Therapy and management of frontal lobe dementia patients.

Abstract:

:Patients with frontal lobe dementia (FLD) include those who suffer from Pick's disease, corticobasal degeneration, FLD without specific histopathologic features, as well as the infrequent families with frontotemporal dementia and parkinsonism associated with chromosome 17. Currently there have been no systematic efforts to manage and to treat patients with FLD. Drawing on the accumulated experience of clinicians and the known therapeutic approaches for patients with other neurodegenerative disorders such as AD and PD, the author discusses possible neurotransmitter replacement and biologic therapeutic approaches for patients with FLD.

journal_name

Neurology

journal_title

Neurology

authors

Litvan I

doi

10.1212/wnl.56.suppl_4.s41

subject

Has Abstract

pub_date

2001-06-01 00:00:00

pages

S41-5

issue

11 Suppl 4

eissn

0028-3878

issn

1526-632X

journal_volume

56

pub_type

杂志文章,评审
  • Evidence for a genetic predisposition for status epilepticus.

    abstract::The role of genetic factors in determining risk for status epilepticus (SE) was examined in twins identified using the population-based Virginia Twin Registry. Concordance rates for SE were 0.38 for monozygotic (MZ) and 0.00 for dizygotic (DZ) twins, with the rate in MZs being significantly increased over DZs. The pre...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.50.2.558

    authors: Corey LA,Pellock JM,Boggs JG,Miller LL,DeLorenzo RJ

    更新日期:1998-02-01 00:00:00

  • Exchange transfusion in neonatal myasthenia gravis.

    abstract::An infant with transient neonatal myasthenia gravis had a double-blood-volume exchange transfusion because of maternal-fetal blood group incompatibility. This seemed to accelerate both decline in antiacetylcholine antibody titer and clinical improvement. ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.31.7.911

    authors: Donat JF,Donat JR,Lennon VA

    更新日期:1981-07-01 00:00:00

  • Motor activation in multiple system atrophy and Parkinson disease: a PET study.

    abstract:BACKGROUND:Multiple system atrophy (MSA) is an atypical parkinsonian syndrome including cerebellar impairment and poor response to levodopa. We assessed right hand motor activation in patients with MSA before and after an acute levodopa challenge in comparison with patients with PD and healthy volunteers (HVs). METHOD...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181f4d78f

    authors: Payoux P,Brefel-Courbon C,Ory-Magne F,Regragui W,Thalamas C,Balduyck S,Durif F,Azulay JP,Tison F,Blin O,Esquerre JP,Rascol O

    更新日期:2010-09-28 00:00:00

  • Cerebral amyloid angiopathy and cognitive function: the HAAS autopsy study.

    abstract:OBJECTIVE:To investigate the relationship between cerebral amyloid angiopathy (CAA), dementia, and cognitive function in an autopsy sample of 211 Japanese-American men from the population-based Honolulu-Asia Aging Study. METHODS:Starting in 1991, participants were assessed with the Cognitive Abilities Screening Instru...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.58.11.1629

    authors: Pfeifer LA,White LR,Ross GW,Petrovitch H,Launer LJ

    更新日期:2002-06-11 00:00:00

  • Folic acid supplementation prevents phenytoin-induced gingival overgrowth in children.

    abstract:OBJECTIVE:Gingival overgrowth is an important adverse effect of phenytoin (PHT) therapy, occurring in about half of the patients. This study aimed to evaluate the effect of oral folic acid supplementation (0.5 mg/day) for the prevention of PHT-induced gingival overgrowth (PIGO) in children with epilepsy aged 6-15 years...

    journal_title:Neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1212/WNL.0b013e3182152844

    authors: Arya R,Gulati S,Kabra M,Sahu JK,Kalra V

    更新日期:2011-04-12 00:00:00

  • Cognitive screening examinations for silent cerebral infarcts in sickle cell disease.

    abstract:OBJECTIVE:In children with sickle cell disease (SCD), silent cerebral infarcts are the most frequent cause of neurologic injury. We determined the sensitivity and specificity of selective neurocognitive measures when separating children with silent cerebral infarcts and SCD from sibling controls. Additionally, we teste...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.50.6.1678

    authors: DeBaun MR,Schatz J,Siegel MJ,Koby M,Craft S,Resar L,Chu JY,Launius G,Dadash-Zadeh M,Lee RB,Noetzel M

    更新日期:1998-06-01 00:00:00

  • Psychiatric adverse events during levetiracetam therapy.

