Zobrazeno 1 - 10
of 147
pro vyhledávání: '"Matthew T, Whitehead"'
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 5, p 1187 (2024)
Abnormalities of dental development and anatomy may suggest the presence of congenital or acquired anomalies. The detection of abnormalities, therefore, is an important skill for radiologists to achieve. Knowledge of dental embryology and an understa
Externí odkaz:
https://doaj.org/article/6f04f36345ba428984bec1589c313961
Autor:
Martine Uittenbogaard, Andrea L. Gropman, Matthew T. Whitehead, Christine A. Brantner, Eliana Gropman, Anne Chiaramello
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 3, p 1386 (2024)
We report the case of a four-year-old male patient with a complex medical history born prematurely as the result of intrauterine growth restriction due to placental insufficiency. His clinical manifestations included severe neurodevelopmental deficit
Externí odkaz:
https://doaj.org/article/5fbd095a83b34a408b6b62f70e9aa8a6
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 32, Iss , Pp 100886- (2022)
Maple syrup urine disease (MSUD) is an autosomal recessive metabolic disease resulting in impaired or absent breakdown of branched-chain amino acids (BCAA) valine, isoleucine, and leucine. Classic MSUD often presents in post-natal periods, at times b
Externí odkaz:
https://doaj.org/article/691566aea8d04341bdbd231462e85c9e
Autor:
Samiat Agunbiade, MD, Ayman Nada, MD, Phd, Sudhir Bhimaniya, MD, Matthew T. Whitehead, MD, Eman S. Mahdi, MD
Publikováno v:
Radiology Case Reports, Vol 15, Iss 4, Pp 382-386 (2020)
Chordomas are rare, slow growing malignant tumors derived from notochord remnants that can arise anywhere along the neuronal axis. Chordomas are particularly rare in patients under 20 years of age and tend to be intracranial in location, as opposed t
Externí odkaz:
https://doaj.org/article/7fd2a9c24b6a420cbc3175d482f1b60b
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
The urea cycle disorders (UCD) are rare genetic disorder due to a deficiency of one of six enzymes or two transport proteins that act to remove waste nitrogen in form of ammonia from the body. In this review, we focus on neuroimaging studies in OTCD
Externí odkaz:
https://doaj.org/article/f5fe6032f49b4b4392cd00ad13f0d97a
Autor:
Taeun Chang, Brenda Poindexter, Gregory M. Sokol, Patrick J Heagerty, Mark Smith, Jessica L Wisnowski, Amit M Mathur, Jeffrey Berman, Ping-Sun Keven Chen, James Dix, Trevor Flynn, Stanley Fricke, Seth D Friedman, Hayden W Head, Chang Y Ho, Beth Kline-Fath, Michael Oveson, Richard Patterson, Sumit Pruthi, Nancy Rollins, Yanerys M Ramos, John Rampton, Jerome Rusin, Dennis W Shaw, Jean Tkach, Shreyas Vasanawala, Arastoo Vossough, Matthew T Whitehead, Duan Xu, Kristen Yeom, Bryan Comstock, Sandra E Juul, Yvonne W Wu, Robert C McKinstry, Kaashif Ahmed, Mariana Beserga, Ellen Bendel-Stenzel, Lina Chalak, John Flibotte, Fernando Gonzalez, Andrea Lampland, Nathalie Maitre, Amit M. Mathur, Dennis Mayock, Ulrike Mietzsch, Rakesh Rao, David Riley, Krisa Van Meurs, Hendrik Weitkamp, Tai-Wei Wu, Toby Yanowitz
Publikováno v:
BMJ Open, Vol 11, Iss 4 (2021)
Introduction MRI and MR spectroscopy (MRS) provide early biomarkers of brain injury and treatment response in neonates with hypoxic-ischaemic encephalopathy). Still, there are challenges to incorporating neuroimaging biomarkers into multisite randomi
Externí odkaz:
https://doaj.org/article/b09a409f0adb4639a6db27d4bf00a9ad
Publikováno v:
Diagnostics, Vol 12, Iss 4, p 861 (2022)
Inborn errors of metabolism (IEM) are a group of disorders due to functional defects in one or more metabolic pathways that can cause considerable morbidity and death if not diagnosed early. While individually rare, the estimated global prevalence of
Externí odkaz:
https://doaj.org/article/eceedb60556a4e168e351536438b5618
Autor:
Rupa Radhakrishnan, Lindsey A.G. Shea, Sumit Pruthi, Victoria M. Silvera, Thangamadhan Bosemani, Nilesh K. Desai, Donald L. Gilbert, Orit A. Glenn, Carolina V. Guimaraes, Mai-Lan Ho, H. F. Samuel Lam, Mohit Maheshwari, David M. Mirsky, Helen R. Nadel, Sonia Partap, Gary R. Schooler, Unni K. Udayasankar, Matthew T. Whitehead, Jason N. Wright, Cynthia K. Rigsby
Publikováno v:
Journal of the American College of Radiology. 19:S240-S255
Autor:
Erica Jacobs, Matthew T. Whitehead
Publikováno v:
Pediatric Radiology. 53:121-130
Autor:
Nathan T, Cohen, Xiaozhen, You, Manu, Krishnamurthy, Leigh N, Sepeta, Anqing, Zhang, Chima, Oluigbo, Matthew T, Whitehead, Taha, Gholipour, Torsten, Baldeweg, Konrad, Wagstyl, Sophie, Adler, William D, Gaillard
Publikováno v:
Annals of Neurology. 92:503-511
The purpose of this study was to evaluate if focal cortical dysplasia (FCD) co-localization to cortical functional networks is associated with the temporal distribution of epilepsy onset in FCD.International (20 center), retrospective cohort from the