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Best matches for "velocardiofacial syndrome":

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Items: 1 to 20 of 591

1.

Speech Therapy in Velocardiofacial Syndrome After Palatopharyngeal Pharyngoplasty.

Jiang L, Yang Y, Liu Q.

J Craniofac Surg. 2018 May 31. doi: 10.1097/SCS.0000000000004629. [Epub ahead of print]

PMID:
29863556
2.

Pierre Robin sequence: A comprehensive narrative review of the literature over time.

Giudice A, Barone S, Belhous K, Morice A, Soupre V, Bennardo F, Boddaert N, Vazquez MP, Abadie V, Picard A.

J Stomatol Oral Maxillofac Surg. 2018 May 17. pii: S2468-7855(18)30118-6. doi: 10.1016/j.jormas.2018.05.002. [Epub ahead of print]

PMID:
29777780
3.

Airway Anomalies in Patients With 22q11.2 Deletion Syndrome: A 5-Year Review.

Jones JW, Tracy M, Perryman M, Arganbright JM.

Ann Otol Rhinol Laryngol. 2018 Jun;127(6):384-389. doi: 10.1177/0003489418771711. Epub 2018 May 7.

PMID:
29732908
4.

Congenital and iatrogenic laryngeal and vocal abnormalities in patients with 22q11.2 deletion.

Ebert B, Sidman J, Morrell N, Roby BB.

Int J Pediatr Otorhinolaryngol. 2018 Jun;109:17-20. doi: 10.1016/j.ijporl.2018.03.006. Epub 2018 Mar 13.

PMID:
29728175
5.

An estimation of the prevalence of genomic disorders using chromosomal microarray data.

Gillentine MA, Lupo PJ, Stankiewicz P, Schaaf CP.

J Hum Genet. 2018 Apr 24. doi: 10.1038/s10038-018-0451-x. [Epub ahead of print]

PMID:
29691480
6.

22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate.

Carpeta S, Pineda T, Martínez MC, Osorio G, Porras-Hurtado GL, Rojas J, Zarante I, Moreno-Niño OM.

Cleft Palate Craniofac J. 2018 Jan 1:1055665618770307. doi: 10.1177/1055665618770307. [Epub ahead of print]

PMID:
29652534
7.

Hypocalcaemia in an adult: the importance of not overlooking the cause.

Abrantes C, Brigas D, Casimiro HJ, Madeira M.

BMJ Case Rep. 2018 Apr 5;2018. pii: bcr-2017-224108. doi: 10.1136/bcr-2017-224108.

PMID:
29622714
8.

Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.

Palmer LD, Butcher NJ, Boot E, Hodgkinson KA, Heung T, Chow EWC, Guna A, Crowley TB, Zackai E, McDonald-McGinn DM, Bassett AS.

Am J Med Genet A. 2018 Apr;176(4):936-944. doi: 10.1002/ajmg.a.38645.

PMID:
29575622
9.

Clinical Significance of the Levator Veli Palatini Muscle in Velocardiofacial Syndrome Patients: Implications in Velopharyngeal Incompetence and Pharyngeal Flap Surgery.

Myung Y, Ahn T, Kim BK, Jeong JH, Baek RM.

Cleft Palate Craniofac J. 2018 Apr;55(4):521-527. doi: 10.1177/1055665617732786. Epub 2017 Dec 14.

PMID:
29554449
10.

The interaction between neurocognitive functioning, subthreshold psychotic symptoms and pharmacotherapy in 22q11.2 deletion syndrome: A longitudinal comparative study.

Weinberger R, Weisman O, Guri Y, Harel T, Weizman A, Gothelf D.

Eur Psychiatry. 2018 Feb;48:20-26. doi: 10.1016/j.eurpsy.2017.10.010. Epub 2018 Jan 10.

PMID:
29331595
11.

Characteristics and outcomes of children with ductal-dependent congenital heart disease and esophageal atresia/tracheoesophageal fistula: A multi-institutional analysis.

