Robert Wollmann to Humans
This is a "connection" page, showing publications Robert Wollmann has written about Humans.
Connection Strength
0.230
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Neuropathological evaluation of an 84-year-old man after 422 ECT treatments. J ECT. 2014 Sep; 30(3):248-50.
Score: 0.016
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Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia. Clin Genet. 2014 Feb; 85(2):166-71.
Score: 0.014
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Synaptic basal lamina-associated congenital myasthenic syndromes. Ann N Y Acad Sci. 2012 Dec; 1275:36-48.
Score: 0.014
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Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE. Clin Genet. 2011 Nov; 80(5):444-51.
Score: 0.012
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Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction. Hum Mol Genet. 2010 Jun 15; 19(12):2370-9.
Score: 0.012
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Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome. J Med Genet. 2009 Mar; 46(3):203-8.
Score: 0.011
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Congenital myasthenic syndrome caused by two non-N88K rapsyn mutations. Clin Genet. 2007 Jul; 72(1):63-5.
Score: 0.010
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Rapsyn mutations in myasthenic syndrome due to impaired receptor clustering. Muscle Nerve. 2003 Sep; 28(3):293-301.
Score: 0.007
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Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis. Muscle Nerve. 2003 Feb; 27(2):180-7.
Score: 0.007
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Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) with hypertrophic spinal radiculopathy mimicking neurofibromatosis. Acta Neuropathol. 2003 Feb; 105(2):185-8.
Score: 0.007
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Presynaptic congenital myasthenic syndrome due to quantal release deficiency. Neurology. 2001 Jul 24; 57(2):279-89.
Score: 0.006
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Disseminated histoplasmosis in an infant with acquired immunodeficiency syndrome. J Infect. 1998 Nov; 37(3):298-301.
Score: 0.005
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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: 0.005
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The clinical significance of extracellular matrix in gangliogliomas. J Neuropathol Exp Neurol. 1996 Dec; 55(12):1246-52.
Score: 0.005
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Pathological case of the month. Globoid cell leukodystrophy (Krabbe's disease). Arch Pediatr Adolesc Med. 1995 Oct; 149(10):1173-4.
Score: 0.004
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Advanced neuroimaging studies in a patient with brain metastases from transitional cell carcinoma of the bladder. J Neuroimaging. 2014 Jul-Aug; 24(4):429-31.
Score: 0.004
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Histopathologic changes in the extraocular muscle in centronuclear myopathy with a Dynamin 2 mutation. Ophthalmic Genet. 2013 Mar-Jun; 34(1-2):83-6.
Score: 0.003
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Six-week-old with fever and fussiness. Pediatr Infect Dis J. 2012 May; 31(5):538, 544.
Score: 0.003
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LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin. Hum Genet. 2012 Jul; 131(7):1123-35.
Score: 0.003
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Inflammation at the neuromuscular junction in myasthenia gravis. Neurology. 1991 Sep; 41(9):1497-504.
Score: 0.003
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A middle-aged woman with nausea, weight loss, and orthostatic hypotension. Neurology. 2011 Aug 02; 77(5):489-95.
Score: 0.003
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Cellular neuropathology of tuberous sclerosis. Ann N Y Acad Sci. 1991; 615:140-8.
Score: 0.003
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Patients with myasthenia gravis and thymoma have in their sera IgG autoantibodies against titin. Clin Exp Immunol. 1990 Nov; 82(2):284-8.
Score: 0.003
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Fatal "hypertensive" intracerebral hemorrhage associated with a cerebral cavernous angioma: case report. Acta Neurochir (Wien). 2011 Feb; 153(2):421-3.
Score: 0.003
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Long-term survival of a patient with glioblastoma. Can J Neurol Sci. 2010 Mar; 37(2):289-92.
Score: 0.003
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A 59 year-old man with sellar lesion. Brain Pathol. 2009 Jan; 19(1):161-2.
Score: 0.003
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Variable phenotypes associated with mutations in DOK7. Muscle Nerve. 2008 Apr; 37(4):448-56.
Score: 0.003
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Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome. J Clin Invest. 2007 Oct; 117(10):2903-12.
Score: 0.002
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A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex. Neuromuscul Disord. 2007 Apr; 17(4):285-9.
Score: 0.002
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Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome model. Neurobiol Dis. 2006 Aug; 23(2):462-70.
Score: 0.002
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N-acetyl-beta-hexosaminidase beta locus defect and juvenile motor neuron disease: a case study. Ann Neurol. 1986 Jun; 19(6):568-72.
Score: 0.002
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Degenerative spine disease : pathologic findings in 985 surgical specimens. Am J Clin Pathol. 2006 Feb; 125(2):193-202.
Score: 0.002
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Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice. Nat Genet. 2006 Feb; 38(2):245-50.
Score: 0.002
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Ganglioneuromatous paraganglioma of the cauda equina--a pathological case study. Hum Pathol. 2005 Apr; 36(4):444-6.
Score: 0.002
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Focal caspase activation underlies the endplate myopathy in slow-channel syndrome. Ann Neurol. 2004 Mar; 55(3):347-52.
Score: 0.002
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Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2. Neurology. 2003 Dec 23; 61(12):1743-8.
Score: 0.002
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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: 0.002
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Venous angiomas of the posterior fossa should be considered as anomalous venous drainage. Surg Neurol. 1983 Jan; 19(1):26-32.
Score: 0.002
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S-100 protein in granular cell tumors (granular cell myoblastomas). Cancer. 1982 May 01; 49(9):1834-8.
