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831 results
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Analysis of blink rate patterns in normal subjects.
Bentivoglio AR, Bressman SB, Cassetta E, Carretta D, Tonali P, Albanese A. Bentivoglio AR, et al. Among authors: albanese a. Mov Disord. 1997 Nov;12(6):1028-34. doi: 10.1002/mds.870120629. Mov Disord. 1997. PMID: 9399231
The subjects were videotaped in a standard setting while performing three different tasks: resting quietly, reading a short passage, talking freely. ...The best curve fit was represented by a log-normal distribution, with the upper tail of each curve having …
The subjects were videotaped in a standard setting while performing three different tasks: resting quietly, reading a short pa …
Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families.
Bentivoglio AR, Cortelli P, Valente EM, Ialongo T, Ferraris A, Elia A, Montagna P, Albanese A. Bentivoglio AR, et al. Among authors: albanese a. Mov Disord. 2001 Nov;16(6):999-1006. doi: 10.1002/mds.10034. Mov Disord. 2001. PMID: 11748730
Affected individuals had a mean age of 57 +/- 8.5 years, and average disease duration was 21 +/- 7.8 years. Parkinsonian features included benign course, early onset of drug-induced dyskinesias, and a good and persistent response to levodopa. ...PARK6 disease is …
Affected individuals had a mean age of 57 +/- 8.5 years, and average disease duration was 21 +/- 7.8 years. Parkinsonian features inc …
Consensus statement on the role of acute dopaminergic challenge in Parkinson's disease.
Albanese A, Bonuccelli U, Brefel C, Chaudhuri KR, Colosimo C, Eichhorn T, Melamed E, Pollak P, Van Laar T, Zappia M. Albanese A, et al. Mov Disord. 2001 Mar;16(2):197-201. doi: 10.1002/mds.1069. Mov Disord. 2001. PMID: 11295770
Available evidence on the practice of acute pharmacological challenge tests in parkinsonian patients was reviewed by a committee of experts, which achieved a general consensus. ...
Available evidence on the practice of acute pharmacological challenge tests in parkinsonian patients was reviewed by a committee of e …
Italian family with cranial cervical dystonia: clinical and genetic study.
Cassetta E, Del Grosso N, Bentivoglio AR, Valente EM, Frontali M, Albanese A. Cassetta E, et al. Among authors: albanese a. Mov Disord. 1999 Sep;14(5):820-5. doi: 10.1002/1531-8257(199909)14:5<820::aid-mds1015>3.0.co;2-i. Mov Disord. 1999. PMID: 10495044
A white Italian family affected by primary torsion dystonia (PTD) is described. The family phenotype most commonly presented with adult onset, cranial cervical involvement, and focal or segmental distribution without progression to generalization. ...The mean age at time o
A white Italian family affected by primary torsion dystonia (PTD) is described. The family phenotype most commonly presented with adu
Apomorphine and levodopa challenge in patients with a focal midbrain lesion.
Moro E, Albanese A. Moro E, et al. Among authors: albanese a. Mov Disord. 1999 Mar;14(2):269-75. doi: 10.1002/1531-8257(199903)14:2<269::aid-mds1012>3.0.co;2-x. Mov Disord. 1999. PMID: 10091621 Review.
Anatomic or etiologic features do not allow us to predict in which cases parkinsonian signs secondary to a midbrain lesion would respond to levodopa or to dopamine agonists. A trial with apomorphine is warranted in all such cases....
Anatomic or etiologic features do not allow us to predict in which cases parkinsonian signs secondary to a midbrain lesion would resp …
Tardive lingual dystonia treated with clozapine.
Raja M, Maisto G, Altavista MC, Albanese A. Raja M, et al. Among authors: albanese a. Mov Disord. 1996 Sep;11(5):585-6. doi: 10.1002/mds.870110521. Mov Disord. 1996. PMID: 8866507 No abstract available.
Acute challenge with apomorphine in Huntington's disease: a double-blind study.
Albanese A, Cassetta E, Carretta D, Bentivoglio AR, Tonali P. Albanese A, et al. Clin Neuropharmacol. 1995 Oct;18(5):427-34. doi: 10.1097/00002826-199510000-00005. Clin Neuropharmacol. 1995. PMID: 8665556 Clinical Trial.
Apomorphine (1.5 or 3 mg) or placebo was acutely administered to choreic patients affected by Huntington's disease in a double-blind fashion. The patients were evaluated before the administration, and at 15-min intervals for 2 h afterward, by means of a rating scale …
Apomorphine (1.5 or 3 mg) or placebo was acutely administered to choreic patients affected by Huntington's disease in a double-blind …
Postural axial tremor in a patient with cerebellar atrophy.
Albanese A, Daniele A, Lo Monaco M, Di Lazzaro V, Restuccia D, Milone M, Tonali P. Albanese A, et al. Mov Disord. 1992;7(3):273-80. doi: 10.1002/mds.870070314. Mov Disord. 1992. PMID: 1620146
The tremor was associated with alternating activity in antagonistic muscles; it was triggered whenever a contraction of lumbar back extensor muscles occurred. Electrical stimulation of the cerebellum did not produce the normal suppression phases of motor responses evoked b …
The tremor was associated with alternating activity in antagonistic muscles; it was triggered whenever a contraction of lumbar back e …
Severe constipation in Parkinson's disease relieved by botulinum toxin.
Albanese A, Maria G, Bentivoglio AR, Brisinda G, Cassetta E, Tonali P. Albanese A, et al. Mov Disord. 1997 Sep;12(5):764-6. doi: 10.1002/mds.870120524. Mov Disord. 1997. PMID: 9380063
A parkinsonian patient with severe outlet-type constipation was treated with injection of botulinum toxin into the puborectalis muscle. ...The present data show that botulinum toxin is a promising tool for treating outlet-type constipation in Parkinson's disease....
A parkinsonian patient with severe outlet-type constipation was treated with injection of botulinum toxin into the puborectalis muscl
Genetically determined cholinergic deficiency in the forebrain of C57BL/6 mice.
Bentivoglio AR, Altavista MC, Granata R, Albanese A. Bentivoglio AR, et al. Among authors: albanese a. Brain Res. 1994 Feb 21;637(1-2):181-9. doi: 10.1016/0006-8993(94)91231-9. Brain Res. 1994. PMID: 8180796
This study demonstrates that a deficiency of forebrain cholinergic neurons occurs in C57BL/6 (C57) mice, a strain characterized by poor learning capabilities. ...These data show that C57 mice can be regarded as a genetic mutant, whose phenotype is characteriz …
This study demonstrates that a deficiency of forebrain cholinergic neurons occurs in C57BL/6 (C57) mice, a strain characterize …
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