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  1. Article: Treatment of Henoch Schonlein nephritis; new trends.

    Nickavar, Azar

    Journal of nephropathology

    2016  Volume 5, Issue 4, Page(s) 116–117

    Language English
    Publishing date 2016-07-28
    Publishing country Iran
    Document type Editorial
    ZDB-ID 2658164-4
    ISSN 2251-8819 ; 2251-8363
    ISSN (online) 2251-8819
    ISSN 2251-8363
    DOI 10.15171/jnp.2016.21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Nutcracker syndrome; a rare cause of hematuria.

    Nickavar, Azar

    Journal of nephropathology

    2016  Volume 5, Issue 4, Page(s) 144–145

    Language English
    Publishing date 2016-07-29
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2658164-4
    ISSN 2251-8819 ; 2251-8363
    ISSN (online) 2251-8819
    ISSN 2251-8363
    DOI 10.15171/jnp.2016.27
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Alkaptonuria, a new association of distal renal tubular acidosis.

    Nickavar, Azar / Azar, Maryam Razzaghy

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

    2018  Volume 29, Issue 4, Page(s) 997–999

    Abstract: Alkaptonuria (ALK) is a rare genetic disorder, characterized by binding of ochronotic pigment to the connective tissues in different tissues. This is the first report of a child presented with primary distal renal tubular acidosis associated with ALK. ... ...

    Abstract Alkaptonuria (ALK) is a rare genetic disorder, characterized by binding of ochronotic pigment to the connective tissues in different tissues. This is the first report of a child presented with primary distal renal tubular acidosis associated with ALK. Both disorders were managed by their specific medical treatments, with no further complication.
    MeSH term(s) Acidosis, Renal Tubular/complications ; Acidosis, Renal Tubular/diagnosis ; Alkaptonuria/complications ; Alkaptonuria/diagnosis ; Child ; Female ; Humans
    Language English
    Publishing date 2018-09-21
    Publishing country Saudi Arabia
    Document type Case Reports
    ZDB-ID 1379955-1
    ISSN 1319-2442
    ISSN 1319-2442
    DOI 10.4103/1319-2442.239645
    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:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  4. Article ; Online: Nutcracker syndrome; a rare cause of hematuria

    Azar Nickavar

    Journal of Nephropathology, Vol 5, Iss 4, Pp 144-

    2016  Volume 145

    Keywords hematuria ; nutcracker syndrome ; children ; Pathology ; RB1-214 ; Internal medicine ; RC31-1245 ; Other systems of medicine ; RZ201-999
    Language English
    Publishing date 2016-10-01T00:00:00Z
    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: Treatment of Henoch Schonlein nephritis; new trends

    Azar Nickavar

    Journal of Nephropathology, Vol 5, Iss 4, Pp 116-

    2016  Volume 117

    Keywords henoch-schönlein nephritis ; chronic kidney disease ; endocapillary proliferation ; Pathology ; RB1-214 ; Internal medicine ; RC31-1245 ; Other systems of medicine ; RZ201-999
    Language English
    Publishing date 2016-10-01T00:00:00Z
    Publisher Society of Diabetic Nephropathy Prevention
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article: Recurrent Macroscopic Hematuria and Abdominal Pain: Questions and Answers.

    Nickavar, Azar

    Iranian journal of public health

    2015  Volume 44, Issue 8, Page(s) 1143–1145

    Abstract: A 6.5 yr old girl was admitted with a category of clinical signs and symptoms including recurrent gross hematuria, abdominal pain, and fever. After different examinations including genetic analysis, the disease was diagnosed as Familial Mediterranean ... ...

    Abstract A 6.5 yr old girl was admitted with a category of clinical signs and symptoms including recurrent gross hematuria, abdominal pain, and fever. After different examinations including genetic analysis, the disease was diagnosed as Familial Mediterranean fever (FMF). It is suggested to consider FMF as a rare cause of recurrent gross hematuria, which is responsive to colchicine treatment.
    Language English
    Publishing date 2015-08
    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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    Inter-library loan at ZB MED

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  7. Article ; Online: Alkaptonuria, a new association of distal renal tubular acidosis

    Azar Nickavar / Maryam Razzaghy Azar

    Saudi Journal of Kidney Diseases and Transplantation, Vol 29, Iss 4, Pp 997-

    2018  Volume 999

    Abstract: Alkaptonuria (ALK) is a rare genetic disorder, characterized by binding of ochronotic pigment to the connective tissues in different tissues. This is the first report of a child presented with primary distal renal tubular acidosis associated with ALK. ... ...

