Alzheimer's disease neuropathologic changes in semantic dementia.

Abstract:

UNLABELLED:Neuropathologic change underlying primary progressive aphasia (PPA) most commonly includes one of the frontotemporal lobar degenerations, such as FTLD-tau or FTLD-ubiquitin. The next most frequent etiology of PPA is Alzheimer's disease (AD). We describe 5 subjects with clinical diagnoses of semantic dementia, who underwent longitudinal clinical evaluation and postmortem neuropathology examination of the central nervous system. This case series examines retrospectively which clinical parameters might have pointed to the neuropathological diagnosis of AD. CONCLUSION:family history of late onset dementia, APOEepsilon4 status, combined features of semantic dementia and progressive non-fluent aphasia present early in illness, or generalized seizures, may indicate AD as the underlying pathology of semantic dementia.

journal_name

Neurocase

journal_title

Neurocase

authors

Chow TW,Varpetian A,Moss T,Vinters HV,Marquez S,Miller C

doi

10.1080/13554790903193174

subject

Has Abstract

pub_date

2010-02-01 00:00:00

pages

15-22

issue

1

eissn

1355-4794

issn

1465-3656

pii

916259346

journal_volume

16

pub_type

杂志文章
  • Complete, bilateral hippocampal ischemia: a case series.

    abstract::Acute and complete ischemia of the hippocampi represents a rare cause of amnesia. This paper describes the features of four such cases presenting to a single tertiary care center over a 3-year period. Interestingly, in three instances, toxicology screening was positive for opioids at the time of presentation, while in...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2016.1213299

    authors: Small JE,Butler PM,Zabar Y,Barash JA

    更新日期:2016-10-01 00:00:00

  • Acute loss of psychic self-activation after cardiac arrest and delayed bilateral pallidal lesions on brain MRI.

    abstract::The delay between cardiac arrest and brain MRI is usually extremely different in the few cerebral imaging studies assessing the affected brain areas. We report an unusual case of loss of psychic self-activation appeared immediately after a cardiac arrest in a middle age patient. The first brain MRI, one month after th...

    journal_title:Neurocase

    pub_type: 临床试验,杂志文章

    doi:10.1080/13554794.2019.1608263

    authors: Martinaud O,Le Goff F,Carlier J,Pouliquen D,Gérardin E,Savouré A

    更新日期:2019-01-01 00:00:00

  • Treatment with L-arginine improves neuropsychological disorders in a child with creatine transporter defect.

    abstract::Creatine transporter deficit (CT1) is an inherited metabolic disorder that causes mental retardation, epilepsy, speech, language and behavioral deficits. Until now, no treatment has been proven to be successful for this condition. We describe 1-year follow-up study of a child, aged 9.6 years, with CT1 defect, on oral ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790802060821

    authors: Chilosi A,Leuzzi V,Battini R,Tosetti M,Ferretti G,Comparini A,Casarano M,Moretti E,Alessandri MG,Bianchi MC,Cioni G

    更新日期:2008-01-01 00:00:00

  • A calendar savant with episodic memory impairments.

    abstract::Patients with memory disorders have severely restricted learning and memory. For instance, patients with anterograde amnesia can learn motor procedures and retain some restricted ability to learn new words and factual information. However, such learning is inflexible and frequently inaccessible to conscious awareness....

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790903405701

    authors: Olson IR,Berryhill ME,Drowos DB,Brown L,Chatterjee A

    更新日期:2010-06-01 00:00:00

  • Cognitive neuropsychological analysis of differential reading and spelling disorder mechanisms in a patient with aphasia.

    abstract::The purpose of this study was to determine if differential reading and spelling mechanisms were involved in a Japanese patient with aphasia. In our case, the patient scored low on all of the administered reading tasks, suggesting that both the reading lexical and non-lexical routes were impaired. In contrast, his writ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2015.1137950

    authors: Hashimoto K,Uno A

    更新日期:2016-06-01 00:00:00

  • The role of the thalamus in recovery from tactile extinction and crossed tactile extinction.

    abstract::A 68-year-old man had a cerebral infarction affecting the right parietal lobe, right insula, and the left prefrontal region. On admission, left hand tactile extinction was noted when the hands were placed both in anatomical and crossed positions, but was noted only in crossed positions from day 20 and later. Five mont...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2012.732082

    authors: Asada T,Takeda K,Okiyama R,Isozaki E,Fukuyama H

    更新日期:2014-01-01 00:00:00

  • Sensory function in severe semilobar holoprosencephaly.

