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Profil bibliographique

Loren McLendon

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

16Publications signalées
233Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Multiple Sclerosis Research StudiesAutoimmune Neurological Disorders and TreatmentsPeripheral Neuropathies and DisordersTraumatic Brain Injury and Neurovascular DisturbancesLong-Term Effects of COVID-19

Les publications récentes

Accès ouvert 2026 article OpenAlex

Role of Tocilizumab in Severe CNS Inflammatory Presentations in Children

Amaar Marefi, E Grasso, Loren McLendon, Sona Narula et autres

OBJECTIVES: Anti-interleukin 6 receptor (anti-IL6R) therapies have been proven to reduce relapse rates in patients with neuromyelitis optica spectrum disorder and are under investigation in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). One anti-IL6R therapy, tocilizumab (TCZ), has been reported as a treatment …

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3 citations Neurology
2025 article OpenAlex

The Continued Need of Pediatric Management Guidelines for Pediatric Stroke with Associated Patent Foramen Ovale: A Case Series (P5-6.007)

Rachna Karumuri, Sam Kamoroff, Loren McLendon, Harry S. Abram

Patent foramen ovale (PFO) is a congenital cardiac anomaly resulting from the incomplete closure of the atrial septum, allowing blood to shunt from the right to the left atrium and bypass pulmonary filtration. This shunting can lead to paradoxical embolism, where emboli …

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2 citations Neurology
2025 article OpenAlex

11-Year-Old Boy With B-ALL–Induced Hypereosinophilic Syndrome Presenting as Acute Encephalopathy

Tristan Loveday, C. Hora, Lauren Chorny, Manisha Bansal et autres

Encephalopathy is a disturbance in neurologic function. It is commonly attributed to infectious and inflammatory etiologies but encompasses a wide differential. Hypereosinophilic syndrome (HES) is a rare cause of encephalopathy that is associated with underlying infection or malignancy. We present a pediatric …

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0 citations PEDIATRICS
Accès ouvert 2025 article OpenAlex

P498: Atypical presentation of Alexander disease in a 4-month-old infant: Emphasizing the importance of integrated genetic and biochemical testing

C. Hora, Loren McLendon

widely spaced teeth), and therefore a diagnosis of a lysosomal storage disorder was suspected.Our patient also presented with hepatosplenomegaly, umbilical hernia, frequent ear infections and mixed conductive/ sensorineural hearing loss (diagnosed via tympanograms, OAEs, and ABRs).Diagnostic Workup: His initial workup found a …

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0 citations Genetics in Medicine Open
Accès ouvert 2024 article OpenAlex

Efficacy of eculizumab in acute refractory pediatric neuromyelitis optica: A case report

Michael Enriquez, Scott Rosenthal, Loren McLendon, Jeffrey L. Bennett et autres

Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune inflammatory disorder of the central nervous system caused by autoantibodies against the aquaporin-4 (AQP4) water channel. Inflammatory injury is often severe and focused on the optic nerves, spinal cord, and other CNS regions with …

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11 citations Neuroimmunology Reports
Accès ouvert 2023 article OpenAlex

Invasive Multimodality Neuromonitoring to Manage Cerebral Edema in Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease

Nina Fainberg, Maya R. Silver, John D. Arena, Elizabeth I. Landzberg et autres

Background: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an inflammatory disorder of the CNS with a variety of clinical manifestations, including cerebral edema. Case Summary: A 7-year-old boy presented with headaches, nausea, and somnolence. He was found to have cerebral edema that …

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1 citation Critical Care Explorations
Accès ouvert 2023 article OpenAlex

Dramatic Response to Anti-IL-6 Receptor Therapy in Children With Life-Threatening Myelin Oligodendrocyte Glycoprotein-Associated Disease

Loren McLendon, Claudia Gambrah-Lyles, Angela N. Viaene, Nina Fainberg et autres

OBJECTIVES: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an immune-mediated neuroinflammatory disorder leading to demyelination of the CNS. Interleukin (IL)-6 receptor blockade is under study in relapsing MOGAD as a preventative strategy, but little is known about the role of such treatment …

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39 citations Neurology Neuroimmunology & Neuroinflammation
Accès ouvert 2023 article OpenAlex

A three‐year‐old with central nervous system graft versus host disease: A rare cause of posthematopoietic stem cell transplant encephalopathy

Poorvi Agrawal, Douglas R. Nordli, Loren McLendon

Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

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0 citations Pediatric Blood & Cancer
Accès ouvert 2022 article OpenAlex

Anti-N-methyl-D-aspartic acid receptor encephalitis after recurrent herpes simplex infection: A case report and literature review

Alexandra B. Kornbluh, Loren McLendon, Brenda Banwell

Familiarize neurologists with the association between herpes simplex encephalitis (HSE) and N-Methyl-D-aspartic acid receptor encephalitis (NMDARE). Case report and literature review We describe the case of a six-year-old boy who experienced neonatal herpes simplex virus (HSV) infection, effective early antiviral therapy, and …

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0 citations Neuroimmunology Reports
Accès ouvert 2022 article OpenAlex

Pediatric anti-NMDA receptor encephalitis with epilepsia partialis continua

Chethan K. Rao, Loren McLendon, Fernando Galán

: We present a patient with anti-N-methyl D-aspartate receptor (NMDAR) encephalitis who presented with focal motor seizures that rapidly progressed to epilepsia partialis continua (EPC) with unilateral background slowing then encephalopathy. : A 12-year-old previously healthy girl presented to our pediatric emergency …

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2 citations Neuroimmunology Reports

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