Cargando…

Vascular Parkinsonism with Dystonia in Moyamoya Disease: An Expansion of Movement Disorder Phenomenology

Detalles Bibliográficos
Autores principales:	Mahale, Rohan R., Dubbal, Rohin, Padmanabha, Hansashree, Mailankody, Pooja
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350800/ https://www.ncbi.nlm.nih.gov/pubmed/35936641 http://dx.doi.org/10.4103/aian.aian_768_21

Ejemplares similares

Cervical Dystonia with Cerebellar Ataxia in KCNA1 Mutation: A Phenotypic Expansion
por: Mahale, Rohan R., et al.
Publicado: (2022)

Childhood-Onset Generalized Dystonia Due to NDUFA9 Gene Mutation: An Expansion of Mutations Causing Leigh’s Syndrome
por: Singh, Raviprakash, et al.
Publicado: (2023)

Kennedy's Disease: A Second Genetically Confirmed Report from India
por: Shah, Rutul, et al.
Publicado: (2021)

Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence
por: Mahale, Rohan, et al.
Publicado: (2022)

Spastic Paraplegia Type 8: A First Report from India
por: Mahale, Rohan, et al.
Publicado: (2023)

Postpartum Optic Neuropathy: Think of Myelin Oligodendrocyte Glycoprotein Immunoglobulin G-Associated Optic Neuritis - Report of Two Cases
por: Mahale, Rohan R., et al.
Publicado: (2021)

Hereditary Spastic Paraplegia due to LYST Gene Mutation: A Novel Causative Gene
por: Mahale, Rohan R., et al.
Publicado: (2023)

DYT30 due to VPS16 Mutation: An Etiology of Childhood-Onset Generalized Dystonia
por: Shashi, Sridhar, et al.
Publicado: (2023)

Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation
por: Mahale, Rohan R., et al.
Publicado: (2021)

Upbeat Nystagmus in Late Onset Cerebellar Ataxia: Think of Anti-Glutamate Decarboxylase 65 Antibody-Associated Cerebellar Ataxia
por: Mahale, Rohan R., et al.
Publicado: (2021)

Autoimmune Antibodies Positivity in Probable Sporadic Creutzfeldt–Jakob Disease: A Mini-Review of Literature
por: Anudeep, Davuluri Durga Srinivas, et al.
Publicado: (2023)

Pseudo-neonatal Adrenoleukodystrophy: A Rare Peroxisomal Disorder
por: Arora, Cheshta, et al.
Publicado: (2022)

ADCY5-Related Dyskinesia: A Genetic Cause of Early-Onset Chorea-Report of Two Cases and a Novel Mutation
por: Padmanabha, Hansashree, et al.
Publicado: (2021)

ANCA-associated Vasculitic Neuropathy Following Anti-SARS-CoV-2 Vaccination: An Epiphenomenon or Causal Association?
por: Jha, Shreyashi, et al.
Publicado: (2023)

A Rare Case of Ataxia-Telangiectasia-Like Disorder With MRE11 Mutation
por: Mahale, Rohan R, et al.
Publicado: (2020)

Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation
por: Mahale, Rohan R., et al.
Publicado: (2021)

COASY Protein-Associated Neurodegeneration: Report from India
por: Mahale, Rohan R., et al.
Publicado: (2023)

CSF1R Related Leukoencephalopathy - Rare Childhood Presentation of An Autosomal Dominant Microgliopathy!
por: Sriram, Neeharika, et al.
Publicado: (2022)

Granulomatous Panuveitis in Multiple Sclerosis: A Rare Occurrence
por: Shah, Rutul, et al.
Publicado: (2022)

Longitudinally Extensive Transverse Myelitis with Optic Neuritis Related to Profound Biotinidase Deficiency: NMOSD Mimic!
por: Ravikumar, Nagaraj Angadi, et al.
Publicado: (2023)

Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with MTHFR Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association
por: Mahale, Rohan R., et al.
Publicado: (2021)

Electroencephalography as a Diagnostic Aid in a Girl with Neuroregression and Stereotypies
por: Dhar, Debjyoti, et al.
Publicado: (2020)

N-Methyl-D-Aspartate Encephalitis our Experience with Diagnostic Dilemmas, Clinical Features, and Outcome
por: Chandra, Sadanandavalli R., et al.
Publicado: (2018)

Clinical, Biochemical, Radiological, and Genetic Profile of Patients with Homocysteine Remethylation Pathway Defect and Spastic Paraplegia
por: Padmanabha, Hansashree, et al.
Publicado: (2021)

Speech-Induced Task-Specific Cranio-Cervical Tardive Dystonia: An Unusual Phenomenology
por: Holla, Vikram Venkappayya
Publicado: (2021)

Status epilepticus in a child with influenza A H1N1 infection: An expansion of neurological abnormalities
por: Mahale, Rohan R., et al.
Publicado: (2016)

Bupropion-Induced Dystonia in a Patient with Parkinson’s Disease
por: Vegda, Monalisa, et al.
Publicado: (2020)

Impact of Disrupted Botulinum Toxin Therapy in Movement Disorders Due to COVID-19 Pandemic
por: Neeraja, Koti, et al.
Publicado: (2021)

Oro-mandibular dystonia in pediatric moyamoya disease: Two cases report
por: Koga, Yuichiro, et al.
Publicado: (2021)

Oculogyric Crisis in a Girl with Infantile Parkinsonism-Dystonia-2
por: Singanamalla, Bhanudeep, et al.
Publicado: (2021)

The phenomenology and natural history of idiopathic lower cranial dystonia
por: Termsarasab, Pichet, et al.
Publicado: (2014)

Dystonia an unusual presentation in pediatric moyamoya disease: Imaging findings of a case
por: Kumar, Suresh, et al.
Publicado: (2016)

Dystonia, myoclonus, and encephalopathy in a single patient: A rare association of moyamoya
por: Roy, Ujjawal, et al.
Publicado: (2016)

Deep Brain Stimulation and Thalamotomy for the Treatment of Dystonia Acquired by Moyamoya Disease with Stroke
por: Wu, Yunhao, et al.
Publicado: (2020)

An expansion for Neutrino Phenomenology
por: Grinstein, Benjamin, et al.
Publicado: (2012)

Slowed Movement Stopping in Parkinson’s Disease and Focal Dystonia is Improved by Standard Treatment
por: Choudhury, Supriyo, et al.
Publicado: (2019)

Generalized dystonia without Parkinsonism in an LRRK2 carrier
por: Díaz-Feliz, Lola, et al.
Publicado: (2022)

Psychiatric disorders in primary focal dystonia and in Parkinson’s disease
por: Dias, Fernando MV, et al.
Publicado: (2011)

An Elderly Woman with Reversal of Clinical Presentation Mimicking Rapid-Onset Dystonia-Parkinsonism
por: Ahn, Byoung June, et al.
Publicado: (2018)

The phenomenological movement : a historical introduction /
por: Spiegelberg, Herbert
Publicado: (1965)

Cannot write session to /tmp/vufind_sessions/sess_v5bhustjergbqv92qhc61cg3vs