Database : MEDLINE
Search on : kluver-bucy and syndrome [Words]
References found : 234 [refine]
Displaying: 1 .. 10   in format [Detailed]

page 1 of 24 go to page                         

  1 / 234 MEDLINE  
              next record last record
select
to print
Photocopy
Full text

[PMID]: 29237192
[Au] Autor:Juliá-Palacios N; Boronat S; Delgado I; Felipe A; Macaya A
[Ad] Address:Pediatric Neurology, Vall d'Hebron Hospital, UAB, Barcelona, Spain.
[Ti] Title:Pediatric Klüver-Bucy Syndrome: Report of Two Cases and Review of the Literature.
[So] Source:Neuropediatrics;, 2017 Dec 13.
[Is] ISSN:1439-1899
[Cp] Country of publication:Germany
[La] Language:eng
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 171213
[Lr] Last revision date:171213
[St] Status:Publisher
[do] DOI:10.1055/s-0037-1609036

  2 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 29061200
[Au] Autor:Gama Marques J
[Ad] Address:1Schizophrenia Department,Hospital Júlio de Matos,Centro Hospitalar Psiquiátrico de Lisboa,Lisboa,Portugal.
[Ti] Title:A neuropsychiatric case report: Klüver-Bucy and Gastaut-Geschwind syndromes in one patient with schizoaffective disorder presenting with brain 99-mTc HMPAO single-photon emission computed tomography showing bilateral discrete decrease of temporal lobes perfusion.
[So] Source:CNS Spectr;:1-3, 2017 Oct 24.
[Is] ISSN:1092-8529
[Cp] Country of publication:United States
[La] Language:eng
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1710
[Cu] Class update date: 171024
[Lr] Last revision date:171024
[St] Status:Publisher
[do] DOI:10.1017/S1092852917000712

  3 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28859570
[Au] Autor:Vannemreddy PSSV; Stone JL
[Ad] Address:Department of Neurosurgery, University of Illinois at Chicago, Illinois; and.
[Ti] Title:Sanger Brown and Edward Schäfer before Heinrich Klüver and Paul Bucy: their observations on bilateral temporal lobe ablations.
[So] Source:Neurosurg Focus;43(3):E2, 2017 Sep.
[Is] ISSN:1092-0684
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Fifty years before a report on the complete bitemporal lobectomy syndrome in primates, known as the Klüver-Bucy syndrome, was published, 2 talented investigators working at the University College in London, England-neurologist Sanger Brown and physiologist Edward Schäfer-also made this discovery. The title of their work was "An investigation into the functions of the occipital and temporal lobes of the monkey's brain," and it involved excisional brain surgery in 12 monkeys. They were particularly interested in the then-disputed primary cortical locations relating to vision and hearing. However, following extensive bilateral temporal lobe excisions in 2 monkeys, they noted peculiar behavior including apparent loss of memory and intelligence resembling "idiocy." These investigators recognized most of the behavioral findings that later came to be known as the Klüver-Bucy syndrome. However, they were working within the late-19th-century framework of cerebral cortical localizations of basic motor and sensory functions. Details of the Brown and Schäfer study and a glimpse of the neurological thinking of that period is presented. In the decades following the pivotal work of Klüver and Bucy in the late 1930s, in which they used a more advanced neurosurgical technique, tools of behavioral observations, and analysis of brain sections after euthanasia, investigators have elaborated the full components of the clinical syndrome and the extent of their resections. Other neuroscientists sought to isolate and determine the specific temporal neocortical, medial temporal, and deep limbic structures responsible for various visual and complex behavioral deficits. No doubt, Klüver and Bucy's contribution led to a great expansion in attention given to the limbic system's role in action, perception, emotion, and affect-a tide that continues to the present time.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1709
[Cu] Class update date: 171116
[Lr] Last revision date:171116
[St] Status:In-Process
[do] DOI:10.3171/2017.6.FOCUS17265

