Author

Somarajan Anandan

Observed name: A Somarajan

Institution: St. Joseph Hospital

Observed institution: St. Joseph Hospital

ORCID: 0000-0002-7449-8468

Observed ORCID: 0000-0002-7449-8468

OpenAlex ID: A5078047548

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

Ataxic form of central pontine myelinolysis

2007 · A Somarajan, MBaby Paul, et al. · Annals of Indian Academy of Neurology · 3

Nine syndrome

2025 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports · 2

PDF

Quadrigeminal cistern lipoma

2024 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports · 2

PDF

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

PDF

Double Trouble: Herpes Simplex Encephalitis Triggering Autoimmune Encephalitis

2025 · Somarajan Anandan, Parameswaran Krishnan · Cureus · 1

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

PDF

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

PDF

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

PDF

Hippocampal dot sign in transient global amnesia

2024 · Somarajan Anandan, Jyothish P Kumar, et al. · Indian Journal of Case Reports · 1

PDF

An interesting case of hemiplegia in a child

2007 · SadanandavalliRetnaswami Chandra, S Syamlal, et al. · Annals of Indian Academy of Neurology · 1

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

PDF

Hidden in plain sight: Duane retraction syndrome diagnosed in an adult

2026 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports

PDF

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

PDF

Hot Cross Bun Sign

2026 · Somarajan Anandan, Sajeesh Rajendran, et al. · European Journal of Case Reports and Clinical Images

PDF

Eyebrow ptosis: Barely mentioned and frequently overlooked

2025 · Somarajan Anandan, Sajeesh S Rajendran, et al. · Indian Journal of Case Reports

PDF

A Curious Case of Abdominal Pain with Reset Osmostat and Rhabdomyolysis

2025 · Somarajan Anandan, Simi Soman, et al. · Journal of the Association of Physicians of India

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

PDF

Works count: 49

Citation count: 21

H-index: 2

I10-index: