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  1. Article: Pachydermodactyly with Broder Hand Span and Long Fingers: A Case Report.

    Rasi, Abbas / Behrangi, Elham / Attar, Bahamin / Azizian, Zahra

    Iranian journal of public health

    2017  Volume 46, Issue 2, Page(s) 258–260

    Abstract: Pachydermodactyly is a rare and benign disease that may be idiopathic, genetic, acquired as a response to repetitive trauma, or associated with several other acquired conditions often pushing the health caregiver to do a bunch of costly lab tests and ... ...

    Abstract Pachydermodactyly is a rare and benign disease that may be idiopathic, genetic, acquired as a response to repetitive trauma, or associated with several other acquired conditions often pushing the health caregiver to do a bunch of costly lab tests and diagnostic workups to rule out other entities. All health care givers must be aware about this disease for reassure the patients and cut unnecessary costs. Moreover, there seems to be an issue of association with certain occupations. A good example might be computer keyboards causing special damages to certain organs like eyes and musculoskeletal system. We have observed deleterious effects of excess work with computer keyboards on fingers in the form of Pachydermodactyly in our case. A 27-yr-old man presented with wider hand span and longer fingers to Dermatology Clinic of Rasoul-E-Akram Hospital in June 2015, especially the ring finger in our case, considered a big symptom who depressed due to their fingers appearance as a rare disease. We gave him an emollient to make his hand smoother. The patient improved both clinically and psychologically on a simple emollient. This disease with its deleterious psychological effects and a simple way of management should be appreciated more by the health care system.
    Language English
    Publishing date 2017-02
    Publishing country Iran
    Document type Journal Article
    ISSN 2251-6085
    ISSN 2251-6085
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Effects of sub-lethal dose of antimicrobial photodynamic therapy on major virulence traits of Streptococcus mutans.

    Afrasiabi, Shima / Pourhajibagher, Maryam / Chiniforush, Nasim / Aminian, Mahdi / Rasi Varaei, Samaneh Sadat / Bahador, Abbas

    Photodiagnosis and photodynamic therapy

    2020  Volume 32, Page(s) 102044

    Abstract: Background: Antimicrobial photodynamic therapy (aPDT) as a complementary step of selective removal of dental caries appears as an ideal choice to help manage caries with minimal interventions. Sub-lethal dose of aPDT (sPDT) impressively effects ... ...

    Abstract Background: Antimicrobial photodynamic therapy (aPDT) as a complementary step of selective removal of dental caries appears as an ideal choice to help manage caries with minimal interventions. Sub-lethal dose of aPDT (sPDT) impressively effects microbial virulence, although it does not kill microorganisms. Therefore, the present study aimed to investigate the influence of sPDT using diode laser plus chlorophyllin-phycocyanin mixture (PhotoActive
    Materials and methods: sPDT using PhotoActive
    Results: In this study, sPDT using 2.4 × 10
    Conclusions: This study demonstrated the potential effect of PhotoActive
    MeSH term(s) Anti-Infective Agents ; Biofilms ; Dental Caries/drug therapy ; Humans ; Photochemotherapy/methods ; Photosensitizing Agents/pharmacology ; Streptococcus mutans/pathogenicity ; Virulence
    Chemical Substances Anti-Infective Agents ; Photosensitizing Agents
    Language English
    Publishing date 2020-10-01
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2149918-4
    ISSN 1873-1597 ; 1572-1000
    ISSN (online) 1873-1597
    ISSN 1572-1000
    DOI 10.1016/j.pdpdt.2020.102044
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Neutrophilic Dermatosis of Dorsal Hands and Legs.

    Behrangi, Elham / Rasi, Abbas / Attar, Bahamin / Azizian, Zahra

    Archives of Iranian medicine

    2016  Volume 19, Issue 12, Page(s) 879–881

    Abstract: We present a case of neutrophilic dermatosis of dorsal hands (NDDH), with lesions on the dorsal part of the hands with pustular features and histologic picture of vasculitis.This case highlights the notion that low dose oral steroid can offer a useful ... ...