Score: 0.002
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Traumatic aneurysm resulting from insertion of an intracranial pressure monitor. Case illustration. J Neurosurg. 2001 Oct; 95(4):720.
Score: 0.002
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Isolated, primary extranodal Hodgkin's disease of the spine: case report. Neurosurgery. 2001 Aug; 49(2):453-6; discussion 456-7.
Score: 0.002
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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: 0.002
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Superior sagittal sinus thrombosis diagnosed by computed tomography. Surg Neurol. 1981 Jan; 15(1):11-4.
Score: 0.002
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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: 0.002
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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: 0.001
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Necrotizing myelopathy complicating Hodgkin's disease. Arch Neurol. 1979 Sep; 36(9):583-5.
Score: 0.001
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Genetic manipulation of AChR responses suggests multiple causes of weakness in slow-channel syndrome. Ann N Y Acad Sci. 1998 May 13; 841:167-80.
Score: 0.001
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A morphologic study of central nervous system aging in Hiroshima, Japan. Folia Psychiatr Neurol Jpn. 1978; 32(2):263-75.
Score: 0.001
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Striational autoantibodies in myasthenia gravis patients recognize I-band titin epitopes. J Neuroimmunol. 1998 Jan; 81(1-2):98-108.
Score: 0.001
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Cluster of wound botulism in California: clinical, electrophysiologic, and pathologic study. Muscle Nerve. 1997 Oct; 20(10):1284-95.
Score: 0.001
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Central pontine myelinolysis in a patient with classic heat stroke. Arch Neurol. 1997 Aug; 54(8):935-6.
Score: 0.001
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Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions. Am J Hum Genet. 1996 Aug; 59(2):400-6.
Score: 0.001
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A transgenic mouse model of the slow-channel syndrome. Muscle Nerve. 1996 Jan; 19(1):79-87.
Score: 0.001
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Clinical and genetic studies of fatal familial insomnia. Neurology. 1995 Jun; 45(6):1068-75.
Score: 0.001
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Function and ultrastructure of the neuromuscular junction in post-polio syndrome. Ann N Y Acad Sci. 1995 May 25; 753:129-37.
Score: 0.001
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The absorption, excretion and metabolic pattern of bromhexine in man after oral and i.v. administration. Arzneimittelforschung. 1975; 25(12):1954-8.
Score: 0.001
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Concomitant chemoradiotherapy, neutron boost, and adjuvant chemotherapy for anaplastic astrocytoma and glioblastoma multiforme. Cancer Invest. 1995; 13(5):453-9.
Score: 0.001
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The human-severe combined immunodeficiency myasthenic mouse model: a new approach for the study of myasthenia gravis. Ann Neurol. 1993 Jul; 34(1):48-56.
Score: 0.001
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Effector mechanisms of myasthenic antibodies. Ann N Y Acad Sci. 1993 Jun 21; 681:264-73.
Score: 0.001
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The hu-SCID myasthenic mouse. A new tool for the investigation of seronegative myasthenia gravis. Ann N Y Acad Sci. 1993 Jun 21; 681:303-5.
Score: 0.001
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SAG: a Schwann cell membrane glycoprotein. J Neurosci. 1992 Jun; 12(6):2177-85.
Score: 0.001
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Late denervation in patients with antecedent paralytic poliomyelitis. N Engl J Med. 1987 Jul 02; 317(1):7-12.
Score: 0.001
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Post-poliomyelitis syndrome: evidence of ongoing denervation in symptomatic and asymptomatic patients. Birth Defects Orig Artic Ser. 1987; 23(4):237-9.
Score: 0.001
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A variant of Fukuyama congenital muscular dystrophy in a non-Japanese child. Pediatr Neurol. 1986 Sep-Oct; 2(5):290-3.
Score: 0.001
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Calcified basal ganglionic mass 12 years after radiation therapy for medulloblastoma. Surg Neurol. 1984 Apr; 21(4):373-6.
Score: 0.000
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Meningeal sarcomatosis and multiple astrocytomas. Arch Neurol. 1983 Mar; 40(3):179-82.
Score: 0.000
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Neuropathy accompanying IgM lambda monoclonal gammopathy. Acta Neuropathol. 1983; 59(4):255-61.
Score: 0.000
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Muscle acid protease activity in amyotrophic lateral sclerosis: correlation with clinical and pathologic features. Neurology. 1982 Aug; 32(8):901-3.
Score: 0.000
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Myopathy induced by epsilon-aminocaproic acid. Case report. J Neurosurg. 1982 Jul; 57(1):130-4.
Score: 0.000
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Distribution of S-100 protein outside the central nervous system. Brain Res. 1982 Feb 25; 234(2):309-17.
Score: 0.000
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S-100 protein in soft-tissue tumors derived from Schwann cells and melanocytes. Am J Pathol. 1982 Feb; 106(2):261-8.
Score: 0.000
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S-100 protein in human chondrocytes. Nature. 1982 Jan 07; 295(5844):63-4.
Score: 0.000
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Immunologic and virologic studies of measles inclusion body encephalitis in an immunosuppressed host: the relationship to subacute sclerosing panencephalitis. Neurology. 1981 Oct; 31(10):1263-70.
Score: 0.000
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Amyotrophic lateral sclerosis with antecedent poliomyelitis. Arch Neurol. 1980 May; 37(5):312-3.
Score: 0.000
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[Ambroxol, studies of biotransformation in man and determination in biological samples (author's transl)]. Arzneimittelforschung. 1978; 28(5a):904-11.
Score: 0.000