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                             24 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 An unusual complication of umbilical catheterisation Costa, Simonetta
2008
167 12 p. 1467-1469
artikel
2 Are ECG abnormalities in Noonan syndrome characteristic for the syndrome? Raaijmakers, R.
2008
167 12 p. 1363-1367
artikel
3 Atypical manifestations of congenital parvovirus B19 infection Savarese, Immacolata
2008
167 12 p. 1463-1466
artikel
4 A variant or a “new” postaxial acrofacial dysostosis syndrome Sułko, Jerzy
2008
167 12 p. 1385-1388
artikel
5 Central precocious puberty and growth hormone deficiency in a boy with Prader-Willi syndrome Crinò, Antonino
2008
167 12 p. 1455-1458
artikel
6 Clinical and radiological findings in Schinzel–Giedion syndrome AL-Mudaffer, Mudaffer
2008
167 12 p. 1399-1407
artikel
7 Clinical features and prognoses of 23 patients with chronic granulomatous disease followed for 21 years by a single hospital in Japan Kobayashi, Shinichi
2008
167 12 p. 1389-1394
artikel
8 Defining chronic diseases and health conditions in childhood (0–18 years of age): national consensus in the Netherlands Mokkink, Lidwine B.
2008
167 12 p. 1441-1447
artikel
9 Effects of antiepileptic drug therapy on vitamin D status and biochemical markers of bone turnover in children with epilepsy Nettekoven, Sina
2008
167 12 p. 1369-1377
artikel
10 Etiology of hemolysis in two patients with hepatitis A infection: glucose-6-phosphate dehydrogenase deficiency or autoimmune hemolytic anemia Ozbay Hosnut, Ferda
2008
167 12 p. 1435-1439
artikel
11 Factors associated with defecation patterns in 0–24-month-old children Tunc, Vildan Taylan
2008
167 12 p. 1357-1362
artikel
12 Increased heme oxygenase-1 expression in premature infants with respiratory distress syndrome Farkas, Ildikó
2008
167 12 p. 1379-1383
artikel
13 Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1 Soylu, Özlem Bekem
2008
167 12 p. 1395-1398
artikel
14 Neuroglial heterotopia causing neonatal airway obstruction: presentation, management, and literature review Husein, Omar F.
2008
167 12 p. 1351-1355
artikel
15 Oculocutaneous albinism accompanied by minor morphologic stigmata Castro-Gago, Manuel
2008
167 12 p. 1475
artikel
16 Outbreaks of human coronavirus in a paediatric and neonatal intensive care unit Gagneur, Arnaud
2008
167 12 p. 1427-1434
artikel
17 Outbreaks of human coronavirus in a paediatric and neonatal intensive care unit Gagneur, Arnaud

167 12 p. 1427-1434
artikel
18 Pseudolipoma in an 18-month-old Caucasian girl: no trauma reported Campos, Marcia S.
2008
167 12 p. 1471-1473
artikel
19 Severe neonatal hypercalcemia caused by subcutaneous fat necrosis without any apparent cutaneous lesion Bonnemains, Laurent
2008
167 12 p. 1459-1461
artikel
20 Splenic infarction in a patient hereditary spherocytosis, protein C deficiency and acute infectious mononucleosis Breuer, Christian
2008
167 12 p. 1449-1452
artikel
21 Splenic infarction in a patient with hereditary spherocytosis, protein C deficiency and acute infectious mononucleosis Breuer, Christian
2008
167 12 p. 1453
artikel
22 The health and economic burden of rotavirus disease in Belgium Bilcke, Joke
2008
167 12 p. 1409-1419
artikel
23 TNF receptor-associated periodic syndrome (TRAPS): Description of a novel TNFRSF1A mutation and response to etanercept Jesus, Adriana A.

167 12 p. 1421-1425
artikel
24 TNF receptor-associated periodic syndrome (TRAPS): Description of a novel TNFRSF1A mutation and response to etanercept Jesus, Adriana A.
2008
167 12 p. 1421-1425
artikel
                             24 gevonden resultaten
 
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