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pro vyhledávání: '"39"'
Publikováno v:
World Neurosurgery. 143:e374-e383
Objective Conus medullaris teratomas are extremely rare, and the treatment experience has been limited. The purpose of the present study was to evaluate the clinical characteristics, radiological features, surgical outcomes, and prognosis of patients
Adverse Outcomes among Low-Risk Pregnancies at 39 to 41 Weeks: Stratified by Birth Weight Percentile
Publikováno v:
American Journal of Perinatology. 38:e269-e283
Objective This study aimed to assess the risk of adverse outcomes among low-risk pregnancies at 39 to 41 weeks, stratified by birth weight percentile. Study Design This retrospective cohort study utilized the U.S. vital statistics datasets (2013–20
Autor:
Casper N. Bang, Lars Idorn, G H Mohr, Gunnar Gislason, Christian Torp-Pedersen, Thomas A. Gerds, Jakob Raunsø, Mohamad El-Chouli, Morten Malmborg, Ole Ahlehoff
Publikováno v:
El-Chouli, M, Mohr, G H, Bang, C N, Malmborg, M, Ahlehoff, O, Torp-Pedersen, C, Gerds, T A, Idorn, L, Raunsø, J & Gislason, G 2021, ' Time Trends in Simple Congenital Heart Disease Over 39 Years : A Danish Nationwide Study ', Journal of the American Heart Association, vol. 10, no. 14, e020375 . https://doi.org/10.1161/JAHA.120.020375
El-Chouli, M, Mohr, G H, Bang, C N, Malmborg, M, Ahlehoff, O, Torp-Pedersen, C, Gerds, T A, Idorn, L, Raunsø, J & Gislason, G 2021, ' Time Trends in Simple Congenital Heart Disease Over 39 Years : A Danish Nationwide Study ', Journal of the American Heart Association, vol. 10, no. 14, 020375 . https://doi.org/10.1161/JAHA.120.020375
El-Chouli, M, Mohr, G H, Bang, C N, Malmborg, M, Ahlehoff, O, Torp-Pedersen, C, Gerds, T A, Idorn, L, Raunsø, J & Gislason, G 2021, ' Time trends in simple congenital heart disease over 39 years : A danish nationwide study ', Journal of the American Heart Association, vol. 10, no. 14, e020375 . https://doi.org/10.1161/JAHA.120.020375
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
El-Chouli, M, Mohr, G H, Bang, C N, Malmborg, M, Ahlehoff, O, Torp-Pedersen, C, Gerds, T A, Idorn, L, Raunsø, J & Gislason, G 2021, ' Time Trends in Simple Congenital Heart Disease Over 39 Years : A Danish Nationwide Study ', Journal of the American Heart Association, vol. 10, no. 14, 020375 . https://doi.org/10.1161/JAHA.120.020375
El-Chouli, M, Mohr, G H, Bang, C N, Malmborg, M, Ahlehoff, O, Torp-Pedersen, C, Gerds, T A, Idorn, L, Raunsø, J & Gislason, G 2021, ' Time trends in simple congenital heart disease over 39 years : A danish nationwide study ', Journal of the American Heart Association, vol. 10, no. 14, e020375 . https://doi.org/10.1161/JAHA.120.020375
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background We describe calendar time trends of patients with simple congenital heart disease. Methods and Results Using the nationwide Danish registries, we identified individuals diagnosed with isolated ventricular septal defect, atrial septal defec
Autor:
Valentina Dini, Angelo Massimiliano D'Erme, Giovanni Bagnoni, Agata Janowska, Marco Romanelli, Paolo Viacava, Teresa Oranges, Cristian Fidanzi, Riccardo Morganti, Flavia Manzo Margiotta, Claudio Spinelli
Pediatric melanoma is a rare form of the tumor whose epidemiology is widely increasing thanks to the improvement of dermoscopic and anatomopathologic diagnostic techniques. Although it is a tumor of considerable interest in adults, little has been de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afa893f6d5d667f09e9bf7e3215f6b5c
http://hdl.handle.net/11568/1117687
http://hdl.handle.net/11568/1117687
Autor:
Michael P. Glotzbecker, Kristin S. Livingston, Daniel J. Hedequist, Benjamin J. Shore, Michael T. Hresko, Patricia E. Miller
Publikováno v:
