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Items: 1 to 20 of 227896

1.

Pharmacotherapeutic Considerations for Individuals with Down Syndrome.

Hefti EJ, Blanco JG.

Pharmacotherapy. 2016 Dec 8. doi: 10.1002/phar.1880. [Epub ahead of print]

PMID:
27931082
2.

The importance of genetic factors for the development of arthropathy: a longitudinal study of children and adolescents with haemophilia A.

Gomperts ED, Schwarz J, Donfield SM, Lail AE, Astermark J, Hoots WK, Winkler CA, Berntorp E.

Thromb Haemost. 2016 Dec 8. [Epub ahead of print]

PMID:
27929201
4.

Evaluation of Pulse Oximetry in the Early Detection of Cyanotic Congenital Heart Disease in Newborns.

Movahedian AH, Mosayebi Z, Sagheb S.

J Tehran Heart Cent. 2016 Apr 13;11(2):73-78.

PMID:
27928258
5.

Hemivertebra Resection With Instrumented Fusion by Posterior Approach in Children.

Piantoni L, Francheri Wilson IA, Tello CA, Noel MA, Galaretto E, Remondino RG, Bersusky ES.

Spine Deform. 2015 Nov;3(6):541-548. doi: 10.1016/j.jspd.2015.04.008.

PMID:
27927556
6.

LAMB2 mutation with different phenotypes in China
.

Zhang H, Cui J, Wang F, Xiao H, Ding J, Yao Y.

Clin Nephrol. 2016 Dec 7. [Epub ahead of print]

PMID:
27925579
7.

Prevalence of non-cardiovascular findings on CT angiography in children with congenital heart disease.

Malik A, Hellinger JC, Servaes S, Schwartz MC, Keller MS, Epelman M.

Pediatr Radiol. 2016 Dec 6. [Epub ahead of print]

PMID:
27924361
8.

Venovenous ECMO Support in an Infant With Single Ventricle Physiology and Catastrophic Pulmonary Venous Abnormalities.

Fernandez RP, Hayes D Jr, McConnell PI, Berman D.

World J Pediatr Congenit Heart Surg. 2016 Dec 6. pii: 2150135116677252. [Epub ahead of print]

PMID:
27923943
9.

Two Rare Vascular Rings With Ductal Origin of the Left Pulmonary Artery: A Previously Unrecognized Syndrome?

Thankavel PP, Guleserian KJ, Anderson RH.

World J Pediatr Congenit Heart Surg. 2016 Dec 6. pii: 2150135116675166. [Epub ahead of print]

PMID:
27923942
10.

Spinal Glomus Arteriovenous Malformation Presenting with a Subarachnoid Hemorrhage.

Jabbour P, Daou B, Atallah E, Al-Saiegh F, Alkhalili K, Tjoumakaris S.

World Neurosurg. 2016 Dec 3. pii: S1878-8750(16)31271-2. doi: 10.1016/j.wneu.2016.11.123. [Epub ahead of print]

PMID:
27923749
11.

Sleep EEG patterns in infants with congenital Zika virus syndrome.

Carvalho MD, Miranda-Filho DB, van der Linden V, Sobral PF, Ramos RC, Rocha MÂ, Cordeiro MT, de Alencar SP, Nunes ML.

Clin Neurophysiol. 2016 Nov 14;128(1):204-214. doi: 10.1016/j.clinph.2016.11.004. [Epub ahead of print]

PMID:
27923187
12.

Changing epidemiology of non-cystic fibrosis bronchiectasis.

Bahçeci S, Karaman S, Nacaroğlu HT, Yazıcı S, Girit S, Ünsal-Karkıner Ş, Can D.

Turk J Pediatr. 2016;58(1):19-26.

PMID:
27922232
13.

Teratogenic Effect of Radotinib: Case Report.

Cheon J, Ahn JW, Park KM, Lee G, Jo YS.

Anticancer Res. 2016 Dec;36(12):6599-6601.

PMID:
27919989
14.

A CGH array procedure to detect PAX6 gene structural defects.

Franzoni A, Russo PD, Baldan F, D'Elia AV, Puppin C, Penco S, Damante G.

Mol Cell Probes. 2016 Dec 2. pii: S0890-8508(16)30117-7. doi: 10.1016/j.mcp.2016.12.001. [Epub ahead of print]

PMID:
27919838
15.

Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber Syndrome.

Huang L, Couto JA, Pinto A, Alexandrescu S, Madsen JR, Greene AK, Sahin M, Bischoff J.

Pediatr Neurol. 2016 Oct 21. pii: S0887-8994(16)30598-7. doi: 10.1016/j.pediatrneurol.2016.10.010. [Epub ahead of print]

PMID:
27919468
16.

A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle.

Murgiano L, Jagannathan V, Piffer C, Diez-Prieto I, Bolcato M, Gentile A, Drögemüller C.

BMC Vet Res. 2016 Dec 5;12(1):276.

17.

Early Postnatal Hyperoxia in Mice Leads to Severe Persistent Vitreoretinopathy.

McMenamin PG, Kenny R, Tahija S, Lim J, Naranjo Golborne C, Chen X, Bouch S, Sozo F, Bui B.

Invest Ophthalmol Vis Sci. 2016 Dec 1;57(15):6513-6526. doi: 10.1167/iovs.16-19928.

PMID:
27918825
18.

Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype.

Skauli N, Wallace S, Chiang SC, Barøy T, Holmgren A, Stray-Pedersen A, Bryceson YT, Strømme P, Frengen E, Misceo D.

Genes (Basel). 2016 Nov 29;7(12). pii: E108.

19.

[Microsurgical management and outcomes of intramedullary spinal arteriovenous malformations: a report of 14 cases].

Zhang L, Jia WQ, Yang J.

Zhonghua Wai Ke Za Zhi. 2016 Dec 1;54(12):919-923. doi: 10.3760/cma.j.issn.0529-5815.2016.12.009. Chinese.

PMID:
27916035
20.

Facial nerve anomalies in paediatric cochlear implant candidates: radiological evaluation.

Palabiyik FB, Hacikurt K, Yazici Z.

J Laryngol Otol. 2016 Dec 5:1-6. [Epub ahead of print]

PMID:
27916008
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