Results 271 to 280 of about 10,435,514 (291)
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Seminars in Neurology, 2007
Huntington's disease is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea and dystonia, incoordination, cognitive decline, and behavioural difficulties. Typically, onset of symptoms is in middle-age after affected individuals have had children, but the disorder can manifest at any time between ...
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Huntington's disease is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea and dystonia, incoordination, cognitive decline, and behavioural difficulties. Typically, onset of symptoms is in middle-age after affected individuals have had children, but the disorder can manifest at any time between ...
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World Journal of Surgery, 1984
AbstractIn 1958, Caroli [1, 2] was the first to describe congenital dilatations of intrahepatic bile ducts concerning a segment, a sector, a lobe, or both halves of the liver. Sometimes the dilatations are associated with congenital hepatic fibrosis as described in 1954 by Grumbach [3], dilatations of biliary ductules (biliary angiomatosis), and ...
M, Mercadier +4 more
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AbstractIn 1958, Caroli [1, 2] was the first to describe congenital dilatations of intrahepatic bile ducts concerning a segment, a sector, a lobe, or both halves of the liver. Sometimes the dilatations are associated with congenital hepatic fibrosis as described in 1954 by Grumbach [3], dilatations of biliary ductules (biliary angiomatosis), and ...
M, Mercadier +4 more
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Plastic and Reconstructive Surgery, 1973
For patients with Peyronie's disease requiring surgery, the authors' treatment is to excise the plaque and replace the diseased area of the tunica with a dermal graft. The goal of the surgery is to create a functional penis without prosthesis. For the first few months, sexual therapy and counseling are very important to help the patient and partner ...
C E, Horton, C J, Devine
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For patients with Peyronie's disease requiring surgery, the authors' treatment is to excise the plaque and replace the diseased area of the tunica with a dermal graft. The goal of the surgery is to create a functional penis without prosthesis. For the first few months, sexual therapy and counseling are very important to help the patient and partner ...
C E, Horton, C J, Devine
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Current Treatment Options in Cardiovascular Medicine, 2004
Kawasaki disease is an acute, self-limited vasculitis of childhood characterized by fever, bilateral nonexudative conjunctivitis, erythema of the lips and oral mucosa, changes in the extremities, rash, and cervical lymphadenopathy. Coronary artery aneurysms or ectasia develop in approximately 15 to 25% of untreated children with the disease and may ...
Jane W, Newburger, David R, Fulton
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Kawasaki disease is an acute, self-limited vasculitis of childhood characterized by fever, bilateral nonexudative conjunctivitis, erythema of the lips and oral mucosa, changes in the extremities, rash, and cervical lymphadenopathy. Coronary artery aneurysms or ectasia develop in approximately 15 to 25% of untreated children with the disease and may ...
Jane W, Newburger, David R, Fulton
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Clinical Nuclear Medicine, 2001
A 15-year-old boy was hospitalized with a 1-month history lumbago and fever. His family history was noncontributory for tuberculosis, and the findings of the physical examination were normal. The sedimentation rate and C-reactive protein level were 55 mm/hour and 48 mg/l, respectively.
Tutus, Ahmet +2 more
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A 15-year-old boy was hospitalized with a 1-month history lumbago and fever. His family history was noncontributory for tuberculosis, and the findings of the physical examination were normal. The sedimentation rate and C-reactive protein level were 55 mm/hour and 48 mg/l, respectively.
Tutus, Ahmet +2 more
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Nursing Standard, 2004
Huntington's disease is a complex degenerative disorder that affects the central nervous system. Although it is a rare condition, nurses are ideally placed to assess and manage patients with the disease, while also providing information and support to family members.
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Huntington's disease is a complex degenerative disorder that affects the central nervous system. Although it is a rare condition, nurses are ideally placed to assess and manage patients with the disease, while also providing information and support to family members.
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2014
Peroxisomal diseases are a group of genetically and clinically divergent diseases due to defects in either the biogenesis of peroxisomes (group 1) or one of its metabolic functions (group 2). Zellweger syndrome and X-linked adrenoleukodystrophy (XALD) are the prototypes for group 1 and 2, respectively.
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Peroxisomal diseases are a group of genetically and clinically divergent diseases due to defects in either the biogenesis of peroxisomes (group 1) or one of its metabolic functions (group 2). Zellweger syndrome and X-linked adrenoleukodystrophy (XALD) are the prototypes for group 1 and 2, respectively.
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Pulseless Disease (Takayasu's Disease)
American Journal of Ophthalmology, 1957openaire +2 more sources