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 |