Results 61 to 70 of about 2,093 (107)

Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant. [PDF]

Front Pediatr
Nguyen TTT, Tran QTH, Nguyen HTT, Pham TQM, Tran D, Fukui K, Tsukaguchi H.   +6 more
europepmc   +1 more source

Simultaneous occurrence of bilateral retroperitoneal neuroblastoma and bifocal malignant mixed germ cell tumor in a pediatric patient with 16p11.2 microdeletion syndrome: a case report. [PDF]

Front Endocrinol (Lausanne)
Fan QX, Zhuang XM, Wen R, Wu XH, Luo HY, Yang HX, Kuang WY, Zhang BS, Zheng MC, Wu P.   +9 more
europepmc   +1 more source

Cephalic Pancreaticoduodenectomy With Right Nephrectomy for Traumatic Ruptured Wilms Tumor. [PDF]

Cureus
Apumayta ED, Sanchez N, Cayo E, Rioja M, Franco E.   +4 more
europepmc   +1 more source

Congenital nephrotic syndrome in a newborn with glycogen storage disease and Wilms tumor 1 (WT1) mutation. [PDF]

CEN Case Rep
Annicchiarico Petruzzelli L, De Marco O, Improda N, Giannattasio P, Luongo I, Carucci M, Brunetti B, Serio V, Minale B, Malgieri G.   +9 more
europepmc   +1 more source

Germline duplication of MYCN predisposes to childhood embryonal tumours. [PDF]

EBioMedicine
Taylor CA, May P, Stone TJ, Ahmed M, Chowdhury T, Tweddle DA, Wilson S, Hanscombe K, Hutchinson JC, Pickles JC, Sebire NJ, Jacques TS.   +11 more
europepmc   +1 more source

Recent advances in neonatal Beckwith-Wiedemann syndrome: from molecular diagnosis to multidisciplinary management-a narrative review. [PDF]

Transl Pediatr
Xue H, Hu Y, Wu X.
europepmc   +1 more source

Developmental reprogramming underlies chemotherapy resistance in favorable-histology Wilms tumor. [PDF]

Cell Rep
Fleming AM, Jablonowski CM, Jin H, Zhang S, Sona S, Lee HW, Dieseldorff Jones KM, Cheng C, Xu B, Morton CL, Woolard MA, Pichavaram P, Gehle DB, Natarajan S, Kodali K, Pagala V, High AA, Kumar Y, Burden S, Valentine V, Daria D, Harbour J, Vocelle D, Chang TC, Easton J, Olsen SR, Neale G, Pinto EM, Rehg JE, Janke L, Santiago T, George RE, Ma X, Zambetti GP, Davidoff AM, Chen T, Wu G, Chen X, Yang J, Murphy AJ.   +39 more
europepmc   +1 more source

Precision Medicine in Pediatric Nephrology: From Shared Clinical Phenotypes to Genotype-Guided Diagnosis and Management. [PDF]

Genes (Basel)
Dotis J, Printza N.
europepmc   +1 more source

A novel <i>de novo QRICH1</i> variant causing Ververi-Brady syndrome with infantile epileptic spasms syndrome: clinical and genetic analysis. [PDF]

Front Neurosci
Fang H, Wu X, Kuang X, Wu L, Zhang X, Wang L, Yang S, Liao H, Ning Z.   +8 more
europepmc   +1 more source