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Nidheesh Cheeyancheri Chencheri

Observed names: Chencheri, Nidheesh, Nidheesh Chencheri
ORCID: 0000-0002-9142-708X
Observed ORCID: 0000-0002-9142-708X
OpenAlex ID: A5024954622
The genomic landscape of rare disorders in the Middle East
2023 · Maha El Naofal, Sathishkumar Ramaswamy, et al. · Genome Medicine · 46
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Case Report: Guillain-Barré Syndrome as Primary Presentation of Systemic Lupus Erythematosus (SLE-GBS) in a Teenage Girl
2022 · Elham Beshir, Ernestina Belt, et al. · Frontiers in Pediatrics · 13
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Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children
2023 · Nidheesh Chencheri, Gail Alexander, et al. · Muscle & Nerve · 10
Early-Onset Epileptic Encephalopathy Responsive to Phenytoin: A Diagnostic Clue for Fibroblast Growth Factor 12 Mutation
2024 · Nadia M Saleem, Nidheesh Chencheri, et al. · Cureus · 6
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The Spectrum of Neurological Manifestations of Human Herpesvirus 6 Infection in Children
2021 · Nidheesh Chencheri, Mohammed Dirawi, et al. · Cureus · 6
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Case Report: Expanding the Phenotypic Spectrum of Timothy Syndrome Type 1: A Sporadic Case With a de novo CACNA1C Pathogenic Variant and Segmental Ileal Dilatation
2021 · Ahmed A. Nugud, Nermeen Mahmoud ELkholy, et al. · Frontiers in Pediatrics · 4
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Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation, and Neuroendocrine Tumor (ROHHADNET) Syndrome: A Case Report
2023 · Mohammed Aldirawi, Lemis Yavuz, et al. · Cureus · 2
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A Rare Cause of Recurrent Febrile Encephalopathy in a Child: The Expanding Spectrum of ATP1A3 Mutations
2021 · Saja Tahir, Nidheesh Chencheri, et al. · Cureus · 2
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Demyelination in Adolescence: A Case Series on Pediatric-onset Multiple Sclerosis in the United Arab Emirates
2026 · Suhaila Ahamed Ahmed, Anjaly Vijayakumar Nair, et al. · Dubai Medical Journal
Hip instability and scoliosis in children with spinal muscular atrophy: a single center retrospective study in the United Arab Emirates
2026 · Hagir Al-Dulaimi, Maryam Alabdullah, et al. · Frontiers in Pediatrics
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Encephalopathy With Guillain-Barré Syndrome Secondary to Extensively Multidrug-Resistant Salmonella Typhi Infection: A Case Report
2026 · Ghadah Al Sharif, Mohamad Shieb, et al. · Cureus
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Pediatric Stroke Associated With a Rare Pathogenic PKP2 Variant: A Diagnostic Challenge
2026 · Alaa Salman, Mohamed O E Babiker, et al. · Cureus
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Clumsy Walking Hides a Rare Neuropathy: A Novel de novo MFN2 Variant Causing Charcot–Marie–Tooth Disease Type 2A in a Child
2025 · Maral Ardalan Azarayesh, Asmaa Khalid Naser, et al. · South Asian Research Journal of Pharmaceutical Sciences
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Case report: Encephalitis with Guillain-Barré Syndrome secondary to extensively multi-drug resistant Salmonella infection
2024 · Mohamad Shieb, Ghadah Al-Sharif, et al. · Journal of the Pediatric Infectious Diseases Society
6136 Hip instability in children with spinal muscular atrophy: a single centre retrospective study in the United Arab Emirates, 2018–2023
2024 · Maryam Alabdullah, Hagir Al-Dulaimi, et al.
Demystifying the Mystery of Vitamin B12 Deficiency in an Infant with Developmental Delay
2022 · Heba Ali Aldarawsha, Sura Ahmed AlDoory, et al. · Dubai Medical Journal
New Era of Curative Therapy for Spinal Muscular Atrophy in Children; Do We Need Implementation of Universal Newborn Screening for Spinal Muscular Atrophy?
2021 · Nidheesh Cheeyancheri Chencheri, Bhavna Gupta · South Asian Research Journal of Medical Sciences
A diagnostic dilemma of two rare stroke mimics in a pediatric patient
2017 · Nidheesh Cheeyancheri Chencheri, Pawan Subhash Kashyape, et al. · International Journal of Contemporary Pediatrics
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A Rare Cause of Quadriparesis
2017 · Nidheesh Cheeyancheri Chencheri, Pawan Subhash Kashyape · Pediatric Neurology
Works count: 23
Citation count: 89
H-index: 5
I10-index: 3
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