    abstract::The prevalence and psychopathologic features of psychiatric adverse events (PAE) in 517 patients taking levetiracetam (LEV) were investigated. Fifty-three (10.1%) patients developed PAE. A significant association was found with previous psychiatric history, history of febrile convulsions, and history of status epilept...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000078031.32904.0d

    authors: Mula M,Trimble MR,Yuen A,Liu RS,Sander JW

    更新日期:2003-09-09 00:00:00

  • Disconnection as a mechanism for social cognition impairment in multiple sclerosis.

    abstract:OBJECTIVE:To assess the contribution of microstructural normal-appearing white matter (NAWM) damage to social cognition impairment, specifically in the theory of mind (ToM), in multiple sclerosis (MS). METHODS:We enrolled consecutively 60 patients with MS and 60 healthy controls (HC) matched on age, sex, and education...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000004060

    authors: Batista S,Alves C,d'Almeida OC,Afonso A,Félix-Morais R,Pereira J,Macário C,Sousa L,Castelo-Branco M,Santana I,Cunha L

    更新日期:2017-07-04 00:00:00

  • Adrenergic innervation in autonomic failure.

    abstract::In 10 patients with chronic autonomic failure, the sympathetic perivascular nerve plexuses from quadriceps muscle biopsies were studied by catecholamine fluorescence and electronmicroscopy. There was almost complete absence of catecholamine fluorescence and fewer than normal numbers of small granular (noradrenergic) v...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.31.12.1501

    authors: Bannister R,Crowe R,Eames R,Burnstock G

    更新日期:1981-12-01 00:00:00

  • Cervical dural sac and spinal cord in juvenile muscular atrophy of distal upper extremity.

    abstract:OBJECTIVE:To investigate specificity and significance of dynamic changes of the cervical dural sac and spinal cord during neck flexion in juvenile muscular atrophy of the distal upper extremity. BACKGROUND:The disorder affects young people-predominantly men-and is progressive for several years. One autopsy case showed...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.54.10.1922

    authors: Hirayama K,Tokumaru Y

    更新日期:2000-05-23 00:00:00

  • Normal fibroblast mitochondrial malic enzyme activity in Friedreich's ataxia.

    abstract::Mitochondrial and cytoplasmic malic isoenzymes were assayed fluorometrically in digitonin-fractionated fibroblasts from three patients with Friedreich's ataxia (FA). Normal activity was found, failing to verify an earlier report of reduced fibroblast mitochondrial malic enzyme activity in FA. The previously reported d...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.36.6.869

    authors: Fernandez RJ,Civantos F,Tress E,Maltese WA,De Vivo DC

    更新日期:1986-06-01 00:00:00

  • Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene.

    abstract::A two-octapeptide repeat deletion of the prion protein gene has been recently observed in a patient with a 2-year history of dementia and a clinical diagnosis of possible Creutzfeldt-Jakob disease (CJD). The authors report a similar deletion in a patient with a definitive diagnosis of CJD. Since the two-repeat deletio...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000035533.86833.28

    authors: Capellari S,Parchi P,Wolff BD,Campbell J,Atkinson R,Posey DM,Petersen RB,Gambetti P

    更新日期:2002-11-26 00:00:00

  • Reduced basal ganglia volumes in Tourette's syndrome using three-dimensional reconstruction techniques from magnetic resonance images.

    abstract::Using a 1.5-tesla GE Signa MR scanner, we imaged the brains of 14 right-handed Tourette's syndrome (TS) patients (11 men, three women), aged 18 to 49 years, who had minimal lifetime neuroleptic exposure. We also studied an equal number of normal controls individually matched for age, sex, and handedness and group-matc...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.43.5.941

    authors: Peterson B,Riddle MA,Cohen DJ,Katz LD,Smith JC,Hardin MT,Leckman JF

    更新日期:1993-05-01 00:00:00

  • Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphism.

    abstract::The association of the STH gene polymorphism with Alzheimer disease (AD) is debated. In the analysis of two genetically and diagnostically distinct groups of Alzheimer patients from the USA and Italy, the authors did not find an association with the STH polymorphism. However, the APOE-4-associated risk of AD greatly i...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000125693.59817.31

    authors: Seripa D,Matera MG,D'Andrea RP,Gravina C,Masullo C,Daniele A,Bizzarro A,Rinaldi M,Antuono P,Wekstein DR,Dal Forno G,Fazio VM

    更新日期:2004-05-11 00:00:00

  • Adiponectin levels in patients with intracranial atherosclerosis.

    abstract:BACKGROUND:Adiponectin is a protein secreted by adipose cells that improves insulin sensitivity and possesses antiatherogenic properties. In this study, we investigated the relationship between adiponectin levels and ischemic stroke subtype. METHODS:Using clinical, imaging, and laboratory data, 231 consecutive patient...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000263186.20988.9f

    authors: Bang OY,Saver JL,Ovbiagele B,Choi YJ,Yoon SR,Lee KH

    更新日期:2007-05-29 00:00:00

  • A short-term randomized MRI study of high-dose oral vs intravenous methylprednisolone in MS.

