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1.
Vox Sang ; 2018 Jun 20.
Article in English | MEDLINE | ID: mdl-29923207

ABSTRACT

BACKGROUND: Although prestorage leucoreduction (LR) of blood components for transfusion has gained favour around the world, evidence of its beneficial clinical effects is ambiguous. STUDY DESIGN AND METHODS: To reveal whether leucocytes and/or platelets in transfused blood are related to transfusion-related adverse effects, a prospective randomized crossover study was performed on patients who donated autologous blood prior to elective surgery. Among 1487 primary enrolees, a total of 192 patients undergoing two-stage, bilateral total hip arthroplasty were randomized to receive autologous blood that was either prestorage leucoreduced, or not, for the first procedure. For the second procedure, each patient was crossed over to receive alternatively processed autologous blood. Length of hospital stay served as a primary end-point, with perioperative infectious/thrombotic complications, pre- and postoperative laboratory values, and body temperature serving as secondary endpoints. RESULTS: No significant differences emerged between prestorage LR and non-LR cohorts in length of hospital stay, as well as perioperative infectious/thrombotic complications, postoperative body temperature and duration of fever. Postoperative laboratory values including white blood cell counts and C-reactive protein levels had no significant differences. CONCLUSION: This study could not prove any superiority of prestorage LR over non-LR for autologous whole blood among patients who underwent total hip arthroplasty.

2.
Vox Sang ; 102(2): 110-5, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21770954

ABSTRACT

BACKGROUND AND OBJECTIVES: This study was aimed at evaluating the feasibility of the ACP215 closed-system cell processor for preparing washed platelet concentrates. MATERIAL AND METHODS: Platelet washing was performed with either the ACP215 system or the manual technique with M-sol. Plasma protein removal and platelet recovery were estimated, and the washed platelet concentrates were stored for 5 days. Samples were collected after washing and on days 1, 3 and 5 of storage to determine the effects of the washing methods on the in vitro platelet qualities (platelet count, platelet volume, pH, glucose and lactate concentrations, hypotonic shock response, aggregation response and CD62P expression level). RESULTS: Platelet recovery was 86·9 ± 2·1% and 85·9 ± 1·9% (P = 0·305), and plasma protein removal was 95·8 ± 0·9% and 96·9 ± 0·7% (P = 0·016) after washing with the ACP215 system and manual technique, respectively. No statistically significant differences in the in vitro platelet qualities were observed between the washing methods. CONCLUSION: The ACP215 system is a feasible alternative to manual, labour-intensive, techniques for preparing washed platelet concentrates.


Subject(s)
Automation, Laboratory/methods , Blood Component Removal/instrumentation , Blood Component Removal/methods , Blood Platelets/cytology , Blood Platelets/physiology , Blood Proteins/isolation & purification , Feasibility Studies , Humans , Platelet Activation
3.
Genome ; 50(8): 735-41, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17893733

ABSTRACT

Black spot disease, which is caused by the Japanese pear pathotype of Alternaria alternata (Fr.) Keissler, is one of the most harmful diseases in Japanese pear cultivation. We identified the exact positions and linkage groups (LGs) of the genes for susceptibility to black spot in the Japanese pear (Pyrus pyrifolia Nakai) cultivars 'Osa Nijisseiki' (gene Ani) and 'Nansui' (gene Ana). Segregation of susceptibility and resistance fitted the expected ratio of 1:1 in progeny of 'Nansui' but showed a slight distortion in progeny of 'Osa Nijisseiki'. We mapped the genes for susceptibility to black spot in both populations using a genome scanning approach. The simple sequence repeat (SSR) markers CH04h02 and CH03d02 showed tight linkage to Ani and Ana. Although Ani and Ana are derived from different sources, both genes are located at the top region of LG 11. Information about the positions of the susceptibility genes and the molecular markers linked to them will be useful for marker-assisted selection in pear breeding programs.


