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                             28 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acute poisoning after oral intake of a toluene-containing paint thinner Malingré, Mirte M.
2002
161 6 p. 354-355
artikel
2 A girl with partial trisomy 5q35→qter and partial trisomy 13pter→q31 derived via a maternal balanced translocation Uchiyama, Atsushi
2002
161 6 p. 360-361
artikel
3 Amitraz poisoning in children Aydin, Kürsad
2002
161 6 p. 349-350
artikel
4 Body mass index measurements and prevalence of overweight and obesity in school-children living in the province of Belgian Limburg Massa, Guy
2002
161 6 p. 343-346
artikel
5 Body mass index measurements and prevalence of overweight and obesity in school-children living in the province of Belgian Limburg Massa, Guy
2002
161 6 p. 343-346
artikel
6 Central heating devices cause childhood injuries but rarely burns: a study in Greece Petridou, Eleni
2002
161 6 p. 347-349
artikel
7 Colloid infusion in the perinatal period and abnormal neurodevelopmental outcome in very low birth weight infants Greenough, Anne
2002
161 6 p. 319-323
artikel
8 Colloid infusion in the perinatal period and abnormal neurodevelopmental outcome in very low birth weight infants Greenough, Anne
2002
161 6 p. 319-323
artikel
9 Colloid infusion in the perinatal period and abnormal neurodevelopmental outcome in very low birth weight infants Greenough, Anne

161 6 p. 319-323
artikel
10 Detection of auto-antibodies against a 70 kDa protein derived from vascular smooth muscle cells in patients with Kawasaki disease Suzuki, Hiroyuki
2002
161 6 p. 324-329
artikel
11 Detection of auto-antibodies against a 70 kDa protein derived from vascular smooth muscle cells in patients with Kawasaki disease Suzuki, Hiroyuki
2002
161 6 p. 324-329
artikel
12 Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain – a review Klepper, Jörg
2002
161 6 p. 295-304
artikel
13 Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain – a review Klepper, Jörg
2002
161 6 p. 295-304
artikel
14 Identification of a novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome presenting with neonatal diabetes mellitus and galactosaemia Yoo, Han-Wook
2002
161 6 p. 351-353
artikel
15 Juvenile dermatomyositis associated with subclinical hypothyroidism due to auto-immune thyroiditis Go, Tohshin
2002
161 6 p. 358-359
artikel
16 Long-term follow-up of children with bacterial meningitis with emphasis on behavioural characteristics Berg, Stefan
2002
161 6 p. 330-336
artikel
17 Long-term follow-up of children with bacterial meningitis with emphasis on behavioural characteristics Berg, Stefan
2002
161 6 p. 330-336
artikel
18 Malignant rhabdoid tumour of the kidney occurring simultaneously with a brain tumour: a report of two cases and review of the literature Luo, Chih-Cheng
2002
161 6 p. 340-342
artikel
19 Malignant rhabdoid tumour of the kidney occurring simultaneously with a brain tumour: a report of two cases and review of the literature Luo, Chih-Cheng
2002
161 6 p. 340-342
artikel
20 Serial bronchoalveolar lavage of preterm infants is not associated with chest radiological changes Vyas, Julian
2002
161 6 p. 313-318
artikel
21 Serial bronchoalveolar lavage of preterm infants is not associated with chest radiological changes Vyas, Julian
2002
161 6 p. 313-318
artikel
22 Small thymus at birth and gestational age Felice, Claudio De
2002
161 6 p. 362-363
artikel
23 Successful resumption of trimethoprim-sulfamethoxazole after oral desensitisation in patients with chronic granulomatous disease Hasui, Masafumi
2002
161 6 p. 356-357
artikel
24 Successful resumption of trimethoprim-sulfamethoxazole after oral desensitisation in patients with chronic granulomatous disease Hasui, Masafumi

161 6 p. 356-357
artikel
25 Sudden infant death: no evidence for linkage to common polymorphisms in the uncoupling protein-1 and the β3-adrenergic receptor genes Fatemi, Ali
2002
161 6 p. 337-339
artikel
26 Sudden infant death: no evidence for linkage to common polymorphisms in the uncoupling protein-1 and the β3-adrenergic receptor genes Fatemi, Ali
2002
161 6 p. 337-339
artikel
27 Uniparental disomy: clinical indications for testing in growth retardation Eggermann, Thomas
2002
161 6 p. 305-312
artikel
28 Uniparental disomy: clinical indications for testing in growth retardation Eggermann, Thomas
2002
161 6 p. 305-312
artikel
                             28 gevonden resultaten
 
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