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Erratum: Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache [Corrigendum]. [PDF]
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National Journal of Neurology, 2015
Sturge-Weber syndrome is the third most common neurocutaneous disorder, after neurofibromatosis and tuberous sclerosis, and impacts approximately 1 in 20000 live births. Sturge-Weber syndrome is not inherited, but rather occurs exclusively sporadically, in both males and females and in all races and ethnic backgrounds. Sturge-Weber syndrome presents at
Z.M. Sadikhova +6 more
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Sturge-Weber syndrome is the third most common neurocutaneous disorder, after neurofibromatosis and tuberous sclerosis, and impacts approximately 1 in 20000 live births. Sturge-Weber syndrome is not inherited, but rather occurs exclusively sporadically, in both males and females and in all races and ethnic backgrounds. Sturge-Weber syndrome presents at
Z.M. Sadikhova +6 more
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Journal of the American Academy of Dermatology, 1999
From the Department of Oral Surgery, Medicine, Pathology, Indiana University,a and the Departments of Dermatologyb and Radiology,c Indiana University Medical Center, Indianapolis; and the University of Missouri School of Medicine, Kansas City.d Reprint requests: Ginat W.
G W, Mirowski +3 more
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From the Department of Oral Surgery, Medicine, Pathology, Indiana University,a and the Departments of Dermatologyb and Radiology,c Indiana University Medical Center, Indianapolis; and the University of Missouri School of Medicine, Kansas City.d Reprint requests: Ginat W.
G W, Mirowski +3 more
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Der Radiologe, 2013
Sturge-Weber syndrome (SWS) is a rare congenital disease which affects the brain, the skin and the eyes. It is a sporadically occurring neurocutaneous syndrome affecting the intracerebral veins (venous angiomatosis). The frequency is estimated to be 1 in 50,000 births [1].
W, Reith, U, Yilmaz, A, Zimmer
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Sturge-Weber syndrome (SWS) is a rare congenital disease which affects the brain, the skin and the eyes. It is a sporadically occurring neurocutaneous syndrome affecting the intracerebral veins (venous angiomatosis). The frequency is estimated to be 1 in 50,000 births [1].
W, Reith, U, Yilmaz, A, Zimmer
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Child's Nervous System, 2006
Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which are facial, mostly unilateral nevi, leptomeningeal angiomatosis, and congenital glaucoma. The interest of this syndrome for pediatric neurosurgeons is mainly related to the association of SWS with epilepsy in 75-90% of the cases.
C, Di Rocco, G, Tamburrini
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Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which are facial, mostly unilateral nevi, leptomeningeal angiomatosis, and congenital glaucoma. The interest of this syndrome for pediatric neurosurgeons is mainly related to the association of SWS with epilepsy in 75-90% of the cases.
C, Di Rocco, G, Tamburrini
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Archives of Neurology, 1969
THE Sturge-Weber syndrome is usually easy to recognize. It consists of angiomatosis of the upper portion of the face and the cerebral leptomeninges, with progressive calcification in the underlying cerebral cortex. 1 These abnormalities are usually unilatera l .
R H, Wilkins, I A, Brody
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THE Sturge-Weber syndrome is usually easy to recognize. It consists of angiomatosis of the upper portion of the face and the cerebral leptomeninges, with progressive calcification in the underlying cerebral cortex. 1 These abnormalities are usually unilatera l .
R H, Wilkins, I A, Brody
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Archives of Dermatology, 1949
PHAKOMATOSES 1 is the term that has been applied to the neurocutaneous syndromes. This term is derived from the Greek root [unk], which means "mother spot" or "mole" and implies a congenital factor. The three diseases which comprise this group and which have cutaneous lesions are (1) tuberous sclerosis, (2) neurofibromatosis of Von Recklinghausen and ...
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PHAKOMATOSES 1 is the term that has been applied to the neurocutaneous syndromes. This term is derived from the Greek root [unk], which means "mother spot" or "mole" and implies a congenital factor. The three diseases which comprise this group and which have cutaneous lesions are (1) tuberous sclerosis, (2) neurofibromatosis of Von Recklinghausen and ...
openaire +2 more sources