Results 351 to 360 of about 367,278 (369)
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Panostotic Fibrous Dysplasia A New Craniotubular Dysplasia
Clinical Nuclear Medicine, 1992The authors describe the radiographic-scintigraphic features of an unusual craniotubular dysplasia characterized by diffuse osteopenia with bone expansion and a "ground glass" appearance, markedly increased skeletal turnover, myelofibrosis, hypophosphatemia, and pigmented "coast-of-Maine" patches.
Caroline Reinhold +4 more
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European Journal of Cancer, 1995
Lethal carcinomas are still found inadvertently in patients under surveillance; some may not be preceded by conventional dysplasia. However, there is a survival advantage for cancers detected endoscopically rather than symptomatically, and, therefore, by preventing them by colectomy when dysplasia first becomes apparent.
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Lethal carcinomas are still found inadvertently in patients under surveillance; some may not be preceded by conventional dysplasia. However, there is a survival advantage for cancers detected endoscopically rather than symptomatically, and, therefore, by preventing them by colectomy when dysplasia first becomes apparent.
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Dysplasia epiphysealis capitis femoris. Meyer's dysplasia
The Journal of Bone and Joint Surgery. British volume, 1991We made a prospective longitudinal clinical and radiological study of 18 children diagnosed as having dysplasia epiphysealis capitis femoris. Half the cases were bilateral. Boys were affected five times more often than girls. There were no symptoms or clinical signs in most but some of the bilateral cases had an inconsistent waddling gait. The imaging
O Khermosh, S Wientroub
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Journal of the American Academy of Dermatology, 2007
Digitocutaneous dysplasia is a rare X-linked dominant genetic syndrome characterized by multiple digital fibromas, atrophic plaques, dental anomalies, dysmorphic features, and bone anomalies. We report the case of a 2-year-old Mexican girl with this rare condition and discuss the clinical, histologic, and genetic features.
Arash, Izadpanah +4 more
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Digitocutaneous dysplasia is a rare X-linked dominant genetic syndrome characterized by multiple digital fibromas, atrophic plaques, dental anomalies, dysmorphic features, and bone anomalies. We report the case of a 2-year-old Mexican girl with this rare condition and discuss the clinical, histologic, and genetic features.
Arash, Izadpanah +4 more
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Hormone Research in Paediatrics, 2002
<i>Definition:</i> Fibrous dysplasia (FD) of bone is a non-inheritable congenital disorder affecting both genders. It is characterized by expanding fibrous lesions, which contain bone-forming mesenchymal cells. <i>Pathophysiology:</i> FD is caused by a somatic activating mutation of the alpha subunit of the Gs protein (Gsα ...
Eckhard, Schoenau, Frank, Rauch
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<i>Definition:</i> Fibrous dysplasia (FD) of bone is a non-inheritable congenital disorder affecting both genders. It is characterized by expanding fibrous lesions, which contain bone-forming mesenchymal cells. <i>Pathophysiology:</i> FD is caused by a somatic activating mutation of the alpha subunit of the Gs protein (Gsα ...
Eckhard, Schoenau, Frank, Rauch
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Dysplasia and Dysplasia Mimics in Barrett’s Mucosa
2013Dysplasia in the gastrointestinal tract, including that in Barrett’s mucosa, is defined as epithelium that is unequivocally neoplastic, a determination that is currently the responsibility of pathologists. Pathologists identify unequivocally neoplastic epithelium based on a set of microscopic features that are both cytologic and architectural.
Scott R. Owens, Henry D. Appelman
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Clinics in Chest Medicine
Bronchopulmonary dysplasia (BPD) is a chronic lung disease, associated with premature birth, that arises during the infantile period. It is an evolving disease process with an unchanged incidence due to advancements in neonatal care which allow for the survival of premature infants of lower gestational ages and birth weights.
Katelyn G, Enzer +2 more
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Bronchopulmonary dysplasia (BPD) is a chronic lung disease, associated with premature birth, that arises during the infantile period. It is an evolving disease process with an unchanged incidence due to advancements in neonatal care which allow for the survival of premature infants of lower gestational ages and birth weights.
Katelyn G, Enzer +2 more
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American Journal of Medical Genetics, 2002
Enilze Maria de Souza Fonseca Ribeiro +1 more
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Enilze Maria de Souza Fonseca Ribeiro +1 more
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