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Pediatric Anesthesia, 2021
AbstractBronchopulmonary dysplasia is the most frequent adverse outcome of prematurity. Before implementation of antenatal steroids and surfactant therapy, bronchopulmonary dysplasia was mostly characterized by fibrotic, scarred, and hyper‐inflated lungs due to pulmonary injury following mechanical ventilation and oxygen toxicity.
Alexander R. Schmidt +1 more
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AbstractBronchopulmonary dysplasia is the most frequent adverse outcome of prematurity. Before implementation of antenatal steroids and surfactant therapy, bronchopulmonary dysplasia was mostly characterized by fibrotic, scarred, and hyper‐inflated lungs due to pulmonary injury following mechanical ventilation and oxygen toxicity.
Alexander R. Schmidt +1 more
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New England Journal of Medicine, 2004
The most common clinical manifestations of fibromuscular dysplasia (FMD) are hypertension due to renal artery involvement and transient ischemic attack or stroke due to carotid or vertebral artery involvement. Patients with renal artery FMD and hypertension should undergo primary angioplasty with the goal of curing the hypertension.
David P, Slovut, Jeffrey W, Olin
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The most common clinical manifestations of fibromuscular dysplasia (FMD) are hypertension due to renal artery involvement and transient ischemic attack or stroke due to carotid or vertebral artery involvement. Patients with renal artery FMD and hypertension should undergo primary angioplasty with the goal of curing the hypertension.
David P, Slovut, Jeffrey W, Olin
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Acrofacial dysplasia resembling geleophysic dysplasia
American Journal of Medical Genetics, 1984AbstractWe report on a 12‐year‐old girl with acrofacial dysplasia, growth retardation, joint contractures, mitral valve incompetence and focal hepatic storage of material reacting histochemically as glycoprotein. The patient's phenotype resembles that of patients with geleophysic dysplasia but differs with respect to facial appearance, milder changes ...
J, Spranger +4 more
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A variant of fibrous dysplasia (osteofibrous dysplasia).
The Journal of Bone & Joint Surgery, 1982We are reporting the cases of five patients with a tumor-like lesion that has recently been called osteofibrous dysplasia but has also been called osteogenic fibroma, monostotic cortical fibrous dysplasia, and a variant of fibrous dysplasia. The lesions in our patients developed in childhood and were located in the diaphysis of the tibia, which was ...
C J, Campbell, T, Hawk
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Otodental dysplasia: a “new” ectodermal dysplasia
Clinical Genetics, 1975Otodental dysplasia is an ectodermal dysplasia characterized by abnormal crown morphology of the teeth and sensorineural hearing loss. It was documented in six generations of a kindred of Italian extraction. Thirty‐three of the 119 examined family members were affected. Twenty‐six persons had characteristic dental anomalies combined with a hearing loss.
L S, Levin, R J, Jorgenson, R A, Cook
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METAPHYSEAL DYSPLASIA, EPIPHYSEAL DYSPLASIA, DIAPHYSEAL DYSPLASIA, AND RELATED CONDITIONS
A.M.A. Archives of Internal Medicine, 1954PROGRESSIVE diaphyseal dysplasia, so-named by Neuhauser, Schwachman, Wittenborg, and Cohen, in 1948,8is also known as Engelmann's disease.* Fairbank6believes that Cockayne4described the first case in 1920 and mentions the other few reports of the syndrome. Affected patients are weak and thin and are shorter than normal in stature.
W P, JACKSON, J, HANELIN, F, ALBRIGHT
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Acta Oto-Laryngologica, 2005
Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth of the skull base or craniofacial bones and abnormal remodeling of the metaphyses of the long bones. We present a sporadic case of craniometaphyseal dysplasia associated with facial paralysis observed in a 4-year-old female, which emphasizes the ...
Young Ho, Kim +3 more
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Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth of the skull base or craniofacial bones and abnormal remodeling of the metaphyses of the long bones. We present a sporadic case of craniometaphyseal dysplasia associated with facial paralysis observed in a 4-year-old female, which emphasizes the ...
Young Ho, Kim +3 more
openaire +2 more sources