Robert Wollmann to Child
This is a "connection" page, showing publications Robert Wollmann has written about Child.
Connection Strength
0.127
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Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis. Muscle Nerve. 2003 Feb; 27(2):180-7.
Score: 0.025
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Presynaptic congenital myasthenic syndrome due to quantal release deficiency. Neurology. 2001 Jul 24; 57(2):279-89.
Score: 0.023
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Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A. Mol Genet Genomic Med. 2018 05; 6(3):434-440.
Score: 0.018
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The clinical significance of extracellular matrix in gangliogliomas. J Neuropathol Exp Neurol. 1996 Dec; 55(12):1246-52.
Score: 0.016
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Inflammation at the neuromuscular junction in myasthenia gravis. Neurology. 1991 Sep; 41(9):1497-504.
Score: 0.011
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Cellular neuropathology of tuberous sclerosis. Ann N Y Acad Sci. 1991; 615:140-8.
Score: 0.011
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A family with seizures and minor features of tuberous sclerosis and a novel TSC2 mutation. Neurology. 2003 Aug 12; 61(3):409-12.
Score: 0.007
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Distribution of the neuronal specific protein, 14-3-2, in central nervous system lesions of tuberous sclerosis. Acta Neuropathol. 1981; 53(2):113-7.
Score: 0.005
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Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome. Acta Neuropathol. 2000 Dec; 100(6):635-46.
Score: 0.005
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Distribution of glial fibrillary acidic protein in central nervous system lesions of tuberous sclerosis. Acta Neuropathol. 1980; 52(2):135-40.
Score: 0.005