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Sajeesh S Rajendran

Observed names: Sajeesh Rajendran, Sajeesh S. Rajendran
Observed institution: Mar Sleeva Medicity Palai
ORCID: 0009-0005-4026-6262
Observed ORCID: 0009-0005-4026-6262
OpenAlex ID: A5101390984
A Very Rare Side Effect of a Very Commonly Used Drug: Pantoprazole-induced Seizure
2024 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Journal of the Association of Physicians of India · 3
Nine syndrome
2025 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports · 2
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Quadrigeminal cistern lipoma
2024 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports · 2
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A Stitch in Time Saves Nine: A Case of Anti LGI1 Encephalitis Presenting as Goose Bumps
2024 · Somarajan Anandan, Sajeesh S. Rajendran, et al. · Neurology India · 2
Tea and Porridge Syndrome: A Rare Cause of Severe Hyponatremia
2025 · Somarajan Anandan, Sajeesh Rajendran, et al. · Cureus · 1
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Late Postpartum Eclampsia with “Normal” Blood Pressure
2024 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Journal of the Association of Physicians of India · 1
Claude syndrome
2024 · Somarajan Anandan, Divine S Shajee, et al. · Indian Journal of Case Reports · 1
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Very Early Onset Familial Alzheimer’s Disease Due to Mutation in PSEN1 I143T – First Case Report from South Asia
2024 · Somarajan Anandan, Sajeesh S. Rajendran, et al. · Neurology India · 1
A rare cause for seizures in an adult male – First report of a rare mutation in HMBS gene (c.730_731del) from India
2024 · Somarajan Anandan, Sajeesh S Rajendran, et al. · IP Indian Journal of Neurosciences · 1
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Double seronegative myasthenia gravis but double positive - A case of LRP4/Agrin antibody positive myasthenia gravis
2024 · Somarajan Anandan, Sajeesh S Rajendran, et al. · IP Indian Journal of Neurosciences · 1
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A rare Anti-GQ1b antibody syndrome- ataxic variant of Guillain Barre syndrome
2026 · Somarajan Anandan, Sajeesh Rajendran, et al. · IP Indian Journal of Neurosciences
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Addison's Disease Mimicking Cerebral Salt Wasting Syndrome: A Case of Severe Hyponatremia
2026 · Somarajan Anandan, Sajeesh Rajendran, et al. · Cureus
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Globus Pallidus Streak Sign in Mitochondrial Membrane Protein-associated Neurodegeneration
2026 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Current Medical Issues
Hippocampal Dot Sign with Cingulate Gyrus Dot-like Lesion in Transient Global Amnesia
2026 · Somarajan Anandan, Sajeesh S. Rajendran, et al. · Archives of Medicine and Health Sciences
Primary Familial Brain Calcification (Fahr Disease) Due to a Novel Mutation in Solute Carrier 20 A2 Gene
2026 · Somarajan Anandan, Sajeesh S. Rajendran, et al. · Annals of African Medicine
A Rare Stroke due to a Rare Mechanism- Embolic Recurrent Artery of Heubner Infarct
2026 · Anandhu Suresh, Sajeesh Rajendran, et al. · Eastern Journal of Medical Sciences
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Hidden in plain sight: Duane retraction syndrome diagnosed in an adult
2026 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports
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Two Syndrome Progressing to Nine Syndrome
2026 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Journal of the Association of Physicians of India
Trinucleotide repeat containing adaptor 6B protein deficiency syndrome – A rare cause for language delay and attention deficit hyperactivity disorder
2026 · Somarajan Anandan, Sajeesh Rajendran, et al. · Indian Journal of Case Reports
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Hot Cross Bun Sign
2026 · Somarajan Anandan, Sajeesh Rajendran, et al. · European Journal of Case Reports and Clinical Images
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Eyebrow ptosis: Barely mentioned and frequently overlooked
2025 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports
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Emery Dreifuss muscular dystrophy masquerading as limb girdle muscular dystrophy type 2 due to a novel mutation in emerin gene
2025 · Somarajan Anandan, Sajeesh Rajendran, et al. · IP Indian Journal of Neurosciences
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Opalski syndrome with ipsilateral upper motor neuron type facial palsy
2025 · Somarajan Anandan, Sajeesh S. Rajendran, et al. · Acta Neurologica Belgica
Xanthogranuloma of the choroid plexus
2025 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports
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Elastin Microfibril Interface-Located Protein 1 (EMILIN1) Mutation Mimicking Axonal Hereditary Motor Sensory Neuropathy
2025 · Somarajan Anandan, Sajeesh Rajendran, et al. · Cureus
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Works count: 38
Citation count: 15
H-index: 2
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