    abstract:OBJECTIVE:To compare the efficacy, tolerability, and safety of IV methylprednisolone (IV MP) vs oral methylprednisolone (oMP) at equivalent high doses in patients with multiple sclerosis (MS) experiencing a recent relapse. METHODS:Patients with a clinical relapse within the previous 2 weeks and at least 1 gadolinium (...

    journal_title:Neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1212/WNL.0b013e3181c3fd5b

    authors: Martinelli V,Rocca MA,Annovazzi P,Pulizzi A,Rodegher M,Martinelli Boneschi F,Scotti R,Falini A,Sormani MP,Comi G,Filippi M

    更新日期:2009-12-01 00:00:00

  • A presenilin 1 R278I mutation presenting with language impairment.

    abstract::Presenilin (PSEN)1 mutations are responsible for many cases of autosomal dominant Alzheimer disease (AD), although the clinical spectrum has not been fully defined. The authors describe two members of a kindred with a novel PSEN1 mutation (R278I) presenting with language impairment and relative preservation of memory....

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000143060.98164.1a

    authors: Godbolt AK,Beck JA,Collinge J,Garrard P,Warren JD,Fox NC,Rossor MN

    更新日期:2004-11-09 00:00:00

  • Migraine in pregnancy.

    abstract::Migraine does not increase the risk for complications of pregnancy for the mother or for the fetus: the incidences of toxemia, miscarriages, abnormal labour, congenital anomalies, and stillbirths are comparable to those of the general population. Several retrospective studies have shown a tendency for migraine to impr...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:

    authors: Aubé M

    更新日期:1999-01-01 00:00:00

  • Venous drainage in multiple sclerosis: a combined MRI and ultrasound study.

    abstract:BACKGROUND:Chronic cerebrospinal venous insufficiency (CCSVI) was proposed as the causal trigger for developing multiple sclerosis (MS). However, current data are contradictory and a gold standard for venous flow assessment is missing. OBJECTIVE:To compare structural magnetic resonance venography (MRV) and dynamic ext...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e318236f0ea

    authors: Doepp F,Würfel JT,Pfueller CF,Valdueza JM,Petersen D,Paul F,Schreiber SJ

    更新日期:2011-11-08 00:00:00

  • Double-blind comparison of pramipexole and bromocriptine treatment with placebo in advanced Parkinson's disease. International Pramipexole-Bromocriptine Study Group.

    abstract::Pramipexole is a new, selective, nonergoline dopamine agonist that acts on D2 and preferentially on D3 dopamine receptors. Phase II and III clinical trials have shown this drug to be useful in treating both early and advanced Parkinson's disease (PD) patients. A double-blind, randomized, multicenter study was performe...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,多中心研究,随机对照试验

    doi:10.1212/wnl.49.4.1060

    authors: Guttman M

    更新日期:1997-10-01 00:00:00

  • Efficacy and safety of add-on divalproex sodium in the treatment of complex partial seizures. The M88-194 Study Group.

    abstract::We studied the efficacy of divalproex sodium in patients with complex partial seizures taking concomitant carbamazepine or phenytoin as monotherapy. Patients were selected because of inadequate seizure control by current therapy. The primary efficacy measure was median reduction of seizure frequency during add-on trea...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1212/wnl.46.1.49

    authors: Willmore LJ,Shu V,Wallin B

    更新日期:1996-01-01 00:00:00

  • Effect of a CYP2D6 polymorphism on the efficacy of donepezil in patients with Alzheimer disease.

    abstract:OBJECTIVE:To evaluate the influence of the single nucleotide polymorphism rs1080985 in the cytochrome P450 2D6 (CYP2D6) gene on the efficacy of donepezil in patients with mild to moderate Alzheimer disease (AD). METHODS:This was a multicenter, prospective cohort study of 127 white patients with AD according to the Nat...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1212/WNL.0b013e3181b6bbe3

    authors: Pilotto A,Franceschi M,D'Onofrio G,Bizzarro A,Mangialasche F,Cascavilla L,Paris F,Matera MG,Pilotto A,Daniele A,Mecocci P,Masullo C,Dallapiccola B,Seripa D

    更新日期:2009-09-08 00:00:00

  • Fetal akinesia deformation sequence (Pena-Shokeir phenotype) associated with acquired intrauterine brain damage.