Subject(s)
Alternaria/pathogenicity , Chromosome Mapping , Genes, Plant , Genetic Predisposition to Disease , Plant Diseases/genetics , Pyrus/genetics , Amplified Fragment Length Polymorphism Analysis , Chromosomes, Plant/genetics , DNA, Plant/genetics , DNA, Plant/isolation & purification , Genetic Linkage , Genetic Markers , Microsatellite Repeats , Plant Diseases/microbiology , Pyrus/microbiology , Random Amplified Polymorphic DNA Technique
4.
Kyobu Geka ; 60(6): 500-3, 2007 Jun.
Article in Japanese | MEDLINE | ID: mdl-17564069

ABSTRACT

A 77-year-old female was admitted to our hospital with a diagnosis of severe mitral regurgitation. Cardiopulmonary revival was done by an emergent resuscitation for the ventricular fibrillation before admission. She had mild anoxic brain damage and brain magnetic resonance imaging (MRI) revealed severe brain atrophy. Chest X-ray showed severe cardiomegaly and congestion. Beating heart mitral valve replacement was planned for the prevention of reperfusion injury. A cardiopulmonary bypass was established by bicaval drainage and aortic return. The prolapse of anterior leaflet was recognized through transeptal approach after aortic clamp. We selected continuous infusion of antegrade cardioplegia for intraoperative coronary perfusion. Mitral valve replacement was done successfully. During intraoperation and postoperation, ventricular fibrillation did not occur. On-pump beating mitral valve replacement is a good procedure to prevent perioperative ventricular arrhythmia especially such the case with a decompressed myocardial function and with a preoperative episode of lethal ventricular arrhythmia necessary for cardiopulmonary resuscitation.


Subject(s)
Cardiopulmonary Bypass/methods , Heart Valve Prosthesis Implantation , Mitral Valve Insufficiency/surgery , Ventricular Fibrillation , Aged , Cardiomegaly/complications , Cardiopulmonary Resuscitation , Female , Humans , Hypoxia, Brain/complications , Hypoxia, Brain/pathology , Intra-Aortic Balloon Pumping , Magnetic Resonance Imaging , Ventricular Fibrillation/complications
5.
Theor Appl Genet ; 113(4): 743-52, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16838137

ABSTRACT

Pear scab (caused by Venturia nashicola) is one of the most harmful diseases of pears, especially Japanese and Chinese pear species. The molecular identification and early selection of resistant plants could greatly improve pear breeding. We have identified the position of the scab resistance gene, designated Vnk in an indigenous Japanese pear cultivar Kinchaku, within the pear genome by using simple sequence repeat (SSR) markers derived from pear and apple. The position of Vnk was identified in the central region of linkage group 1 of Kinchaku. Several amplified fragment length polymorphism (AFLP) markers linked to Vnk were obtained by bulked segregant analysis. Among them, the AFLP marker closest to Vnk was converted into a sequence tagged site (STS) marker. Four random amplified polymorphic DNA (RAPD) markers previously found to be loosely associated with Vnk (Iketani et al. 2001) were successfully converted into STS markers. Six markers (one SSR Hi02c07 and five STSs converted from AFLP and RAPD) showed tight linkages to Vnk, being mapped with distances ranging from 2.4 to 12.4 cM. The SSR CH-Vf2, which was isolated from a BAC clone of the contig containing the apple scab gene Vf, was mapped at the bottom of linkage group 1 in Kinchaku, suggesting that the Vnk and Vf loci are located in different genomic regions of the same homologous linkage group.


Subject(s)
Genes, Plant , Plant Diseases/genetics , Pyrus/genetics , Ascomycota/physiology , Chromosome Mapping , Chromosomes, Artificial, Bacterial , Cloning, Molecular , Genetic Linkage , Genetic Markers , Immunity, Innate/genetics , Malus/genetics , Malus/microbiology , Microsatellite Repeats , Plant Diseases/microbiology , Plant Leaves/anatomy & histology , Plant Leaves/genetics , Plant Leaves/microbiology , Polymorphism, Genetic , Prunus/genetics , Prunus/microbiology , Pyrus/anatomy & histology , Pyrus/microbiology
6.
Kyobu Geka ; 57(6): 488-91, 2004 Jun.
Article in Japanese | MEDLINE | ID: mdl-15202271

ABSTRACT

We report an extremely rare case of multi-vessel dissection including left carotid artery, ascending aorta and thoracoabdominal aorta independently. A 65-year-old man suffered from cerebral infarction due to left carotid artery dissection. Five days later, he complained of severe back pain and was diagnosed as acute DeBakey type IIIb aortic dissection. He had been treated medically. One month later, computed tomography (CT) scan demonstrated DeBakey type II as well as type IIIb aortic dissections. The ascending aorta was replaced on August 8, 2001. Then replacement of the descending thoracic aorta with reconstruction of the eighth and tenth intercostal arteries was performed on September 26, 2001. The left carotid artery dissection has been treated medically.


