Results 81 to 90 of about 33,018 (284)
Gomal Journal of Medical Sciences, 2012 Background: Fibrous dysplasia and ossifying fibroma are amongst maxillofacial fibro-osseous lesions and their incidence is reported to be approximately 37.1% and 22.9% respectively of all the jaw tumours.
Rabia Zafar +5 more
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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
Multiple problems in siblings with Gardner’s syndrome [PDF]
, 1998 The problems encountered in the diagnosis of two siblings suffering from a high penetration variant of Gardner’s syndrome are presented. The importance of recognizing the extra colonic manifestations of the syndrome at an early stage and technical ...
Borg, Hermann Karl, Swain, Charles
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Polyostotic Fibrous Dysplasia With and Without McCune-Albright Syndrome-Clinical Features in a Nordic Pediatric Cohort [PDF]
, 2018 Objective: Fibrous dysplasia (FD) presents as skeletal lesions in which normal bone is replaced by abnormal fibrous tissue due to mosaic GNAS mutation.
Bjornsdottir, Sigridur +4 more
core +1 more source
Aging Cell, EarlyView.cTAGE5 regulates LBR trafficking between the ER and the nucleus membrane to maintain the integrity of both the ER and the nuclear envelope. cTAGE5 KO results in LBR retention in the ER, reduced stability, and subsequent disruption of nuclear envelope integrity. ABSTRACT cTAGE5/MEA6 plays a pivotal role in COPII complex assembly, ER‐to‐Golgi trafficking,
Yaqing Wang +9 more
wiley +1 more source
, 2005 Since 1995, according to the World Health Organisation’s classification of cardiomyopathies, Naxos disease has been considered as the recessive form of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C).1 It is a stereotype association of
Protonotarios, Nikos +1 more
core +2 more sources
Clinical Genetics, EarlyView.We report a 2‐year‐old male with clinical features of Takenouchi‐Kosaki syndrome, bilateral colobomas, and a de novo, likely pathogenic missense variant in CDC42. Supportive evidence includes a Cdc42 conditional knock‐out mouse model with colobomas.
Diana Brightman +11 more
wiley +1 more source
p53-sensitive epileptic behavior and inflammation in Ft1 hypomorphic mice [PDF]
, 2018 Epilepsy is a complex clinical condition characterized by repeated spontaneous seizures. Seizures have been linked to multiple drivers including DNA damage accumulation.
Alessandro, Vercelli +10 more
core +2 more sources
Piezo2 in Mechanosensory Biology: From Physiological Homeostasis to Disease‐Promoting Mechanisms
Cell Proliferation, EarlyView.Piezo2 channels are essential mechanotransducers regulating touch, proprioception and visceral mechanosensation across physiological systems, emerging as therapeutic targets for pathological mechanical hypersensitivity and neurogenic disorders. ABSTRACT Piezo2, a mechanically activated ion channel, serves as the key molecular transducer for touch ...
Zhebin Cheng +4 more
wiley +1 more source
Journal of Orthopaedic Reports, 2022 Introduction: Fibrous dysplasia is a non-inheritable congenital disorder characterized by bone-forming expansile fibrous lesions that disrupt normal bone architecture.
Mitali Mokashi +3 more
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