| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An unusual case of transient neonatal pustular melanosis: a diagnostic puzzle
|
Brazzelli, Valeria
|
|
2013
|
173 |
12 |
p. 1655-1658
|
artikel
|
| 2 |
An unusual cause of fetal hypomobility:congenital central hypoventilation syndrome associated with hirschsprung disease
|
Montpellier, Sybille De
|
|
2013
|
173 |
12 |
p. 1607-1609
|
artikel
|
| 3 |
Anuria in a solitary kidney with Candida bezoars managed conservatively
|
Schilperoort, Jaap V.
|
|
2013
|
173 |
12 |
p. 1623-1625
|
artikel
|
| 4 |
A pediatric case of gluten sensitivity with severe neurological presentation
|
Jorge, R.
|
|
2014
|
173 |
12 |
p. 1699-1702
|
artikel
|
| 5 |
A rare cause of short stature: transsphenoidal encephalocele
|
Bayram, Özhan
|
|
2013
|
173 |
12 |
p. 1611-1613
|
artikel
|
| 6 |
Association of trisomy 18 with hepatoblastoma and its implications
|
Tan, Zhen Han
|
|
2013
|
173 |
12 |
p. 1595-1598
|
artikel
|
| 7 |
Bitter lupine beans ingestion in a child: a disregarded cause of acute anticholinergic toxicity
|
Daverio, Marco
|
|
2013
|
173 |
12 |
p. 1549-1551
|
artikel
|
| 8 |
Bubbles in the heart as first sign of gastric pneumatosis
|
Müller, Béatrice
|
|
2013
|
173 |
12 |
p. 1587-1589
|
artikel
|
| 9 |
Cayler cardiofacial syndrome with situs inversus totalis
|
Rai, Birendra
|
|
2014
|
173 |
12 |
p. 1675-1678
|
artikel
|
| 10 |
Celiac crisis presenting with status epilepticus and encephalopathy
|
Hijaz, Nadia M.
|
|
2013
|
173 |
12 |
p. 1561-1564
|
artikel
|
| 11 |
Celiac crisis presenting with status epilepticus and encephalopathy
|
Hijaz, Nadia M.
|
|
|
173 |
12 |
p. 1561-1564
|
artikel
|
| 12 |
Clinical and molecular characteristics of two transaldolase-deficient patients
|
Tylki-Szymanska, Anna
|
|
2014
|
173 |
12 |
p. 1679-1682
|
artikel
|
| 13 |
Congenital central hypoventilation syndrome and carbon dioxide sensitivity
|
Rossor, Thomas
|
|
2014
|
173 |
12 |
p. 1727-1730
|
artikel
|
| 14 |
Congenital lobar emphysema causing discrepancy between size and symptoms of ventricular septal defect
|
Noten, Anna M. E.
|
|
2014
|
173 |
12 |
p. 1671-1673
|
artikel
|
| 15 |
Deep peroneal nerve palsy during growth spurt: a case report
|
Eleftheriou, Kyriacos I.
|
|
2013
|
173 |
12 |
p. 1603-1605
|
artikel
|
| 16 |
Different course of lung disease in two siblings with novel ABCA3 mutations
|
Hallik, Maarja
|
|
2013
|
173 |
12 |
p. 1553-1556
|
artikel
|
| 17 |
Diffuse lung metastases in a child with blastic plasmacytoid dendritic cell neoplasm and review
|
Zhong, Xiao-dan
|
|
2014
|
173 |
12 |
p. 1667-1670
|
artikel
|
| 18 |
Early treatment of a child with NAGS deficiency using N-carbamyl glutamate results in a normal neurological outcome
|
Leynseele, Anouk Van
|
|
2013
|
173 |
12 |
p. 1635-1638
|
artikel
|
| 19 |
Extracorporeal life support for a 5-week-old infant with idiopathic pulmonary hemosiderosis
|
Gutierrez, Sherrill
|
|
2013
|
173 |
12 |
p. 1573-1576
|
artikel
|
| 20 |
False negative newborn screen and neonatal cholestasis in a premature child with cystic fibrosis
|
Heidendael, J. F.
