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Journal Abstract Search

199 related items for PubMed ID: 10215551

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  • 22. Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings.
    Chen CP, Lin SP, Liu YP, Tsai JD, Chen CY, Shih SL, Tsai FJ, Wu PC, Wang W.
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):212-6. PubMed ID: 21791310
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  • 28. Late-onset growth restriction in Galloway-Mowat syndrome: a case report.
    Kang L, Kuo PL, Lee KH, Liu YC, Chang CH, Chang FM, Lin SJ.
    Prenat Diagn; 2005 Feb; 25(2):159-62. PubMed ID: 15712336
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  • 30. Kidney in Galloway-Mowat syndrome: clinical spectrum with description of pathology.
    Cohen AH, Turner MC.
    Kidney Int; 1994 May; 45(5):1407-15. PubMed ID: 8072253
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  • 32. Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome.
    Colin E, Huynh Cong E, Mollet G, Guichet A, Gribouval O, Arrondel C, Boyer O, Daniel L, Gubler MC, Ekinci Z, Tsimaratos M, Chabrol B, Boddaert N, Verloes A, Chevrollier A, Gueguen N, Desquiret-Dumas V, Ferré M, Procaccio V, Richard L, Funalot B, Moncla A, Bonneau D, Antignac C.
    Am J Hum Genet; 2014 Dec 04; 95(6):637-48. PubMed ID: 25466283
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  • 33. Microcephaly and early-onset nephrotic syndrome--confusion in Galloway-Mowat syndrome.
    Sano H, Miyanoshita A, Watanabe N, Koga Y, Miyazawa Y, Yamaguchi Y, Fukushima Y, Itami N.
    Pediatr Nephrol; 1995 Dec 04; 9(6):711-4. PubMed ID: 8747110
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  • 34. Diagnosis delay a family of Galloway-Mowat Syndrome caused by a classical splicing mutation of Lage3.
    Chen Y, Yang Y, Yang Y, Rao J, Bai H.
    BMC Nephrol; 2023 Feb 08; 24(1):29. PubMed ID: 36755238
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  • 35. Corrected head circumference centiles as a possible predictor of developmental performance in high-risk neonatal intensive care unit survivors.
    Bolduc FV, Shevell MI.
    Dev Med Child Neurol; 2005 Nov 08; 47(11):766-70. PubMed ID: 16225741
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  • 38. A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report.
    Hyun HS, Kim SH, Park E, Cho MH, Kang HG, Lee HS, Miyake N, Matsumoto N, Tsukaguchi H, Cheong HI.
    BMC Med Genet; 2018 Jul 27; 19(1):131. PubMed ID: 30053862
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  • 39. An unusual case of nephrotic syndrome in a microcephalic infant: Answers.
    Baker E, Weaver D, Massengill S, Mittag D, Juusola J, Demmer L.
    Pediatr Nephrol; 2019 Nov 27; 34(11):2327-2329. PubMed ID: 31069511
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