Dmytriw, Adam Andrew Alrashed, Abdullah Enriquez-Marulanda, Alejandro Medhi, Gorky Mendes Pereira, Vitor
Published in
Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences
The natural history and outcome of unruptured posterior circulation dissecting fusiform aneurysms is not fully understood. These have a high risk of morbidity and mortality, not only due to natural history but also due to the challenging and controversial treatment approaches currently available compared to other types of intracranial aneurysms. We...
Abul-Kasim, Kasim Persson, Erik Levinsson, Anders Strömbeck, Anita Selariu, Eufrozina Ohlin, Acke
Published in
The neuroradiology journal
To determine the prevalence of vertebral hemangiomas (VHs), establish a new classification of VHs based on their MRI-signal pattern, and study their natural history. MRI of 1000 consecutive patients who underwent at least two MRI with an interval of at least 3 years. Growth rate and change of MRI-signal pattern during the follow-up period were the ...
card, daren c. jennings, w. bryan edwards, scott v.
Non-avian reptiles comprise a large proportion of amniote vertebrate diversity, with squamate reptiles—lizards and snakes—recently overtaking birds as the most species-rich tetrapod radiation. Despite displaying an extraordinary diversity of phenotypic and genomic traits, genomic resources in non-avian reptiles have accumulated more slowly than the...
Goodspeed, Kimberly Mosca, Lindsay R. Weitzel, Nicole C. Horning, Kyle Simon, Elijah W. Pfalzer, Anna C. Xia, Maya Langer, Katherine Freed, Amber Bone, Megan
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Published in
Frontiers in Neuroscience
Introduction SLC6A1 Neurodevelopmental Disorder (SLC6A1-NDD), first described in 2015, is a rare syndrome caused by a mutation in the SLC6A1 gene which encodes for the GABA Transporter 1 (GAT-1) protein. Epilepsy is one of the most common symptoms in patients and is often the primary treatment target, though the severity of epilepsy is variable. Th...
cavallina, ilaria d’alessandro, rossella brusa, chiara panero, elisa rolle, enrica rossi, francesca mongini, tiziana ricci, federica silvia
Congenital muscular dystrophies (CMDs) are a heterogeneous group of genetic neuromuscular disorders. They usually occur at birth or in early childhood, with delayed acquisition of motor milestones, and diffuse muscle weakness. A dystrophic pattern is evident on the muscle biopsy. They are highly variable both in terms of severity and clinical evolu...
Otero-Losada, Matilde Gubellini, Paolo Capani, Francisco Perez-Lloret, Santiago
Published in
Frontiers in Pharmacology
Miriti, Maria N Rawson, Ariel J Mansfield, Becky
Published in
Ecological applications : a publication of the Ecological Society of America
Natural history, loosely defined as the observational study of organisms in the habitats where they occur, is recognized at the roots of ecology. Although the centrality of natural history in ecology has shifted over time, natural history is currently in resurgence: many again consider it to be the foundation of ecological and evolutionary inquiry ...
cheloni, riccardo jackson, daniel moosajee, mariya
X-linked retinitis pigmentosa (RP) is a severe form of RP, often with early macular involvement. This study aimed to characterise the natural history of patients with a diagnosis of X-linked RP due to RP2 mutations. Clinical details, best-corrected visual acuity (BCVA) and multimodal retinal imaging were retrospectively collected from patients with...
Zhang, Jason Harish, Keerthi Speranza, Giancarlo Hartwell, Charlotte Garg, Karan Jacobowitz, Glenn Sadek, Mikel Maldonado, Thomas Kim, Danny Rockman, Caron
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Published in
Journal of vascular surgery
The existing RAA literature is largely comprised of reports of patients who underwent intervention. The objective of this study was to review the natural history of RAA. This single-institution retrospective analysis studied all patients with RAA diagnosed by CT imaging between 2015 and 2019, identified by our institutional radiology database. Imag...
Mohareb, Amir M Liu, Anne F Kim, Arthur Y Coffie, Patrick A Kouamé, Menan Gérard Freedberg, Kenneth A Boyd, Anders Hyle, Emily P
Published in
The Journal of infectious diseases
In people with hepatitis B virus (HBV) infection, persistence of hepatitis B e antigen (HBeAg) is associated with clinical progression and need for treatment. HBeAg loss represents partial immune control and is a critical event in the natural history of chronic HBV. We conducted a systematic review and meta-analysis of cohort studies that report HB...