Results 81 to 90 of about 131,137 (361)
Extramedullary Plasmacytoma of Soft Tissues and Gingiva [PDF]
, 2012 Extramedullary plasmacytoma (EMP) is a rare plasma cell neoplasm of soft tissue without bone marrow involvement or other systemic characteristics of multiple myeloma. It accounts for 3% of all plasma cell tumors.
Jena, M, Kaler, AK, Shankar, A
core
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani +17 more
wiley +1 more source
‘old foley’s in a new bottle’- USE OF FOLEY’S CATHETER IN ANTERIOR MAXILLARY WALL FRACTURES [PDF]
, 2013 Management of comminuted zygomaticomaxillary fractures are is an entity that has always tested the skill of surgeons. A variety of methods have been coined over the years for management of these fractures.
Kothandaraman, Srikamakshi +2 more
core +1 more source
A Novel Method to Combine Maxilla-Based Coordinate System and Mandibular Voxel-Based Superimposition with Cone-Bean Computed Tomography [PDF]
, 2022 Chenghao Zhang +5 more
openalex +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes +3 more
wiley +1 more source
, 2013 Nose is the most prominent part of the face, hence it is likely to be the most common structure to be injured in the face. Although fractures involving the nasal bones are very common, it is often ignored by the patient.
Thiagarajan, Balasubramanian +1 more
core +1 more source
Ewing′s sarcoma of maxilla in an adolescent boy
Journal of International Clinical Dental Research Organization, 2010 Ewing′s sarcoma is a rarer malignancy, occurring usually in childhood. In majority of reported cases, the occurrence of this tumor is predominantly in the mandible than in the maxilla. Prognosis remains poor in most of the cases; however, better survival
Dattaprasad P Dadhe +2 more
doaj +1 more source
International Forum of Allergy &Rhinology, EarlyView.ABSTRACT Background Nasal airway obstruction (NAO) is prevalent with substantial health and quality of life burdens. Nasal valve collapse (NVC) is one structural cause of NAO. Temperature‐controlled radiofrequency (TCRF) nasal valve remodeling offers an alternative to invasive surgery.
David W. Kennedy +7 more
wiley +1 more source
Hyphessobrycon nicolasi (Teleostei: Characidae) a new species from the Uruguay River basin in the Mesopotamian Region, Argentina [PDF]
, 2010 Hyphessobrycon nicolasi is described from the Uruguay River basin in the Mesopotamian Region, Entre Ríos, Argentina. The new species can be distinguished from all congeners by the presence of a well-defined oblique and marginal black stripe on each lobe ...
Lopez, Hugo Luis +1 more
core +3 more sources