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Pytel, Peter

One or more keywords matched the following items that are connected to Pytel, Peter

Item Type	Name
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-Barr? 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