Em homenagem ao pisca-pisca, orochinho, reizinho das mitadas e piscadas, PedroNaruto123, o maior beat boxer que já existiu. Descanse em paz Pedro, eternamente em nossos corações.
Scariest thing that has ever happened in my life...
lala
NO
Submitted by:anonymous
NO
Completely wrong. Even after having an essay wrote on these variations you still can’t see the difference. Lmao. I guess that’s why I’ve beaten people like Serral and have a >65% PvZ win-rate during ApeCraft 2 and you’re in bronze league despite massive balance issues favoring your race.
Submitted by:starcraft
starcraft
Completely wrong. Even after having an essay wrote on these variations you still can’t see the difference. Lmao. I guess that’s why I’ve beaten people like Serral and have a >65% PvZ win-rate during ApeCraft 2 and you’re in bronze league despite massive balance issues favoring your race.
Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is an invariably fatal degenerative brain disorder.[4][1] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances.[4] Later symptoms include dementia, involuntary movements, blindness, weakness, and coma.[4] About 70% of people die within a year of diagnosis.[4] The name Creutzfeldt–Jakob disease was introduced by Walther Spielmeyer in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob.[6]
Submitted by:Overqwil7
Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is an invariably fatal degenerative brain disorder.[4][1] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances.[4] Later symptoms include dementia, involuntary movements, blindness, weakness, and coma.[4] About 70% of people die within a year of diagnosis.[4] The name Creutzfeldt–Jakob disease was introduced by Walther Spielmeyer in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob.[6]
Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is an invariably fatal degenerative brain disorder.[4][1] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances.[4] Later symptoms include dementia, involuntary movements, blindness, weakness, and coma.[4] About 70% of people die within a year of diagnosis.[4] The name Creutzfeldt–Jakob disease was introduced by Walther Spielmeyer in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob.[6]