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Search Results to Robert Wollmann

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Wollmann, Robert

Item TypeName
Concept Acquired Immunodeficiency Syndrome
Concept Demyelinating Diseases
Concept Syndrome
Concept Postpoliomyelitis Syndrome
Concept Hereditary Central Nervous System Demyelinating Diseases
Concept Myasthenic Syndromes, Congenital
Concept Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Academic Article A transgenic mouse model of the slow-channel syndrome.
Academic Article Genetic manipulation of AChR responses suggests multiple causes of weakness in slow-channel syndrome.
Academic Article Presynaptic congenital myasthenic syndrome due to quantal release deficiency.
Academic Article Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome.
Academic Article Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) with hypertrophic spinal radiculopathy mimicking neurofibromatosis.
Academic Article Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis.
Academic Article Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome.
Academic Article Focal caspase activation underlies the endplate myopathy in slow-channel syndrome.
Academic Article Rapsyn mutations in myasthenic syndrome due to impaired receptor clustering.
Academic Article Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2.
Academic Article K+ channel blockade impairs remyelination in the cuprizone model.
Academic Article Variable phenotypes associated with mutations in DOK7.
Academic Article Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome model.
Academic Article Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome.
Academic Article Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction.
Academic Article Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE.
Academic Article Congenital myasthenic syndrome caused by two non-N88K rapsyn mutations.
Academic Article Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome.
Academic Article The L-coding region of the DA strain of Theiler's murine encephalomyelitis virus causes dysfunction and death of myelin-synthesizing cells.
Academic Article A subgenomic segment of Theiler's murine encephalomyelitis virus RNA causes demyelination.
Academic Article A variant of Fukuyama congenital muscular dystrophy in a non-Japanese child.
Academic Article Function and ultrastructure of the neuromuscular junction in post-polio syndrome.
Academic Article LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin.
Academic Article Post-poliomyelitis syndrome: evidence of ongoing denervation in symptomatic and asymptomatic patients.
Academic Article The effect of short-term and chronic immunosuppression on Theiler's virus demyelination.
Academic Article DA strain of Theiler's murine encephalomyelitis virus induces demyelination in nude mice.
Academic Article Disseminated histoplasmosis in an infant with acquired immunodeficiency syndrome.
Academic Article Synaptic basal lamina-associated congenital myasthenic syndromes.
Academic Article Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia.
Academic Article Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A.

Search Criteria
  • Acquired
  • demyelinating
  • syndromes