Results 111 to 120 of about 43,622 (268)

Segmentation-by-Detection: A Cascade Network for Volumetric Medical Image Segmentation

, 2017
We propose an attention mechanism for 3D medical image segmentation. The method, named segmentation-by-detection, is a cascade of a detection module followed by a segmentation module. The detection module enables a region of interest to come to attention
Cobzas, Dana, Jagersand, Martin, Jaremko, Jacob L., Tang, Min, Zhang, Zichen   +4 more
core   +1 more source

Red‐light flashing pens and seizures in children

Developmental Medicine &Child Neurology, EarlyView.
Guidelines exist to limit seizure‐provoking visual stimuli. However, existing recommendations are not universally applied, and poorly regulated flickering lights are easily encountered in consumer products. Two girls experienced prolonged absence seizures triggered by a red‐light flickering pen.
Simone Gasparini, Alice Dainelli, Francesca Piras, Simona Balestrini, Renzo Guerrini   +4 more
wiley   +1 more source

The lateral hip instability test: Diagnostic accuracy for lateral or posterolateral femoral head undercoverage

Journal of Experimental Orthopaedics
Purpose To (i) describe the lateral hip instability test, developed to discriminate between stable versus unstable hips with lateral or posterolateral femoral head undercoverage, (ii) evaluate differences between painful hips that tested positive versus ...
Michael Wettstein, Kinga Michalewska, Sonia Ramos‐Pascual, Stefan Hefer, Elyazid Mouhsine, Mo Saffarini   +5 more
doaj   +1 more source

Hip dysplasia research at Ghent University: towards a new approach to assess hip quality? [PDF]

, 2006
C
Comhaire, Frank, Coopman, Frank, de Brabander, Katrien, Saunders, Jimmy, Schoonjans, Frank, van Bree, Henri   +5 more
core   +2 more sources

Neonates born at term with periventricular haemorrhagic infarction: Risk factors and clinical presentation

Developmental Medicine &Child Neurology, EarlyView.
This case series describes infants born near term with periventricular hemorrhagic infarction (PVHI), highlighting seizures as a common early symptom. Neonatal complications during delivery and pro‐thrombotic genetic mutations were slightly more common. MRI‐classified involvement was predominantly in the caudate vein territory.
Aleksandra Zaykova, Jeroen Dudink, Floris Groenendaal, Maarten H. Lequin, Manon J.N.L. Benders, Maria Luisa Tataranno, Elise Roze   +6 more
wiley   +1 more source

Hip dysplasia and dislocation in children with congenital disorders treated at a national rehabilitation institute

Revista Habanera de Ciencias Médicas, 2023
Introduction: Congenital musculoskeletal disorders often present hip malformations that affect gait and functional activities, therefore the importance of detecting them in a timely manner.
Erika Betzabé Oropeza Soria, Jenny Aurora Cornejo López, Herminio Teófilo Camacho Conchucos   +2 more
doaj  

La displasia congénita de cadera y el grupo sanguíneo [PDF]

, 1990
Este trabajo analiza la relación existente entre la displasia congénita de la cadera y el grupo sanguíneo. El estudio comprende 116 recién nacidos diagnosticados de displasia congenita de cadera a los que se le aplican los parámetros de grupo sanguí- neo
Camba Bouzas, S., Fernández, H.R., Fraga, M., León, R., Mosquera, S., Nieto, E., Villar González, José Luis   +6 more
core  

Epidemiology of cerebral palsy in Brazil through the lens of the International Classification of Functioning, Disability and Health framework

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To establish an overall description of people with cerebral palsy (CP) in Brazil, including the epidemiology, clinical features, functioning, and access to rehabilitation and equipment, through the lens of the International Classification of Functioning, Disability and Health (ICF) framework, using preliminary data from the Brazilian ...
Hércules Ribeiro Leite, Luana Cristina da Silva, Elton Duarte Dantas Magalhães, Israt Jahan, Nadia Badawi, Gulam Khandaker, Maysa Ferreira Martins Ribeiro, Juliana de Alcântara Moreira Pereira, Luma Sthephanine Viana Roque da Silva, Maria de las Mercedes Ruiz Brunner, Paula Silva de Carvalho Chagas   +10 more
wiley   +1 more source

Further evidence for the involvement of EFL1 in a Shwachman-Diamond-like syndrome and expansion of the phenotypic features. [PDF]

, 2018
Recent evidence has implicated EFL1 in a phenotype overlapping Shwachman-Diamond syndrome (SDS), with the functional interplay between EFL1 and the previously known causative gene SBDS accounting for the similarity in clinical features. Relatively little
Bacino, Carlos A, Bonner, Melanie J, Butler, Megan W, Cope, Heidi, Frush, Donald P, Jiang, Yong-Hui, Lachman, Ralph S, Lee, Brendan, McCall, Chad M, McDonald, Marie T, Pena, Loren DM, Pendse, Avani A, Rothman, Jennifer A, Shashi, Vandana, Spillmann, Rebecca C, Stong, Nicholas, Tan, Queenie K-G, Undiagnosed Diseases Network, Walley, Nicole   +18 more
core  

Regulation of PHOX2B gene expression by the long non‐coding natural antisense RNA PHOX2B‐AS1

The FEBS Journal, EarlyView.
PHOX2B is a transcription factor essential for autonomic nervous system development. We identify and characterize PHOX2B‐AS1, a human long non‐coding antisense transcript at the PHOX2B locus, along with its murine counterpart. Our findings reveal bidirectional transcription and reciprocal regulation: PHOX2B activates PHOX2B‐AS1, whereas PHOX2B‐AS1 ...
Simona Di Lascio, Ana Lucia Cuadros Gamboa, Martina Bertocchi, Filippo Chiesa, Francesca Cargnin, Ettore Mosca, Paride Pelucchi, Viviana Tritto, Stefania Corti, Isabella Ceccherini, Paola Riva, Roberta Benfante, Diego Fornasari   +12 more
wiley   +1 more source