|
|
2013
|
173 |
12 |
p. 1581-1583
|
artikel
|
| 21 |
Food protein-induced enterocolitis syndrome to trivial oral mucosal contact
|
Mane, Shikha K.
|
|
2013
|
173 |
12 |
p. 1545-1547
|
artikel
|
| 22 |
Heart transplant and 2-year follow up in a child with generalized arterial calcification of infancy
|
Giovannoni, Isabella
|
|
2014
|
173 |
12 |
p. 1735-1740
|
artikel
|
| 23 |
Hypertensive encephalopathy as a late complication of autonomic dysreflexia in a 12-year-old boy with a previous spinal cord injury
|
Bjelakovic, Bojko
|
|
2014
|
173 |
12 |
p. 1683-1684
|
artikel
|
| 24 |
Hypoparathyroidism and central diabetes insipidus: in search of the link
|
Eyal, Ori
|
|
2014
|
173 |
12 |
p. 1731-1734
|
artikel
|
| 25 |
Infant deaths in slings
|
Madre, Chrystèle
|
|
2013
|
173 |
12 |
p. 1659-1661
|
artikel
|
| 26 |
Interventional closure of RPA-to-LA communication in an oligosymptomatic neonate
|
Benz, Dominik C.
|
|
2014
|
173 |
12 |
p. 1703-1705
|
artikel
|
| 27 |
Isolated hepatobiliary cryptococcosis manifesting as obstructive jaundice in an immunocompetent child: case report and review of the literature
|
Zhang, Chi
|
|
2013
|
173 |
12 |
p. 1569-1572
|
artikel
|
| 28 |
Ketotifen-induced nocturnal bruxism
|
Italiano, Domenico
|
|
2013
|
173 |
12 |
p. 1585-1586
|
artikel
|
| 29 |
Life-threatening QT prolongation in a boy with attention-deficit/hyperactivity disorder on atomoxetine
|
Yamaguchi, Hiroshi
|
|
2013
|
173 |
12 |
p. 1631-1634
|
artikel
|
| 30 |
Malonic aciduria: long-term follow-up of new patients detected by newborn screening
|
Baertling, Fabian
|
|
2014
|
173 |
12 |
p. 1719-1722
|
artikel
|
| 31 |
Neonatal hemolytic anemia due to pyknocytosis
|
Vos, Michel J.
|
|
2014
|
173 |
12 |
p. 1711-1714
|
artikel
|
| 32 |
Neonatal limb ischemia: caudal blockade and NIRS monitoring
|
Piersigilli, Fiammetta
|
|
2013
|
173 |
12 |
p. 1599-1601
|
artikel
|
| 33 |
Neurofibromatosis type 1 (NF1) with an unusually severe phenotype due to digeny for NF1 and ryanodine receptor 1 associated myopathy
|
Martin, Florence
|
|
2014
|
173 |
12 |
p. 1691-1694
|
artikel
|
| 34 |
Neuroleptic malignant syndrome in an adolescent with CYP2D6 deficiency
|
Butwicka, Agnieszka
|
|
2013
|
173 |
12 |
p. 1639-1642
|
artikel
|
| 35 |
Persistent eyelid swelling in a child: lest myiasis be forgot
|
Karadag-Oncel, Eda
|
|
2013
|
173 |
12 |
p. 1649
|
artikel
|
| 36 |
Persistent multifocal atrial tachycardia in infant with encephalocraniocutaneous lipomatosis: a case report
|
Pregowska, Katarzyna
|
|
2013
|
173 |
12 |
p. 1577-1580
|
artikel
|
| 37 |
Persistent pure red cell aplasia in dicygotic twins with persistent congenital parvovirus B19 infection—remission following high dose intravenous immunoglobulin
|
Lejeune, Alice
|
|
|
173 |
12 |
p. 1723-1726
|
artikel
|
| 38 |
Persistent pure red cell aplasia in dicygotic twins with persistent congenital parvovirus B19 infection—remission following high dose intravenous immunoglobulin
|
Lejeune, Alice
|
|
2014
|
173 |
