Results 11 to 20 of about 46,879 (178)
Substructured formulations of nonlinear structure problems - influence of the interface condition [PDF]
, 2015 We investigate the use of non-overlapping domain decomposition (DD) methods for nonlinear structure problems. The classic techniques would combine a global Newton solver with a linear DD solver for the tangent systems. We propose a framework where we can
Gosselet, Pierre +3 more
core +4 more sources
Endotracheal intubation using a three-dimensional printed airway model in a patient with Pierre Robin sequence and a history of tracheostomy -a case report- [PDF]
Korean Journal of Anesthesiology, 2021 Background Pierre Robin sequence (PRS) patients have an increased risk of difficult intubation due to anatomical airway abnormalities, and intubation simulation with a three-dimensional (3D) printed airway model before anesthesia may facilitate safe ...
Seyeon Park +4 more
doaj +1 more source
Acoustic characteristics of glottal stop associated to Pierre Robin Sequence : case study [PDF]
, 2013 A fissura de palato, em associação à Sequência de Pierre Robin, pode favorecer o desenvolvimento de produções atípicas (compensatórias), na fala da criança, como é o caso da oclusiva glotal (golpe de glote) comumente observada em substituição aos sons ...
Berti, Larissa Cristina +2 more
core +1 more source
Identical twins with Pierre Robin syndrome; unusual encounter
Electronic Physician, 2017 New born babies could suffer from multiple craniofacial abnormalities, such as Pierre Robin syndrome, which consists of micrognathia and relative macroglossia with or without cleft palate. Although Pierre Robin syndrome is well described in literature,
Nabil Shdaifat +4 more
doaj +1 more source
Feeding plate for a neonate with Pierre Robin sequence
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2011 Pierre Robin Sequence is a congenital condition involving a combination of micrognathia and glossoptosis with or without a cleft palate. Feeding problems are often associated with cleft anamoly which make it difficult for the infant to maintain adequate ...
J Radhakrishnan, A Sharma
doaj +1 more source
Identification of Novel Craniofacial Regulatory Domains Located far Upstream of SOX9 and Disrupted in Pierre Robin Sequence. [PDF]
, 2014 Mutations in the coding sequence of SOX9 cause campomelic dysplasia (CD), a disorder of skeletal development associated with 46,XY disorders of sex development (DSDs). Translocations, deletions, and duplications within a ∼2 Mb region upstream of SOX9 can
Abadie, V. +16 more
core +3 more sources
Convergence of a Finite Volume Scheme for a Corrosion Model [PDF]
, 2014 In this paper, we study the numerical approximation of a system of partial dif-ferential equations describing the corrosion of an iron based alloy in a nuclear waste repository.
Chainais-Hillairet, Claire +2 more
core +5 more sources
Siblings with pierre robin sequence
CHRISMED Journal of Health and Research, 2017 Pierre Robin anomalad is a syndrome characterized by cleft of the palate, micrognathia of the mandible, and glossoptosis. This syndrome can occur as an individual presentation, or it may be associated with a wide variety of syndromes and anomalies.
Medhini Madi +5 more
doaj +1 more source
Early Communication Intervention with Young Children with Pierre Robin Sequence
South African Journal of Communication Disorders, 1998 Young children with Pierre Robin sequence are at considerable risk to develop delayed or disordered communication development. This study investigated the effectiveness of early communication intervention with four young children with Pierre Robin ...
Lisl Fair, Brenda Louw
doaj +1 more source
Molecular Genetics and Metabolism Reports, 2015 Catel–Manzke syndrome is a rare autosomal recessive disorder characterized by Pierre Robin sequence with hyperphalangy and clinodactyly of the index finger. Recently, homozygous or compound heterozygous pathogenic variants in TGDS have been discovered to
Rachel Pferdehirt +4 more
doaj +1 more source