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Journal Abstract Search
90 related items for PubMed ID: 18212429
1. Late-onset nephrotic syndrome in galloway-mowat syndrome: a case report. Hazza I, Najada AH. Saudi J Kidney Dis Transpl; 1999; 10(2):171-4. PubMed ID: 18212429 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
12. Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy. Cooperstone BG, Friedman A, Kaplan BS. Am J Med Genet; 1993 Aug 15; 47(2):250-4. PubMed ID: 8213914 [Abstract] [Full Text] [Related]
13. 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 15; 9(6):711-4. PubMed ID: 8747110 [Abstract] [Full Text] [Related]
15. Galloway-Mowat syndrome: neurologic features in two sibling pairs. Ekstrand JJ, Friedman AL, Stafstrom CE. Pediatr Neurol; 2012 Aug 15; 47(2):129-32. PubMed ID: 22759691 [Abstract] [Full Text] [Related]
16. [Association of early-onset nephrotic syndrome and microcephaly. Apropos of 4 cases in 2 families]. Gaudelus J, Leverger G, Rault G, Nathanson M, Giorno JL, Boccon-Gibod L, Levy M, Broyer M. Arch Fr Pediatr; 1984 Aug 15; 41(6):409-15. PubMed ID: 6487044 [Abstract] [Full Text] [Related]
17. Infantile nephrotic syndrome with microcephaly and global developmental delay: the Galloway Mowat Syndrome. Krishnamurthy S, Rajesh NG, Ramesh A, Zenker M. Indian J Pediatr; 2012 Aug 15; 79(8):1087-90. PubMed ID: 22144119 [Abstract] [Full Text] [Related]
18. Neuropathological homology in true Galloway-Mowat syndrome. Keith J, Fabian VA, Walsh P, Sinniah R, Robitaille Y. J Child Neurol; 2011 Apr 15; 26(4):510-7. PubMed ID: 21233460 [Abstract] [Full Text] [Related]
19. Nephrotic syndrome, microcephaly, and developmental delay: three separate syndromes. Meyers KE, Kaplan P, Kaplan BS. Am J Med Genet; 1999 Jan 29; 82(3):257-60. PubMed ID: 10215551 [Abstract] [Full Text] [Related]
20. Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype. Lin PY, Tseng MH, Zenker M, Rao J, Hildebrandt F, Lin SH, Lin CC, Chang JH, Hsu CH, Lee MD, Lin SP, Tsai JD. Orphanet J Rare Dis; 2018 Dec 17; 13(1):226. PubMed ID: 30558655 [Abstract] [Full Text] [Related] Page: [Next] [New Search]