These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
199 related items for PubMed ID: 10215551
1. 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]
2. 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 29; 79(8):1087-90. PubMed ID: 22144119 [Abstract] [Full Text] [Related]
3. Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay. de Vries BB, van'tHoff WG, Surtees RA, Winter RM. Clin Dysmorphol; 2001 Apr 29; 10(2):115-21. PubMed ID: 11310991 [Abstract] [Full Text] [Related]
4. Galloway-Mowat syndrome. Akhtar N, Kiran S, Hafeez F. J Coll Physicians Surg Pak; 2008 Aug 29; 18(8):520-1. PubMed ID: 18798594 [Abstract] [Full Text] [Related]
5. 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]
6. Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome. Steiss JO, Gross S, Neubauer BA, Hahn A. Neuropediatrics; 2005 Oct 15; 36(5):332-5. PubMed ID: 16217710 [Abstract] [Full Text] [Related]
7. [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 Oct 15; 41(6):409-15. PubMed ID: 6487044 [Abstract] [Full Text] [Related]
8. The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patients. Hershkovitz E, Shalitin S, Levy J, Leiberman E, Weinshtock A, Varsano I, Gorodischer R. Isr J Med Sci; 1995 May 15; 31(5):293-7. PubMed ID: 7538982 [Abstract] [Full Text] [Related]
10. Anesthetic management of a patient with Galloway-Mowat syndrome. Bailey A, Georges L. Paediatr Anaesth; 2007 Nov 15; 17(11):1111-2. PubMed ID: 17897280 [No Abstract] [Full Text] [Related]
11. Congenital microcephaly, hiatus hernia and nephrotic syndrome: an autosomal recessive syndrome. Shapiro LR, Duncan PA, Farnsworth PB, Lefkowitz M. Birth Defects Orig Artic Ser; 1976 Nov 15; 12(5):275-8. PubMed ID: 953231 [No Abstract] [Full Text] [Related]
12. Podocyte proteins in Galloway-Mowat syndrome. Srivastava T, Whiting JM, Garola RE, Dasouki MJ, Ruotsalainen V, Tryggvason K, Hamed R, Alon US. Pediatr Nephrol; 2001 Dec 15; 16(12):1022-9. PubMed ID: 11793093 [Abstract] [Full Text] [Related]
13. 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]
16. Congenital nephrotic syndrome with microcephaly: report of a case. Yu CH, Tsai WS, Wang PJ, Tsau YK, Tseng GC, Wang TR. J Formos Med Assoc; 1994 Jun 15; 93(6):528-30. PubMed ID: 7858445 [Abstract] [Full Text] [Related]
17. Collapsing glomerulopathy in Galloway-Mowat syndrome: a case report and review of the literature. Sartelet H, Pietrement C, Noel LH, Sabouraud P, Birembaut P, Oligny LL, Roussel B, Doco-Fenzy M. Pathol Res Pract; 2008 Jun 15; 204(6):401-6. PubMed ID: 18276083 [Abstract] [Full Text] [Related]
18. Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face. Winter RM. Am J Med Genet; 1993 Nov 01; 47(6):917-20. PubMed ID: 7506485 [Abstract] [Full Text] [Related]
19. Recurrence of Galloway Mowat syndrome and associated prenatal imaging findings. Horton AL, Smith JK, Strauss RA. Prenat Diagn; 2009 Mar 01; 29(3):280-2. PubMed ID: 19177459 [No Abstract] [Full Text] [Related]