    abstract::We report a 4-year-old child with severe semi-lobar holoprosencephaly (HPE) not expected to survive after birth. Magnetic resonance imaging (MRI) revealed agenesis of the corpus callosum, absence of the third ventricle, fused thalami and basal ganglia. To investigate sensory function, visual, auditory and somatosensor...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790802631936

    authors: Liasis A,Hildebrand D,Clark C,Katz X,Gunny R,Stieltjes B,Taylor D

    更新日期:2009-01-01 00:00:00

  • Action-based memory in Alzheimer's disease: a longitudinal look at tea making.

    abstract::In this paper we report the results of a longitudinal study which examined memory for a single routine activity of daily living in people with dementia of the Alzheimer type. We assessed memory in a natural setting, visiting volunteers in their homes. We video-taped performance on the selected task and analysed the re...

    journal_title:Neurocase

    pub_type: 临床试验,杂志文章

    doi:10.1093/neucas/8.1.111

    authors: Rusted J,Sheppard L

    更新日期:2002-01-01 00:00:00

  • A slice of pi : an exploratory neuroimaging study of digit encoding and retrieval in a superior memorist.

    abstract::Subject PI demonstrated superior memory using a variant of a Method of Loci (MOL) technique to recite the first digits of the mathematical constant pi to more than 2(16) decimal places. We report preliminary behavioral, functional magnetic resonance imaging (fMRI), and brain volumetric data from PI. fMRI data collecte...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790902776896

    authors: Raz A,Packard MG,Alexander GM,Buhle JT,Zhu H,Yu S,Peterson BS

    更新日期:2009-10-01 00:00:00

  • A paradigm for awake intraoperative memory mapping during forniceal stimulation.

    abstract::A case report is presented detailing the successful use of awake intraoperative memory testing while using white matter stimulation in order to isolate the fornix tracks involved in memory function. The identification of the white matter tracks of the fornix that were involved in memory function was used to tailor the...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2010.547509

    authors: Brandling-Bennett EM,Bookheimer SY,Horsfall JL,Moftakhar P,Sedrak M,Barkulis CT,Gertsch JH,MacDougall MG,Boucharel W,Nuwer MR,Bergsneider M

    更新日期:2012-02-01 00:00:00

  • A case of prosopometamorphopsia caused by infarction of the splenium of the corpus callosum and major forceps.

    abstract::An adult female complained of enlargement of right eyes in other people. Diffusion-weighted imaging detected an abnormal high-intensity area in the region from the splenium of the corpus callosum to the major forceps on the right side. The patient reported that right eyes appeared larger in size, which suggested proso...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2020.1797819

    authors: Ogawa K,Akimoto T,Takahashi K,Hara M,Morita A,Kamei S,Nakajima H,Fujishiro M,Suzuki Y,Soma M,Shikata E,Futamura A,Kawamura M

    更新日期:2020-10-01 00:00:00

  • Progression of neuropsychiatric and cognitive features due to exons 2 to 5 deletion in the epsilon-sarcoglycan gene: a case report.

    abstract::Physical symptoms of myoclonus dystonia due to epsilon-sarcoglycan mutations are well documented; however, the progression of neuropsychiatric and cognitive symptoms remains unclear. We present a case of a 34-year-old woman with early childhood onset of myoclonic jerks, dystonic posture and developmental delay due to ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2015.1120312

    authors: Multani N,Moro E,Lang A,Zurowski M,Duff Canning S,Tartaglia MC

    更新日期:2016-01-01 00:00:00

  • Case report: diagnosis and treatment of attention deficit hyperactivity disorder and autism spectrum disorder in patients diagnosed with oculocutaneous albinism.

    abstract::Oculocutaneous albinism (OCA) is a group of autosomal recessive disorders characterized by impairment in the melanin synthesis. We report two siblings with OCA who presented with symptoms of autism spectrum disorder and attention deficit hyperactivity disorder (ADHD). Ocular side effects occured after methylphenidate ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2020.1853174

    authors: Ünsel Bolat G

    更新日期:2020-12-01 00:00:00

  • Influence of motor disorders on the visual perception of human movements in a case of peripheral dysgraphia.

    abstract::We report the case of a 71 year-old female patient (DC) with a left parietal lesion resulting in a peripheral dysgraphia essentially characterized by difficulties in letter sequences writing. The aim of our experiments was to analyze the influence of motor difficulties on the visual perception of both writing and reac...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790490495113

    authors: Chary C,Méary D,Orliaguet JP,David D,Moreaud O,Kandel S

    更新日期:2004-06-01 00:00:00

  • FDG-PET measurement is more accurate than neuropsychological assessments to predict global cognitive deterioration in patients with mild cognitive impairment.

