勇者を狂牛に変身させるモッさんの新型コロナクチンは全てのタイプ全部アウト！

 Creutzfeldt-Jakob Disease After the COVID-19

Vaccination

ABSTRACT Reports of neurological problems are increasing for the clinical presentation of COVID-
19. The clinical presentation reported in this study seemed to be a combination of nonspecific
complications of the systemic disease, inflammation of the cerebrovascular system, and the
effects of a direct viral infection. Creutzfeldt–Jakob disease, a spongiform encephalopathy
caused by prions, is characterized by a severe neurological destruction, which has an extremely
high mortality. In this publication, we presented a patient who was admitted to the Pamukkale
University Anesthesiology Intensive Care Units with the neurological findings that developed after
the COVID-19 vaccine (CoronaVac, Sinovac Life Sciences, Beijing, China). The patient died due to
the progressive neurological disorders. In cases where rapidly progressive neurological disorders
are observed, Creutzfeldt–Jakob disease should be considered and the role of immunity-related
conditions in the progression of the disease should be investigated.
Keywords: Covid-19, Vaccine, Creutzfeldt–Jakob disease, Prion protein

Case Report
A 82-year-old female patiet with a known diagnosis of hypertension and dementia started to have tremors and weakness on the right side of her body. The patient’s findings emerged one day after the first dose of COVID-19 CoronaVac vaccine was administered. She admitted to the hospital with the addition of symptoms such as regression in her state of consciousness, inability to recognize the people around her, impaired vision, impaired place-time orientation and meaningless shouts at the following month. She was admitted to our neurology unit hospital with a diagnosis of encephalitis and subdural hematoma.
On admission, she has myoclonic contractions and disorientation in her right extremities. She has no findings in cranial nerve examinations. Clonus, rigidity and hyperreflexia
were present in the right half of the body. Glasgow Coma Scale (GCS) was 10/15 on neurological examination. Laboratory studies such as liver and kidney function tests, electrolytes, complete blood count, blood gas analysis, coagulation tests,
thyroid function tests, autoimmune markers, viral encephalitis markers were done. CSF samples were taken and examined. Electroencephalograghy(EEG) examination was performed.
Blood, urine, respiratory secretions and cerebrospinal fluid (CSF) cultures were made. No abnormal laboratory finding was found in blood tests. Autoimmune en- cephalopathy
panels were negative. EEG showed paroxysmal mixed sharp and sharply slow paroxysms, diffuse slowing of cerebral bioelectrical activity without lateralization and localization.
She received pulse steroid and intravenous immunoglobulin g (IVIG) therapy with a diagnosis of autoimmune encephalitis in the neurology service. When GCS dropped to 4 in the neurology service, she was intubated and hospitalized in our intensive care unit. Brain and thorax computed tomography and cranial MRI examinations were performed. She received empirical antibiotics and antiepileptic therapy for meningitis prophylaxis in addition to pulse steroid and intravenous IVIG therapy in the intensive care unit. Transesophageal echocardiography was performed for infective endocarditis.
Diffusion-weighted MRI revealed cortical diffusion restriction in the left parietal, occipital, temporal lobes and the right occipital lobe. In the FLAIR examination, hyperintensity was
observed in the same regions (Figure 1).
The patient was diagnosed with sporadic CJD after the 14-3-3 protein test was positive, MRI findings, physical examination, and evaluation of the clinical history. As a
result of her examinations, viral encephalitis, autoimmune encephalitis and subdural hematoma were excluded. The patient died as a result of the progressive course of the
disease.


https://cms.galenos.com.tr/Uploads/Article_50671/TYBD-0-0.pdf

Towards the emergence of a new form of the neurodegenerative Creutzfeldt-Jakob disease: Twenty six cases of CJD declared a few days after a COVID-19 “vaccine” Jab

• May 2022

DOI:10.13140/RG.2.2.14427.03366

Abstract

Towards the emergence of a new form of the neurodegenerative Creutzfeldt-Jakob disease: Twenty six cases of CJD declared a few days after a COVID-19 “vaccine” Jab Jean Claude Perez, PhD Maths§Computer Science Bordeaux University ; Retired (IBM European Research center on Artificial Intelligence Montpellier France) ; Bordeaux metropole France; https://orcid.org/0000-0001-6446-2042 France jeanclaudeperez2@gmail.com Claire Moret-Chalmin, MD. Neurologist, 13 rue Roger Martin du Gard 60600 Clermont France clmoret@gmail.com Luc Montagnier RIP MD. Virologist, Fondation Luc Montagnier Quai Gustave-Ador 62 1207 Genève, Switzerland KEYWORDS Creutzfeldt-Jakob desease (CJD), Prion protein, SARS-CoV2 Variants, Spike, COVID-19 mRNA Vaccines, survival, Neuropsychiatric disease, Evolution. ABSTRACT We highlight the presence of a Prion region in the different Spike proteins of the original SARS-CoV2 virus as well as of all its successive variants but also of all the “vaccines” built on this same sequence of the Spike SARS-CoV2 from Wuhan. Paradoxically, with a density of mutations 8 times greater than that of the rest of the spike, the possible harmfulness of this Prion region disappears completely in the Omicron variant. We analyze and explain the causes of this disappearance of the Prion region of the Spike of Omicron. At the same time, we are analyzing the concomitance of cases, which occurred in various European countries, between the first doses of Pfizer or Moderna mRNA vaccine and the sudden and rapid onset of the first symptoms of Creutzfeldt-Jakob disease, which usually requires several years before observing its first symptoms. We are studying 26 Creutzfeld Jakob Diseases, in 2021, from an anamnestic point of view, centered on the chronological aspect of the

 

evolution of this new prion disease, without being able to have an explanation of the etiopathogenic aspect of this new entity. We subsequently recall the usual history of this dreadfull subacute disease, and compare it with this new, extremely acute, prion disease, following closely vaccinations. In a few weeks, more 50 cases of almost spontaneous emergence of Creutzfeldt-Jakob disease have appeared in France and Europe very soon after the injection of the first or second dose of Pfizer, Moderna or AstraZeneka vaccines. To summarize, of the 26 cases analyzed, the first symptoms of CJD appeared on average 11.38 days after the injection of the COVID-19 "vaccine". Of these 26 cases, 20 had died at the time of writing this article while 6 were still alive. The 20 deaths occurred only 4.76 months after the injection. Among them, 8 of them lead to a sudden death (2.5 months). All this confirms the radically different nature of this new form of CJD, whereas the classic form requires several decades.

https://www.researchgate.net/publication/358661859_Towards_the_emergence_of_a_new_form_of_the_neurodegenerative_Creutzfeldt-Jakob_disease_Twenty_six_cases_of_CJD_declared_a_few_days_after_a_COVID-19_vaccine_Jab

2022年1月15日土曜日

ペンギンみたいなべーやんの好物の佐隈さんのカレーと佐天さんの鯖カレーと人間を牛にするモッさんと大麻が好きな・・・

https://tokumei10.blogspot.com/2022/01/blog-post_62.html

 

DeNA斎藤隆チーフ投手コーチが「小脳の脳梗塞」 - 匿名党

http://tokumei10.blogspot.com › 2022/03 › dena

DeNA斎藤隆チーフ投手コーチ、入院は「小脳の脳梗塞」だった 現場復帰し明かす「今は落ち着いている」 ... やっぱ「脳」に、、、（爆wwwwwwwwwwww.

新型コロナクチンは全てのタイプ全部アウトあるね。牛肉みたいに輸入・生産禁止にせんとあかん。（爆ｗｗｗｗｗｗｗｗｗｗｗ