    Abstract Alkaptonuria (ALK) is a rare genetic disorder, characterized by binding of ochronotic pigment to the connective tissues in different tissues. This is the first report of a child presented with primary distal renal tubular acidosis associated with ALK. Both disorders were managed by their specific medical treatments, with no further complication.
    Keywords Medicine ; R
    Language English
    Publishing date 2018-01-01T00:00:00Z
    Publisher Wolters Kluwer Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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    Inter-library loan at ZB MED

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  8. Article ; Online: Recurrent Macroscopic Hematuria and Abdominal Pain

    Azar NICKAVAR

    Iranian Journal of Public Health, Vol 44, Iss

    Questions and Answers

    2015  Volume 8

    Abstract: A 6.5 yr old girl was admitted with a category of clinical signs and symptoms including recurrent gross hematuria, ab-dominal pain, and fever. After different examinations including genetic analysis, the disease was diagnosed as Familial Mediterranean ... ...

    Abstract A 6.5 yr old girl was admitted with a category of clinical signs and symptoms including recurrent gross hematuria, ab-dominal pain, and fever. After different examinations including genetic analysis, the disease was diagnosed as Familial Mediterranean fever (FMF). It is suggested to consider FMF as a rare cause of recurrent gross hematuria, which is re-sponsive to colchicine treatment.
    Keywords Familial Mediterranean fever ; Hematuria ; Fever ; Pain ; Iran ; Public aspects of medicine ; RA1-1270
    Language English
    Publishing date 2015-10-01T00:00:00Z
    Publisher Tehran University of Medical Sciences
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    Full text online

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    Inter-library loan at ZB MED

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  9. Article: Utility of Urine N-acetyl-β-D-glucosaminidase for Prediction of Renal Damage in Obese Children.

    Safaeian, Baranak / Nickavar, Azar / Zaeri, Hossein / Lahootian, Lida / Behnampour, Nasser

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

    2022  Volume 32, Issue 3, Page(s) 699–702

    Abstract: The incidence of obesity has increased globally in children and adults. In addition, renal dysfunction is an important complication of childhood obesity. This study was performed to identify the diagnostic value of N-acetyl-β-D-glucosaminidase (NAG), a ... ...

    Abstract The incidence of obesity has increased globally in children and adults. In addition, renal dysfunction is an important complication of childhood obesity. This study was performed to identify the diagnostic value of N-acetyl-β-D-glucosaminidase (NAG), a renal injury marker, for the early determination of renal damage in childhood obesity. Totally, 115 obese children and 115 healthy normal weight controls were enrolled in a cross-sectional case-control study. Urine NAG was measured in sample urine and normalized by urine creatinine (CR). In addition, correlation of urine NAG with other variables such as blood pressure (BP), blood glucose, and urine albumin was evaluated. Mean systolic BP (P <0.001), serum glucose (P = 0.047), urine albumin/Cr (P = 0.049), and urine NAG/Cr (P = 0.037) were significantly higher in obese children, compared with normal healthy controls. There was no correlation between urine NAG and urine albumin excretion. Urinary NAG/Cr was a simple and safe screening test for early determination of renal damage in children with obesity.
    MeSH term(s) Acetylglucosaminidase/urine ; Acute Kidney Injury/diagnosis ; Acute Kidney Injury/urine ; Adolescent ; Albuminuria/urine ; Biomarkers/urine ; Body Weight/physiology ; Case-Control Studies ; Child ; Child, Preschool ; Creatinine/urine ; Cross-Sectional Studies ; Humans ; Pediatric Obesity/complications ; Pediatric Obesity/diagnosis
    Chemical Substances Biomarkers ; Creatinine (AYI8EX34EU) ; Acetylglucosaminidase (EC 3.2.1.52)
    Language English
    Publishing date 2022-02-10
    Publishing country Saudi Arabia
    Document type Journal Article
    ZDB-ID 1379955-1
    ISSN 1319-2442
    ISSN 1319-2442
    DOI 10.4103/1319-2442.336764
    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:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  10. Article: Prevention of renal damage by treating hyperuricemia.

    Nickavar, Azar

    International journal of preventive medicine

    2013  Volume 4, Issue 11, Page(s) 1318–1320

    Abstract: Nephrolithiasis, obstructive renal failure, essential hypertension, and chronic tubulointerstitial nephritis have been considered as the renal complications of hyperuricemia. Massive proteinuria has been rarely reported as the primary manifestation of ... ...

    Abstract Nephrolithiasis, obstructive renal failure, essential hypertension, and chronic tubulointerstitial nephritis have been considered as the renal complications of hyperuricemia. Massive proteinuria has been rarely reported as the primary manifestation of increased serum uric acid. This is the report of a child presented with proteinuira, hypertension, and glomerular scelrosis secondary to hypouricosuric hyperuricemia, who was treated by uric acid lowering management.
    Language English
    Publishing date 2013-12-05
    Publishing country Iran
    Document type Case Reports
    ZDB-ID 2574680-7
    ISSN 2008-8213 ; 2008-7802
    ISSN (online) 2008-8213
    ISSN 2008-7802
    Database MEDical Literature Analysis and Retrieval System OnLINE

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