    Abstract We present a case of neutrophilic dermatosis of dorsal hands (NDDH), with lesions on the dorsal part of the hands with pustular features and histologic picture of vasculitis.This case highlights the notion that low dose oral steroid can offer a useful first therapeutic option for NDDH. Interstingly, in this case, a few additional lesions were located on the legs, making it different from some previously described cases of NDDH. As with other authors, we believe that this recently described neutrophilic dermatosis is a localized and acral variant of SS. To our knowledge, this is the first case report of NDDH from Iran.
    MeSH term(s) Female ; Glucocorticoids/therapeutic use ; Hand Dermatoses/diagnosis ; Hand Dermatoses/drug therapy ; Humans ; Leg ; Middle Aged ; Prednisolone/therapeutic use ; Sweet Syndrome/diagnosis ; Sweet Syndrome/drug therapy
    Chemical Substances Glucocorticoids ; Prednisolone (9PHQ9Y1OLM)
    Language English
    Publishing date 2016-12
    Publishing country Iran
    Document type Case Reports ; Journal Article
    ZDB-ID 2204979-4
    ISSN 1735-3947 ; 1029-2977
    ISSN (online) 1735-3947
    ISSN 1029-2977
    DOI 0161912/AIM.0012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Pachydermodactyly with Broder Hand Span and Long Fingers

    Abbas RASI / Elham BEHRANGI / Bahamin ATTAR / Zahra AZIZIAN

    Iranian Journal of Public Health, Vol 46, Iss

    A Case Report

    2017  Volume 2

    Abstract: Pachydermodactyly is a rare and benign disease that may be idiopathic, genetic, acquired as a response to repetitive trauma, or associated with several other acquired conditions often pushing the health caregiver to do a bunch of costly lab tests and ... ...

    Abstract Pachydermodactyly is a rare and benign disease that may be idiopathic, genetic, acquired as a response to repetitive trauma, or associated with several other acquired conditions often pushing the health caregiver to do a bunch of costly lab tests and diagnostic workups to rule out other entities. All health care givers must be aware about this disease for reassure the patients and cut unnecessary costs. Moreover, there seems to be an issue of association with certain occupations. A good example might be computer keyboards causing special damages to certain organs like eyes and musculoskeletal system. We have observed deleterious effects of excess work with computer keyboards on fingers in the form of Pachydermodactyly in our case. A 27-yr-old man presented with wider hand span and longer fingers to Dermatology Clinic of Rasoul-E-Akram Hospital in June 2015, especially the ring finger in our case, considered a big symptom who depressed due to their fingers appearance as a rare disease. We gave him an emollient to make his hand smoother. The patient improved both clinically and psychologically on a simple emollient. This disease with its deleterious psychological effects and a simple way of management should be appreciated more by the health care system.
    Keywords Pachydermodactyly ; Digital fibromatosis ; Soft tissue swelling ; Public aspects of medicine ; RA1-1270
    Subject code 006
    Language English
    Publishing date 2017-02-01T00:00:00Z
    Publisher Tehran University of Medical Sciences
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: The Prevalence of Sleep Disorders in Patients with Alopecia Areata

    Gholamhossein Ghafarpour / Abbas Zamanian / Abbas Rasi / Sepideh Asadbeigi / Shiva Ghods

    مجله دانشکده پزشکی اصفهان, Vol 33, Iss 365, Pp 2296-

    2016  Volume 2301

    Abstract: Background: Alopecia areata is a chronic inflammatory disorder that causes nonscarring hair loss. The cause is unknown, but an interaction between autoimmune and psychological factors may trigger the disease. Sleep deprivation is associated with a ... ...

    Abstract Background: Alopecia areata is a chronic inflammatory disorder that causes nonscarring hair loss. The cause is unknown, but an interaction between autoimmune and psychological factors may trigger the disease. Sleep deprivation is associated with a variety of adverse consequences including the effects on both psychological and physical health. Sleep deprivation can adversely affect immune function and exacerbate autoimmunity. Poor sleep quality is also associated with stress. Method: A case control study was conducted on 92 patients divided into two groups of 46, those diagnosed with alopecia areata and a healthy population. The demographic information of both groups was gathered with a questionnaire and the sleep quality was evaluated using Pittsburgh Sleep Quality Index (PSQI), a self-rated questionnaire that assesses sleep quality and disturbances over a 1-month time interval. SPSS16 was used to analyze the data. P value of less than 0.05 was considered significant. Findings: 45.7% of patients with alopecia areata and 21.7% of the control group had sleep disorders. The difference between these percentages was significant (P < 0.05). There was not any significant difference in the scores of PSQI between the two groups (mean score = 5.37 and 4.04 in alopecia areata and control groups, respectively). The mean night sleep hours in patients with alopecia areata (6.73 hours) was significantly lower than the normal population (7.76 hours). Conclusion: The results of this study revealed that the poor sleep quality is more common among patients with alopecia areata compared to the normal population; but the difference of the severity of sleep disturbances between the two groups was not statistically significant.
    Keywords Alopecia areata ; Pittsburgh Sleep Quality Index ; Sleep disorder ; Medicine ; R ; Medicine (General) ; R5-920
    Subject code 150
    Language Persian
    Publishing date 2016-02-01T00:00:00Z
    Publisher Vesnu Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article: Prioritization of non-revenue water reduction scenarios using a risk-based group decision-making approach