Journal of Pediatric Orthopaedics. 36:685-690
BACKGROUND Compartment syndrome in the absence of fracture is rare and poorly described within the pediatric literature. The purpose of this study was to report the varying etiologies, risk factors, and treatment outcomes associated with pediatric no
Publikováno v:
Journal of Neuroradiology. 43:148-154
Summary Objective MR imaging using diffusion-weighted (DW) images and delayed gadolinium-enhanced T1-weighted images is evolving into an alternative to second look surgery in detection of recurrent cholesteatomas. The aim of this study was to retrosp
Publikováno v:
Ginekologia polska. 88(7)
Objectives: The purpose of this study was to retrospectively analyze maternal and neonatal outcomes in pregnant women with mild gestational diabetes mellitus at 39 weeks compared to 40 weeks. Material and methods: Clinical data of 372 cases of mild g
Autor:
Chenglong Zhao, Qi Jia, Yan Lou, Dongyu Peng, Wei Wan, Zhipeng Wu, Nanzhe Zhong, Xinghai Yang, Xiaopan Cai, Jianru Xiao, Jian Yang
Publikováno v:
World Journal of Surgical Oncology
Background The surgical treatment of upper cervical spine metastases are controversial up to now. By summarizing and analyzing the clinical data of the upper cervical spine involved metastases treated surgically in our center, we mainly aimed to inve
Autor:
Aurélia Jacquette, Alice Goldenberg, Thierry Frebourg, Julien Thevenon, David Geneviève, Anne-Marie Guerrot, Andrée Delahaye-Duriez, Yline Capri, Bruno Leheup, François Lecoquierre, Florence Riccardi, Tiffany Busa, Laurent Villard, Pierre Cacciagli, Vincent Gatinois, Julien Mancini, Chantal Missirian, Lionel Van Maldergem, Massimiliano Rossi, Laurence Perrin, Catherine Vincent-Delorme, Pascale Saugier-Veber, Philippe Khau Van Kien, Gwenaël Nadeau, Annick Toutain, Alain Verloes, Sandrine Marlin, Rolph Pfundt, Elise Schaefer, Arthur Sorlin, Vincent Michaud, Christel Thauvin-Robinet, Philippe Parent, Cyril Mignot, Charles Coutton, Nicole Philip, Véronique Satre, Aude Tessier
Publikováno v:
American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, Wiley, 2016, 170 (11), pp.2847-2859. 〈10.1002/ajmg.a.37878〉
American Journal of Medical Genetics. Part A, 170, 2847-2859
American Journal of Medical Genetics Part A, Wiley, 2016, 170 (11), pp.2847-2859. ⟨10.1002/ajmg.a.37878⟩
American Journal of Medical Genetics Part A, 2016, 170 (11), pp.2847-2859. ⟨10.1002/ajmg.a.37878⟩
American Journal of Medical Genetics. Part A, 170, 11, pp. 2847-2859
American Journal of Medical Genetics Part A, Wiley, 2016, 170 (11), pp.2847-2859. 〈10.1002/ajmg.a.37878〉
American Journal of Medical Genetics. Part A, 170, 2847-2859
American Journal of Medical Genetics Part A, Wiley, 2016, 170 (11), pp.2847-2859. ⟨10.1002/ajmg.a.37878⟩
American Journal of Medical Genetics Part A, 2016, 170 (11), pp.2847-2859. ⟨10.1002/ajmg.a.37878⟩
American Journal of Medical Genetics. Part A, 170, 11, pp. 2847-2859
Item does not contain fulltext KBG syndrome, due to ANKRD11 alteration is characterized by developmental delay, short stature, dysmorphic facial features, and skeletal anomalies. We report a clinical and molecular study of 39 patients affected by KBG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9893a4cf738da58e20ba8d0b0c43ef2
https://hal.archives-ouvertes.fr/hal-01469066
https://hal.archives-ouvertes.fr/hal-01469066
Autor:
J. Mercier, J. Giordanetto, Hélios Bertin, Jean-Philippe Perrin, A. Cohen, Sang-Hwy Lee, N. Cohen, Pierre Corre
Publikováno v:
Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery. 45(6)
Repair of the mandibular deformity in hemifacial microsomia (HFM) remains controversial, and there is scant information in the literature regarding the late outcomes. The aim of this study was to evaluate architectural and aesthetic long-term outcome