- Speech-Induced Task-Specific Cranio-Cervical Tardive Dystonia: An Unusual Phenomenology
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Holla VV
- KMID: 2511495
- J Mov Disord.
- 2021 Jan;14(1):84-85.
- doi: 10.14802/jmd.20067
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- Myoclonus-Dystonic Presentation of Childhood Onset DYT-GCH1: A Report From India
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Sharma P, Holla VV, Gurram S, Kamble N, Yadav R, Pal PK
- KMID: 2539029
- J Mov Disord.
- 2023 Jan;16(1):101-103.
- doi: 10.14802/jmd.22106
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- Dystonic Opisthotonus in Kufor-Rakeb Syndrome: Expanding the Phenotypic and Genotypic Spectrum
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Gurram S, Holla VV, Kumari R, Dhar D, Kamble N, Yadav R, Muthusamy B, Pal PK
- KMID: 2545935
- J Mov Disord.
- 2023 Sep;16(3):343-346.
- doi: 10.14802/jmd.23098
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- “Face of the Giant Panda” Sign and Bilateral Thalamic Hyperintensity in Isoniazid-Induced Ataxia
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Holla VV, Netravathi M, Kamble N, Saini J, Pal PK
- KMID: 2551217
- J Mov Disord.
- 2024 Jan;17(1):99-101.
- doi: 10.14802/jmd.23112
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- Movement Disorders Associated With Radiotherapy and Surgical Procedures
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Surisetti BK, Prasad S, Holla VV, Kamble N, Yadav R, Pal PK
- KMID: 2539019
- J Mov Disord.
- 2023 Jan;16(1):42-51.
- doi: 10.14802/jmd.22092
Occasionally, movement disorders can occur following interventional procedures including but not limited to radiotherapy, dental procedures, and cardiac, cerebral and spinal surgeries. The majority of these disorders tend to be... -
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- Sialidosis Type I without a Cherry Red Spot— Is There a Genetic Basis?
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Neeraja K, Holla VV, Prasad S, Surisetti BK, Rakesh K, Kamble N, Yadav R, Pal PK
- KMID: 2511490
- J Mov Disord.
- 2021 Jan;14(1):65-69.
- doi: 10.14802/jmd.20083
Sialidosis is an inborn error of metabolism due to a defect in the NEU1 gene and manifests as two phenotypes: mild type I and severe type II. The cherry red... -
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- Utility of Clinical Exome Sequencing in Dystonia: A Single-Center Study From India
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Holla VV, Neeraja K, Stezin A, Prasad S, Surisetti BK, Netravathi M, Kamble N, Yadav R, Pal PK
- KMID: 2530222
- J Mov Disord.
- 2022 May;15(2):156-161.
- doi: 10.14802/jmd.21146
Objective With the use of next-generation sequencing in clinical practice, several genetic etiologies of dystonia have been identified. This study aimed to ascertain the utility of clinical exome sequencing (CES)... -
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- Clinical and Imaging Profile of Patients with Joubert Syndrome
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Surisetti BK, Holla VV, Prasad S, Neeraja K, Kamble N, Yadav R, Pal PK
- KMID: 2547821
- J Mov Disord.
- 2021 Sep;14(3):231-235.
- doi: 10.14802/jmd.21066
Objective Joubert syndrome (JS) is a rare syndrome characterized by ataxia and the molar tooth sign (MTS) on imaging. The present study aims to explore the clinical and radiological features... -
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- Deep Brain Stimulation Battery Exhaustion during the COVID-19 Pandemic: Crisis within a Crisis
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Holla VV, Neeraja K, Surisetti BK, Prasad S, Kamble N, Srinivas D, Yadav R, Pal PK
- KMID: 2506750
- J Mov Disord.
- 2020 Sep;13(3):218-222.
- doi: 10.14802/jmd.20073
Objective The novel coronavirus disease (COVID-19) pandemic and public health measures to control it have resulted in unique challenges in the management of patients with deep brain stimulation (DBS). We... -
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- Patient Knowledge, Attitude and Perceptions towards Botulinum Toxin Treatment for Movement Disorders in India
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Mol TN, Kamble N, Holla VV, Mahale R, Pal PK, Yadav R
- KMID: 2516385
- J Mov Disord.
- 2021 May;14(2):126-132.
- doi: 10.14802/jmd.20094
Objective There is limited literature on the knowledge, attitude, and perceptions (KAP) of botulinum toxin (BoNT) treatment among patients and caregivers. The objective of this study was to assess the... -
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- The Non-Motor Symptom Profile of Progressive Supranuclear Palsy
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Chaithra SP, Prasad S, Holla VV, Stezin A, Kamble N, Yadav R, Pal PK
- KMID: 2503077
- J Mov Disord.
- 2020 May;13(2):118-126.
- doi: 10.14802/jmd.19066
Objective Non-motor symptoms (NMSs) significantly contribute to increased morbidity and poor quality of life in patients with parkinsonian disorders. This study aims to explore the profile of NMSs in patients... -
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- KMT2B-Related Dystonia in Indian Patients With Literature Review and Emphasis on Asian Cohort
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Dhar D, Holla VV, Kumari R, Sriram N, Saini J, Yadav R, Pandey A, Kamble N, Muthusamy B, Pal PK
- KMID: 2545925
- J Mov Disord.
- 2023 Sep;16(3):285-294.
- doi: 10.14802/jmd.23035
ObjectiveaaMutations in the KMT2B gene have been identified in patients previously diagnosed with idiopathic dystonia. Literature on KMT2B-related dystonia is sparse in the Indian and Asian populations. MethodsaaWe report seven patients... -
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