Subject(s)
Aortic Aneurysm/diagnosis , Aortic Dissection/diagnosis , Blood Vessel Prosthesis Implantation , Carotid Artery Diseases/diagnosis , Aged , Aortic Dissection/surgery , Aortic Aneurysm/surgery , Aortic Aneurysm, Abdominal/diagnosis , Aortic Aneurysm, Abdominal/surgery , Aortic Aneurysm, Thoracic/diagnosis , Aortic Aneurysm, Thoracic/surgery , Cerebral Infarction/complications , Humans , Magnetic Resonance Imaging , Male , Tomography, X-Ray Computed , Ultrasonography , Vascular Surgical Procedures/methods
8.
Pediatr Cardiol ; 25(1): 56-7, 2004.
Article in English | MEDLINE | ID: mdl-14534759

ABSTRACT

A neonate with Ebstein's anomaly presented with severe cyanosis because of massive right-to-left shunt through an atrial septal defect and reduced blood flow through an unobstructed right ventricular outflow tract. This atypical patient underwent a right modified Blalock-Taussig shunt, which resolved the respiratory.


Subject(s)
Ebstein Anomaly/surgery , Heart Bypass, Right , Heart Bypass, Right/methods , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Male
9.
Aktuelle Urol ; 34(4): 265-6, 2003 Jul.
Article in English | MEDLINE | ID: mdl-14566681

ABSTRACT

The prognosis of urinary epithelial cancer is still poor, and early detection of this cancer is strongly desirable. The sensitivity of conventional urinary cytology is not satisfactory enough. It is hoped that a specific tumor marker will be established. In recent years, it has been reported that urine NMP 22 is very useful and that urine BFP is also relatively useful. We have now determined urine NMP22 and BFP and studied their clinical usefulness as a tumor marker. Using patients diagnosed with histologically confirmed urinary epithelial cancer as the subjects, we retrospectively studied the usefulness of NMP 22, BFP and cytology mainly with regard to the sensitivity (positivity rate), and also in relation to atypia, degree of infiltration and clinical course.


Subject(s)
Biomarkers, Tumor/urine , Carcinoma/diagnosis , Carcinoma/urine , Nuclear Proteins/urine , Urinary Bladder Neoplasms/diagnosis , Urinary Bladder Neoplasms/urine , Female , Humans , Kidney Neoplasms/diagnosis , Kidney Neoplasms/urine , Kidney Pelvis , Linear Models , Male , Middle Aged , Multivariate Analysis , Ureteral Neoplasms/diagnosis , Ureteral Neoplasms/urine , Urine/cytology
10.
Neuroradiology ; 45(7): 493-7, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12761601

ABSTRACT

We report two fatal cases of methotrexate (MTX)-induced disseminated necrotising leukoencephalopathy (DNL) in which MRI was repeated from the onset. Initial T2-weighted images showed multiple areas of high signal, mainly in deep cerebral white matter, which on follow-up, spread and coalesced to involve the entire white matter. Small irregular low-signal foci on T2-weighted images were seen within the high-signal lesions. Multiple areas of contrast enhancement corresponded to these low-signal foci. The condition of both patients deteriorated and they died. We compared their MRI findings with those of seven patients with mild MTX-related leukoencephalopathy, six of whom were asymptomatic; one had transient neurological symptoms. They showed no contrast enhancement, but rather mild-to-moderate diffuse high signal in deep white matter, which later disappeared. These findings suggest that multiple low-signal foci on T2-weighted images with contrast enhancement may be characteristic of DNL, and that contrast-enhanced imaging is useful to differentiate this condition from mild leukoencephalopathy.


