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81Publicado 1990“…We propose that this type of ganglion cell desensitization under dim backgrounds is due to a post-receptoral gain control driven by quantal fluctuations, and term it noise adaptation in contrast to the Weber adaptation (desensitization proportional to the mean background intensity) of rods, horizontal cells, and ganglion cells at higher background intensities.…”
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83por Purkait, Radheshyam, Samanta, Tryambak, Sinhamahapatra, Tapankumar, Chatterjee, Mridula“…Sturge–Weber syndrome is a rare sporadic condition of mesodermal phakomatosis, characterized by purple-colored flat cutaneous cranial (face) hemangiomas (most commonly along the trigeminal nerve), glaucoma and vascular lesions in the ipsilateral brain and meninges. …”
Publicado 2011
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87“…Weber's law—the observation that the ability to perceive changes in magnitudes of stimuli is proportional to the magnitude—is a widely observed psychophysical phenomenon. …”
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88por Parisi, Lucia, Di Filippo, Teresa, La Grutta, Sabina, Lo Baido, Rosa, Epifanio, Maria Stella, Esposito, Maria, Carotenuto, Marco, Roccella, Michele“…Sturge-Weber-Krabe syndrome (SWS), also known as encephalotrigeminalangiomatosis and named the forthfacomatosis, recall the names of the authors who first describedit in its basic clinical, radiological andanatomopathological aspects. …”
Publicado 2013
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89“…Epilepsy is a major morbidity in Sturge Weber syndrome, a segmental vascular neurocutaneous disorder classically associated with facial angiomas, glaucoma, and leptomeningeal capillary-venous type vascular malformations. …”
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90“…BACKGROUND: Sturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder. …”
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92“…BACKGROUND: Numerous reporting biases have been known to affect spontaneous reporting databases. The Weber effect, which constitutes a peak in adverse event (AE) reporting of a drug at the end of second year after regulatory approval followed by a continuous decline thereafter, has been considered an important bias for a long time. …”
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94por Su, Wei-Wen“…PURPOSE: Sturge-Weber syndrome (SWS) is a neurocutaneous disorder characterized by facial cutaneous venous dilatation (port-wine stain), leptomeningeal angioma, and ocular abnormalities. …”
Publicado 2018
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95por Tortora, Annalisa, Riccioni, Maria Elena, Gaetani, Eleonora, Ojetti, Veronica, Holleran, Grainne, Gasbarrini, Antonio“…Hereditary hemorrhagic teleangectasia (HHT, or Rendu-Osler-Weber disease) is a rare inherited syndrome, characterized by arterio-venous malformations (AVMs or Telangiectasia). …”
Publicado 2019
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96por Kellam, Patrick, DeKeyser, Graham J., Higgins, Thomas F., Rothberg, David, Haller, Justin, Marchand, Lucas S.“…CONCLUSION: AO 44-B1 fractures have a varying rate of syndesmotic injury. Weber B fractures that end between the level of the plafond and the physeal scar (Zone 2) are 2.6 times more likely to have a syndesmotic injury compared to those that end below the plafond (Zone 1). …”
Publicado 2020
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97por Nikyar, Zahra, Hatami, Parvaneh, Aryanian, Zeinab, Kamyab Hesari, Kambiz, Goodarzi, Azadeh, Borzouei, Anahita“…Neonatal lupus erythematous (NLE) is a rare condition presented by lupus dermatitis shortly after birth or later following sun exposure. Sturge–Weber syndrome (SWS) is also an uncommon congenital condition characterized by extensive capillary malformation and ophthalmic and/or neurologic involvement. …”
Publicado 2021
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98por Pathak, Bishnu Deep, Sharma, Shriya, Adhikari, Aakriti, Simkhada, Nabin, Ghimire, Bhuwan, Aryal, Nirjala“…Sturge–Weber syndrome is a rare congenital neurocutaneous disorder characterized by dermatological, ophthalmological, and neurological manifestations. …”
Publicado 2022
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99“…Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome. …”
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100por Sheikh Hassan, Mohamed, Osman Sidow, Nor, Adam, Bakar Ali, Adani, Abdulkamil Abdullahi“…INTRODUCTION: and importance: Weber's syndrome is a rare type of brain stem stroke syndrome that is characterized by ipsilateral oculomotor nerve palsy and contralateral hemiparesis. …”
Publicado 2022
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