Issa S. Alawneh

Nablus, WBK, Palestine

Last Updated: 09/26/2026

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Found 17 publications

MOG Antibody-Associated Disease With Bilateral Deep Gray Matter Involvement in a Child: Unique MRI Findings and Therapeutic Response.

MOG Antibody-Associated Disease With Bilateral Deep Gray Matter Involvement in a Child: Unique MRI Findings and Therapeutic Response.

Journal: Case reports in pediatrics

Published: January 24, 2026

Salbutamol in Congenital Myasthenic Syndrome: A Systematic Review.

Salbutamol in Congenital Myasthenic Syndrome: A Systematic Review.

Journal: BMC neurology

Published: September 16, 2025

Hyperreflexia and Preserved Reflexes in Pediatric Guillain-Barré Syndrome: A Case Report and Literature Review.

Hyperreflexia and Preserved Reflexes in Pediatric Guillain-Barré Syndrome: A Case Report and Literature Review.

Journal: Cureus

Published: June 01, 2025

Pediatric Cohort of Charcot-Marie-Tooth Disease: Clinical Features and Genetic Distribution.

Pediatric Cohort of Charcot-Marie-Tooth Disease: Clinical Features and Genetic Distribution.

Journal: Neurology. Genetics

Published: May 16, 2025

From initial suspicion to accurate diagnosis: unmasking rabies in a case of suspected Guillain-Barre syndrome.

From initial suspicion to accurate diagnosis: unmasking rabies in a case of suspected Guillain-Barre syndrome.

Journal: BMC pediatrics

Published: January 16, 2025

Pediatric Chronic Inflammatory Demyelinating Polyneuropathy: Challenges in Diagnosis and Therapeutic Strategies.

Pediatric Chronic Inflammatory Demyelinating Polyneuropathy: Challenges in Diagnosis and Therapeutic Strategies.

Journal: Paediatric drugs

Published: July 21, 2024

Neuromyotonia in a 16-year-old female with dramatic improvement after IVIG therapy: Case report and literature review.

Neuromyotonia in a 16-year-old female with dramatic improvement after IVIG therapy: Case report and literature review.

Journal: Neuromuscular disorders : NMD

Published: May 17, 2024

A novel deep intronic variant in LAMA2 identified by RNA sequencing.

A novel deep intronic variant in LAMA2 identified by RNA sequencing.

Journal: Neuromuscular disorders : NMD

Published: February 04, 2024

Expanding the spectrum of LAMB2: Pierson syndrome associated with neuromuscular junction disorder in two patients.

Expanding the spectrum of LAMB2: Pierson syndrome associated with neuromuscular junction disorder in two patients.

Journal: Neuromuscular disorders : NMD

Published: January 19, 2024

Muscle MRI patterns for limb girdle muscle dystrophies: systematic review.

Muscle MRI patterns for limb girdle muscle dystrophies: systematic review.

Journal: Journal of neurology

Published: February 14, 2023

Titin related myopathy with ophthalmoplegia. A novel phenotype.

Titin related myopathy with ophthalmoplegia. A novel phenotype.

Journal: Neuromuscular disorders : NMD

Published: January 26, 2023

CAMK4-related Case of Hyperkinetic Movement Disorder.

CAMK4-related Case of Hyperkinetic Movement Disorder.

Journal: Movement disorders clinical practice

Published: November 14, 2022

Showing 1-12 of 17

Last Updated: 09/26/2026