    abstract::The accurate prediction, at a pre-dementia stage of Alzheimer's disease (AD), of the subsequent clinical evolution of patients would be a major breakthrough from both therapeutic and research standpoints. Amnestic mild cognitive impairment (MCI) is presently the most common reference to address the pre-dementia stage ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790490896938

    authors: Chételat G,Eustache F,Viader F,De La Sayette V,Pélerin A,Mézenge F,Hannequin D,Dupuy B,Baron JC,Desgranges B

    更新日期:2005-02-01 00:00:00

  • Dementia with Lewy bodies presenting as Logopenic variant primary progressive Aphasia.

    abstract::We report a patient presenting with clinical features of logopenic variant primary progressive aphasia (lvPPA) who was later diagnosed with probable dementia with Lewy bodies. LvPPA is a neurodegenerative disease that is characterized by anomia, word-finding difficulty, impaired comprehension, and phonological errors....

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2020.1795204

    authors: Boes S,Botha H,Machulda M,Lowe V,Graff-Radford J,Whitwell JL,Utianski RL,Duffy JR,Josephs KA

    更新日期:2020-10-01 00:00:00

  • Sign language aphasia following right hemisphere damage in a left-hander: a case of reversed cerebral dominance in a deaf signer?

    abstract::Recent lesion studies have shown that left hemisphere lesions often give rise to frank sign language aphasias in deaf signers, whereas right hemisphere lesions do not, suggesting similar patterns of hemispheric asymmetry for signed and spoken language. We present here a case of a left-handed, deaf, life-long signer wh...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790590944717

    authors: Pickell H,Klima E,Love T,Kritchevsky M,Bellugi U,Hickok G

    更新日期:2005-06-01 00:00:00

  • Clinical and imaging progression over 10 years in a patient with primary progressive apraxia of speech and autopsy-confirmed corticobasal degeneration.

    abstract::Primary progressive apraxia of speech (PPAOS) is a neurodegenerative disorder in which AOS is the sole presenting complaint. We report clinical and neuroimaging data spanning 10 years from disease onset-to-death in a 49 year-old male PPAOS patient, DY, who died with corticobasal degeneration. He presented with AOS wit...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2018.1477963

    authors: Tetzloff KA,Duffy JR,Strand EA,Machulda MM,Boland SM,Utianski RL,Botha H,Senjem ML,Schwarz CG,Josephs KA,Whitwell JL

    更新日期:2018-04-01 00:00:00

  • Lack of orientation due to a congenital brain malformation: a case study.

    abstract::Topographical disorientation is usually described in patients who have lost the ability to orient themselves as a consequence of acquired focal brain damage. Here, we describe the case of a 20-year-old woman with a congenital brain malformation who has never been able to orient herself within the environment. We addre...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790500423602

    authors: Iaria G,Incoccia C,Piccardi L,Nico D,Sabatini U,Guariglia C

    更新日期:2005-12-01 00:00:00

  • Cross-examining dissociative identity disorder: neuroimaging and etiology on trial.

    abstract::Dissociative identity disorder (DID) is probably the most disputed of psychiatric diagnoses and of psychological forensic evaluations in the legal arena. The iatrogenic proponents assert that DID phenomena originate from psychotherapeutic treatment while traumagenic proponents state that DID develops after severe and ...

    journal_title:Neurocase

    pub_type: 杂志文章,评审

    doi:10.1080/13554790801992768

    authors: Reinders AA

    更新日期:2008-01-01 00:00:00

  • A case of semantic variant primary progressive aphasia with Pick's pathology.

    abstract::Neurodegenerative diseases are caused by aggregation of specific proteins that catalyze a cascade of changes that ultimately lead to neurodegeneration. This concept guides current diagnostic approaches, as well as clinical trials, that focus on detecting or removing amyloid or tau from the brain. The semantic variant ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2018.1447134

    authors: Caplan A,Marx G,Elofson J,Lis C,Grinberg L,Miller B,Rosen H

    更新日期:2018-04-01 00:00:00

  • Preserved cognition and functional independence after a large right posterior cerebral artery infarct: longitudinal clinical and neuropathological findings.

    abstract::BVR was 77 years old when he sustained a large posterior cerebral artery territory infarct. Medical, cognitive and functional data collected on four occasions over 10 years initially revealed circumscribed neurological signs, no functional or cognitive deficits. BVR became significantly impaired only after two other s...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554790500502918

    authors: Piguet O,Bennett HP,Waite LM,Kril JJ,Creasey H,Anthony Broe G,Halliday GM

    更新日期:2006-04-01 00:00:00

  • Temporal lobe epilepsy masquerading as psychosis--a case report and literature review.

    abstract::The psychoses of epilepsy are well recognized complications of seizure disorders, diagnosed easily from the history. However, in the absence of recognized seizures, the diagnosis can be challenging. We present a 27-year-old female, who suffered a treatment refractory psychosis for 6 years. She did not report, or dis...

