Similar articles for PMID: 15122424

Year	Number of Results
1869	1
1876	1
1896	1
1912	1
1917	1
1922	1
1924	2
1932	1
1937	1
1948	1
1949	2
1955	1
1957	1
1959	1
1962	1
1977	1
1978	2
1979	2
1982	2
1985	2
1990	2
1991	2
1993	5
1994	6
1995	3
1996	4
1997	2
1998	3
1999	3
2000	4
2001	6
2002	4
2003	4
2004	1
2005	5
2007	1
2008	4
2009	2
2010	4
2011	5
2012	5
2013	3
2014	7
2015	11
2016	1
2017	5
2018	2
2020	4
2021	1
2022	5
2024	0

1

Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosis.

Albano LM, Sakae PP, Mataloun MM, Leone CR, Bertola DR, Kim CA. Albano LM, et al. Rev Hosp Clin Fac Med Sao Paulo. 2004 Apr;59(2):89-92. doi: 10.1590/s0041-87812004000200008. Epub 2004 Apr 26. Rev Hosp Clin Fac Med Sao Paulo. 2004. PMID: 15122424

2

Schinzel-Giedion syndrome and congenital megacalyces.

Herman TE, Sweetser DA, McAlister WH, Dowton SB. Herman TE, et al. Pediatr Radiol. 1993;23(2):111-2. doi: 10.1007/BF02012399. Pediatr Radiol. 1993. PMID: 8516031

3

Three new cases of the Schinzel-Giedion syndrome and review of the literature.

Labrune P, Lyonnet S, Zupan V, Imbert MC, Goutieres F, Hubert P, Le Merrer M. Labrune P, et al. Am J Med Genet. 1994 Mar 1;50(1):90-3. doi: 10.1002/ajmg.1320500120. Am J Med Genet. 1994. PMID: 8160760 Review.

4

Schinzel-Giedion syndrome: report of two sibs.

Antich J, Manzanares R, Camarasa F, Krauel X, Vila J, Cusi V. Antich J, et al. Am J Med Genet. 1995 Oct 23;59(1):96-9. doi: 10.1002/ajmg.1320590119. Am J Med Genet. 1995. PMID: 8849020

5

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.

Lehman AM, McFadden D, Pugash D, Sangha K, Gibson WT, Patel MS. Lehman AM, et al. Am J Med Genet A. 2008 May 15;146A(10):1299-306. doi: 10.1002/ajmg.a.32277. Am J Med Genet A. 2008. PMID: 18398855

6

Schinzel-Giedion syndrome.

Verloes A, Moës D, Palumbo L, Elmer C, François A, Bricteux G. Verloes A, et al. Eur J Pediatr. 1993 May;152(5):421-3. doi: 10.1007/BF01955902. Eur J Pediatr. 1993. PMID: 8319710

7

The Schinzel-Giedion syndrome. A case report and review of the literature.

Pul M, Yilmaz N, Komsuoglu B. Pul M, et al. Clin Pediatr (Phila). 1990 Apr;29(4):235-9. doi: 10.1177/000992289002900407. Clin Pediatr (Phila). 1990. PMID: 2184969 Review.

8

Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features.

Carvalho E, Honjo R, Magalhães M, Yamamoto G, Rocha K, Naslavsky M, Zatz M, Passos-Bueno MR, Kim C, Bertola D. Carvalho E, et al. Am J Med Genet A. 2015 May;167A(5):1039-46. doi: 10.1002/ajmg.a.36789. Epub 2015 Feb 7. Am J Med Genet A. 2015. PMID: 25663181

9

Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotype.

Ozkinay FF, Akisü M, Kültürsay N, Oral R, Tansug N, Sapmaz G. Ozkinay FF, et al. Clin Genet. 1996 Sep;50(3):145-8. doi: 10.1111/j.1399-0004.1996.tb02369.x. Clin Genet. 1996. PMID: 8946113

10

Progressive brain atrophy in Schinzel-Giedion syndrome with a SETBP1 mutation.

Takeuchi A, Okamoto N, Fujinaga S, Morita H, Shimizu J, Akiyama T, Ninomiya S, Takanashi J, Kubo T. Takeuchi A, et al. Eur J Med Genet. 2015 Aug;58(8):369-71. doi: 10.1016/j.ejmg.2015.05.006. Epub 2015 Jun 19. Eur J Med Genet. 2015. PMID: 26096993

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

132 results

Results by year