| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aborted Tracheo-esophageal Fistula in a Neonate
|
Hallett, John M
|
|
2018
|
21 |
5 |
p. 475-479
|
artikel
|
| 2 |
Abstracts from the meeting of the Paediatric Pathology Society, Lisbon, Portugal, September 7–9, 2017
|
|
|
2018
|
21 |
5 |
p. NP1
|
artikel
|
| 3 |
A Case of Juvenile Onset Neuronal Intranuclear Inclusion Disease With a Negative Antemortem Skin Biopsy
|
Pilson, Keith
|
|
2018
|
21 |
5 |
p. 494-496
|
artikel
|
| 4 |
Anatomical Pathology of the Umbilical Cord and Its Maternal and Fetal Clinical Associations in 434 Newborns
|
Olaya-C, Mercedes
|
|
2018
|
21 |
5 |
p. 467-474
|
artikel
|
| 5 |
Author’s Reply: TK2-related Myopathic Mitochondrial Depletion Syndrome
|
Martín-Hernández, Elena
|
|
2018
|
21 |
5 |
p. 509-510
|
artikel
|
| 6 |
Bronchial Mucoepidermoid Carcinoma With the Classic MAML2 Gene Rearrangement in a 2-year-old Boy
|
Szymanski, Linda J
|
|
2018
|
21 |
5 |
p. 480-485
|
artikel
|
| 7 |
Ectopic Liver Within the Placental Parenchyma of a Stillborn Fetus
|
Saluja, Rasleen
|
|
2018
|
21 |
5 |
p. 486-488
|
artikel
|
| 8 |
Expanding the Phenotype of ALK-positive Histiocytosis: A Report of 2 Cases
|
Huang, Huiya
|
|
2018
|
21 |
5 |
p. 449-455
|
artikel
|
| 9 |
FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family
|
Ferro, Elisa
|
|
2018
|
21 |
5 |
p. 456-460
|
artikel
|
| 10 |
Martha Wollstein of Babies Hospital in New York City (1868–1939)—The First North American Pediatric Pathologist
|
Wright, James R
|
|
2018
|
21 |
5 |
p. 437-443
|
artikel
|
| 11 |
Measles Lymphadenopathy in a Child With PFAPA Syndrome
|
Terry, Jefferson
|
|
2018
|
21 |
5 |
p. 497-501
|
artikel
|
| 12 |
Occult Massive Visceral Fat Necrosis Following Therapeutic Hypothermia for Neonatal Encephalopathy
|
Khedr, Salwa
|
|
2018
|
21 |
5 |
p. 502-506
|
artikel
|
| 13 |
Plaque-like Myofibroblastic Tumor: 2 Cases of This Unusual Dermal Tumor Which Occurs in Infancy and Early Childhood
|
Sekar, Thivya
|
|
2018
|
21 |
5 |
p. 444-448
|
artikel
|
| 14 |
Rare MYC-amplified Neuroblastoma With Large Cell Histology
|
Matsuno, Ryosuke
|
|
2018
|
21 |
5 |
p. 461-466
|
artikel
|
| 15 |
Systemic Juvenile Xanthogranuloma Involving the Bone Marrow, Multiple Bones, and the Skin That Developed During Treatment of Acute Lymphoblastic Leukemia in Remission State
|
Cheon, Eunjae
|
|
2018
|
21 |
5 |
p. 489-493
|
artikel
|
| 16 |
TK2-related Myopathic Mitochondrial Depletion Syndrome
|
Finsterer, Josef
|
|
2018
|
21 |
5 |
p. 507-508
|
artikel
|
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