    Tabesh, Massoud / Roozbahani, Abbas / Roghani, Bardia / Salehi, Sattar / Rasi Faghihi, Niousha / Heydarzadeh, Reza

    Stochastic environmental research and risk assessment. 2020 Nov., v. 34, no. 11

    2020  

    Abstract: This study investigates the effectiveness of the reduction policies of the apparent and real losses of non-revenue water. For this purpose, using technique for order of preference by similarity to ideal solution (TOPSIS) model, a decision matrix is ... ...

    Abstract This study investigates the effectiveness of the reduction policies of the apparent and real losses of non-revenue water. For this purpose, using technique for order of preference by similarity to ideal solution (TOPSIS) model, a decision matrix is proposed, involving apparent and real losses risk reduction values induced by the implementation of each non-revenue water reduction policy. First, decision criteria, including technical, economic, and social criteria, were selected and introduced. Then, the technical criterion was calculated using a fuzzy Bayesian model. In the following, using group decision-making and analytic hierarchy process method, the criteria were weighted. In the next step, the bests of decision criteria were determined by the TOPSIS method. This method was applied in the water distribution network of district 4 of Tehran, Iran. The results indicated that the most basic non-revenue water reduction policy by risk-based group decision-making is to identify unauthorized connections in the apparent water loss sector and increase the speed and quality of maintenance and repairs in the real water loss sector.
    Keywords Bayesian theory ; decision making ; issues and policy ; models ; prioritization ; risk reduction ; water distribution ; Iran
    Language English
    Dates of publication 2020-11
    Size p. 1713-1724.
    Publishing place Springer Berlin Heidelberg
    Document type Article
    ZDB-ID 1481263-0
    ISSN 1436-3259 ; 1435-151X ; 1436-3240 ; 0931-1955
    ISSN (online) 1436-3259 ; 1435-151X
    ISSN 1436-3240 ; 0931-1955
    DOI 10.1007/s00477-020-01858-1
    Database NAL-Catalogue (AGRICOLA)

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  7. Article ; Online: Measuring Equity in Iranian Healthcare System Financing

    Abdolvahed Khodamoradi / Shahram Ghaffari / Amir Abbas Fazaeli / Reza Toyserkanmanesh / Vahid Rasi / Fariba Bigdeli

    Journal of Evidence Based Health Policy, Management & Economics, Vol 3, Iss 2, Pp 87-

    Experiences of Recent Health Reform Plan

    2019  Volume 95

    Abstract: Background: One of the main goals of the health system is the fair contribution of people to healthcare financing. Therefore, the current study not only evaluated the status of fair financial contribution, but also investigated the impacts of the health ... ...

    Abstract Background: One of the main goals of the health system is the fair contribution of people to healthcare financing. Therefore, the current study not only evaluated the status of fair financial contribution, but also investigated the impacts of the health reform plan on the financial pillars of the Iranian healthcare system. Methods: To conduct this retrospective descriptive study, the data of Income and Expenditure Survey (2011-2015) commissioned by Statistical Center of Iran were used. To measure fairness of financing, four indices were used. Data were analyzed using the Excel and SPSS software. Results: The results show that although the health reform plan has increased insurance coverage of both rural and urban households, out of pocket, and even its proportion to household capacity to pay continues to rise. Prevalence of catastrophic health expenditures in the baseline year in rural and urban areas was 2.19% and 1.04%, reaching 3.69% and 2.39% at the end of the study, respectively. Accordingly, fair financial contribution in rural and urban areas was obtained 0.830% and 0.850% in the baseline year, reaching 0.823% and 0.850% in the last year of the study, respectively. Conclusion: Although indices of fair financial contribution during the 5-year period varied, they ultimately showed a worse situation compared to the baseline year. Thus, it is assumed that the health reform plan has not yet been successful in meeting the goal of improving fair financial contribution to the health system.
    Keywords Health Expenditures ; Health System Financing ; Health Equity ; Fair Financial Contribution ; Catastrophic Healthcare Expenditures ; Medicine ; R ; Public aspects of medicine ; RA1-1270
    Subject code 360
    Language English
    Publishing date 2019-07-01T00:00:00Z
    Publisher Shahid Sadoughi University of Medical Sciences
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Comparison of the Frequency of Personality Disorders in Patients Diagnosed with Alopecia Areata and the Normal Population

    Gholamhosein Ghafarpour / Abbas Zamanian / Abbas Rasi / Shiva Ghods / Sepideh Asadbeigi

    مجله دانشکده پزشکی اصفهان, Vol 32, Iss 316, Pp 2286-

    2015  Volume 2294

    Abstract: Background: Alopecia areata is a recurrent inflammatory disorder causes non-scarring hair loss. The condition most commonly presents with discrete patches of alopecia on the scalp but can include total loss of scalp or body hair. While occurring in men ... ...

