Results 101 to 110 of about 11,914 (280)
Monostotic fibrous dysplasia of fibula: a rare case report [PDF]
, 2021 Fibrous dysplasia is a developmental anomaly of bone formation that may exist in monostotic or polyostotic form. Monostotic fibrous dysplasia of fibula is a rare case with unusual site and most common sites being facial bones, ribs, proximal femur and ...
Roy, Dipen, Sil, Bhupes, V., Naveen
core +2 more sources
Skeletal Phenotype in Mulibrey Nanism, A Monogenic Skeletal Dysplasia With Fibrous Dysplasia
Clinical Genetics, Volume 107, Issue 3, Page 271-277, March 2025.We present a cross‐sectional detailed radiographic evaluation of the skeletal phenotype in 33 patients, aged 4.5–48 years, with Mulibrey nanism (MUL). This study confirms MUL as a skeletal dysplasia with prenatal‐onset growth failure, slender bones, vertebral changes, and a high prevalence of fibrous dysplasia and fractures.
Susann Karlberg +3 more
wiley +1 more source
Convolutional neural networks for automatic detection of Focal Cortical Dysplasia [PDF]
arXiv, 2020 Focal cortical dysplasia (FCD) is one of the most common epileptogenic lesions associated with cortical development malformations. However, the accurate detection of the FCD relies on the radiologist professionalism, and in many cases, the lesion could be missed.
arxiv
Undulation Instability of Epithelial Tissues [PDF]
Phys. Rev. Lett. 106, 158101 (2011), 2011 Treating the epithelium as an incompressible fluid adjacent to a viscoelastic stroma, we find a novel hydrodynamic instability that leads to the formation of protrusions of the epithelium into the stroma. This instability is a candidate for epithelial fingering observed in vivo.
arxiv +1 more source
Head &Neck, Volume 46, Issue 1, Page E1-E5, January 2024.Abstract Background McCune‐Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia (FD), café‐au‐lait skin pigmentation, and endocrine dysfunction. Extensive FD in the craniofacial region can present significant challenges in terms of disease control and carries a high risk of permanent visual impairment.
Moataz D. Abouammo +5 more
wiley +1 more source
Molecular Genetics &Genomic Medicine, Volume 12, Issue 1, January 2024.This study revealed three patients with familial gigantiform cementoma (FGC) carried the heterozygous mutation c.1067G>A (p.Cys356Tyr) in the ANO5 gene which was not found in 8 juvenile ossifying fibromas, 5 polyostotic fibrous dysplasia and 5 florid cemento‐osseous dysplasia.
Zheng Zhou +5 more
wiley +1 more source
Failure regime in (1+1) dimensions in fibrous materials [PDF]
Phy. Rev. E 63,025104 (2001), 2000 In this paper, we introduce a model for fracture in fibrous materials that takes into account the rupture height of the fibers, in contrast with previous models. Thus, we obtain the profile of the fracture and calculate its roughness, defined as the variance around the mean height.
arxiv +1 more source
Fracture toughness in fibrous materials [PDF]
Phy. Rev. E 65,011502 (2001), 2002 In the present paper, a fiber bundle model in (1+1)-dimensions that simulates the rupture process of a fibrous material pulled by an uniaxial force F is analyzed. In this model the load of a broken fiber is shifted in equal portions onto the nearest unbroken fibers.
arxiv +1 more source
McCune-Albright Syndrome: A-rare-case report [PDF]
, 2022 McCune-Albright syndrome (MAS) is a rare genetic disordered originally recognized by the triad of polyostotic fibrous dysplasia, precocious puberty, and cafe-au-late spots. We report a case of 2 years-11-month-old girl who came with complaints ...
Angriani, Hadia +3 more
core +2 more sources
Fibrous Dysplasia: Clinicopathologic Presentation of 36 Cases
Türk Patoloji Dergisi, 2018 Objective: Fibrous dysplasia is a slowly progressing bone lesion resulting from displacement of the normal medullary bone with abnormal fibroosseous tissue.
Mine ÖZŞEN +3 more
doaj +1 more source