| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A child presenting with disordered consciousness, hallucinations, screaming episodes and abdominal pain
|
Hussain, Khalid
|
|
2001
|
161 |
2 |
p. 127-129
|
artikel
|
| 2 |
A girl with bilateral ovarian tumours: Frasier syndrome
|
Shimoyama, Hironobu
|
|
2001
|
161 |
2 |
p. 81-83
|
artikel
|
| 3 |
A girl with bilateral ovarian tumours: Frasier syndrome
|
Shimoyama, Hironobu
|
|
2001
|
161 |
2 |
p. 81-83
|
artikel
|
| 4 |
Eosinophilic fasciitis successfully treated with oral hydroxyzine: a new therapeutic use of an old drug?
|
Uçkun, Aysin
|
|
2001
|
161 |
2 |
p. 118-119
|
artikel
|
| 5 |
High density lipoprotein-cholesterol changes in children with high cholesterol levels at birth
|
Bastida, Sara
|
|
2001
|
161 |
2 |
p. 94-98
|
artikel
|
| 6 |
High density lipoprotein-cholesterol changes in children with high cholesterol levels at birth
|
Bastida, Sara
|
|
2001
|
161 |
2 |
p. 94-98
|
artikel
|
| 7 |
Impact of pneumococcal vaccination in Senegalese HIV-1-infected children
|
Dieye, Tandakha
|
|
2001
|
161 |
2 |
p. 122-123
|
artikel
|
| 8 |
Low molecular weight heparin in children
|
Albisetti, Manuela
|
|
2001
|
161 |
2 |
p. 71-77
|
artikel
|
| 9 |
Low molecular weight heparin in children
|
Albisetti, Manuela
|
|
2001
|
161 |
2 |
p. 71-77
|
artikel
|
| 10 |
Neutrophil adherence receptor deficiency regressing with granulocyte-colony stimulating factor therapy in a case of glycogen storage disease type Ib
|
Latger-Cannard, Véronique
|
|
2001
|
161 |
2 |
p. 87-93
|
artikel
|
| 11 |
Neutrophil adherence receptor deficiency regressing with granulocyte-colony stimulating factor therapy in a case of glycogen storage disease type Ib
|
Latger-Cannard, Véronique
|
|
2001
|
161 |
2 |
p. 87-93
|
artikel
|
| 12 |
Pepper syndrome, truncus arteriosus communis and abnormal pulmonary venous return: an unusual association
|
Nouet, Natacha
|
|
2001
|
161 |
2 |
p. 114-115
|
artikel
|
| 13 |
Presymptomatic diagnosis of Wilson disease associated with a novel mutation of the ATP713 gene
|
Ohya, Kazuhiro
|
|
2001
|
161 |
2 |
p. 124-126
|
artikel
|
| 14 |
Recurrent herpetic whitlow in an immune competent girl without vesicular lesions
|
Kopriva, Frantisek
|
|
2001
|
161 |
2 |
p. 120-121
|
artikel
|
| 15 |
Reply
|
Carolis, Maria Pia De
|
|
2002
|
161 |
2 |
p. 131
|
artikel
|
| 16 |
Serum hepatocyte growth factor combined with vascular endothelial growth factor as a predictive indicator for the occurrence of coronary artery lesions in Kawasaki disease
|
Ohno, Takuro
|
|
2001
|
161 |
2 |
p. 105-111
|
artikel
|
| 17 |
Serum hepatocyte growth factor combined with vascular endothelial growth factor as a predictive indicator for the occurrence of coronary artery lesions in Kawasaki disease
|
Ohno, Takuro
|
|
2001
|
161 |
2 |
p. 105-111
|
artikel
|
| 18 |
Severe hypoalbuminaemia in a systemic lupus erythematosus-like patient
|
Gattorno, Marco
|
|
2001
|
161 |
2 |
p. 84-86
|
artikel
|
| 19 |
Severe hypoalbuminaemia in a systemic lupus erythematosus-like patient
|
Gattorno, Marco
|
|
2001
|
161 |
2 |
p. 84-86
|
artikel
|
| 20 |
The first case of the FRAXE form of inherited mental retardation in Croatia
|
Hećimović, Silva
|
|
2001
|
161 |
2 |
p. 112-113
|
artikel
|
| 21 |
38th Workshop for Pediatric Research held at the Max- Planck-Institut for Experimental Medicine, Göttingen, February 21-22, 2002
|
|
|
2002
|
161 |
2 |
p. R1-R10
|
artikel
|
| 22 |
Umbilical artery catheters: more dangerous than useful?
|
Messer, Jean
|
|
2001
|
161 |
2 |
p. 130
|
artikel
|
| 23 |
Unilateral CHARGE association
|
Trip, Jeroen
|
|
2001
|
161 |
2 |
p. 78-80
|
artikel
|
| 24 |
Unilateral CHARGE association
|
Trip, Jeroen
|
|
2001
|
161 |
2 |
p. 78-80
|
artikel
|
| 25 |
Unilateral decompressive craniectomy for children with severe brain injury. Report of seven cases and review of the relevant literature
|
Hejazi, Nedal
|
|
2001
|
161 |
2 |
p. 99-104
|
artikel
|
| 26 |
Unilateral decompressive craniectomy for children with severe brain injury. Report of seven cases and review of the relevant literature
|
Hejazi, Nedal
|
|
2001
|
161 |
2 |
p. 99-104
|
artikel
|
| 27 |
Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies
|
Toscano, Alessandra
|
|
2001
|
161 |
2 |
p. 116-117
|
artikel
|
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