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  1. Article: CTNS Mutations Causing Autosomal Recessive Cystinosis in a Subset of Iranian Population: Report of Two New Variants.

    Mohammadi Chermahini, Zahra / Salehi, Mansoor / Gheissari, Alaleh / Ahmadi Beni, Faeze / Khosravian, Farinaz / Kazemi, Mohammad

    Advanced biomedical research

    2024  Volume 13, Page(s) 2

    Abstract: Background: Nephropathic cystinosis (NC) is an uncommon autosomal recessive disease with abnormality in lysosomal storage that appearances in patients with mutations in the : Materials and methods: Twenty Iranian cystinosis patients referring to Imam ...

    Abstract Background: Nephropathic cystinosis (NC) is an uncommon autosomal recessive disease with abnormality in lysosomal storage that appearances in patients with mutations in the
    Materials and methods: Twenty Iranian cystinosis patients referring to Imam Hossein Hospital of Isfahan were employed in this case-series study. After extraction of genomic DNA, the promoter and entire coding regions of
    Results: The large deletion was not seen in any NC patients. Molecular analysis which conducted to screen the
    Conclusion: The mutational spectrum in the Iranian patients is the same as previously reported mutations except that two new mutations were found. The present findings will present suggestions for regular molecular diagnosis of cystinosis in Iran.
    Language English
    Publishing date 2024-01-30
    Publishing country India
    Document type Journal Article
    ZDB-ID 2672524-1
    ISSN 2277-9175
    ISSN 2277-9175
    DOI 10.4103/abr.abr_149_23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Focal segmental glomerulosclerosis and end-stage kidney disease in children.

    Gheissari, Alaleh

    Journal of nephropharmacology

    2015  Volume 4, Issue 2, Page(s) 61–62

    Language English
    Publishing date 2015-05-17
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2756100-8
    ISSN 2345-4202
    ISSN 2345-4202
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Acute kidney injury and renal angina.

    Gheissari, Alaleh

    Journal of renal injury prevention

    2013  Volume 2, Issue 2, Page(s) 33–34

    Language English
    Publishing date 2013-06-01
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2747305-3
    ISSN 2345-2781
    ISSN 2345-2781
    DOI 10.12861/jrip.2013.12
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Acute kidney injury and renal angina

    Gheissari Alaleh

    Journal of Renal Injury Prevention, Vol 2, Iss 2, Pp 33-

    2013  Volume 34

    Abstract: Implication for health policy/practice/research/medical education:Recently, the term renal angina (RA) has been described to straighten using biomarkers in at-risk patients who have a combination of illness severity/risk and even small changes in kidney ... ...

    Abstract Implication for health policy/practice/research/medical education:Recently, the term renal angina (RA) has been described to straighten using biomarkers in at-risk patients who have a combination of illness severity/risk and even small changes in kidney function. RA is a valuable guideline to identify high risk patients and improve the positive predictive value of serum and urine biomarkers to predict early stages of AKI and its severity.
    Keywords Acute kidney injury ; Chronic kidney disease ; Renal angina ; Diseases of the genitourinary system. Urology ; RC870-923 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Urology ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language English
    Publishing date 2013-06-01T00:00:00Z
    Publisher Society of Diabetic Nephropathy Prevention
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: The Effect of Parental Consanguinity on Clinical Course and Outcome of Children with Focal Segmental Glomerulosclerosis, a Report from Isfahan, Iran.

    Gheissari, Alaleh / Meamar, Rokhsareh / Kheirollahi, Majid / Abedini, Amin

    Iranian journal of kidney diseases

    2020  Volume 14, Issue 5, Page(s) 348–357

    Abstract: Introduction: Focal segmental glomerulosclerosis (FSGS) accounts for 20% of nephrotic syndromes among children as well as 75% of the steroid resistant nephrotic syndrome (SRNS). The aim of the present study was to evaluate the influence of parental ... ...

    Abstract Introduction: Focal segmental glomerulosclerosis (FSGS) accounts for 20% of nephrotic syndromes among children as well as 75% of the steroid resistant nephrotic syndrome (SRNS). The aim of the present study was to evaluate the influence of parental consanguinity on clinical course and outcome of FSGS in children.
    Methods: This historical cohort was carried out on 69 children affected by steroid resistant FSGS. Patients' data were recorded at the initial and the final analyses and response to therapeutic measures. Subjects were also questioned about the history of parental consanguinity.
    Results: Forty-four participants (63.8%) were male with a male to female proportion of 1.76:1. Mean baseline age was 5.69 ± 2.39 (range: 1 to 10). Fifty-one patients (73.9%) reported consanguinity. A more significant resistance to cyclosporine A and cyclophosphamide was observed in participants denoting parental consanguinity than those with no kinship. The average renal survival time obtained significantly lower among those reporting consanguinity compared to the others (8.33 vs. 10.44 years, P < .05). According to univariate analysis results, parental consanguinity was a risk factor for developing chronic kidney disease (HR = 4.56, 95% CI: 1.06 to 19.47; P < .05).
    Conclusion: Patients with FSGS plus parental consanguinity presented less renal survival time with more resistance to cures being more predisposed to the development of CKD.
    MeSH term(s) Child ; Consanguinity ; Female ; Glomerulosclerosis, Focal Segmental/diagnosis ; Glomerulosclerosis, Focal Segmental/genetics ; Humans ; Iran ; Male ; Nephrotic Syndrome ; Parents
    Language English
    Publishing date 2020-09-14
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2388271-2
    ISSN 1735-8604 ; 1735-8582
    ISSN (online) 1735-8604
    ISSN 1735-8582
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  6. Article ; Online: Cutaneous microvascular occlusion syndrome as the first manifestation of catastrophic lupus-associated antiphospholipid antibody syndrome: a case report.

