Results 171 to 180 of about 1,142,799 (204)
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Moyamoya in a patient with Sneddon's syndrome
Clinical Neurology and Neurosurgery, 2015NEUROFARBA Department, Neuroscience Section, University of Florence, Florence, Italy SOD Neurologia 2, Neuroscience Department, Azienda Ospedaliero Universitaria Careggi, Florence, Italy SOD Oculistica, Department of Translational Surgery and Medicine, Florence, Italy Department of Surgery and Translational Medicine, Division of Dermatology, University
FIERINI, FABIO +6 more
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Moyamoya disease and down syndrome
The Indian Journal of Pediatrics, 2005Moyamoya disease is an obstruction of the internal carotids and of the afferent and efferent channels of Willis polygon, which causes a collateral circulation, responsible for the typical angiographic image of a "puff of smoke" (Moyamoya, in Japanese). Its etiology is unknown, and it might be congenital or acquired.
Muferet, Erguven +2 more
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Zentralblatt fur Neurochirurgie, 1979
The Moyamoya vascular convolutions are interpreted as an unspecific collateral system in unilateral and bilateral progressive stenosing of the A. carotis interna and additional transdural externainterna anastomoses. In such cases one should speak of a Moyamoya syndrome. The designation Moyamoya disease only applies to the congenital form.
G, Gemende, K O, Kagel
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The Moyamoya vascular convolutions are interpreted as an unspecific collateral system in unilateral and bilateral progressive stenosing of the A. carotis interna and additional transdural externainterna anastomoses. In such cases one should speak of a Moyamoya syndrome. The designation Moyamoya disease only applies to the congenital form.
G, Gemende, K O, Kagel
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Cardio-facio-cutaneous syndrome and moyamoya syndrome
Brain and Development, 2002We reported a patient with cardio-facio-cutaneous (CFC) syndrome associated with moyamoya syndrome. The patient was referred at 6 years 5 months with left hemiplegia and right-sided eye deviation. He had an apparently short stature, macrocephaly, left ptosis and atopic skin, and was odd looking.
Yoshiko, Ishiguro +6 more
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Journal of neurosurgery. Pediatrics, 2009
Seckel syndrome is an autosomal recessive disorder characterized by intrauterine and postnatal growth delay, microcephaly with mental retardation, and facial dysmorphisms including micrognathia, a recessed forehead, and a large beaked nose. Occurring in 1 in 10,000 children without sex preference, it is the most common primordial microcephalic ...
Patrick J, Codd +2 more
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Seckel syndrome is an autosomal recessive disorder characterized by intrauterine and postnatal growth delay, microcephaly with mental retardation, and facial dysmorphisms including micrognathia, a recessed forehead, and a large beaked nose. Occurring in 1 in 10,000 children without sex preference, it is the most common primordial microcephalic ...
Patrick J, Codd +2 more
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Moyamoya Syndrome in a Child With Trisomy 12p Syndrome
Pediatric Neurology, 2006A female, 2 years and 7 months of age, was admitted to the hospital with stupor and nystagmus following projectile vomiting. She had been prenatally diagnosed with trisomy 12p with a familial pericentric inversion of chromosome 12 originating from her mother.
Young Ok, Kim +4 more
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Comparison between moyamoya disease and moyamoya syndrome in Israel
Journal of Stroke and Cerebrovascular DiseasesMoyamoya is a chronic brain vasculopathy involving the distal intracranial internal carotid artery (ICA) or proximal middle cerebral artery (MCA). Moyamoya patients can be divided into those with primary moyamoya disease (MMD) and those with moyamoya secondary to other known causes such as intracranial atherosclerosis (moymoya syndrome [MMS]).
Y. Schwartzmann +8 more
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Moyamoya Disease and Syndrome: A National Inpatient Study of Ischemic Stroke Predictors
Journal of Stroke and Cerebrovascular Diseases, 2021Santiago Unda +2 more
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