| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A 12-month-old boy with a localized verrucous tumor
|
Möhrenschlager, Matthias
|
|
2009
|
169 |
4 |
p. 513-515
|
artikel
|
| 2 |
A novel L1CAM mutation in a fetus detected by prenatal diagnosis
|
Piccione, Maria
|
|
2009
|
169 |
4 |
p. 415-419
|
artikel
|
| 3 |
A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum
|
Koehler, Udo
|
|
2009
|
169 |
4 |
p. 463-468
|
artikel
|
| 4 |
A patient with Lemierre syndrome
|
Vargiami, Efthimia G.
|
|
2010
|
169 |
4 |
p. 491-493
|
artikel
|
| 5 |
Behçet disease: treatment of vascular involvement in children
|
Ozen, Seza
|
|
2009
|
169 |
4 |
p. 427-430
|
artikel
|
| 6 |
Clinical practice:
|
Khalil, Basem A.
|
|
2009
|
169 |
4 |
p. 395-402
|
artikel
|
| 7 |
Clinical practice
|
Kantor, Paul F.
|
|
2010
|
169 |
4 |
p. 403-410
|
artikel
|
| 8 |
Diagnosis, treatment and follow-up of 25 patients with melamine-induced kidney stones complicated by acute obstructive renal failure in Beijing Children’s Hospital
|
Sun, Qiang
|
|
2009
|
169 |
4 |
p. 483-489
|
artikel
|
| 9 |
Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy of the central nervous system—a novel entity?
|
Helbig, Ingo
|
|
2009
|
169 |
4 |
p. 495-500
|
artikel
|
| 10 |
Eponym
|
Vargiami, Efthimia G.
|
|
2010
|
169 |
4 |
p. 411-414
|
artikel
|
| 11 |
Familial primary carpal tunnel syndrome with possible skipped generation
|
Senel, Saliha
|
|
2009
|
169 |
4 |
p. 453-455
|
artikel
|
| 12 |
Gradenigo's syndrome with lateral venous sinus thrombosis: successful conservative treatment
|
Scardapane, Alessandra
|
|
2009
|
169 |
4 |
p. 437-440
|
artikel
|
| 13 |
Involvement of tryptophan hydroxylase 2 (TPH2) gene polymorphisms in susceptibility to coronary artery lesions in Korean children with Kawasaki disease
|
Park, Sung Wook
|
|
2009
|
169 |
4 |
p. 457-461
|
artikel
|
| 14 |
LEOPARD syndrome with recurrent PTPN11 mutation Y279C and different cutaneous manifestations: two case reports and a review of the literature
|
Kalev, Ingrid
|
|
2009
|
169 |
4 |
p. 469-473
|
artikel
|
| 15 |
Microcephaly, sensorineural deafness and Currarino triad with duplication–deletion of distal 7q
|
Pavone, Piero
|
|
2009
|
169 |
4 |
p. 475-481
|
artikel
|
| 16 |
Mycoplasma pneumoniae associated opsoclonus–myoclonus syndrome in three cases
|
Huber, Benedikt Maria
|
|
2009
|
169 |
4 |
p. 441-445
|
artikel
|
| 17 |
Mycoplasma pneumoniae associated opsoclonus–myoclonus syndrome in three cases
|
Huber, Benedikt Maria
|
|
|
169 |
4 |
p. 441-445
|
artikel
|
| 18 |
Non-accidental chlorpyrifos poisoning—an unusual cause of profound unconsciousness
|
Lee, Jiun-Chang
|
|
2009
|
169 |
4 |
p. 509-511
|
artikel
|
| 19 |
Ochoa syndrome: a spectrum of urofacial syndrome
|
Aydogdu, Ozgu
|
|
2009
|
169 |
4 |
p. 431-435
|
artikel
|
| 20 |
Prevalence of flexible flatfoot in Taiwanese school-aged children in relation to obesity, gender, and age
|
Chang, Jen-Huei
|
|
2009
|
169 |
4 |
p. 447-452
|
artikel
|
| 21 |
Rapid diagnosis of herpetic encephalitis in children by PCR-microarray technology for simultaneous detection of seven human herpes viruses
|
Shi, Jianrong
|
|
2009
|
169 |
4 |
p. 421-425
|
artikel
|
| 22 |
Reply to correspondence letter by Luis Ignacio Gonzalez-Granado
|
Aytekin, Caner
|
|
2009
|
169 |
4 |
p. 519
|
artikel
|
| 23 |
Sclerosing cholangitis and combination antifungal therapy for PNP deficiency patients
|
Gonzalez-Granado, Luis Ignacio
|
|
2009
|
169 |
4 |
p. 517
|
artikel
|
| 24 |
Submandibular lymphadenitis caused by Mycobacterium interjectum: contribution of new diagnostic tools
|
Tuerlinckx, David
|
|
2009
|
169 |
4 |
p. 505-508
|
artikel
|
| 25 |
Virilizing adrenocortical carcinoma in a child with Turner syndrome and somatic TP53 gene mutation
|
Ko, Jung-Hee
|
|
2009
|
169 |
4 |
p. 501-504
|
artikel
|
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