One Wiki Lab

Júne's One Wiki LAB [OWL] is a collective platform to organize and manage personal & private information of Júne's. This iki is also for providing practical manuals of operating working machines and solving technical problems.

currently accessing from with FreshpingBot/1.0 (+

Júne's Wiki COVID-19 Medical info

Getting starting

  • AI, machine learning and the reasoning machine with Dr. Geoff Gordon — LINK

codex de novo prioritas Updated on 2024/04/17 18:50

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refero de for de novo Updated on 2024/04/17 18:50

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refero de free domainsOut of service — Updated on 2021/01/22 02:16

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sui hosting in manibus Updated on 2024/04/17 19:13

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public keys for authorized_keys Updated on 2024/04/17 19:24

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message of the day (motd) Updated on 2020/08/06 01:16

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scripts for machines — Updated on 2018/09/02 09:07

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configuration for machines — Updated on 2018/09/07 18:10

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Nginx confinguration Updated on 2020/08/06 01:11

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Router settings for iPTiME routers — Updated on 2019/03/31 19:23

COVID-19 Dashboard by Broad Institute — by Broad Institute of MIT and Harvard

interactive maps of COVID-19 — by Johns Hopkins

Statistical Status of COVID-19 — by oogle

Statistical Status of COVID-19 in South Korea — by ikipedia

COVID-19 MATLAB R&D — by Mathworks, Inc

Statistics and Research — by Our World in Data

NCBI SARS-CoV-2 Resources

Coronavirus (COVID-19) NEJM

Novel Coronavirus Information Center — Elsevier’s free health and medical research on the novel coronavirus (SARS-CoV-2) and COVID-19

Searched results — from ScienceDirect

DOI: 10.1056/NEJMsr2005760 — Renin–Angiotensin–Aldosterone System Inhibitors in Patients with Covid-19

DOI: 10.1056/NEJMc2005073 — SARS-CoV-2 Infection in Children

DOI: 10.1016/S1473-3099(20)30651-4 — COVID-19 and multisystem inflammatory syndrome in children and adolescents –

LAB TEST ONLINE — The American Association for Clinical Chemistry (AACC) | 한국어판 — 대한진단검사의학회


  • Anti-Müllerian HormoneAMH AMH Hormone Test Müllerian-inhibiting Hormone MIH Müllerian Inhibiting Factor MIF Müllerian-Inhibiting Substance MIS – In women, to assess ovarian function and menopausal status; in the evaluation of polycystic ovary syndrome (PCOS) or to evaluate the effectiveness of ovarian cancer treatment; in an infant, to evaluate the presence of external sex organs that are not clearly male or female (ambiguous genitalia) and/or function of the testicles in an infant boy
  • C-Reactive Protein (CRP)CRP – To identify the presence of inflammation and to monitor response to treatment for an inflammatory disorder

MSD Manual Consumer Version — by MSD | 한국어판

MSD Manual Profession Version — by MSD


  • Capgras SyndromeCapgras syndrome is a psychological condition. It’s also known as “imposter syndrome” or “Capgras delusion.” — Updated on 2019/06/10 14:07


International Classification of Diseases by WHO, What is it? — ICD




Genetic Disorder

Genetic Home Reference — U.S. National Library of Medicine

  • Noonan syndromeNoonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.
  • Williams syndromeWilliams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems.
  • Duchenne and Becker muscular dystrophyMuscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). The Duchenne and Becker types of muscular dystrophy are two related conditions that primarily affect skeletal muscles, which are used for movement, and heart (cardiac) muscle. These forms of muscular dystrophy occur almost exclusively in males.
  • Down syndromeDown syndrome is a chromosomal condition that is associated with intellectual disability, a characteristic facial appearance, and weak muscle tone (hypotonia) in infancy. All affected individuals experience cognitive delays, but the intellectual disability is usually mild to moderate. Trisomy 21
  • Trisomy 13Trisomy 13, also called Patau syndrome, is a chromosomal condition associated with severe intellectual disability and physical abnormalities in many parts of the body.
  • Trisomy 18Trisomy 18, also called Edwards syndrome, is a chromosomal condition associated with abnormalities in many parts of the body. Individuals with trisomy 18 often have slow growth before birth (intrauterine growth retardation) and a low birth weight.
  • Crouzon syndromeCrouzon syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face.
  • Wolff-Parkinson-White syndrome (WPW)Wolff-Parkinson-White (WPW) syndrome is a condition in which there is an extra electrical pathway in the heart that leads to periods of rapid heart rate (tachycardia).

Miltefosine — amebic meningoencephalitis

Oseltamivir — antiviral medication used to treat and prevent influenza A and B

List of Sulfonamides

  • Bacterial infections: eg, sulfamethoxazole/trimethoprim, sulfisoxazole
  • Crohn’s disease: eg, sulfasalazine
  • Diabetes: eg, glyburide, tolbutamide
  • Fluid retention: eg, chlorothiazide, furosemide, hydrochlorothiazide
  • Gout: eg, probenecid
  • High blood pressure: eg, chlorothiazide, hydrochlorothiazide
  • Pain and inflammation: eg, celecoxib
  • Rheumatoid arthritis: eg, sulfasalazine
  • Ulcerative colitis: eg, sulfasalazine.

Amiodarone Oral — antiarrhythmia


Ipratropium Bromide Solution

Azathioprine — immunosuppressants , COMMON BRAND(S): Imuran


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  • Last modified: 2024/04/17 19:24
  • by Júne Park