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                             25 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male Yang, Yonghui
2012
172 1 p. 127-129
artikel
2 A disease severity scoring system for children with type 1 Gaucher disease Kallish, Staci
2012
172 1 p. 39-43
artikel
3 Association of adipokines with cardiovascular risk factors in low birth weight children: a case–control study Strufaldi, Maria Wany Louzada
2012
172 1 p. 71-76
artikel
4 Atlantooccipital septic arthritis complicating recurrent otitis media Asher, Zoe
2012
172 1 p. 123-125
artikel
5 Blood pressure-to-height ratio as a screening measure for identifying children with hypertension Lu, Qiang
2012
172 1 p. 99-105
artikel
6 Cartographers in an uncharted terrain—the importance of going the extra mile Jünger, Saskia
2012
172 1 p. 1-3
artikel
7 Don’t forget to report “simple” finding on CT: the hypodense eye lens Taslakian, Bedros
2012
172 1 p. 131-132
artikel
8 Grisel syndrome as a complication of Kawasaki disease: a case report and review of the literature Nozaki, Fumihito
2012
172 1 p. 119-121
artikel
9 High prevalence of complementary and alternative medicine use in the Dutch pediatric oncology population: a multicenter survey Singendonk, Maartje
2012
172 1 p. 31-37
artikel
10 Images in pediatrics: The thymic sail sign and thymic wave sign Alves, Nuno D.
2012
172 1 p. 133
artikel
11 Long-term quality of life of patients treated in paediatric intensive care unit Polic, Branka
2012
172 1 p. 85-90
artikel
12 Management of unstable pediatric hemato-oncology patient: results of a web-based survey to pediatric oncologists in Spain García-Salido, Alberto
2012
172 1 p. 51-58
artikel
13 Neurologic manifestations of Fusobacterium infections in children Megged, Orli
2012
172 1 p. 77-83
artikel
14 Pain in cognitively impaired children: a focus for general pediatricians Massaro, M.
2012
172 1 p. 9-14
artikel
15 Plasminogen activator inhibitor-1 gene polymorphism in Iranian Azeri Turkish patients with FMF disease and its association with amyloidosis Bonyadi, M.
2012
172 1 p. 91-98
artikel
16 Renal complications of seasonal and pandemic influenza A virus infections Watanabe, Toru
2012
172 1 p. 15-22
artikel
17 Renal complications of seasonal and pandemic influenza A virus infections Watanabe, Toru

172 1 p. 15-22
artikel
18 Renal Doppler ultrasonography in the diagnosis of nutcracker syndrome. Park, Se Jin
2012
172 1 p. 135-136
artikel
19 Renal phenotypic variability in HDR syndrome: glomerular nephropathy as a novel finding Chenouard, Alexis
2012
172 1 p. 107-110
artikel
20 Reply to the correspondence letter by Park et al. “Renal Doppler ultrasonography in the diagnosis of nutcracker syndrome” Waseem, Muhammad
2012
172 1 p. 137
artikel
21 Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene Fencl, Filip
2012
172 1 p. 45-49
artikel
22 Simultaneous EMG–fMRI during startle inhibition in monosymptomatic enuresis—an exploratory study Schulz-Juergensen, Sebastian
2012
172 1 p. 23-30
artikel
23 The controversy regarding the need for hormonal treatment in boys with unilateral cryptorchidism goes on: a review of the literature Ludwikowski, Barbara
2012
172 1 p. 5-8
artikel
24 The needs of professionals in the palliative care of children and adolescents Bergstraesser, Eva
2012
172 1 p. 111-118
artikel
25 Waist circumference percentiles among Turkish children under the age of 6 years Hatipoglu, Nihal
2012
172 1 p. 59-69
artikel
                             25 gevonden resultaten
 
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