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One or more keywords matched the following items that are connected to Pytel, Peter
Item TypeName
Concept Acquired Immunodeficiency Syndrome
Concept Carpal Tunnel Syndrome
Concept Immunologic Deficiency Syndromes
Concept Hamartoma Syndrome, Multiple
Concept Sjogren's Syndrome
Concept Opsoclonus-Myoclonus Syndrome
Concept Lambert-Eaton Myasthenic Syndrome
Concept Myasthenic Syndromes, Congenital
Concept Guillain-Barre Syndrome
Concept Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Academic Article Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) with hypertrophic spinal radiculopathy mimicking neurofibromatosis.
Academic Article Minor salivary gland inflammation in Devic's disease and longitudinally extensive myelitis.
Academic Article Disseminated intravascular large-cell lymphoma with initial presentation mimicking Guillain-Barré syndrome.
Academic Article Opsoclonus-myoclonus and anti-Hu positive limbic encephalitis in a patient with neuroblastoma.
Academic Article Progressive intracranial fusiform aneurysms and T-cell immunodeficiency.
Academic Article Systemic transthyretin amyloidosis in a patient with bent spine syndrome.
Academic Article Selective inhibition of caspases in skeletal muscle reverses the apoptotic synaptic degeneration in slow-channel myasthenic syndrome.
Academic Article Fluoxetine is neuroprotective in slow-channel congenital myasthenic syndrome.
Academic Article Cervicomedullary compression as the main manifestation of wild-type transthyretin amyloidosis.
Academic Article Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmission.
Academic Article A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5.
Academic Article Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A.
Academic Article Rare Epstein-Barr Virus-Associated Smooth Muscle Tumor in a Patient with AIDS: A Case Report.
Academic Article Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations.
Academic Article A Novel TBK1 Variant (Lys694del) Presenting With Corticobasal Syndrome in a Family With FTD-ALS Spectrum Diseases: Case Report.
Search Criteria
  • Acquired
  • demyelinating
  • syndromes