Results 281 to 290 of about 856,105 (317)
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Seminars in Fetal and Neonatal Medicine, 2005
Congenital hyperinsulinism is a cause of persistent hypoglycaemia in the neonatal period. It is a heterogeneous disease with respect to clinical presentation, molecular biology, genetic aetiology and response to medical therapy. The clinical heterogeneity may range from severe life-threatening disease to very mild clinical symptoms.
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Congenital hyperinsulinism is a cause of persistent hypoglycaemia in the neonatal period. It is a heterogeneous disease with respect to clinical presentation, molecular biology, genetic aetiology and response to medical therapy. The clinical heterogeneity may range from severe life-threatening disease to very mild clinical symptoms.
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1983
The early diagnosis of congenital nephropathies, sometimes before birth, is mandatory for the optimal management of affected children. While they do not always modify the final outcome of the disease, preventive measures can attenuate the consequences, and sometimes significantly delay the progression of the nephropathy.
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The early diagnosis of congenital nephropathies, sometimes before birth, is mandatory for the optimal management of affected children. While they do not always modify the final outcome of the disease, preventive measures can attenuate the consequences, and sometimes significantly delay the progression of the nephropathy.
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2020 ESC Guidelines for the management of adult congenital heart disease
European Heart Journal, 2021Helmut Baumgartner +2 more
exaly
Congenital melanocytic naevus and congenital strabismus
Clinical and Experimental Dermatology, 2018C. Dubois +5 more
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Otolaryngologic Clinics of North America
Congenital cholesteatoma is a cyst of keratinizing squamous cell epithelium in the setting of an intact tympanic membrane, in a patient without a history of otorrhea, tympanic membrane perforation, or otologic surgery. The most common presentation of a congenital cholesteatoma is that of an asymptomatic pearly white mass in the anterosuperior quadrant ...
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Congenital cholesteatoma is a cyst of keratinizing squamous cell epithelium in the setting of an intact tympanic membrane, in a patient without a history of otorrhea, tympanic membrane perforation, or otologic surgery. The most common presentation of a congenital cholesteatoma is that of an asymptomatic pearly white mass in the anterosuperior quadrant ...
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Topical therapy for regression and melanoma prevention of congenital giant nevi
Cell, 2022Tal Hadad Erlich +2 more
exaly