, 2010, v. 25, n. 11, p. 1577, doi. 10.1002/mds.22857
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- Publication type:
- Article
ATP13A2 variants in early-onset Parkinson's disease patients and controls.
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- Movement Disorders, 2009, v. 24, n. 14, p. 2104, doi. 10.1002/mds.22728
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- Publication type:
- Article
The first cinematic presentation of a possible rhythmic movement disorder in a Disney film precedes its scientific debut by 60 years.
- Published in:
- Movement Disorders, 2009, v. 24, n. 1, p. 143, doi. 10.1002/mds.22232
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- Publication type:
- Article
Multiple rhythmic movement disorders in a teenage boy with excellent response to clonazepam.
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- Movement Disorders, 2008, v. 23, n. 5, p. 767, doi. 10.1002/mds.21969
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- Publication type:
- Article
Delayed-onset dystonia due to perinatal asphyxia: A prospective study.
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- Movement Disorders, 2007, v. 22, n. 16, p. 2426, doi. 10.1002/mds.21747
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- Publication type:
- Article
Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in serbian family with Myofibrillogenesis regulator 1 gene mutation.
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- Movement Disorders, 2006, v. 21, n. 11, p. 2010, doi. 10.1002/mds.21095
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- Publication type:
- Article
Changes in cortical inhibition during task-specific contractions in primary writing tremor patients.
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- Movement Disorders, 2006, v. 21, n. 6, p. 855, doi. 10.1002/mds.20807
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- Publication type:
- Article
Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients.
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- Movement Disorders, 2006, v. 21, n. 2, p. 187, doi. 10.1002/mds.20687
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- Publication type:
- Article
Reply: Bilateral chorea-ballism associated with hyperthyroidism.
- Published in:
- Movement Disorders, 2005, v. 20, n. 4, p. 512, doi. 10.1002/mds.20428
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- Publication type:
- Article
Incidence of vascular hemiballism in the population of Belgrade.
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- Movement Disorders, 2004, v. 19, n. 12, p. 1469, doi. 10.1002/mds.20256
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- Publication type:
- Article
Bilateral chorea-ballism associated with hyperthyroidism.
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- Movement Disorders, 2004, v. 19, n. 8, p. 982, doi. 10.1002/mds.20119
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- Publication type:
- Article
Prevalence of primary late-onset focal dystonia in the Belgrade population.
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- Movement Disorders, 2003, v. 18, n. 11, p. 1389, doi. 10.1002/mds.10615
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- Publication type:
- Article
Therapeutic efficacy of bilateral prefrontal slow repetitive transcranial magnetic stimulation in depressed patients with Parkinson's disease: An open study.
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- Movement Disorders, 2002, v. 17, n. 3, p. 528, doi. 10.1002/mds.10109
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- Publication type:
- Article
Dystonia in Wilson's disease.
- Published in:
- Movement Disorders, 2001, v. 16, n. 4, p. 719, doi. 10.1002/mds.1118
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- Publication type:
- Article
Penicillamine-induced lethal status dystonicus in a patient with Wilson's disease.
- Published in:
- 2001
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- Publication type:
- journal article
Bereitschaftspotential in depressed and non-depressed patients with Parkinson's disease.
- Published in:
- Movement Disorders, 2001, v. 16, n. 2, p. 294, doi. 10.1002/mds.1059
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- Publication type:
- Article
Visuomotor skill learning on serial reaction time task in patients with early Parkinson's disease.
- Published in:
- Movement Disorders, 2000, v. 15, n. 6, p. 1095, doi. 10.1002/1531-8257(200011)15:6<1095::AID-MDS1006>3.0.CO;2-R
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- Publication type:
- Article
Adherence to Medication among Parkinson's Disease Patients Using the Adherence to Refills and Medications Scale.
- Published in:
- 2022
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- Publication type:
- journal article
Craniocervical Dystonia Questionnaire (CDQ-24): Validation and Cross-Cultural Adaptation in Serbian Patients.
