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/vufind/Search/Results?lookfor=%22Canpolat%2C+Nur%22&type=Person&page=5
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PubPharm (262)
41
A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature
enthalten in:
Pediatric nephrology
| 2022
von
Tastemel Ozturk, T.
|
Canpolat, N.
|
Saygili, S.
| +4
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42
A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature
enthalten in:
Pediatric nephrology
| 2022
von
Tastemel Ozturk, T.
|
Canpolat, N.
|
Saygili, S.
| +4
Wird geladen...
43
A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature
enthalten in:
Pediatric nephrology
| 2022
von
Tastemel Ozturk, T.
|
Canpolat, N.
|
Saygili, S.
| +4
Wird geladen...
44
Omalizumab may facilitate drug desensitization in patients failing standard protocols
enthalten in:
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
| 2022
von
Gemici Karaaslan, H.
|
Karabag Yilmaz, E.
|
Gulmez, R.
| +3
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45
Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome : a multicentric retrospective study
enthalten in:
Journal of nephrology
| 2022
von
Baskin, E.
|
Fidan, K.
|
Gulhan, B.
| +7
ErratumIn: J Nephrol. 2022 Feb 7;:. - PMID 35129816
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46
Correction to : Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study
enthalten in:
Journal of nephrology
| 2022
von
Baskin, E.
|
Fidan, K.
|
Gulhan, B.
| +7
ErratumFor: J Nephrol. 2022 May;35(4):1213-1222. - PMID 35060104
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47
Findings from 4C-T Study demonstrate an increased cardiovascular burden in girls with end stage kidney disease and kidney transplantation
enthalten in:
Kidney international
| 2022
von
Sugianto, R.
|
Memaran, N.
|
Schmidt, B.
| +27
CommentIn: Kidney Int. 2022 Mar;101(3):459-462. - PMID 35190033
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48
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome
enthalten in:
Clinical genetics
| 2022
von
Canpolat, N.
|
Liu, D.
|
Atayar, E.
| +17
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49
Correction to: Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study
enthalten in:
Journal of nephrology
| 2022
von
Baskin, E.
|
Fidan, K.
|
Gulhan, B.
| +7
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50
Increased risk for kidney sequelae surrogates in survivors of Wilms tumor
enthalten in:
Pediatric nephrology
| 2022
von
Arslan, E.
|
Saygili, S.
|
Celkan, T.
| +8
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