    Hosseini, Nastaran-Sadat / Babaei, Sharareh / Rahimi, Hamid / Gheissari, Alaleh / Sedaghat, Banafsheh / Pourmahdi-Boroujeni, Mahsa / Abtahi-Naeini, Bahareh

    Journal of medical case reports

    2023  Volume 17, Issue 1, Page(s) 375

    Abstract: Background: Antiphospholipid syndrome (APS), defined by thrombotic events or obstetric complications in the presence of persistently high antiphospholipid antibodies, is characterized by a wide variety of clinical presentations and the effects of ... ...

    Abstract Background: Antiphospholipid syndrome (APS), defined by thrombotic events or obstetric complications in the presence of persistently high antiphospholipid antibodies, is characterized by a wide variety of clinical presentations and the effects of vascular occlusion can impact almost any organ system or tissue. Since adult-onset APS classification criteria are not well verified in pediatrics (where pregnancy-related problems are rare), estimating childhood prevalence is challenging. Stroke and pulmonary embolism are thromboembolic events occurring in children that can cause considerable long-term morbidity. Children with APS are more prone to recurrent thromboembolism than adults. Cutaneous symptoms are prominent and typically represent the first clue of APS. Although dermatologic findings are exceedingly heterogeneous, it is essential to consider which dermatological symptoms justify the investigation of antiphospholipid syndrome and the required further management.
    Case presentation: We describe a seven-year-old Iranian boy with retiform purpura and acral cutaneous ischemic lesions as the first clinical presentation of antiphospholipid syndrome in the setting of systemic lupus erythematous.
    Conclusion: APS in pediatrics, is associated with a variety of neurologic, dermatologic, and hematologic symptoms. Therefore, it is essential for pediatricians to be aware of the rare appearance of Catastrophic APS as an initial indication of APS.
    MeSH term(s) Adult ; Male ; Female ; Humans ; Child ; Pregnancy ; Antiphospholipid Syndrome/complications ; Antiphospholipid Syndrome/diagnosis ; Iran ; Pulmonary Embolism ; Stroke/etiology
    Language English
    Publishing date 2023-08-22
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 2269805-X
    ISSN 1752-1947 ; 1752-1947
    ISSN (online) 1752-1947
    ISSN 1752-1947
    DOI 10.1186/s13256-023-04068-9
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  7. Article: Essential hypertension in children, a growing worldwide problem.

    Sabri, Mohammadreza / Gheissari, Alaleh / Mansourian, Marjan / Mohammadifard, Noushin / Sarrafzadegan, Nizal

    Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences

    2019  Volume 24, Page(s) 109

    Abstract: Hypertension is one of the most common diseases worldwide. For many decades, it was considered as a problem related to adult population; however, its incidence in children has also been increased in recent years. Although secondary causes of hypertension ...

    Abstract Hypertension is one of the most common diseases worldwide. For many decades, it was considered as a problem related to adult population; however, its incidence in children has also been increased in recent years. Although secondary causes of hypertension are more common in children, few studies have been published focusing on the growing epidemic rate of essential hypertension in children and adolescents. Considering the importance of essential hypertension and its cardiovascular consequences, we review briefly its epidemiology and risk factors in children.
    Language English
    Publishing date 2019-12-23
    Publishing country India
    Document type Journal Article ; Review
    ZDB-ID 2513029-8
    ISSN 1735-7136 ; 1735-1995
    ISSN (online) 1735-7136
    ISSN 1735-1995
    DOI 10.4103/jrms.JRMS_641_19
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    In stock of ZB MED Cologne/Königswinter

    Zs.A 6810: Show issues Location:
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  8. Article ; Online: Essential hypertension in children, a growing worldwide problem

    Mohammadreza Sabri / Alaleh Gheissari / Marjan Mansourian / Noushin Mohammadifard / Nizal Sarrafzadegan

    Journal of Research in Medical Sciences, Vol 24, Iss 1, Pp 109-

    2019  Volume 109

    Abstract: Hypertension is one of the most common diseases worldwide. For many decades, it was considered as a problem related to adult population; however, its incidence in children has also been increased in recent years. Although secondary causes of hypertension ...

    Abstract Hypertension is one of the most common diseases worldwide. For many decades, it was considered as a problem related to adult population; however, its incidence in children has also been increased in recent years. Although secondary causes of hypertension are more common in children, few studies have been published focusing on the growing epidemic rate of essential hypertension in children and adolescents. Considering the importance of essential hypertension and its cardiovascular consequences, we review briefly its epidemiology and risk factors in children.
    Keywords adolescent ; cardiovascular disease ; child ; essential hypertension ; obesity ; Medicine ; R
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Wolters Kluwer Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Is CKD Screening Program Necessary in Developing Countries?

