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                             49 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abstracts
22 12 p. 2151-2175
artikel
2 Abstracts 2007
22 12 p. 2151-2175
artikel
3 Antenatal and postnatal risk factors for neonatal hypertension and infant follow-up Seliem, Wael A.
2007
22 12 p. 2081-2087
artikel
4 Antenatal and postnatal risk factors for neonatal hypertension and infant follow-up Seliem, Wael A.

22 12 p. 2081-2087
artikel
5 Chronic kidney disease in children: the global perspective Warady, Bradley A.

22 12 p. 1999-2009
artikel
6 Chronic kidney disease in children: the global perspective Warady, Bradley A.
2007
22 12 p. 1999-2009
artikel
7 Correlation between finger-prick and venous ciclosporin levels: association with gingival overgrowth and hypertrichosis Webb, Nicholas J. A.

22 12 p. 2111-2118
artikel
8 Correlation between finger-prick and venous ciclosporin levels: association with gingival overgrowth and hypertrichosis Webb, Nicholas J. A.
2007
22 12 p. 2111-2118
artikel
9 Cystic renal dysplasia as a leading sign of inherited metabolic disease Distelmaier, Felix

22 12 p. 2119-2124
artikel
10 Cystic renal dysplasia as a leading sign of inherited metabolic disease Distelmaier, Felix
2007
22 12 p. 2119-2124
artikel
11 Efficacy of urine screening at school: experience in Shanghai, China Zhai, Yi-Hui

22 12 p. 2073-2079
artikel
12 Efficacy of urine screening at school: experience in Shanghai, China Zhai, Yi-Hui
2007
22 12 p. 2073-2079
artikel
13 Hemodialysis in children weighing less than 15 kg: a single-center experience Kovalski, Yael

22 12 p. 2105-2110
artikel
14 Hemodialysis in children weighing less than 15 kg: a single-center experience Kovalski, Yael
2007
22 12 p. 2105-2110
artikel
15 Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder Sharma, Ajay P.

22 12 p. 2097-2103
artikel
16 Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder Sharma, Ajay P.
2007
22 12 p. 2097-2103
artikel
17 Identification of a urinary proteomic signature for lupus nephritis in children Suzuki, Michiko

22 12 p. 2047-2057
artikel
18 Identification of a urinary proteomic signature for lupus nephritis in children Suzuki, Michiko
2007
22 12 p. 2047-2057
artikel
19 Mechanisms of progression of chronic kidney disease Fogo, Agnes B.

22 12 p. 2011-2022
artikel
20 Mechanisms of progression of chronic kidney disease Fogo, Agnes B.
2007
22 12 p. 2011-2022
artikel
21 Molecular mechanism of edema formation in nephrotic syndrome: therapeutic implications Doucet, Alain

22 12 p. 1983-1990
artikel
22 Molecular mechanism of edema formation in nephrotic syndrome: therapeutic implications Doucet, Alain
2007
22 12 p. 1983-1990
artikel
23 NGAL is an early predictive biomarker of contrast-induced nephropathy in children Hirsch, Russel

22 12 p. 2089-2095
artikel
24 NGAL is an early predictive biomarker of contrast-induced nephropathy in children Hirsch, Russel
2007
22 12 p. 2089-2095
artikel
25 NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome Berdeli, Afig
2007
22 12 p. 2031-2040
artikel
26 NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome Berdeli, Afig

22 12 p. 2031-2040
artikel
27 Perinatal asphyxia may present with features of neonatal atypical hemolytic uremic syndrome Biran, Valérie

22 12 p. 2129-2132
artikel
28 Perinatal asphyxia may present with features of neonatal atypical hemolytic uremic syndrome Biran, Valérie
2007
22 12 p. 2129-2132
artikel
29 Rabson-Mendenhall syndrome: medullary sponge kidney, a new component Harris, Andrew M.
2007
22 12 p. 2141-2144
artikel
30 Rabson-Mendenhall syndrome: medullary sponge kidney, a new component Harris, Andrew M.

22 12 p. 2141-2144
artikel
31 Reduced albumin levels and utilization of arteriovenous access in pediatric patients with systemic lupus erythematosus (SLE) Sule, Sangeeta D.
2007
22 12 p. 2041-2046
artikel
32 Reduced albumin levels and utilization of arteriovenous access in pediatric patients with systemic lupus erythematosus (SLE) Sule, Sangeeta D.

22 12 p. 2041-2046
artikel
33 Reviews submitted from August 1st, 2006 to August 31st, 2007
22 12 p. 2145-2149
artikel
34 Reviews submitted from August 1st, 2006 to August 31st, 2007 2007
22 12 p. 2145-2149
artikel
35 Serum levels of galactose-deficient IgA in children with IgA nephropathy and Henoch-Schönlein purpura Lau, Keith K.
2007
22 12 p. 2067-2072
artikel
36 Serum levels of galactose-deficient IgA in children with IgA nephropathy and Henoch-Schönlein purpura Lau, Keith K.

22 12 p. 2067-2072
artikel
37 Splenic peliosis in the course of IgA nephropathy Stojanović, Vesna
2007
22 12 p. 2137-2140
artikel
38 Splenic peliosis in the course of IgA nephropathy Stojanović, Vesna

22 12 p. 2137-2140
artikel
39 Splenic peliosis in the course of IgA nephropathy Stojanović, Vesna

22 12 p. 2137-2140
artikel
40 Teaching molecular genetics: chapter 4—positional cloning of genetic disorders Puliti, Aldamaria
2007
22 12 p. 2023-2029
artikel
41 Teaching molecular genetics: chapter 4—positional cloning of genetic disorders Puliti, Aldamaria

22 12 p. 2023-2029
artikel
42 Thrombotic microangiopathy as a complication in a patient with focal segmental glomerulosclerosis Benz, Kerstin

22 12 p. 2125-2128
artikel
43 Thrombotic microangiopathy as a complication in a patient with focal segmental glomerulosclerosis Benz, Kerstin
2007
22 12 p. 2125-2128
artikel
44 Transplantation of renal primordia: renal organogenesis Hammerman, Marc R.

22 12 p. 1991-1998
artikel
45 Transplantation of renal primordia: renal organogenesis Hammerman, Marc R.
2007
22 12 p. 1991-1998
artikel
46 Treatment with mycophenolate mofetil and prednisolone for steroid-dependent nephrotic syndrome Afzal, Kamran

22 12 p. 2059-2065
artikel
47 Treatment with mycophenolate mofetil and prednisolone for steroid-dependent nephrotic syndrome Afzal, Kamran
2007
22 12 p. 2059-2065
artikel
48 WT1 mutation and podocyte molecular expression in a Chinese Frasier syndrome patient Li, Jianguo

22 12 p. 2133-2136
artikel
49 WT1 mutation and podocyte molecular expression in a Chinese Frasier syndrome patient Li, Jianguo
2007
22 12 p. 2133-2136
artikel
                             49 gevonden resultaten
 
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