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