Subject(s)
Drug-Related Side Effects and Adverse Reactions , Leukoencephalopathy, Progressive Multifocal/chemically induced , Leukoencephalopathy, Progressive Multifocal/diagnosis , Magnetic Resonance Imaging , Methotrexate/adverse effects , Adolescent , Brain Diseases/diagnosis , Child , Child, Preschool , Encephalomyelitis, Acute Disseminated/diagnosis , Encephalomyelitis, Acute Disseminated/pathology , Female , Follow-Up Studies , Humans , Image Enhancement , Male , Radiotherapy, Adjuvant/adverse effects
11.
Kyobu Geka ; 55(13): 1149-52, 2002 Dec.
Article in Japanese | MEDLINE | ID: mdl-12476567

ABSTRACT

Surgery for constrictive pericarditis after coronary artery bypass grafting (CABG) needs complete pericardiectomy without injury to bypass grafts. We performed pericardiectomy for post-CABG constrictive pericarditis 15 months after the first surgery. Preoperative multislice helical 3-dimensional computed tomography (CT) clearly demonstrated the patent bypass grafts and anatomical relationship between grafts and surrounding organs. Among surgical approaches, we chose bilateral thoracotomy to avoid injury to the bypass grafts and to obtain a good surgical exposure, especially for pericardiectomy of the left side of the heart. Additionally, with the use of intraoperative doppler ultrasound blood flowmetry, we could safely achieve complete pericardiectomy. We conclude that the combined application of 3-dimensional CT, bilateral thoracotomy and doppler ultrasound blood flowmetry was a supreme strategy for the operation of constrictive pericarditis after CABG.


Subject(s)
Coronary Artery Bypass/adverse effects , Pericardiectomy/methods , Pericarditis, Constrictive/surgery , Humans , Imaging, Three-Dimensional , Male , Middle Aged , Myocardial Ischemia/surgery , Pericarditis, Constrictive/diagnostic imaging , Pericarditis, Constrictive/etiology , Postoperative Complications/surgery , Tomography, X-Ray Computed , Ultrasonography, Doppler
13.
Theor Appl Genet ; 106(1): 9-18, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12582866

ABSTRACT

Genetic linkage maps of the European pear ( Pyrus communis L.) cultivar 'Bartlett' and the Japanese pear ( Pyrus pyrifolia Nakai) cultivar 'Housui' were constructed based on AFLPs, SSRs from pear, apple and Prunus, isozymes and phenotypic traits by using their F(1) progenies. The map of the female parent Bartlett consisted of 226 loci including 175 AFLPs, 49 SSRs, one isozyme and one S locus on 18 linkage groups over a total length of 949 cM, while that for 'Housui' contained 154 loci including 106 AFLPs, 42 SSRs, two phenotypic traits and the other four markers on 17 linkage groups encompassing a genetic distance of 926 cM. These maps were partially aligned using 20 codominant markers which showed segregating alleles in both parents. Compared with the reports of apple genetic maps, these pear maps were not saturated but were near saturation. Distorted segregation was observed in two and one regions of the genome of Bartlett and Housui, respectively. The position of 14 SSRs originating from apple could be successfully determined in pear maps, which enabled us to compare the two maps. Some SSRs developed from Prunus (peach, cherry) were also mapped. The relationships between pear and the other species belonging to the Rosaceae were discussed based on the position of SSRs.


Subject(s)
Chromosome Mapping , Hybridization, Genetic , Pyrus/genetics , Genetic Markers , Isoenzymes/genetics , Microsatellite Repeats , Pyrus/enzymology , Rosaceae/genetics
14.
Int J Cancer ; 94(1): 35-43, 2001 Oct 01.
Article in English | MEDLINE | ID: mdl-11668476

ABSTRACT

p53 protein is a transcription factor involved in multiple tumor-suppressor activities including cell cycle control and apoptosis. TP53 gene is frequently mutated in glioblastoma, suggesting the importance of inactivation of this gene product in gliomagenesis. Restoration of p53 function in glioblastoma cell lines deficient for p53 has shown that p53 induces growth arrest or apoptosis depending on the cell line and vector used to transduce wild-type TP53 alleles. Considering that astrocytes grow and express p53, it is not clear whether these results reflect physiologic responses or the result of p53 overexpression in combination with cellular responses to viral vector infection. Here, we reassessed this issue using a glioblastoma cell line (LN382) that expresses an endogenous temperature-sensitive mutant p53. This cell line expresses TP53 alleles (100% as determined by a p53 transcriptional assay in yeast) mutated at codon 197 GTG (Val) > CTG (Leu). We found that the p53 protein in these cells acted as an inactive mutant at 37 degrees C and as a functional wild-type p53 below 34 degrees C as demonstrated by several lines of evidence, including (i) restoration of transactivating ability in yeast, (ii) induction of p53-modulated genes such as CDKN1(p21) and transforming growth factor-alpha, (iii) disappearance of accumulated p53 protein in the nucleus and (iv) decrease in steady state p53 protein levels. This temperature switch allowed p53 levels, which were close to physiological levels to dramatically reduce LN382 cell proliferation by inducing a G(1)/S cell cycle block, but not to induce apoptosis. The lack of apoptosis was considered to be a result of the low level p53 expression, because increasing wild-type p53 levels by adenoviral-mediated gene transfer caused apoptosis in these cells. The LN382 cell line will be extremely useful for investigations into the roles of p53 in cellular responses to a variety of stimuli or damages.