- Published in:
- Collegium Antropologicum, 2009, v. 33, n. 4, p. 1185
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- Publication type:
- Article
Factors associated with deterioration of health-related quality of life in multiple system atrophy: 1-year follow-up study.
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- Acta Neurologica Belgica, 2018, v. 118, n. 4, p. 589, doi. 10.1007/s13760-018-0962-4
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- Publication type:
- Article
Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center.
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- Neurogenetics, 2024, v. 25, n. 3, p. 193, doi. 10.1007/s10048-024-00766-8
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- Publication type:
- Article
DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery.
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- Neurogenetics, 2024, v. 25, n. 2, p. 141, doi. 10.1007/s10048-024-00752-0
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- Publication type:
- Article
The Diagnosis of Dementia Is Unspecified – Report of a Pilot Survey of Dementia in Belgrade.
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- Gerontology, 2004, v. 50, n. 4, p. 260, doi. 10.1159/000078357
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- Publication type:
- Article
An Expert System for Quantification of Bradykinesia Based on Wearable Inertial Sensors.
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- Sensors (14248220), 2019, v. 19, n. 11, p. 2644, doi. 10.3390/s19112644
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- Publication type:
- Article
Quantification of Finger-Tapping Angle Based on Wearable Sensors.
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- Sensors (14248220), 2017, v. 17, n. 2, p. 203, doi. 10.3390/s17020203
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- Publication type:
- Article
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia.
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- Movement Disorders Clinical Practice, 2024, v. 11, n. 6, p. 626, doi. 10.1002/mdc3.14020
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- Publication type:
- Article
Laboratory‐Supported Multiple System Atrophy beyond Autonomic Function Testing and Imaging: A Systematic Review by the MoDiMSA Study Group.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 322, doi. 10.1002/mdc3.13158
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- Publication type:
- Article
The Pathophysiology of Fatigue in Parkinson's Disease and its Pragmatic Management.
- Published in:
- Movement Disorders Clinical Practice, 2016, v. 3, n. 4, p. 323, doi. 10.1002/mdc3.12343
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- Publication type:
- Article
Dystonia in Patients With Spinocerebellar Ataxia Type 2.
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- Movement Disorders Clinical Practice, 2016, v. 3, n. 3, p. 292, doi. 10.1002/mdc3.12274
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- Publication type:
- Article
Changes of Phenotypic Pattern in Functional Movement Disorders: A Prospective Cohort Study.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.582215
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- Publication type:
- Article
Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.
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- Genes, 2020, v. 11, n. 9, p. 1037, doi. 10.3390/genes11091037
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- Publication type:
- Article
Variants in the 3′UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression.
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- European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1265, doi. 10.1038/ejhg.2012.84
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- Publication type:
- Article
A laboratory-based study on patients with Parkinson's disease and seborrheic dermatitis: the presence and density of Malassezia yeasts, their different species and enzymes production.
- Published in:
- BMC Dermatology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-5945-14-5
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- Publication type:
- Article
A laboratory-based study on patients with Parkinson's disease and seborrheic dermatitis: the presence and density of Malassezia yeasts, their different species and enzymes production.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Health-related quality of life as a predictor of recurrent falling in Parkinson's disease: 1-year follow-up study.
- Published in:
- Psychogeriatrics, 2016, v. 16, n. 6, p. 362, doi. 10.1111/psyg.12178
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- Publication type:
- Article
Quality of life in Serbian patients with Parkinson's disease.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.
- Published in:
- Genes, 2017, v. 8, n. 10, p. 276, doi. 10.3390/genes8100276
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- Publication type:
- Article
Neuropsychiatric symptoms in early onset Alzheimer's disease and frontotemporal dementia: Neuropsychiatry and behavioral neurology/Assessment/Measurement of neuropsychiatric/Behavioral and psychological symptoms.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.044068
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- Publication type:
- Article
Screening for gene mutation in early onset Alzheimer's disease and frontotemporal dementia: Report from a Serbian tertiary referral center: Genetics/genetic factors of non‐Alzheimer's tauopathies.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.041807
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- Publication type:
- Article