288 related articles for article (PubMed ID: 26958139)
1. Williams-Beuren syndrome associated with single kidney and nephrocalcinosis: a case report.
Abidi K; Jellouli M; Ben Rabeh R; Hammi Y; Gargah T
Pan Afr Med J; 2015; 22():276. PubMed ID: 26958139
[TBL] [Abstract][Full Text] [Related]
2. [Diagnosis of a case with Williams-Beuren syndrome with nephrocalcinosis using chromosome microarray analysis].
Jin SJ; Liu M; Long WJ; Luo XP
Zhonghua Er Ke Za Zhi; 2016 Dec; 54(12):941-945. PubMed ID: 27938597
[No Abstract] [Full Text] [Related]
3. Williams syndrome with severe hypercalcaemia.
Gupta V; Pandita A; Panghal A; Kallem VR
BMJ Case Rep; 2018 Sep; 2018():. PubMed ID: 30262523
[TBL] [Abstract][Full Text] [Related]
4. Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome.
Baştuğ F; Nalçacıoğlu H; Baş VN; Tekatlı-Çelik B; Çetinkaya H; Yel S
Turk J Pediatr; 2018; 60(2):210-215. PubMed ID: 30325132
[TBL] [Abstract][Full Text] [Related]
5. FISH analysis in both classical and atypical cases of Williams-Beuren syndrome.
Hou JW; Wang JK; Wang TR
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1998; 39(6):398-403. PubMed ID: 9926515
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Clinical expression of familial Williams-Beuren syndrome in a Turkish family.
Parlak M; Nur BG; Mıhçı E; Durmaz E; Karaüzüm SB; Akcurin S; Bircan İ
J Pediatr Endocrinol Metab; 2014 Jan; 27(1-2):153-8. PubMed ID: 24057591
[TBL] [Abstract][Full Text] [Related]
9. [Syndromes 5. Williams-Beuren Syndrome].
Hoff M; van Hagen JM; Baart JA; Vissink A
Ned Tijdschr Tandheelkd; 1998 Oct; 105(10):368-9. PubMed ID: 11928452
[TBL] [Abstract][Full Text] [Related]
10. [Early revealing of Williams-Beuren syndrome by digestive disorders].
de Montgolfier-Aubron I; Burglen L; Chavet MS; Tevissen H; Perrot C; Baudon JJ; Gold F
Arch Pediatr; 2000 Oct; 7(10):1085-7. PubMed ID: 11075265
[TBL] [Abstract][Full Text] [Related]
11. Williams-Beuren syndrome: an update and review for the primary physician.
Lashkari A; Smith AK; Graham JM
Clin Pediatr (Phila); 1999 Apr; 38(4):189-208. PubMed ID: 10326175
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH).
Sugayama SM; Koch VH; Furusawa EA; Leone C; Kim CA
Rev Hosp Clin Fac Med Sao Paulo; 2004 Oct; 59(5):266-72. PubMed ID: 15543398
[TBL] [Abstract][Full Text] [Related]
14. Recurrent achalasia in a child with Williams-Beuren syndrome.
Pereza N; Barbarić I; Ostojić S; Cace N; Kapović M
Coll Antropol; 2011 Sep; 35(3):941-4. PubMed ID: 22053584
[TBL] [Abstract][Full Text] [Related]
15. Incidence and spectrum of renal abnormalities in Williams-Beuren syndrome.
Pankau R; Partsch CJ; Winter M; Gosch A; Wessel A
Am J Med Genet; 1996 May; 63(1):301-4. PubMed ID: 8723124
[TBL] [Abstract][Full Text] [Related]
16. Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms.
Brøndum-Nielsen K; Beck B; Gyftodimou J; Hørlyk H; Liljenberg U; Petersen MB; Pedersen W; Petersen MB; Sand A; Skovby F; Stafanger G; Zetterqvist P; Tommerup N
Hum Genet; 1997 Jan; 99(1):56-61. PubMed ID: 9003495
[TBL] [Abstract][Full Text] [Related]
17. Echocardiographic findings in patients with Williams-Beuren syndrome.
Scheiber D; Fekete G; Urban Z; Tarjan I; Balaton G; Kosa L; Nagy K; Vajo Z
Wien Klin Wochenschr; 2006 Sep; 118(17-18):538-42. PubMed ID: 17009066
[TBL] [Abstract][Full Text] [Related]
18. Cardiovascular spectrum in Williams-Beuren syndrome: the Mexican experience in 40 patients.
De Rubens Figueroa J; Rodríguez LM; Hach JL; Del Castillo Ruíz V; Martínez HO
Tex Heart Inst J; 2008; 35(3):279-85. PubMed ID: 18941598
[TBL] [Abstract][Full Text] [Related]
19. Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study.
Yau EK; Lo IF; Lam ST
Hong Kong Med J; 2004 Feb; 10(1):22-7. PubMed ID: 14967851
[TBL] [Abstract][Full Text] [Related]
20. Williams syndrome and the elastin gene in Thai patients.
Ruangdaraganon N; Tocharoentanaphol C; Kotchabhakdi N; Khowsathit P
J Med Assoc Thai; 1999 Nov; 82 Suppl 1():S174-8. PubMed ID: 10730539
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
