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PubPharm (261)
1
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
enthalten in:
Kidney international
| 2024
von
Riedhammer, K.
|
Nguyen, T.
|
Koşukcu, C.
| +57
UpdateOf: medRxiv. 2023 Mar 22;:. - PMID 36993625
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2
Artificial Intelligence in Pediatrics : Learning to Walk Together
enthalten in:
Turkish archives of pediatrics
| 2024
von
Can Demirbaş, K.
|
Yıldız, M.
|
Saygılı, S.
| +2
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3
Complement gene mutations in children with C3 glomerulopathy : do they affect the response to mycophenolate mofetil?
enthalten in:
Pediatric nephrology (Berlin, Germany)
| 2024
von
Günay, N.
|
Dursun, .
|
Gökçe, .
| +30
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4
A case of crescentic glomerulonephritis with exacerbation of pre-existing IgA nephropathy after COVID-19
enthalten in:
The Turkish journal of pediatrics
| 2024
von
Yılmaz, E.
|
Saygılı, S.
|
Musayeva, G.
| +4
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5
Long-term Effects of Kidney Transplantation Compared With Dialysis on Intima-media Thickness in Children-Results From the 4C-T Study
enthalten in:
Transplantation
| 2024
von
Grabitz, C.
|
Sugianto, R.
|
Doyon, A.
| +82
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6
Magnetic resonance imaging based kidney volume assessment for risk stratification in pediatric autosomal dominant polycystic kidney disease
enthalten in:
Frontiers in pediatrics
| 2024
von
Yilmaz, K.
|
Saygili, S.
|
Canpolat, N.
| +18
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7
Outcome of immunosuppression in children with IgA vasculitis-related nephritis
enthalten in:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
| 2024
von
Rohner, K.
|
Marlais, M.
|
Ahn, Y.
| +48
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8
Children With Type 1 Spinal Muscular Atrophy Are at Increased Risk for Nephrolithiasis
enthalten in:
Pediatric neurology
| 2024
von
Gök, A.
|
Saygılı, S.
|
Kuruğoğlu, S.
| +2
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9
A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)
enthalten in:
Clinical genetics
| 2023
von
Saygılı, S.
|
Koşukcu, C.
|
Baştuğ, T.
| +7
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10
Complement gene mutations in children with C3 glomerulopathy: Do they affect clinical outcome?
enthalten in:
ResearchSquare.com
| 2023
von
Günay, N.
|
Dursun, I.
|
Gökce, .
| +30
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3
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3
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38
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26
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20
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17
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