Subject(s)
Apoptosis , Glioblastoma/pathology , Mutation , Tumor Suppressor Protein p53/physiology , Cell Cycle , Cell Division , Glioblastoma/genetics , Humans , Temperature , Transcription, Genetic , Tumor Cells, Cultured , Tumor Suppressor Protein p53/chemistry , Tumor Suppressor Protein p53/genetics
15.
AJNR Am J Neuroradiol ; 22(7): 1283-90, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11498415

ABSTRACT

BACKGROUND AND PURPOSE: Clinical diagnosis of lymphomatoid granulomatosis (LG) of the brain, in patients without skin or chest lesions, usually is difficult because of the nonspecific neurologic manifestations, laboratory data, and CT appearance. Our aim was to characterize the MR appearance of LG of the brain. METHODS: We retrospectively reviewed the MR images in four patients (35 to 72 years old) with histologically confirmed LG of the brain. RESULTS: On T2-weighted images, we noted diffuse hyperintense lesions in the cerebral white matter bilaterally (n = 3), in the brain stem and cerebellar hemisphere (n = 1), and patchy hyperintense lesions the brain stem (n = 2). On contrast-enhanced T1-weighted images, we observed multiple punctate or linear enhancements residing along the perivascular space (n = 4), nodular enhancements (n = 2), ringlike enhancements (n = 1), and a large, enhanced mass (n = 1). All patients had multifocal lesions. CONCLUSION: Although the MR appearance of LG of the brain varies, multiple punctate or linear enhancements that reside along the perivascular space suggest LG.


Subject(s)
Brain Diseases/diagnosis , Lymphomatoid Granulomatosis/diagnosis , Magnetic Resonance Imaging , Adult , Aged , Biopsy , Brain/pathology , Dominance, Cerebral/physiology , Female , Humans , Male , Middle Aged , Neurologic Examination , Retrospective Studies
17.
Brain Pathol ; 11(3): 296-305, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11414472

ABSTRACT

The p53 gene is normally wild type in meningiomas. Since all three members of the p53 gene family recognize the same DNA sequence, tumors containing wild type p53 could decrease transactivation of p53 target genes by mutating either p63 or p73. In meningiomas the most likely target is p73, because loss of heterozygosity of the chromosomal band containing p73 is the commonest genetic lesion in these tumors. To screen p73 for mutations we have developed a functional assay which tests the ability of p73 to activate transcription from a p53-responsive promoter in yeast. The assay correctly identified p73 mutants with mutations equivalent to hotspot mutations in p53, demonstrating that the assay can detect transcriptionally inactive p73. No mutations in p73 were identified in meningiomas. p73 RNA level was higher in more advanced tumors, but there was no correlation between the expression level of p73 and p21, a known p53 target gene. The yeast assay was also used to measure the intrinsic sensitivity of the p73 protein to mutagenesis. Like p53, p73 is exceptionally easy to inactivate as a transcription factor by point mutation. Taken together, these results indicate that p53 and p73 serve very different functions in tumors.


