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BMC Research Notes|April 3, 2016
Central venous catheter infection-related glomerulonephritis under long-term parenteral nutrition: a report of two casesMari Okada, Mai Sato, Masao Ogura, et al.
Pediatric Nephrology (Berlin, Germany)|March 13, 2024
Nail-patella syndrome with nephropathy in a de novo LMX1B mutation: triangular lunula of the thumb and lack of finger creases as cluesYoshinori Banno, Masako Ikemiyagi, Riku Hamada, et al.
Neurologia Medico-Chirurgica|March 27, 2010
Meningeal melanocytoma extruded from the skull of a neonate--case reportKuniaki Nakahara, Nobuhito Morota, Satoshi Ihara, et al.
European Journal of Human Genetics : EJHG|February 19, 2015
Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome)Masayo Kagami, Kenji Kurosawa, Osamu Miyazaki, et al.
Pediatric Blood & Cancer|December 30, 2015
Gorham-Stout Disease of the Skull Base With Hearing Loss: Dramatic Recovery and Antiangiogenic TherapyAkifumi Nozawa, Michio Ozeki, Bunya Kuze, et al.
Children (Basel, Switzerland)|March 29, 2023
A Fatal Case of Neuroblastoma Complicated by Posterior Reversible Encephalopathy with Rapidly Evolving Transplantation-Associated Thrombotic MicroangiopathyMotohiro Matsui, Atsushi Makimoto, Yuya Saito, et al.
Fetal Diagnosis and Therapy|January 24, 2015
Twin anemia-polycythemia sequence after laser surgery for twin-twin transfusion syndrome and maternal morbidityKosuke Taniguchi, Masahiro Sumie, Rika Sugibayashi, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 4, 2011
Neuroblastomas with discordant genotype-phenotype relationships: report of four cases with MYCN amplification and favorable histologyAtsuko Nakagawa, Kentaro Matsuoka, Hajime Okita, et al.
Pediatric Blood & Cancer|January 26, 2016
Clinical Features and Prognosis of Generalized Lymphatic Anomaly, Kaposiform Lymphangiomatosis, and Gorham-Stout DiseaseMichio Ozeki, Akihiro Fujino, Kentaro Matsuoka, et al.
Pediatric Nephrology (Berlin, Germany)|January 24, 2024
WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasiaMari Kurokawa, Manao Nishimura, Kei Nishiyama, et al.
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