  4 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28859563
[Au] Autor:Sloffer CA
[Ad] Address:Bronson Neuroscience Center, and Western Michigan University Homer Stryker School of Medicine, Kalamazoo, Michigan.
[Ti] Title:Editorial. The Klüver-Bucy syndrome and the golden age of localization.
[So] Source:Neurosurg Focus;43(3):E3, 2017 09.
[Is] ISSN:1092-0684
[Cp] Country of publication:United States
[La] Language:eng
[Pt] Publication type:EDITORIAL; COMMENT
[Em] Entry month:1709
[Cu] Class update date: 171116
[Lr] Last revision date:171116
[St] Status:In-Process
[do] DOI:10.3171/2017.6.FOCUS17416

  5 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy

[PMID]: 28730259
[Au] Autor:Hreniuc NC; NeamTu C; Sferdian MF; Ghib Para CG; Precup CV; Ioiart I
[Ad] Address:General Surgery Unit, Emergency County Hospital, Arad, Romania; carmen.neamtu@gmail.com.
[Ti] Title:Clinical manifestations and morphological changes in one case with post-stroke Klüver-Bucy syndrome.
[So] Source:Rom J Morphol Embryol;58(2):665-669, 2017.
[Is] ISSN:1220-0522
[Cp] Country of publication:Romania
[La] Language:eng
[Ab] Abstract:We present the case of a 71-year-old right-handed male, admitted to the Department of Neurology, Emergency County Hospital of Arad, Romania, on November 2015, with a rare case of Klüver-Bucy syndrome (KBS), following an ischemic stroke of the right temporal lobe, which was previously diagnosed in December 2014 and was treated accordingly. At the moment of second hospital admission, the patient was found somnolent and confused at home, with traumatic signs of biting of the tongue and urine emission. A couple days after admission, our patient became alert and presented hypersexuality, hypermetamorphosis, increased oral tendency, behavior changes including apathy with loss of anger and fear, and a very increased appetite, transient visual agnosia and right-left disorientation. In the initial phase, the patient could not recognize any members of his family, but he had a tendency to touch everything within his reach and place it into his mouth. The KBS presented in this case, following an ischemic stroke of the right temporal lobe provides distinct and intriguing insights into the possible pathophysiology of this syndrome. Often disruption of consciousness during recovery period may hide the clinical manifestation of the syndrome.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1707
[Cu] Class update date: 170721
[Lr] Last revision date:170721
[St] Status:In-Process

  6 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28009619
[Au] Autor:Loo D; Evans D; Abbott CC; Quinn DK
[Ad] Address:University of New Mexico, Albuquerque, NM daloo@salud.unm.edu.
[Ti] Title:Left Anterior-Right Temporal Electroconvulsive Therapy for Catatonia After Epilepsy Surgery: A Case Report.
[So] Source:J ECT;33(1):e4-e6, 2017 Mar.
[Is] ISSN:1533-4112
[Cp] Country of publication:United States
[La] Language:eng
[Mh] MeSH terms primary: Catatonia/etiology
Catatonia/therapy
Electroconvulsive Therapy/methods
Epilepsy, Complex Partial/surgery
Kluver-Bucy Syndrome/therapy
Neurosurgical Procedures/adverse effects
Postoperative Complications/therapy
[Mh] MeSH terms secundary: Anterior Temporal Lobectomy/adverse effects
Epilepsy, Complex Partial/complications
Female
Humans
Kluver-Bucy Syndrome/psychology
Middle Aged
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Em] Entry month:1710
[Cu] Class update date: 171023
[Lr] Last revision date:171023
[Js] Journal subset:IM
[Da] Date of entry for processing:161224
[St] Status:MEDLINE
[do] DOI:10.1097/YCT.0000000000000372

