Results 1 to 10 of about 20 (20)
Clinical and Experimental Dental Research, Volume 8, Issue 6, Page 1655-1663, December 2022., 2022 Abstract Objectives The primary aim of this ex vivo study was to evaluate thermal damage and cutting efficiency of micro and super pulsed diode lasers. The secondary aim was to suggest a guideline to perform simple surgical excisions adequate for histopathological evaluation.
Mariliza C. O. Prado +5 more
wiley +1 more source
Molecular testing of soft tissue tumors
Diagnostic Cytopathology, Volume 51, Issue 1, Page 12-25, January 2023., 2023 Abstract Background The diagnosis of soft tissue tumors is challenging, especially when the evaluable material procured is limited. As a result, diagnostic ancillary testing is frequently needed. Moreover, there is a trend in soft tissue pathology toward increasing use of molecular results for tumor classification and prognostication. Hence, diagnosing
Douglas Rottmann +2 more
wiley +1 more source
Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting
Human Mutation, Volume 43, Issue 12, Page 1956-1969, December 2022., 2022 Abstract Tuberous sclerosis complex (TSC) is a multi‐system genetic disorder. Most patients have germline mutations in TSC1 or TSC2 but, 10%–15% patients do not have TSC1/TSC2 mutations detected on routine clinical genetic testing. We investigated the contribution of low‐level mosaic TSC1/TSC2 mutations in unsolved sporadic patients and families with ...
Zimeng Ye +31 more
wiley +1 more source
Veterinary Record, Volume 192, Issue 1, 7/14 January 2023., 2023 Abstract Background A cross‐species jump was confirmed in 2018, when a novel recombinant myxoma virus (MYXV) (ha‐MYXV) caused high mortality in Iberian hare (Lepus granatensis) in the Iberian Peninsula. Method The aim of this study was to evaluate the main lesions, tissular distribution and target cells of ha‐MYXV in Iberian hare.
Irene Agulló‐Ros +9 more
wiley +1 more source
Craniofacial microsomia – more than a structural malformation
Orthodontics &Craniofacial Research, Volume 26, Issue 1, Page 117-122, February 2023., 2023 Abstract Objectives To analyse the prevalence and distribution of craniofacial microsomia (CFM) cases in Finland and their most frequent comorbidities. The second aim was to analyse the patients' need for specialized healthcare services. Materials and methods Data were gathered from two complementary registers: The Register of Congenital Malformations ...
Louhi Kuu‐Karkku +2 more
wiley +1 more source
Dental implantology and fibrous dysplasia: A 6‐year follow‐up case report and a literature review
Oral Surgery, Volume 16, Issue 1, Page 126-132, February 2023., 2023 Abstract Background and Aim It is unclear if fibrous dysplasia (FD) represents a contraindication for implant borne rehabilitation, and only two successful cases are reported in the literature with a 4–2‐year follow‐up. The present paper discusses this issue reporting a full‐arch maxillary rehabilitation with a >5‐year follow‐up.
Giuseppe Lizio +4 more
wiley +1 more source
Orthopaedic Surgery, Volume 14, Issue 12, Page 3431-3440, December 2022., 2022 This article described a surgical technique of allogeneic tendon transplantation technique for children with absence of patellar ligament. At 4‐year postoperative follow‐up, the knee range of motion was in the range of 0°–120°, and the child walked normally without any external help.
Min Zhou +10 more
wiley +1 more source
Orthopaedic Surgery, Volume 14, Issue 12, Page 3171-3177, December 2022., 2022 Percutaneous curettage and impaction of allogenic bone graft mixed with autogenic bone marrow aspirate can induce complete resolution of the primary ABCs without use of other adjuvants or any form of internal fixation. Objective Recurrence is the main hinderance in treatment of aneurysmal bone cysts (ABCs).
Mohamad Yasin +4 more
wiley +1 more source
Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio +13 more
wiley +1 more source
Management of post‐implant fibrous dysplasia in the maxilla: A case study
Clinical Advances in Periodontics, EarlyView.Abstract Background Fibrous dysplasia is generally rare, and even rarer in older adults. Special care is needed when altering the alveolar bone in these cases, especially if an implant is involved. This case study highlights such a scenario. Methods This case study details the experience of a 63‐year‐old African American female who presented with a ...
Yousef Taha Y. Amrou +4 more
wiley +1 more source