    Abstract Background: Alopecia areata is a recurrent inflammatory disorder causes non-scarring hair loss. The condition most commonly presents with discrete patches of alopecia on the scalp but can include total loss of scalp or body hair. While occurring in men and women of all ages and races, onset most frequently occurs in young people. Psychosomatic changes caused by this disease can lead to psychological long-term problems such as anxiety and depression. Personality disorders can alter clinical presentation of the disease. This study sought to determine the correlation of personality disorders with the occurrence of alopecia areata. Methods: A case-control study was conducted in 84 patients divided in two groups of patients diagnosed with alopecia areata and the normal population. The demographic information of both groups was gathered with a questionnaire and the personality disorder was evaluated with the Millon Clinical Multiaxial Inventory-III (MCMI-III). Findings: Patients with alopecia areata tended to have statistically more personality disorders compared to the control group (P < 0.05). Personality disorders among women were more common compared with men (0.27 vs. 0.05). The difference was significant in women compared with control group (P < 0.05), but was not statistically significant between the two groups of men (P > 0.05). Conclusion: Based on the significant role of adolescence in society and the correlation between personality disorder and alopecia areata, we recommend psychiatric counseling, clinical evaluation, psychological diagnosis and treatment along with the other treatments.
    Keywords Alopecia areata ; Personality disorder ; Millon clinical multiaxial inventory-III (MCMI-III) ; Medicine ; R ; Medicine (General) ; R5-920
    Subject code 150
    Language Persian
    Publishing date 2015-03-01T00:00:00Z
    Publisher Vesnu Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Hypertrichosis Is Not so Prevalent in Becker's Nevus

    Abbas Rasi / Hoda Berenji Ardestani / Seyed Mehdi Tabaie

    ISRN Dermatology , Vol

    Analysis of 47 Cases

    2014  Volume 2014

    Keywords Dermatology ; RL1-803 ; Medicine ; R
    Language English
    Publishing date 2014-01-01T00:00:00Z
    Publisher Hindawi Publishing Corporation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article: Hypertrichosis Is Not so Prevalent in Becker's Nevus: Analysis of 47 Cases.

    Rasi, Abbas / Berenji Ardestani, Hoda / Tabaie, Seyed Mehdi

    ISRN dermatology

    2014  Volume 2014, Page(s) 953747

    Abstract: Becker's nevus is a relatively common cutaneous hamartoma, but is often overlooked or misdiagnosed. This nevus usually begins during the second decade of life as a circumscribed, hyperpigmented patch with irregular outline that gradually enlarges with ... ...

    Abstract Becker's nevus is a relatively common cutaneous hamartoma, but is often overlooked or misdiagnosed. This nevus usually begins during the second decade of life as a circumscribed, hyperpigmented patch with irregular outline that gradually enlarges with associated hypertrichosis, developing several years later. The purpose of this study was to determine the prevalence of lesional hypertrichosis associated with Becker's nevus. Methods. 47 patients who had sharply demarcated brown patch with or without coarse hair, presence or enlargement of the lesion at the time of puberty, and compatible Wood's light examination were enrolled. Patients who had axillary freckling, previous skin inflammation, and gray pigmentation of the lesions were excluded. Results. In summary, the mean age of onset was 11.89 (range 0-19). The most commonly involved site was the arm (34%), followed by shoulder (23.4%), chest, face, flank, buttock, and leg. Lesional hypertrichosis was found in only 8 (17%) of the 47 patients. In 29 cases (61.7%) the lesions were in the right side of the body. Conclusion. Hypertrichosis was not so frequent among patients with Becker's nevus. There was a higher preponderance of the lesions on the right side.
    Language English
    Publishing date 2014-04-30
    Publishing country Egypt
    Document type Journal Article
    ZDB-ID 2612990-5
    ISSN 2090-4606 ; 2090-4592
    ISSN (online) 2090-4606
    ISSN 2090-4592
    DOI 10.1155/2014/953747
    Database MEDical Literature Analysis and Retrieval System OnLINE

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