12 |
p. 1723-1726
|
artikel
|
| 39 |
Premature ovarian failure due to tetrasomy X in an adolescent girl
|
Kara, Cengiz
|
|
2013
|
173 |
12 |
p. 1627-1630
|
artikel
|
| 40 |
Primary hypothyroidism: an unusual manifestation of Wolcott–Rallison syndrome
|
Ersoy, Betül
|
|
2013
|
173 |
12 |
p. 1565-1568
|
artikel
|
| 41 |
Purpura, petechiae, and bullae as first signs of juvenile granulomatosis with polyangiitis
|
Rawn, Saara
|
|
|
173 |
12 |
p. 1685-1689
|
artikel
|
| 42 |
Purpura, petechiae, and bullae as first signs of juvenile granulomatosis with polyangiitis
|
Rawn, Saara
|
|
2014
|
173 |
12 |
p. 1685-1689
|
artikel
|
| 43 |
Reversible pulmonary arterial hypertension in cobalamin-dependent cobalamin C disease due to a novel mutation in the MMACHC gene
|
Gündüz, Mehmet
|
|
2014
|
173 |
12 |
p. 1707-1710
|
artikel
|
| 44 |
Severe infantile Bordetella pertussis pneumonia in monozygotic twins with a congenital C3 deficiency
|
Kurvers, Roel A. J.
|
|
2013
|
173 |
12 |
p. 1591-1594
|
artikel
|
| 45 |
Severe infantile Bordetella pertussis pneumonia in monozygotic twins with a congenital C3 deficiency
|
Kurvers, Roel A. J.
|
|
|
173 |
12 |
p. 1591-1594
|
artikel
|
| 46 |
Successful remission induced by plasma exchange combined with leukocytapheresis against refractory systemic juvenile idiopathic arthritis
|
Miyazono, Akinori
|
|
|
173 |
12 |
p. 1557-1560
|
artikel
|
| 47 |
Successful remission induced by plasma exchange combined with leukocytapheresis against refractory systemic juvenile idiopathic arthritis
|
Miyazono, Akinori
|
|
2013
|
173 |
12 |
p. 1557-1560
|
artikel
|
| 48 |
Superior mesenteric artery syndrome in a 15-year-old boy during Ramadan
|
Bakker, M. E. C.
|
|
2013
|
173 |
12 |
p. 1619-1621
|
artikel
|
| 49 |
Syngnathia and obstructive apnea in a case of popliteal pterygium syndrome
|
Posey, Jennifer E.
|
|
2014
|
173 |
12 |
p. 1741-1744
|
artikel
|
| 50 |
The emergence of CD20−/CD19− tumor cells after rituximab therapy for Epstein–Barr virus-associated post-transplant lymphoproliferative disorder complicated with hemophagocytic lymphohistiocytosis
|
Yamamoto, Nobuyuki
|
|
2013
|
173 |
12 |
p. 1615-1618
|
artikel
|
| 51 |
The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation
|
Overwater, E.
|
|
2014
|
173 |
12 |
p. 1695-1698
|
artikel
|
| 52 |
Thiamine-responsive megaloblastic anemia syndrome with Ebstein anomaly: a case report
|
Akbari, Mohammad Taghi
|
|
2013
|
173 |
12 |
p. 1663-1665
|
artikel
|
| 53 |
Transient leukemia in a newborn without Down syndrome: case report and review of the literature
|
Rozen, Laurence
|
|
2013
|
173 |
12 |
p. 1643-1647
|
artikel
|
| 54 |
Unilateral atelectasis in a preterm infant monitored with electrical impedance tomography: a case report
|
Burg, P. S. van der
|
|
2014
|
173 |
12 |
p. 1715-1717
|
artikel
|
| 55 |
Vasopressin as an adjunct therapy for pulmonary hypertension: a case report
|
Malikiwi, Andra
|
|
2013
|
173 |
12 |
p. 1651-1654
|
artikel
|
Tijdschrift beschrijving