117 related articles for article (PubMed ID: 19597063)
1. Images in cardiovascular medicine. Dynamic left main coronary artery obstruction associated with Williams syndrome.
Yan BP; Kiernan TJ; Rosenfield K; Garasic JM; de Moor M
Circulation; 2009 Jul; 120(2):181-2. PubMed ID: 19597063
[No Abstract] [Full Text] [Related]
2. [Genetic diagnosis of Williams syndrome].
Urbán Z; Kiss E; Kádár K; Szabolcs J; Csiszár K; Boyd DC; Fekete G
Orv Hetil; 1997 Jul; 138(27):1749-52. PubMed ID: 9273487
[TBL] [Abstract][Full Text] [Related]
3. [Williams syndrome--developmental syndrome's common cardiovascular disorders].
Peippo M; Hiippala A; Raatikka M; Westerlund A; Johansson R; Arvio M; Eronen M
Duodecim; 2001; 117(5):505-12. PubMed ID: 12116777
[No Abstract] [Full Text] [Related]
4. Infantile spasms in two children with Williams syndrome.
Tsao CY; Westman JA
Am J Med Genet; 1997 Jul; 71(1):54-6. PubMed ID: 9215769
[TBL] [Abstract][Full Text] [Related]
5. Williams-Beuren Syndrome and Burkitt Leukemia.
Zhukova N; Naqvi A
J Pediatr Hematol Oncol; 2013 Jan; 35(1):e30-2. PubMed ID: 23018576
[TBL] [Abstract][Full Text] [Related]
6. Progressive left main coronary artery obstruction leading to myocardial infarction in a child with Williams syndrome.
Bonnet D; Cormier V; Villain E; Bonhoeffer P; Kachaner J
Eur J Pediatr; 1997 Oct; 156(10):751-3. PubMed ID: 9365061
[TBL] [Abstract][Full Text] [Related]
7. Molecular cytogenetic diagnosis of Williams syndrome.
Hirota H; Matsuoka R; Kimura M; Imamura S; Joh-o K; Ando M; Takao A; Momma K
Am J Med Genet; 1996 Aug; 64(3):473-7. PubMed ID: 8862624
[TBL] [Abstract][Full Text] [Related]
8. Coronary Artery Involvement of Williams Syndrome in Infants and Surgical Revascularization Strategy.
Federici D; Ranghetti A; Merlo M; Terzi A; Di Dedda GB; Marcora S; Marrone C; Ciuffreda M; Seddio F; Galletti L
Ann Thorac Surg; 2016 Jan; 101(1):359-61. PubMed ID: 26694280
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.
Brewer CM; Morrison N; Tolmie JL
Arch Dis Child; 1996 Jan; 74(1):59-61. PubMed ID: 8660051
[TBL] [Abstract][Full Text] [Related]
10. Arterial hypertension in a child with Williams-Beuren syndrome (7q11.23 chromosomal deletion).
Sylos Cd; Pereira AC; Azeka E; Miura N; Mesquita SM; Ebaid M
Arq Bras Cardiol; 2002 Aug; 79(2):173-80. PubMed ID: 12219191
[TBL] [Abstract][Full Text] [Related]
11. Williams-Beuren syndrome and West "syndrome:" causal association or contiguous gene deletion syndrome?
Tercero MF; Cabrera López JC; Herrero MM; Rodríguez-Quiñones F
Am J Med Genet A; 2005 Mar; 133A(2):213-5. PubMed ID: 15633183
[No Abstract] [Full Text] [Related]
12. [Williams syndrome(Williams-Beuren syndrome), elfin face syndrome].
Ehara H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):263-5. PubMed ID: 11057222
[No Abstract] [Full Text] [Related]
13. Pelvic hypoplastic kidney in a patient with Williams-Beuren syndrome.
Stathaki M; Papadopoulou E; Koukouraki S; Sifakis S; Papadaki E; Kalmanti M; Karkavitsas N
Hell J Nucl Med; 2011; 14(2):160-2. PubMed ID: 21761019
[TBL] [Abstract][Full Text] [Related]
14. A new case of keratoconus associated with Williams-Beuren syndrome.
Viana MM; Frasson M; Leão LL; Stofanko M; Gonçalves-Dornelas H; Cunha Pda S; de Aguiar MJ
Ophthalmic Genet; 2013 Sep; 34(3):174-7. PubMed ID: 23167938
[TBL] [Abstract][Full Text] [Related]
15. Non-Hodgkin lymphoma in a child with Williams syndrome.
Amenta S; Moschovi M; Sofocleous C; Kostaridou S; Mavrou A; Fryssira H
Cancer Genet Cytogenet; 2004 Oct; 154(1):86-8. PubMed ID: 15381380
[TBL] [Abstract][Full Text] [Related]
16. Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome.
Leme DE; Souza DH; Mercado G; Pastene E; Dias A; Moretti-Ferreira D
Genet Mol Res; 2013 Sep; 12(3):3407-11. PubMed ID: 24065682
[TBL] [Abstract][Full Text] [Related]
17. Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion.
Gagliardi C; Bonaglia MC; Selicorni A; Borgatti R; Giorda R
J Med Genet; 2003 Jul; 40(7):526-30. PubMed ID: 12843326
[No Abstract] [Full Text] [Related]
18. Acute occlusion of the left anterior descending artery following intravascular ultrasound examination of left main coronary artery.
Lee CH; Lim IH; Tan HC
Int J Cardiol; 2007 Sep; 120(3):407-9. PubMed ID: 17250905
[No Abstract] [Full Text] [Related]
19. [Williams syndrome without cardiovascular abnormalities].
Cincinnati P; Genuardi M; Rutiloni C
Minerva Pediatr; 1998 Nov; 50(11):467-71. PubMed ID: 10207296
[TBL] [Abstract][Full Text] [Related]
20. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes.
Botta A; Novelli G; Mari A; Novelli A; Sabani M; Korenberg J; Osborne LR; Digilio MC; Giannotti A; Dallapiccola B
J Med Genet; 1999 Jun; 36(6):478-80. PubMed ID: 10874638
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]