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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 2
1980 1
1981 1
1983 1
1988 1
1989 1
1996 1
2001 1
2004 1
2010 1
2016 1
2024 0

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12 results

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Page 1
Nerve pathologic features differentiate POEMS syndrome from CIDP.
Piccione EA, Engelstad J, Dyck PJ, Mauermann ML, Dispenzieri A, Dyck PJ. Piccione EA, et al. Acta Neuropathol Commun. 2016 Oct 31;4(1):116. doi: 10.1186/s40478-016-0389-1. Acta Neuropathol Commun. 2016. PMID: 27799073 Free PMC article.
A significantly higher number of epineurial vessels was present in POEMS biopsies, with a total count of 120 epineurial vessels predicted as best cutoff to differentiate both conditions (77 % specific and 54 % sensitive).In conclusion, nerve biopsy can be helpful in distin …
A significantly higher number of epineurial vessels was present in POEMS biopsies, with a total count of 120 epineurial vessels predicted …
Sural nerve biopsy in chronic inflammatory demyelinating polyneuropathy: are supportive pathologic criteria useful in diagnosis?
Kulkarni GB, Mahadevan A, Taly AB, Nalini A, Shankar SK. Kulkarni GB, et al. Neurol India. 2010 Jul-Aug;58(4):542-8. doi: 10.4103/0028-3886.68673. Neurol India. 2010. PMID: 20739789 Free article.
PATIENTS AND METHODS: Forty-six patients with idiopathic CIDP (32 with progressive course and 14 with relapsing-remitting course) satisfying AAN clinical and electrophysiologic criteria evaluated between January 1991 and August 2004 were reviewed. ...Endoneurial inf …
PATIENTS AND METHODS: Forty-six patients with idiopathic CIDP (32 with progressive course and 14 with relapsing-remitting course …
Chronic immune sensory polyradiculopathy: a possibly treatable sensory ataxia.
Sinnreich M, Klein CJ, Daube JR, Engelstad J, Spinner RJ, Dyck PJ. Sinnreich M, et al. Neurology. 2004 Nov 9;63(9):1662-9. doi: 10.1212/01.wnl.0000142507.12763.58. Neurology. 2004. PMID: 15534252
RESULTS: All patients had gait ataxia, large fiber sensory loss, and paresthesias, and nine had frequent falls. The disease course was chronic and progressive (median duration 5 years, range 3 months to 18 years). ...
RESULTS: All patients had gait ataxia, large fiber sensory loss, and paresthesias, and nine had frequent falls. The disease course wa …
Hypertrophic neuritis due to chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): a postmortem pathological study.
Matsuda M, Ikeda S, Sakurai S, Nezu A, Yanagisawa N, Inuzuka T. Matsuda M, et al. Muscle Nerve. 1996 Feb;19(2):163-9. doi: 10.1002/(SICI)1097-4598(199602)19:2<163::AID-MUS6>3.0.CO;2-C. Muscle Nerve. 1996. PMID: 8559164
We speculate that visceral autonomic nerves as well as somatic peripheral nerves are involved in patients with a long clinical CIDP course and that peripheral nerve pathology in this disorder shows more heterogeneous changes than previously recognized....
We speculate that visceral autonomic nerves as well as somatic peripheral nerves are involved in patients with a long clinical CIDP cours …
Acute idiopathic polyneuritis. A clinical and electrophsiological follow-up study.
McLeod JG, Walsh JC, Prineas JW, Pollard JD. McLeod JG, et al. J Neurol Sci. 1976 Feb;27(2):145-62. doi: 10.1016/0022-510x(76)90057-5. J Neurol Sci. 1976. PMID: 1249583
It is suggested that a subacute onset of the illness,electromyographic evidence of denervation or gross slowing of conduction, and significant reduction of numbers of myelinated fibres or onion-bulb formation on sural nerve biopsy are factors which may indicate a prolonged cou …
It is suggested that a subacute onset of the illness,electromyographic evidence of denervation or gross slowing of conduction, and significa …
A suspected case of proximal diabetic neuropathy predominantly presenting with scapulohumeral muscle weakness and deep aching pain.
Ogawa K, Sasaki H, Kishi Y, Yamasaki H, Okamoto K, Yamamoto N, Hanabusa T, Nakao T, Nishi M, Nanjo K. Ogawa K, et al. Diabetes Res Clin Pract. 2001 Oct;54(1):57-64. doi: 10.1016/s0168-8227(01)00249-2. Diabetes Res Clin Pract. 2001. PMID: 11532331
The pain and muscle weakness had persisted more severely in the shoulder than in the thigh throughout the clinical course. His unbearable symptoms could be partially alleviated by an administration of a selective serotonin reuptake inhibitor, fluvoxamine maleate. ...
The pain and muscle weakness had persisted more severely in the shoulder than in the thigh throughout the clinical course. His unbear …
Congenital hypomyelination with axonopathy.
Vital A, Vital C, Coquet M, Hernandorena X, Demarquez JM. Vital A, et al. Eur J Pediatr. 1989 Feb;148(5):470-2. doi: 10.1007/BF00595918. Eur J Pediatr. 1989. PMID: 2920756
We report a case of congenital neuropathy taking a rapidly fatal clinical course. Ultrastructural features of the peripheral nerve were unusual with sparsity of myelinated fibres, lack of "onion bulb" formation and presence of axonal damage. ...
We report a case of congenital neuropathy taking a rapidly fatal clinical course. Ultrastructural features of the peripheral nerve we …
Congenital hypomyelination neuropathy: glial bundles in cranial and spinal nerve roots.
Towfighi J. Towfighi J. Ann Neurol. 1981 Dec;10(6):570-3. doi: 10.1002/ana.410100614. Ann Neurol. 1981. PMID: 7325606
Autopsy examination of a 3 1/4-year-old child with a severe congenital hypomyelination neuropathy showed the anterior spinal nerve roots and motor cranial nerves to be almost devoid of myelin in their subarachnoid course. The posterior spinal nerve roots and peripheral ner …
Autopsy examination of a 3 1/4-year-old child with a severe congenital hypomyelination neuropathy showed the anterior spinal nerve roots and …
Juvenile metachromatic leukodystrophy. Clinical, biochemical, and neuropathologic studies in nine new cases.
Haltia T, Palo J, Haltia M, Icén A. Haltia T, et al. Arch Neurol. 1980 Jan;37(1):42-6. doi: 10.1001/archneur.1980.00500500072011. Arch Neurol. 1980. PMID: 6101304
Seven patients had the juvenile form; in two others, the age at onset was 1 year, but the clinical course was different from the late infantile form. The age at onset ranged from 1 to 18 years; the duration ranged from three to 17 years. ...
Seven patients had the juvenile form; in two others, the age at onset was 1 year, but the clinical course was different from the late …
12 results