Venous thromboembolism in COVID-19 patients and prediction model: a multicenter cohort study von Lee, Yi, Jehangir, Qasim, Li, Pin, Gudimella, Deepthi, Mahale, Pooja, Lin, Chun-Hui, Apala, Dinesh R, Krishnamoorthy, Geetha, Halabi, Abdul R, Patel, Kiritkumar, Poisson, Laila, Balijepally, Venugopal, Sule, Anupam A, Nair, Girish B

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Hereditary Spastic Paraplegia due to LYST Gene Mutation: A Novel Causative Gene von Mahale, Rohan, Arunachal, Gautam, Singh, Raviprakash, Padmanabha, Hansashree, Mailankody, Pooja

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Childhood-onset generalized dystonia due to NDUFA9 gene mutation: An expansion of mutations causing leigh's syndrome von Singh, Raviprakash, Padmanabha, Hansashree, Arunachal, Gautam, Mailankody, Pooja, Mahale, Rohan

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Adult-onset cranio-cervical segmental dystonia due to ADAR1 gene mutation: A novel phenotype von Mahale, Rohan, Arunachal, Gautham, Padmanabha, Hansashree, Mailankody, Pooja

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Autoimmune Antibodies Positivity in Probable Sporadic Creutzfeldt–Jakob Disease: A Mini-Review of Literature von Anudeep, Davuluri Srinivas, Padmanabha, Hansashree, Mailankody, Pooja, Mathuranath, P, Mahale, Rohan

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Early-onset levodopa responsive parkinsonism in PPP2R5D mutation von Mahale, Rohan, Arunachal, Gautham, Chadha, Deepak, Padmanabha, Hansashree, M, Pooja, Pavagada, Mathuranath

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ANCA-associated vasculitic neuropathy following Anti-SARS-CoV-2 vaccination: An epiphenomenon or causal association? von Jha, Shreyashi, Hema, A, Padmanabha, Hansashree, Mahadevan, Anitha, Mailankody, Pooja, Mathuranath, P, Mahale, Rohan

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Postural Orthostatic Tachycardia Syndrome (POTS) as a Cause of Dizziness – Expanding the Etiological Spectrum von Baskar, Dipti, Mailankody, Pooja, Sathyaprabha, Talakad Narasappa, Mathuranath, P S, Mahale, Rohan R, Padmanabha, Hansashree

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The phenotypic conundrum of Trp748Ser variant in POLG gene: a report of two patients von Rathore, Abhishek, Arunachal, Gautham, Mahale, Rohan R, Padmanabha, Hansashree, Mailankody, Pooja

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Spastic Ataxia with Sensory Neuropathy Sans Cerebral Leukodystrophy in Probable Adult Polyglucosan Body Disease von Mahale, Rohan, Shashi, Sridhar, Mahadevan, Anitha, Singh, Raviprakash, Potluri, Vivek, Padmanabha, Hansashree, Mailankody, Pooja, Pavagada, Mathuranath S

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Neuro-Bechet’s disease: a case series from India von Mahale, Rohan R, Kamath, Sneha, Ravindranadh, C. M, Padmanabha, Hansashree, Mailankody, Pooja, Pavagada, Mathuranath

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DYT30 due to VPS16 mutation: An etiology of childhood-onset generalized dystonia von Shashi, Sridhar, Nashi, Saraswati, Arunachal, Gautham, Venkatachalam, N, Padmanabha, Hansashree, Mailankody, Pooja, Menon, Deepak, Arshad, Faheem, Alladi, Suvarna, Mathuranath, Pavagada, Mahale, Rohan

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Cerebral abscesses due to Pseudallescheria boydii mycoses: a diagnostic and therapeutic conundrum von Padmanabha, Hansashree, Chandrashekar, Nagarathna, Shukla, Dhaval, Pooja, M, Mahale, Rohan

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Human placental extract a miracle that heals the wound faster von Katkurwar, Ankita, Chaudhari, Dipali, Mahale, Swapna, Mahale, Arunkumar, Kadam, Pooja

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Vascular Parkinsonism with Dystonia in Moyamoya Disease: An Expansion of Movement Disorder Phenomenology von Mahale, Rohan, Dubbal, Rohin, Padmanabha, Hansashree, Mailankody, Pooja

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Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype von Mahale, Rohan, Padmanabha, Hansashree, Mailankody, Pooja, Pavagada, Mathuranath

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Cerebral Sparganosis - An Unusual Parasitic Infection Mimicking Cerebral Tuberculosis: Isolation of a Live Plerocercoid Larva of Spirometra mansoni von Rathore, Abhishek, Padmanabha, Hansashree, Mahale, Rohan, Arora, Ankit, Goyal, Aditi, Reddy, Jeevika, Sipani, Mahak, Pruthi, Nupur, Lingaraju, T S, Nagarathna, S, Yasha, T C, Saini, Jitender, Nashi, Saraswati, Pooja, M, Mathuranath, P S

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Rare Encephalitis-Like Presentation of a Pediatric Patient with Dual Positive Aquaporin-4 and Myelin Oligodendrocyte Antibodies: A Case Report with Review of Literature von Dhar, Debjyoti, Mahadevan, Anita, Nagaraj, A R, Mahale, Rohan, Prasad, Chandrajit, Shreedevi, Athyadi U, Mailankody, Pooja, Mathuranath, P S, Padmanabha, Hansashree

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Autosomal dominant cerebral small vessel disease in HTRA1 gene mutation von Mahale, Rohan, Agarwal, Aakash, Gautam, Jyothi, Varghese, Nibu, Kovoor, Jennifer, Mailankody, Pooja, Padmanabha, Hansashree, Pavagada, Mathuranath

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Spastic paraplegia type 8: A first report from India von Mahale, Rohan, Arunachal, Gautam, Davuluri, Anudeep, Padmanabha, Hansashree, Mailankody, Pooja

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