  7 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 27827379
[Au] Autor:Hu H; Hübner C; Lukacs Z; Musante L; Gill E; Wienker TF; Ropers HH; Knierim E; Schuelke M
[Ad] Address:Max Planck Institute for Molecular Genetics, Berlin, Germany.
[Ti] Title:Klüver-Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C).
[So] Source:Eur J Hum Genet;25(2):253-256, 2017 Feb.
[Is] ISSN:1476-5438
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Klüver-Bucy syndrome (KBS) comprises a set of neurobehavioral symptoms with psychic blindness, hypersexuality, disinhibition, hyperorality, and hypermetamorphosis that were originally observed after bilateral lobectomy in Rhesus monkeys. We investigated two siblings with KBS from a consanguineous family by whole-exome sequencing and autozygosity mapping. We detected a homozygous variant in the heparan-α-glucosaminidase-N-acetyltransferase gene (HGSNAT; c.518G>A, p.(G173D), NCBI ClinVar RCV000239404.1), which segregated with the phenotype. Disease-causing variants in this gene are known to be associated with autosomal recessive Mucopolysaccharidosis type IIIC (MPSIIIC, Sanfilippo C). This lysosomal storage disease is due to deficiency of the acetyl-CoA:α-glucosaminidase-N-acetyltransferase, which was shown to be reduced in patient fibroblasts. Our report extends the phenotype associated with MPSIIIC. Besides MPSIIIA and MPSIIIB, due to variants in SGSH and NAGLU, this is the third subtype of Sanfilippo disease to be associated with KBS. MPSIII should be included in the differential diagnosis of young patients with KBS.
[Mh] MeSH terms primary: Acetyltransferases/genetics
Kluver-Bucy Syndrome/genetics
Mucopolysaccharidosis III/genetics
[Mh] MeSH terms secundary: Child
Exome
Female
Genes, Recessive
Homozygote
Humans
Kluver-Bucy Syndrome/complications
Kluver-Bucy Syndrome/diagnosis
Male
Mucopolysaccharidosis III/complications
Mucopolysaccharidosis III/diagnosis
Phenotype
Siblings
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Nm] Name of substance:EC 2.3.1.- (Acetyltransferases); EC 2.3.1.78 (HGSNAT protein, human)
[Em] Entry month:1707
[Cu] Class update date: 170705
[Lr] Last revision date:170705
[Js] Journal subset:IM
[Da] Date of entry for processing:161110
[St] Status:MEDLINE
[do] DOI:10.1038/ejhg.2016.149

  8 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 27530874
[Au] Autor:Jha KK; Singh SK; Kumar P; Arora CD
[Ad] Address:Department of Psychiatry, All India Institute of Medical Sciences Patna, Patna, Bihar, India.
[Ti] Title:Partial Kluver-Bucy syndrome secondary to tubercular meningitis.
[So] Source:BMJ Case Rep;2016, 2016 Aug 16.
[Is] ISSN:1757-790X
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Tubercular meningitis (TBM) is a devastating extra pulmonary manifestation of tuberculosis and demonstrates a high neurological morbidity. A rare complication of this condition is Kluver-Bucy syndrome (KBS), which is a neurobehavioral disorder characterised by hyper-sexuality, visual agnosia, bulimia, placidity, hyperorality and memory deficits caused by lesions to the amygdala. The amygdala lesions can be due to many causes, including traumatic brain injury, systemic conditions and infections such as tuberculosis. Here, we present a case of partial KBS in a patient undergoing treatment for TBM.
[Mh] MeSH terms primary: Kluver-Bucy Syndrome/microbiology
Tuberculosis, Meningeal/complications
[Mh] MeSH terms secundary: Antipsychotic Agents/therapeutic use
Antitubercular Agents/therapeutic use
Humans
Magnetic Resonance Imaging
Male
Risperidone/therapeutic use
Treatment Outcome
Young Adult
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Nm] Name of substance:0 (Antipsychotic Agents); 0 (Antitubercular Agents); L6UH7ZF8HC (Risperidone)
[Em] Entry month:1702
[Cu] Class update date: 170221
[Lr] Last revision date:170221
[Js] Journal subset:IM
[Da] Date of entry for processing:160818
[St] Status:MEDLINE

  9 / 234 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
PubMed Central Full text
Full text