Puri K, Morris SA, Mery CM, Wang Y, Moffett BS, Heinle JS, Rodriguez JR, Shekerdemian LS, Cabrera AG.

Surgery. 2018 Apr;163(4):847-853. doi: 10.1016/j.surg.2017.09.010. Epub 2018 Jan 8.

PMID:
29325785
12.

The Scientific Knowledge Base for Treatment of Patients with Cleft Lip, Alveolus and Palate [Internet].

Forsetlund L, Semb G, Farah MG, Flottorp S.

Oslo, Norway: Knowledge Centre for the Health Services at The Norwegian Institute of Public Health (NIPH); 2009 Oct.

13.

Congenital respiratory tract disorders in 22q11.2 deletion syndrome.

Verheij E, Speleman L, Mink van der Molen AB, Thomeer HGXM.

Int J Pediatr Otorhinolaryngol. 2018 Jan;104:1-4. doi: 10.1016/j.ijporl.2017.10.028. Epub 2017 Oct 20.

PMID:
29287846
14.

Pediatric healthcare costs for patients with 22q11.2 deletion syndrome.

Benn P, Iyengar S, Crowley TB, Zackai EH, Burrows EK, Moshkevich S, McDonald-McGinn DM, Sullivan KE, Demko Z.

Mol Genet Genomic Med. 2017 Nov;5(6):631-638. doi: 10.1002/mgg3.310. Epub 2017 Aug 12.

15.

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

Homans JF, Tromp IN, Colo D, Schlösser TPC, Kruyt MC, Deeney VFX, Crowley TB, McDonald-McGinn DM, Castelein RM.

Am J Med Genet A. 2017 Nov 21. doi: 10.1002/ajmg.a.38545. [Epub ahead of print]

PMID:
29159873
16.

Psychosis Beyond the 22q11.2 Deletion: Do Additional Genetic Factors Play a Role?

Goes FS, Sawa A.

Am J Psychiatry. 2017 Nov 1;174(11):1027-1029. doi: 10.1176/appi.ajp.2017.17080910. No abstract available.

PMID:
29088933
17.

Health-related quality of life in 22q11.2 deletion syndrome: The child's perspective.

Joyce P, O'Rourke C, McDermott B, Heussler H.

J Paediatr Child Health. 2018 Mar;54(3):311-315. doi: 10.1111/jpc.13746. Epub 2017 Oct 30.

PMID:
29083072
18.

Adults with 22q11.2 deletion syndrome have a different velopharyngeal anatomy with predisposition to velopharyngeal insufficiency.

Filip C, Impieri D, Aagenæs I, Breugem C, Høgevold HE, Særvold T, Aukner R, Lima K, Tønseth K, Abrahamsen TG.

J Plast Reconstr Aesthet Surg. 2018 Apr;71(4):524-536. doi: 10.1016/j.bjps.2017.09.006. Epub 2017 Sep 22.

19.

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.

Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, Michaelovsky E, Schneider M, Eliez S, Antonarakis SE, Coleman K, Tomita-Mitchell A, Mitchell ME, Digilio MC, Dallapiccola B, Marino B, Philip N, Busa T, Kushan-Wells L, Bearden CE, Piotrowicz M, Hawuła W, Roberts AE, Tassone F, Simon TJ, van Duin EDA, van Amelsvoort TA, Kates WR, Zackai E, Johnston HR, Cutler DJ, Agopian AJ, Goldmuntz E, Mitchell LE, Wang T, Emanuel BS, Morrow BE; International 22q11.2 Consortium/Brain and Behavior Consortium*.

Circ Cardiovasc Genet. 2017 Oct;10(5). pii: e001690. doi: 10.1161/CIRCGENETICS.116.001690.

20.

Comparing the broad socio-cognitive profile of youth with Williams syndrome and 22q11.2 deletion syndrome.

Weisman O, Feldman R, Burg-Malki M, Keren M, Geva R, Diesendruck G, Gothelf D.

J Intellect Disabil Res. 2017 Dec;61(12):1083-1093. doi: 10.1111/jir.12424. Epub 2017 Oct 8.

PMID:
28990288

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