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Items: 1 to 20 of 86

1.

Case report of schizophrenia in adolescent with Russell-Silver syndrome.

Inoue K, Natsuyama T, Miyaoka H.

Psychiatry Clin Neurosci. 2014 Jul;68(7):582. doi: 10.1111/pcn.12169. Epub 2014 Apr 13. No abstract available.

2.

Ophthalmological findings in children and adolescents with Silver-Russell syndrome.

Andersson Grönlund M, Dahlgren J, Aring E, Kraemer M, Hellström A.

Br J Ophthalmol. 2011 May;95(5):637-41. doi: 10.1136/bjo.2010.184457. Epub 2010 Aug 30.

PMID:
20805133
3.

Generalized lichen nitidus in Russell-Silver syndrome.

Kanai C, Terao M, Tanemura A, Miyoshi Y, Ozono K, Katayama I.

Pediatr Dermatol. 2013 Jan-Feb;30(1):150-1. doi: 10.1111/j.1525-1470.2011.01613.x. Epub 2012 Feb 14.

PMID:
22329413
4.

The first case of Silver-Russell syndrome accompanied by linea alba hernia in China.

Wong KF, Wong WW, Li BX, Song YZ.

Singapore Med J. 2010 Jan;51(1):e9-e11.

5.

Myoclonus-dystonia syndrome associated with Russell Silver syndrome.

Augustine EF, Blackburn J, Pellegrino JE, Miller R, Mink JW.

Mov Disord. 2013 Jun;28(6):841-2. doi: 10.1002/mds.25483. Epub 2013 May 23. No abstract available.

6.

Autistic regression in a child with Silver-Russell syndrome and maternal UPD 7.

Vardi O, Davidovitch M, Vinkler C, Michelson M, Lerman-Sagie T, Lev D.

Eur J Paediatr Neurol. 2012 Jan;16(1):95-8. doi: 10.1016/j.ejpn.2011.05.009. Epub 2011 Jul 12.

PMID:
21752678
7.

Peripubertal hypoglycemia--an unusual cause.

Gangadhar P, Walia R, Bhansali A.

J Pediatr Endocrinol Metab. 2012;25(1-2):199-201.

PMID:
22570977
8.

Neonatal Silver-Russell syndrome with maternal uniparental heterodisomy, trisomy 7 mosaicism, and dysplasia of the cerebellum.

Abdelhedi F, El Khattabi L, Cuisset L, Tsatsaris V, Viot G, Druart L, Lebbar A, Dupont JM.

Am J Clin Pathol. 2014 Aug;142(2):248-53. doi: 10.1309/AJCPBLMPRXKU1JUE.

PMID:
25015868
9.

Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients.

Bruce S, Hannula-Jouppi K, Puoskari M, Fransson I, Simola KO, Lipsanen-Nyman M, Kere J.

J Med Genet. 2010 Dec;47(12):816-22. doi: 10.1136/jmg.2009.069427. Epub 2009 Sep 14.

PMID:
19752157
10.

Dilated cardiomyopathy in a 32-year-old woman with Russell-Silver syndrome.

Ryan TD, Gupta A, Gupta D, Goldenberg P, Taylor MD, Lorts A, Jefferies JL.

Cardiovasc Pathol. 2014 Jan-Feb;23(1):21-7. doi: 10.1016/j.carpath.2013.08.004. Epub 2013 Sep 24.

PMID:
24075556
11.

[Russell Silver syndrome: report of three cases and review of the literature].

Lamzouri A, Ratbi I, Sefiani A.

Pan Afr Med J. 2013 Mar 8;14:91. doi: 10.11604/pamj.2013.14.91.1645. Print 2013. Review. French. No abstract available.

12.

Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7.

Stark Z, Ryan MM, Bruno DL, Burgess T, Savarirayan R.

Am J Med Genet A. 2010 Sep;152A(9):2342-5. doi: 10.1002/ajmg.a.33590.

PMID:
20684011
13.

Family caregiver distress with children having rare genetic disorders: a qualitative study involving Russell-Silver Syndrome in Taiwan.

Weng HJ, Niu DM, Turale S, Tsao LI, Shih FJ, Yamamoto-Mitani N, Chang CC, Shih FJ.

J Clin Nurs. 2012 Jan;21(1-2):160-9. doi: 10.1111/j.1365-2702.2010.03583.x. Epub 2011 Mar 16.

PMID:
21410572
14.

17p13.1 microduplication in a boy with Silver-Russell syndrome features and intellectual disability.

Coutton C, Devillard F, Vieville G, Amblard F, Lopez G, Jouk PS, Satre V.

Am J Med Genet A. 2012 Oct;158A(10):2564-70. doi: 10.1002/ajmg.a.35553. Epub 2012 Aug 17.

PMID:
22903743
15.

Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features.

Eggermann T, Spengler S, Begemann M, Binder G, Buiting K, Albrecht B, Spranger S.

Clin Genet. 2012 Mar;81(3):298-300. doi: 10.1111/j.1399-0004.2011.01719.x. Epub 2011 Dec 28. No abstract available.

PMID:
22211632
16.

Russell-Silver syndrome due to paternal H19/IGF2 hypomethylation in a patient conceived using intracytoplasmic sperm injection.

Chopra M, Amor DJ, Sutton L, Algar E, Mowat D.

Reprod Biomed Online. 2010 Jun;20(6):843-7. doi: 10.1016/j.rbmo.2010.02.025. Epub 2010 Mar 4.

PMID:
20385510
17.

Clinical utility gene card for: Silver-Russell syndrome.

Eggermann T, Buiting K, Temple IK.

Eur J Hum Genet. 2011 Mar;19(3). doi: 10.1038/ejhg.2010.202. Epub 2010 Dec 8. No abstract available.

18.

Epigenetic signatures of Silver-Russell syndrome.

Abu-Amero S, Wakeling EL, Preece M, Whittaker J, Stanier P, Moore GE.

J Med Genet. 2010 Mar;47(3):150-4. doi: 10.1136/jmg.2009.071316. Review. No abstract available.

PMID:
20305090
19.

Anaesthesia for orphan disease: management of an infant with Silver-Russell syndrome.

Passier RH, Verwijs E, Driessen JJ.

Eur J Anaesthesiol. 2014 Jun;31(6):336-8. doi: 10.1097/EJA.0000000000000013. No abstract available.

PMID:
24276373
20.

[Silver syndrome: report of a family with 5 cases].

Cen ZD, Wang ZZ, Lu XJ, Ouyang ZY, Xie F, Luo W.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):500. doi: 10.3760/cma.j.issn.1003-9406.2013.04.024. Chinese. No abstract available.

PMID:
23926023

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