Subject(s)
DNA-Binding Proteins/genetics , Gene Expression Regulation, Neoplastic , Meningeal Neoplasms/genetics , Meningioma/genetics , Neoplasm Proteins/genetics , Nuclear Proteins/genetics , Aged , Codon/genetics , Cyclin-Dependent Kinase Inhibitor p21 , Cyclins/biosynthesis , Cyclins/genetics , DNA Mutational Analysis , DNA, Neoplasm/genetics , DNA-Binding Proteins/biosynthesis , DNA-Binding Proteins/physiology , Disease Progression , Female , Genes, Tumor Suppressor , Humans , Male , Meningeal Neoplasms/metabolism , Meningeal Neoplasms/pathology , Meningioma/metabolism , Meningioma/pathology , Middle Aged , Neoplasm Proteins/biosynthesis , Nuclear Proteins/biosynthesis , Nuclear Proteins/physiology , RNA Splicing , RNA, Messenger/biosynthesis , RNA, Neoplasm/biosynthesis , Recombinant Fusion Proteins/physiology , Reverse Transcriptase Polymerase Chain Reaction , Saccharomyces cerevisiae/genetics , Transcriptional Activation , Tumor Protein p73 , Tumor Suppressor Protein p53/physiology , Tumor Suppressor Proteins
18.
Neuropathology ; 21(2): 129-37, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11396678

ABSTRACT

JC virus (JCV) together with Simian virus 40 (SV40) and BK virus (BKV), belong to the polyomavirus group and these viruses are neuro-oncogenic to rodents by expression of large T antigen (LT), which binds to cellular p53 and pRB thus reducing the anticancer potential of the cell. The function of LT has not been clarified because small t antigen (st) is transcribed from the same start codon as the overlapping reading frame of LT, and is translated as a different protein with the same N-terminal residues (1-81 amino acids) by a splice-site variant of mRNA. To elucidate the function of LT without st, we constructed plasmids that express LT only by deleting the splicing region including the C-terminus of st, and consequently stable cell lines were established that express only JCLT, SV40LT and BKLT. The growth rates of these cells were examined in colonies on soft agar and it was found that LT alone has a transforming capacity; the order of efficiency being SV40LT, BKLT and JCLT. In addition, to verify the involvement of JCV in human medulloblastoma, eight cases of medulloblastoma, six cases of frozen material and five cases of paraffin-embedded tissues which included three cases of frozen tissues, were examined. PCR assay, genomic Southern blotting, and in situ hybridization were applied to detect the JCV genome, and LT and st were examined by immunohistochemistry; the results were compared with JCV-infected tissues as a positive control. All methods failed to detect not only JCV genome but also LT protein in medulloblastoma and it was concluded that JCV LT has transforming activities in rodent cells, but is not related to human medulloblastoma.


Subject(s)
Antigens, Polyomavirus Transforming/pharmacology , Brain Stem Neoplasms/pathology , Cell Transformation, Neoplastic/drug effects , JC Virus/metabolism , Medulloblastoma/pathology , 3T3 Cells , Animals , Blotting, Southern , Blotting, Western , Cells, Cultured , Culture Media , DNA/genetics , Humans , Immunohistochemistry , In Situ Hybridization , Insect Vectors/genetics , Mice , Rats , Reverse Transcriptase Polymerase Chain Reaction
19.
No To Shinkei ; 53(5): 457-62, 2001 May.
Article in Japanese | MEDLINE | ID: mdl-11424357

ABSTRACT

Image-guided stereotactic surgery of the ventralis intermedius nucleus of the thalamus, globus pallidus, and subthalamic nucleus is a prevailing modality as a treatment of movement disorders. This technical note describes a method of minimally-invasive stereotactic functional surgery for patients with parkinsonian symptom or various tremors. Patients were administered propofol, an intravenous anesthetic, during placement of a burr hole and a stereotactic frame, but not the period when the patients were necessary to be awake. The intravenous anesthesia was very beneficial to relieve local pain and mental stress of the patients. Radionics ImageFusion and AtlasPlan were used for defining the target localization without an intraoperative ventriculography. ImageFusion efficiently fused high-resolution MR images on CT images. AtlasPlan accurately corrected the localization of the tentative target point after measurements from the midpoint of the anterior commissure-posterior commissure line on the modified MRI, and enabled us to reduce the degree of an intraoperative correction to fix a final target. Stereotactic functional surgery has been thought to be less-invasive, however further modifications of surgical procedure and intraoperative medication can make this type of surgery much more less-invasive.


Subject(s)
Anesthesia, Intravenous , Anesthetics, Intravenous , Brain/surgery , Minimally Invasive Surgical Procedures/methods , Movement Disorders/surgery , Propofol , Stereotaxic Techniques , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Parkinson Disease/surgery , Tomography, Emission-Computed
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