[PMID]: 27446793
[Au] Autor:Cho AR; Lim YH; Chung SH; Choi EH; Lim JY
[Ad] Address:Department of Rehabilitation Medicine, Hallym University Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Chuncheon, Korea.
[Ti] Title:Bilateral Anterior Opercular Syndrome With Partial Kluver-Bucy Syndrome in a Stroke Patient: A Case Report.
[So] Source:Ann Rehabil Med;40(3):540-4, 2016 Jun.
[Is] ISSN:2234-0645
[Cp] Country of publication:Korea (South)
[La] Language:eng
[Ab] Abstract:Bilateral anterior opercular syndrome and partial Kluver-Bucy syndrome are associated with bilateral middle cerebral artery lesions. The combination of these two syndromes has only been reported in a child with limbic encephalitis. In this case, a 44-year-old woman with bilateral middle cerebral artery infarction, which occurred 2 years prior, could walk independently. However, she showed automatic-voluntary dissociation and anarthria with preserved writing skills. She also presented hypersexuality, hypermetamorphosis, and memory disturbances. Here, we report a case of an adult stroke patient who suffered from bilateral anterior opercular syndrome accompanied by partial Kluver-Bucy syndrome.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1607
[Cu] Class update date: 170220
[Lr] Last revision date:170220
[Da] Date of entry for processing:160723
[St] Status:PubMed-not-MEDLINE
[do] DOI:10.5535/arm.2016.40.3.540

  10 / 234 MEDLINE  
              first record previous record
select
to print
Photocopy
Full text

[PMID]: 27380585
[Au] Autor:Caro MA; Jimenez XF
[Ad] Address:Department of Psychiatry and Psychology, Cleveland Clinic Foundation, 9500 Euclid Ave P57, Cleveland, OH, 44195. mario.caro@yale.edu.
[Ti] Title:Mesiotemporal Disconnection and Hypoactivity in Klüver-Bucy Syndrome: Case Series and Literature Review.
[So] Source:J Clin Psychiatry;77(8):e982-8, 2016 Aug.
[Is] ISSN:1555-2101
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:OBJECTIVE: Klüver-Bucy syndrome (KBS) is often perceived as rare and limited to cases with bilateral amygdala destruction. In fact, various alternate mechanisms may be involved, warranting exploration of the syndrome's presentation, pathophysiology, prognosis, and management. DATA SOURCES: Clinical management and the electronic medical records were examined for 2 patients diagnosed with partial KBS (ICD-10 F07.0) after experiencing ≥ 3 of the following: placidity, indiscriminate dietary behavior, hyperorality, hypersexuality, visual agnosia, and hypermetamorphosis. A literature search was performed in April 2015 by using the keyword Kluver-Bucy in PubMed and Ovid databases for English language publications since inception. Additionally, the authors reviewed the reference list of these publications in order to identify additional reports. STUDY SELECTION: Studies were included if they had information about presentation, pathophysiology, syndrome treatment or management, and course of KBS. DATA EXTRACTION: Information about our KBS cases was obtained by reviewing electronic medical records and by direct observation of the patients. A total of 186 (PubMed) and 137 (Ovid) publications were identified in each database. We ultimately reviewed 109 articles containing information about KBS, finding 51 publications addressing relevant aspects of this syndrome. RESULTS: The first case demonstrates KBS secondary to mesiotemporal structural atrophy, and the second illustrates transient KBS due to functional, postictal, hypoactivity within such structures. Literature review and discussion regarding both prognosis and treatment of KBS follows. CONCLUSIONS: Klüver-Bucy syndrome may be underreported due to a limited understanding of the syndrome as one necessitating bilateral amygdaloid destruction. The syndrome can be seen with damage/hypofunction of the hippocampal-amygdaloid complex and its projections. The prognosis of KBS is variable, and its treatment is based on a combination of environmental and pharmacologic measures.
[Mh] MeSH terms primary: Kluver-Bucy Syndrome/pathology
Kluver-Bucy Syndrome/physiopathology
[Mh] MeSH terms secundary: Humans
Kluver-Bucy Syndrome/therapy
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Entry month:1706
[Cu] Class update date: 170630
[Lr] Last revision date:170630
[Js] Journal subset:IM
[Da] Date of entry for processing:160706
[St] Status:MEDLINE
[do] DOI:10.4088/JCP.14r09497


page 1 of 24 go to page                         
   


Refine the search
  Database : MEDLINE Advanced form   

    Search in field  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/PAHO/WHO - Latin American and Caribbean Center on Health Sciences Information