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Best matches for "22q11 deletion":

22q11 deletion syndrome: current perspective. Hacıhamdioğlu B et al. Appl Clin Genet. (2015)

Fetal phenotype associated with the 22q11 deletion. Noël AC et al. Am J Med Genet A. (2014)

Immunological features of 22q11 deletion syndrome. Gennery AR et al. Curr Opin Pediatr. (2013)

Search results

Items: 1 to 20 of 693

1.

Perioperative and Anesthetic Considerations in Interrupted Aortic Arch.

Burbano-Vera N, Zaleski KL, Latham GJ, Nasr VG.

Semin Cardiothorac Vasc Anesth. 2018 May 1:1089253218775954. doi: 10.1177/1089253218775954. [Epub ahead of print]

PMID:
29742969
2.

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
3.

Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington's Disease.

Farrell M, Lichtenstein M, Crowley JJ, Filmyer DM, Lázaro-Muñoz G, Shaughnessy RA, Mackenzie IR, Hirsch-Reinshagen V, Stowe R, Evans JP, Berg JS, Szatkiewicz J, Josiassen RC, Sullivan PF.

Am J Psychiatry. 2018 May 1;175(5):400-407. doi: 10.1176/appi.ajp.2017.17060638. No abstract available.

PMID:
29712475
4.

DiGeorge syndrome : Relevance of psychiatric symptoms in undiagnosed adult patients.

Kraus C, Vanicek T, Weidenauer A, Khanaqa T, Stamenkovic M, Lanzenberger R, Willeit M, Kasper S.

Wien Klin Wochenschr. 2018 Apr;130(7-8):283-287. doi: 10.1007/s00508-018-1335-y. Epub 2018 Apr 18.

5.

The psychosocial impact of 22q11 deletion syndrome on patients and families: A systematic review.

Vo OK, McNeill A, Vogt KS.

Am J Med Genet A. 2018 Mar 25. doi: 10.1002/ajmg.a.38673. [Epub ahead of print]

PMID:
29575505
6.

Characteristics of prenatally detected right aortic arch cases in a single institution.

Velipasaoglu M, Sentürk M, Ayaz R, Atesli B, Tanir HM.

J Obstet Gynaecol. 2018 Mar 19:1-4. doi: 10.1080/01443615.2018.1430126. [Epub ahead of print]

PMID:
29553860
7.

Attentional functioning in individuals with 22q11 deletion syndrome: insight from ERPs.

Mannarelli D, Pauletti C, Accinni T, Carlone L, Frascarelli M, Lattanzi GM, Currà A, Fattapposta F.

J Neural Transm (Vienna). 2018 Jul;125(7):1043-1052. doi: 10.1007/s00702-018-1873-5. Epub 2018 Mar 8.

PMID:
29520614
8.

Platelet parameters in children with chromosome 22q11 deletion and conotruncal heart defects.

Anilkumar A, Vasudevan DM, Kappanayil M, Sundaram KR, Krishna Kumar R, Nampoothiri S.

Congenit Heart Dis. 2018 May;13(3):483-487. doi: 10.1111/chd.12600. Epub 2018 Mar 5.

PMID:
29508558
9.

Atypical microdeletion in 22q11 deletion syndrome reveals new candidate causative genes: A case report and literature review.

Shi H, Wang Z.

Medicine (Baltimore). 2018 Feb;97(8):e9936. doi: 10.1097/MD.0000000000009936. Review.

10.

22q11 Deletion Syndrome with Vascular Anomalies.

Maldjian P, Sanders AE.

J Clin Imaging Sci. 2018 Jan 22;8:1. doi: 10.4103/jcis.JCIS_66_17. eCollection 2018.

11.

Altered auditory processing and effective connectivity in 22q11.2 deletion syndrome.

Larsen KM, Mørup M, Birknow MR, Fischer E, Hulme O, Vangkilde A, Schmock H, Baaré WFC, Didriksen M, Olsen L, Werge T, Siebner HR, Garrido MI.

Schizophr Res. 2018 Jan 30. pii: S0920-9964(18)30048-3. doi: 10.1016/j.schres.2018.01.026. [Epub ahead of print]

PMID:
29395612
12.

Young Adult Outcomes for Children With 22q11 Deletion Syndrome and Comorbid ADHD.

Taylor LE, Kates WR, Fremont W, Antshel KM.

J Pediatr Psychol. 2018 Jan 25. doi: 10.1093/jpepsy/jsy002. [Epub ahead of print]

PMID:
29378061
13.

Association Between Tetralogy of Fallot and Tracheobronchial Branching Abnormalities: A New Clue for Pathogenesis?

Chassagnon G, Lefort B, Meot M, Carpentier E, Sirinelli D, Chantepie A, Morel B.

J Am Heart Assoc. 2017 Dec 29;7(1). pii: e006921. doi: 10.1161/JAHA.117.006921.

14.

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
15.

Resource Use and Morbidities in Pediatric Cardiac Surgery Patients with Genetic Conditions.

Furlong-Dillard J, Bailly D, Amula V, Wilkes J, Bratton S.

J Pediatr. 2018 Feb;193:139-146.e1. doi: 10.1016/j.jpeds.2017.09.085. Epub 2017 Dec 12.

PMID:
29246465
16.

Chromosome 22q11 deletion in a patient with pulmonary atresia, intact ventricular septum, and confluent branch pulmonary arteries.

Aggarwal V, Imamura M, Acuna C, Cabrera AG.

Cardiol Young. 2018 Mar;28(3):467-470. doi: 10.1017/S104795111700227X. Epub 2017 Dec 13.

PMID:
29233233
17.

Dopamine in high-risk populations: A comparison of subjects with 22q11.2 deletion syndrome and subjects at ultra high-risk for psychosis.

Vingerhoets C, Bloemen OJN, Boot E, Bakker G, de Koning MB, da Silva Alves F, Booij J, van Amelsvoort TAMJ.

Psychiatry Res Neuroimaging. 2018 Feb 28;272:65-70. doi: 10.1016/j.pscychresns.2017.11.014. Epub 2017 Nov 21.

PMID:
29174435
18.

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
19.

22q11 deletion syndrome: Parents' and children's experiences of educational and healthcare provision in the United Kingdom.

Cohen W, McCartney E, Crampin L.

J Child Health Care. 2017 Jun;21(2):142-152. doi: 10.1177/1367493516686203. Epub 2017 Jan 18.

PMID:
29119811
20.

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

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