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JMIR Research Protocols|November 28, 2024
Sleep Treatment Education Program for Cancer Survivors: Protocol for an Efficacy TrialBriana L Bice, Alexis L Michaud, Katherine G McCormick, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutationsJoanna McCauley, Navta Masand, Ruth McGowan, et al.
International Journal of Environmental Research and Public Health|December 24, 2016
Social Disparities in Exposure to Point-of-Sale Cigarette MarketingMohammad Siahpush, Paraskevi A Farazi, Jungyoon Kim, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|November 1, 1988
[Cardiac transplantation at the University Hospital Center of Nantes. 2 years' experience]T Petit, M Train, M Treilhaud, et al.
Biospectroscopy|August 26, 1998
FTIR characterization of heterocycles lumazine and violapterin in solution: effects of solvent on anionic formsA L Michaud, J A Herrick, J E Duplain, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|August 15, 2019
Association Between Weight Loss and Glycemic Outcomes: A Post Hoc Analysis of a Remote Patient Monitoring Program for Diabetes ManagementTzeyu L Michaud, Mohammad Siahpush, Paul Estabrooks, et al.
Science Advances|October 27, 2021
Ectopic expression of Irx3 and Irx5 in the paraventricular nucleus of the hypothalamus contributes to defects in Sim1 haploinsufficiencyJoe Eun Son, Zhengchao Dou, Siyi Wanggou, et al.
Annals of Clinical and Translational Neurology|June 9, 2022
Assessment of burden and segregation profiles of CNVs in patients with epilepsyClaudia Moreau, Frédérique Tremblay, Stefan Wolking, et al.
AJNR. American Journal of Neuroradiology|October 2, 2007
Diffusion tensor MR imaging reveals persistent white matter alteration after traumatic brain injury experienced during early childhoodW Yuan, S K Holland, V J Schmithorst, et al.
American Journal of Human Genetics|March 1, 1994
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophyL M Brzustowicz, B A Allitto, D Matseoane, et al.
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