    Gheissari, Alaleh / Riahinejad, Maryam / Mehrkash, Mehryar / Merrikhi, Alireza / Madihi, Yahya / Farajzadegan, Ziba / Esteki, Behnoosh / Amini, Niloufar / Saeidi, Minoo / Vard, Bahareh / Kermani, Rasool / Kelishadi, Roya / Pourmirzaiee, Mohammad Ali / Ghanei, Amirmohammad / Azin, Neda

    Iranian journal of kidney diseases

    2023  Volume 1, Issue 1, Page(s) 37–46

    Abstract: Introduction: The prevalence of congenital anomaly of kidney and urinary tract (CAKUT) and related chronic kidney disease (CKD) may be increased in countries with higher rate of consanguineous marriage. Therefore, we evaluated the prevalence of CKD by ... ...

    Abstract Introduction: The prevalence of congenital anomaly of kidney and urinary tract (CAKUT) and related chronic kidney disease (CKD) may be increased in countries with higher rate of consanguineous marriage. Therefore, we evaluated the prevalence of CKD by biochemical and kidney ultrasound measurements in the firstgrade pupils.
    Methods: This cross -sectional study was carried on children aged 6 to 7 years. Urine analysis, serum creatinine, urine microalbumin to creatinine ratio and kidney ultrasound have been evaluated for participants.
    Results: 653 children were recruited to the study. Stage 1 and stage 2 systolic hypertension have been found in 6.5 and 1%, respectively. The percentage of stage 1 and stage 2 diastolic hypertension were 1.3 and 0.3%, respectively. Both weight Z-score and waist Z-score had positive correlation with systolic and diastolic blood pressure. Microalbuminuria (in 2.5%) did not have any correlation with the following factors: hypertension, body mass index, microscopic hematuria, glomerular filtration rate, kidney sonographic abnormalities or kidney parenchymal thickness and family history of kidney transplantation. GFR less than 90 mL/ min /1.73 m2 has been detected in 1.8% of the students. Only 1.7% had urine RBC more than 5 in each high-power field (hpf). Approximately 1.5% had anatomical abnormality of kidney and urinary tract (hydronephrosis or hydroureter).
    Conclusion: Considering the higher prevalence of elevated blood pressure and microalbuminuria in Iranian children, a CKD screening program based on evaluating microalbuminuria and blood pressure measurement is needed. However, irrespective of high prevalence of consanguineous marriage in Iran, using kidney ultrasound as a screening tool has not been recommended.  DOI: 10.52547/ijkd.7306.
    MeSH term(s) Child ; Humans ; Iran/epidemiology ; Developing Countries ; Renal Insufficiency, Chronic/diagnosis ; Renal Insufficiency, Chronic/epidemiology ; Kidney ; Hypertension/diagnosis ; Hypertension/epidemiology ; Albuminuria/diagnosis ; Albuminuria/epidemiology ; Glomerular Filtration Rate ; Hematuria ; Prevalence ; Risk Factors
    Language English
    Publishing date 2023-02-04
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2388271-2
    ISSN 1735-8604 ; 1735-8582
    ISSN (online) 1735-8604
    ISSN 1735-8582
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  10. Article: The place of ultrasound in renal medicine.

    Gheissari, Alaleh

    Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia

    2006  Volume 17, Issue 4, Page(s) 540–548

    Abstract: Today, ultrasound is one of the most commonly used diagnostic tools, the reasons being that it is non-invasive, reliable, widely available, and affordable. In this paper, we review the place of ultrasound in the diagnosis and follow-up of patients with ... ...

    Abstract Today, ultrasound is one of the most commonly used diagnostic tools, the reasons being that it is non-invasive, reliable, widely available, and affordable. In this paper, we review the place of ultrasound in the diagnosis and follow-up of patients with kidney diseases. We briefly discuss a wide range of kidney diseases for which ultrasound imaging is still performed as one of the initial steps of diagnosis. To achieve this, five following categories are addressed: congenital anomalies of the kidney; renal cystic diseases; renal infections; kidney stones; and kidney tumors. The sonographic findings of these diseases are discussed.
    MeSH term(s) Humans ; Kidney/abnormalities ; Kidney/anatomy & histology ; Kidney/diagnostic imaging ; Kidney Diseases/diagnostic imaging ; Kidney Neoplasms/diagnostic imaging ; Polycystic Kidney, Autosomal Dominant/diagnostic imaging ; Pyelonephritis/diagnostic imaging ; Ultrasonography/trends ; Urologic Diseases/diagnostic imaging
    Language English
    Publishing date 2006-12
    Publishing country Saudi Arabia
    Document type Journal Article ; Review
    ZDB-ID 1379955-1
    ISSN 1319-2442
    ISSN 1319-2442
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 4735: Show issues Location:
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    Jg. 1995 - 2021: Lesesall (2.OG)
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