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Best matches for "DiGeorge Syndrome":

Perioperative management of patients with DiGeorge syndrome undergoing cardiac surgery. Yeoh TY et al. J Cardiothorac Vasc Anesth. (2014)

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). McDonald-McGinn DM et al. Medicine (Baltimore). (2011)

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan. Jonas RK et al. Biol Psychiatry. (2014)

Search results

Items: 1 to 20 of 2353

1.

Gene expression profiling in the developing secondary palate in the absence of Tbx1 function.

Zoupa M, Xavier GM, Bryan S, Theologidis I, Arno M, Cobourne MT.

BMC Genomics. 2018 Jun 4;19(1):429. doi: 10.1186/s12864-018-4782-y.

2.

Syndromes with aortic involvement: pictorial review.

Zucker EJ.

Cardiovasc Diagn Ther. 2018 Apr;8(Suppl 1):S71-S81. doi: 10.21037/cdt.2017.09.14. Review.

3.

The effects of aberrant expression of LncRNA DGCR5/miR-873-5p/TUSC3 in lung cancer cell progression.

Luo J, Zhu H, Jiang H, Cui Y, Wang M, Ni X, Ma C.

Cancer Med. 2018 May 23. doi: 10.1002/cam4.1566. [Epub ahead of print]

4.

Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series.

Butcher NJ, Boot E, Lang AE, Andrade D, Vorstman J, McDonald-McGinn D, Bassett AS.

Am J Med Genet A. 2018 May 19. doi: 10.1002/ajmg.a.38708. [Epub ahead of print]

PMID:
29777584
5.

Immunodeficiency.

Justiz Vaillant AA, Qurie A.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2018 Jan-.
2018 May 2.

6.

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
7.

The rarest aortic arch anomaly a case report of asymptomatic isolation of the subclavian artery.

Taliana N, Gatt A, Borg A, Grech V.

Images Paediatr Cardiol. 2017 Apr-Jun;19(2):9-12.

8.

Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.

Liu N, Schoch K, Luo X, Pena LDM, Bhavana VH, Kukolich MK, Stringer S, Powis Z, Radtke K, Mroske C, Deak KL, McDonald MT, McConkie-Rosell A, Markert ML, Kranz PG, Stong N, Need AC, Bick D, Amaral MD, Worthey EA, Levy S; Undiagnosed Diseases Network (UDN), Wangler MF, Bellen HJ, Shashi V, Yamamoto S.

Hum Mol Genet. 2018 May 2. doi: 10.1093/hmg/ddy146. [Epub ahead of print]

PMID:
29726930
9.

Role of DiGeorge syndrome critical region gene 9, a long noncoding RNA, in gastric cancer.

Ni C, Yang P, Guo J, Ye M.

Onco Targets Ther. 2018 Apr 19;11:2259-2267. doi: 10.2147/OTT.S162253. eCollection 2018.

10.

DiGeorge Syndrome with Sacral Myelomeningocele and Epilepsy.

Alkan G, Emiroglu MK, Kartal A.

J Pediatr Neurosci. 2017 Oct-Dec;12(4):344-345. doi: 10.4103/jpn.JPN_92_17.

11.

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.

12.

Preoperative Physiology, Imaging, and Management of Interrupted Aortic Arch.

Friedman K.

Semin Cardiothorac Vasc Anesth. 2018 Apr 1:1089253218770198. doi: 10.1177/1089253218770198. [Epub ahead of print]

PMID:
29649938
13.

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
14.

The Combinational Use of CRISPR/Cas9 and Targeted Toxin Technology Enables Efficient Isolation of Bi-Allelic Knockout Non-Human Mammalian Clones.

Watanabe S, Sakurai T, Nakamura S, Miyoshi K, Sato M.

Int J Mol Sci. 2018 Apr 4;19(4). pii: E1075. doi: 10.3390/ijms19041075.

15.

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
16.

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
17.

Genetic Syndromes Associated with Congenital Cardiac Defects and Ophthalmologic Changes - Systematization for Diagnosis in the Clinical Practice.

Oliveira PHA, Souza BS, Pacheco EN, Menegazzo MS, Corrêa IS, Zen PRG, Rosa RFM, Cesa CC, Pellanda LC, Vilela MAP.

Arq Bras Cardiol. 2018 Jan;110(1):84-90. doi: 10.5935/abc.20180013. English, Portuguese.

18.

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
19.

22q11.2 Deletion Status and Perioperative Outcomes for Tetralogy of Fallot with Pulmonary Atresia and Multiple Aortopulmonary Collateral Vessels.

Mercer-Rosa L, Elci OU, Pinto NM, Tanel RE, Goldmuntz E.

Pediatr Cardiol. 2018 Jun;39(5):906-910. doi: 10.1007/s00246-018-1840-9. Epub 2018 Mar 8.

PMID:
29520463
20.

Pulmonary Alveolar Proteinosis.

Carrington JM, Hershberger DM.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2018 Jan-.
2018 Mar 20.

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