    abstract::An infant with Pena-Shokeir phenotype was born to a cocaine-using mother. The pathologic findings included polyhydramnios, facial anomalies, arthrogryposis, camptodactyly, pulmonary hypoplasia, and tetralogy of Fallot. The neuropathologic findings were diffuse brainstem and spinal cord neuronal degeneration and focal ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.41.9.1467

    authors: Lavi E,Montone KT,Rorke LB,Kliman HJ

    更新日期:1991-09-01 00:00:00

  • Abeta1-42 promotes cholinergic sprouting in patients with AD and Lewy body variant of AD.

    abstract:BACKGROUND:The neurodegenerative process in Alzheimer's disease (AD) and in the Lewy body variant of AD (LBV) patients is characterized by cholinergic dysfunction and deposition of amyloid beta-peptide (Abeta) 1-40 and 1-42; however, the differential effects of Abeta species on the cholinergic system are not completely...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000073987.79060.4b

    authors: Masliah E,Alford M,Adame A,Rockenstein E,Galasko D,Salmon D,Hansen LA,Thal LJ

    更新日期:2003-07-22 00:00:00

  • Sex, race, and risk of dementia diagnosis after traumatic brain injury among older veterans.

    abstract:OBJECTIVE:To investigate whether sex and race differences exist in dementia diagnosis risk associated with traumatic brain injury (TBI) among older veterans. METHODS:Using Fine-Gray regression models, we investigated incident dementia diagnosis risk with TBI exposure by sex and race. RESULTS:After the exclusion of ba...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000010617

    authors: Kornblith E,Peltz CB,Xia F,Plassman B,Novakovic-Apopain T,Yaffe K

    更新日期:2020-09-29 00:00:00

  • Patient-centered outcomes: translating clinical efficacy into benefits on health-related quality of life.

    abstract:BACKGROUND:Multiple sclerosis (MS) is a neurodegenerative disease associated with marked impairments in health-related quality of life (HRQoL). Although standard clinical end points such as the Expanded Disability Status Scale and annualized relapse rate remain useful in assessing MS activity and severity, these measur...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181dbb884

    authors: Miller D,Rudick RA,Hutchinson M

    更新日期:2010-04-27 00:00:00

  • Endothelial progenitor cells correlate with lesion volume and growth in acute stroke.

    abstract:OBJECTIVES:Circulating endothelial progenitor cells (EPC) are markers of vascular injury and their numbers decrease in acute stroke. However, the relation of EPC levels to stroke severity has not been quantified. MRI measurements of lesion volume provide an objective method for stroke severity assessment and outcome pr...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e318200d741

    authors: Bogoslovsky T,Chaudhry A,Latour L,Maric D,Luby M,Spatz M,Frank J,Warach S

    更新日期:2010-12-07 00:00:00

  • APOE epsilon4 is not a susceptibility gene in idiopathic or diabetic sensory neuropathy.

    abstract::The presence of an APOE epsilon4 allele may be a risk factor for neuropathy severity in diabetes. The authors assessed the frequency of APOE epsilon4 in patients presenting with sensory predominant neuropathy. APOE epsilon4 frequency among patients with early diabetic neuropathy and impaired glucose tolerance-associat...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.WNL.0000148587.97690.4E

    authors: Zhou Z,Hoke A,Cornblath DR,Griffin JW,Polydefkis M

    更新日期:2005-01-11 00:00:00

  • Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease).

    abstract:OBJECTIVE:To critically re-evaluate cases diagnosed as adult neuronal ceroid lipofuscinosis (ANCL) in order to aid clinicopathologic diagnosis as a route to further gene discovery. METHODS:Through establishment of an international consortium we pooled 47 unsolved cases regarded by referring centers as ANCL. Clinical a...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000002943

    authors: Berkovic SF,Staropoli JF,Carpenter S,Oliver KL,Kmoch S,Anderson GW,Damiano JA,Hildebrand MS,Sims KB,Cotman SL,Bahlo M,Smith KR,Cadieux-Dion M,Cossette P,Jedličková I,Přistoupilová A,Mole SE,ANCL Gene Discovery Consortiu

    更新日期:2016-08-09 00:00:00

  • Conglomerated beads shape of lacunar infarcts on diffusion-weighted MRI: what does it suggest?

    abstract:OBJECTIVE:We aimed to analyze lesion patterns of lacunae-sized infarctions in the perforating arterial territory in terms of shape and to determine whether the particular pattern of conglomerated beads shape affected early neurologic deterioration. METHODS:We consecutively included acute ischemic stroke patients with ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e318253d62f

    authors: Ryu DW,Shon YM,Kim BS,Cho AH

    更新日期:2012-05-01 00:00:00