    journal_title:Neurocase

    pub_type: 杂志文章,评审

    doi:10.1080/13554794.2011.627338

    authors: Needham E,Hamelijnck J

    更新日期:2012-01-01 00:00:00

  • Failure to paint the left quarter of a watercolor and no error in a line drawing: a case report of an art teacher with unilateral spatial neglect.

    abstract::A 54-year-old art teacher, experienced a right putaminal hemorrhage, and thereafter suffered severe left hemiplegia and unilateral spatial neglect, and was transferred to the rehabilitation department of the University Hospital 1 month after the onset. Although the unilateral spatial neglect was improving, the patient...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2011.588175

    authors: Kondo M,Mori T,Makino K,Okazaki T,Hachisuka K

    更新日期:2012-06-01 00:00:00

  • Two different mechanisms for omission and substitution errors in neglect dyslexia.

    abstract::Neglect dyslexia is a reading disorder often associated with right-sided brain lesions. In reading single words, errors are mostly substitutions or omissions of letters that occupy the left-sided positions. Typically, these errors have been thought to depend on a single mechanism. Conversely, we propose that they are ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2010.498382

    authors: Martelli M,Arduino LS,Daini R

    更新日期:2011-01-01 00:00:00

  • Effect of propranolol on naming in chronic Broca's aphasia with anomia.

    abstract::Previous research suggests that the noradrenergic system modulates flexibility of access to the lexical-semantic network, with propranolol benefiting normal subjects in lexical-semantic problem solving tasks. Patients with Broca's aphasia with anomia have impaired ability to access appropriate verbal output for a give...

    journal_title:Neurocase

    pub_type: 临床试验,杂志文章

    doi:10.1080/13554790701595471

    authors: Beversdorf DQ,Sharma UK,Phillips NN,Notestine MA,Slivka AP,Friedman NM,Schneider SL,Nagaraja HN,Hillier A

    更新日期:2007-08-01 00:00:00

  • Chediak-Higashi syndrome: neurocognitive and behavioral data from infancy to adulthood after bone marrow transplantation.

    abstract::Chediak-Higashi syndrome (CHS) is a rare autosomal disorder characterized by immunodeficiency, albinism, and progressive neurologic abnormalities. While survivors of the childhood-onset disease are known to exhibit learning disabilities and neuropsychiatric disorders followed by middle-age dementia, we lack detailed d...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2020.1856384

    authors: Yliranta A,Mäkinen J

    更新日期:2020-12-09 00:00:00

  • A cognitive chameleon: lessons from a novel MAPT mutation case.

    abstract::We report a case of frontotemporal dementia caused by a novel MAPT mutation (Q351R) with a remarkably long amnestic presentation mimicking familial Alzheimer's disease. Longitudinal clinical, neuropsychological and imaging data provide convergent evidence for predominantly bilateral anterior medial temporal lobe invol...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2013.826697

    authors: Liang Y,Gordon E,Rohrer J,Downey L,de Silva R,Jäger HR,Nicholas J,Modat M,Cardoso MJ,Mahoney C,Warren J,Rossor M,Fox N,Caine D

    更新日期:2014-01-01 00:00:00

  • Amnesiacs might get the gist: reduced false recognition in amnesia may be the result of impaired item-specific memory.

    abstract::It is a common finding in tests of false recognition that amnesic patients recognize fewer related lures than healthy controls, and this has led to assumptions that gist memory is damaged in these patients (Schacter, Verfaellie, & Anes, 1997, Neuropsychology, 11; Schacter, Verfaellie, Anes, & Racine, 1998, Journal of ...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2012.701637

    authors: Nissan J,Abrahams S,Sala SD

    更新日期:2013-01-01 00:00:00

  • The GGGGCC repeat expansion in C9ORF72 in a case with discordant clinical and FDG-PET findings: PET trumps syndrome.

    abstract::A hexanucleotide repeat expansion in the chromosome 9 open reading frame 72 (C9ORF72) gene was recently discovered as the cause underlying frontotemporal degeneration (FTD) and/or amyotrophic lateral sclerosis (ALS) linked to chromosome 9 (c9FTD/ALS). In this atypical case of c9FTD/ALS, the proband presented with amne...

    journal_title:Neurocase

    pub_type: 杂志文章

    doi:10.1080/13554794.2012.732090

    authors: Adeli A,Savica R,Lowe VJ,Vemuri P,Knopman DS,Dejesus-Hernandez M,Rademakers R,Fields JA,Crum BA,Jack CR,Petersen RC,Boeve BF

    更新日期:2014-01-01 00:00:00