Αρχειοθήκη ιστολογίου

Τετάρτη 26 Απριλίου 2017

Consideration

Young, CSR; (2005) Consideration. [Solo exhibition]. Paula Cooper Gallery, New York. 16 November 2005 - 20 November 2005.

http://ift.tt/2q4D30W

Body: New Art from the UK

Young, CSR; Coupland, D; Ledwith, C; Grenville, B; (2005) Body: New Art from the UK. [Catalogue]. British Council: London.

http://ift.tt/2ovpWsi

Causal Inference via Algebraic Geometry: Feasibility Tests for Functional Causal Structures with Two Binary Observed Variables

Lee, CM; Spekkens, RW; (2017) Causal Inference via Algebraic Geometry: Feasibility Tests for Functional Causal Structures with Two Binary Observed Variables. Journal of Causal Inference , Article 20160013. 10.1515/jci-2016-0013 .

http://ift.tt/2q4JctZ

Zoology: War of the Worms

Telford, MJ; Copley, RR; (2016) Zoology: War of the Worms. Current Biology , 26 (8) R335-R337. 10.1016/j.cub.2016.03.015 . Green open access

http://ift.tt/2ovpfzm

Clinical failure is more common in young children with acute otitis media who receive a short course of antibiotics compared with standard duration

Venekamp, RP; Schilder, AGM; (2017) Clinical failure is more common in young children with acute otitis media who receive a short course of antibiotics compared with standard duration. Evidence-Based Medicine 10.1136/ebmed-2017-110697 . (In press). Green open access

http://ift.tt/2q4VOBm

Frank-Thomas Ott, Die zweite Philippica als Flugschrift in der späten Republik, Berlin – Boston (De Gruyter), 2013

Manuwald, G; (2016) Frank-Thomas Ott, Die zweite Philippica als Flugschrift in der späten Republik, Berlin – Boston (De Gruyter), 2013. Klio , 98 (2) pp. 773-777. 10.1515/klio-2016-0077 .

http://ift.tt/2ovyrDO

Otorhinolaryngologic manifestations of Hartsfield syndrome: Case series and review of literature

Publication date: July 2017
Source:International Journal of Pediatric Otorhinolaryngology, Volume 98
Author(s): Jeremie D. Oliver, Deanna C. Menapace, Shelagh A. Cofer
Diagnosis of Hartsfield syndrome includes recognition of three distinct clinical anomalies: holoprosencephaly, ectrodactyly, and bilateral cleft-lip and palate syndrome. A family including three male siblings all affected by Hartsfield syndrome presented to our institution for care. An autosomal dominant variant in Fibroblast Growth Factor Receptor 1 (FGFR1) was identified. This report focuses on otorhinolaryngologic manifestationsof Hartsfield syndrome, previously undescribed, including midline defects of holoprosencephaly, bilateral cleft-lip and palate, retrognathia, gastroesophageal reflux disease, external ear anomalies, eustachian tube dysfunction, and midface abnormalities, in addition to multidisciplinary, long-term management strategies. Multidisciplinary management is imperative in the care of these children with modification of approach based on their medical complexity.



http://ift.tt/2phRuys